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Search Results (617)

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Keywords = marine invertebrates

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35 pages, 1644 KiB  
Review
Marine-Derived Polysaccharides and Their Potential Health Benefits in Nutraceutical Applications
by Joana Carrasqueira, Susana Bernardino, Raul Bernardino and Clélia Afonso
Mar. Drugs 2025, 23(2), 60; https://doi.org/10.3390/md23020060 - 28 Jan 2025
Abstract
Marine-derived polysaccharides have sparked immense interest in the nutraceutical industry as they possess a wide range of bioactivities which are highlighted in this review. These include antioxidants, anti-inflammatory, anti-cancer, gut microbiota regulator, anti-diabetic, and anti-obesity. Algae, marine invertebrates, vertebrates, and microorganisms are the [...] Read more.
Marine-derived polysaccharides have sparked immense interest in the nutraceutical industry as they possess a wide range of bioactivities which are highlighted in this review. These include antioxidants, anti-inflammatory, anti-cancer, gut microbiota regulator, anti-diabetic, and anti-obesity. Algae, marine invertebrates, vertebrates, and microorganisms are the main sources of marine polysaccharides, such as alginate, fucoidan, laminarin, carrageenan, chitosan, glycosaminoglycans, and exopolysaccharides. The structure and functional groups of these compounds influence their bioactive properties. Moreover, the functional properties of polysaccharides, such as gelling, thickening, and stabilising capabilities, are also crucial in product development, where they can serve as gluten substitutes in bakery goods and stabilisers in icings, sauces, and yoghurts. The potential of commercial products under development, such as marine polysaccharide supplements, is discussed, along with already commercialised products in the nutraceutical market. This review emphasises the enormous potential of marine-derived polysaccharides as bioactive compounds with health benefits and commercial value. Full article
(This article belongs to the Special Issue Polysaccharides from Marine Environment)
15 pages, 1727 KiB  
Article
Characterizing the Ultraviolet (UV) Screening Ability of L-5-Sulfanylhistidine Derivatives on Human Dermal Fibroblasts
by Alessia Luccarini, Fabio Marcheggiani, Roberta Galeazzi, Annalisa Zuccarotto, Immacolata Castellano and Elisabetta Damiani
Mar. Drugs 2025, 23(2), 57; https://doi.org/10.3390/md23020057 - 24 Jan 2025
Viewed by 308
Abstract
Using sunscreens is one of the most widespread measures to protect human skin from sun ultraviolet radiation (UVR) damage. However, several studies have highlighted the toxicity of certain inorganic and organic UV filters used in sunscreens for the marine environment and human health. [...] Read more.
Using sunscreens is one of the most widespread measures to protect human skin from sun ultraviolet radiation (UVR) damage. However, several studies have highlighted the toxicity of certain inorganic and organic UV filters used in sunscreens for the marine environment and human health. An alternative strategy may involve the use of natural products of marine origin to counteract UVR-mediated damage. Ovothiols are sulfur-containing amino acids produced by marine invertebrates, microalgae, and bacteria, endowed with unique antioxidant and UV-absorption properties. This study aimed to evaluate the protective effect of synthetic L-5-sulfanyl histidine derivatives, inspired by natural ovothiols, on human dermal fibroblasts (HDFs) upon UVA exposure. By using a custom-made experimental set-up to assess the UV screening ability, we measured the levels of cytosolic and mitochondrial reactive oxygen species (ROS), as well as cell viability and apoptosis in HDFs, in the presence of tested compounds, after UVA exposure, using flow cytometry assays with specific fluorescent probes. The results show that L-5-sulfanyl histidine derivatives display a UV screening capacity and prevent loss in cell viability, the production of cytosolic and mitochondrial ROS induced by UVA exposure in HDFs, and subsequent apoptosis. Overall, this study sheds light on the potential applications of marine-inspired sulfur-containing amino acids in developing alternative eco-safe sunscreens for UVR skin protection. Full article
(This article belongs to the Special Issue Marine Bioactive Compounds for Skin Health)
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Figure 1

Figure 1
<p>Absorbance spectra of phosphate-buffer solutions (0.5 mM) of the disulfide forms of (<b>a</b>) 5-thio, (<b>b</b>) me-5-thio, (<b>c</b>) iso-ovoA, and (<b>d</b>) 0.1 mM ovothiol A, (before (black line) and after (red line) exposure to UVA for 20 min (=~540 kJ/m<sup>2</sup>). The chemical structures of the disulfide forms are shown in each panel.</p>
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<p>(<b>a</b>) Representative scheme of the experimental set-up for UVA exposure using marine ovothiol analogs as shielding agents. (<b>b</b>) Time course of cell viability of HDFs exposed to UVA, assessed using the Presto Blue Assay. The effect of increasing concentrations (0.25–1 mM) of, (<b>c</b>) 5-thio (blue bars), (<b>d</b>) 5-me-thio (purple bars), and (<b>e</b>) iso-ovoA (green bars) used as shielding agents on cell viability determined after exposure to UVA for 15 min. Statistical significance was calculated with an ordinary one-way ANOVA using Tukey’s multiple comparison test. * <span class="html-italic">p</span> &lt; 0.05, *** <span class="html-italic">p</span> &lt; 0.0001 vs. CTR; ### <span class="html-italic">p</span> &lt; 0.0001 vs. 0, i.e., in the absence of compounds exposed to UVA. CTR = non-irradiated cells used as the negative control.</p>
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<p>(<b>a</b>) Time course of cell viability in HDFs, measured by flow cytometry using the ViaCount probe, after exposure to UVA for 10, 15, and 20 min. (<b>b</b>) Effects on HDFs cell viability in the presence of 0.5 mM 5-thio, 5-me-thio, and iso-ovoA used as shielding agents and measured after UVA exposure for 10 min. (<b>c</b>) Effects of the presence of the tested compounds at 1 mM on HDFs viability. Statistical significance was calculated with Kruskal–Wallis test using Dunn’s multiple comparison test. * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.0001 vs. CTR. CTR = non-irradiated cells used as negative control.</p>
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<p>(<b>a</b>) Time course of the production of cytosolic high ROS in HDFs measured after UVA exposure for 10, 15, and 20 min using a flow cytometric assay with the ROS-sensitive probe CM-H<sub>2</sub>DCFDA. (<b>b</b>) Percentage of cells with cytosolic high ROS measured after UVA exposure for 10 min in the presence of 0.5 mM and 1 mM 5-thio, me-5-thio, iso-ovoA used as shielding agents. (<b>c</b>) Percentage of cells with mitochondrial high ROS assessed in the same conditions using the probe MitoSOX Red. The statistical significance was calculated with an ordinary one-way ANOVA using Tukey’s multiple comparison test. ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.0001 vs. CTR; # <span class="html-italic">p</span> &lt; 0.05, ## <span class="html-italic">p</span> &lt; 0.01 vs. 0, i.e., in the absence of compounds exposed to UVA. CTR = non-irradiated cells used as negative control.</p>
Full article ">
13 pages, 3688 KiB  
Article
Occurrence of Intersex in the Marine Mussel Perumytilus purpuratus (Mollusca: Bivalvia): Does Gonadal Parasitism Play a Role?
by Pablo A. Oyarzún, Sebastián Diaz, Sara M. Rodríguez, Gonzalo Ruiz-Tagle, José J. Nuñez and Jorge E. Toro
Biology 2025, 14(1), 70; https://doi.org/10.3390/biology14010070 - 14 Jan 2025
Viewed by 547
Abstract
Intersexuality is a reproductive phenomenon that occurs in some gonochoric species and refers to the simultaneous presence of both male and female gametes within the same individual. Although this phenomenon has been reported in various invertebrate species, many aspects remain poorly understood, especially [...] Read more.
Intersexuality is a reproductive phenomenon that occurs in some gonochoric species and refers to the simultaneous presence of both male and female gametes within the same individual. Although this phenomenon has been reported in various invertebrate species, many aspects remain poorly understood, especially in marine mussels. However, it has been suggested that the prevalence of parasites within populations could induce the occurrence of intersex animals. We studied intersexuality in the marine mollusk Perumytilus purpuratus, a key species of the rocky intertidal zone on the southeastern coast of the Pacific Ocean. A total of 6472 mussels from eight locations in northern and southern Chile were analyzed. We estimated the size of the specimens, the sex ratio of the population, and the prevalence of parasites. Additionally, we examined the germ cells of intersex mussels. The results showed that the male-to-female sex ratio (1:1) was maintained in the populations. Intersex mussels were found in six of the eight locations, representing 0.19% of the mussels analyzed. However, no parasites were found in the intersex animals. Additionally, the abundance of intersex individuals was not correlated with parasitism levels in the population. In intersex mussels, the gonadal tissue was compartmentalized, with male and female germ cells remaining separate. It is concluded that intersexuality in Perumytilus purpuratus is a low-frequency reproductive phenomenon, likely resulting from an alteration in the sex determination mechanism. Intersexuality offers a valuable opportunity to explore the biological aspects of sex determination in mussels. Therefore, further research in this area should be pursued. Full article
(This article belongs to the Section Marine Biology)
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Figure 1

Figure 1
<p>Map of the study region along the Chilean coast, showing <span class="html-italic">Perumytilus purpuratus</span> sampling sites in rocky intertidal zones.</p>
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<p>Photograph of a <span class="html-italic">Perumytilus purpuratus</span> bed in the intertidal zone, Chile (<b>A</b>), and examples of the location of reproductive tissue in intersex mussels (<b>B</b>). The female gonad is indicated by brown tissue (FGT: female gonadal tissue), while the male gonad is indicated by yellow tissue (MGT: male gonadal tissue). The bar corresponds to 1 cm.</p>
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<p>Proportion of intersex individuals and prevalence of parasites in <span class="html-italic">Perumytilus purpuratus</span> beds in the lower, middle, and high intertidal zones of the analyzed localities in Chile.</p>
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<p>Percentage of reproductive tissue (GVF) in the gonads of gonochoric (male and female) and intersex individuals of the bivalve <span class="html-italic">Perumytilus purpuratus</span> from Reñaca and Pichilemu, Chile. The asterisk represents the tissue of intersex mussels.</p>
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<p>Percentage of oocyte stages (previtellogenic, vitellogenic, mature, atresic) within the gonadal tissue of gonochoric and intersex females of <span class="html-italic">Perumytilus purpuratus</span> from Reñaca and Pichilemu, Chile.</p>
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42 pages, 2146 KiB  
Review
Aquatic Invertebrate Antimicrobial Peptides in the Fight Against Aquaculture Pathogens
by Tomás Rodrigues, Francisco Antonio Guardiola, Daniela Almeida and Agostinho Antunes
Microorganisms 2025, 13(1), 156; https://doi.org/10.3390/microorganisms13010156 - 14 Jan 2025
Viewed by 852
Abstract
The intensification of aquaculture has escalated disease outbreaks and overuse of antibiotics, driving the global antimicrobial resistance (AMR) crisis. Antimicrobial peptides (AMPs) provide a promising alternative due to their rapid, broad-spectrum activity, low AMR risk, and additional bioactivities, including immunomodulatory, anticancer, and antifouling [...] Read more.
The intensification of aquaculture has escalated disease outbreaks and overuse of antibiotics, driving the global antimicrobial resistance (AMR) crisis. Antimicrobial peptides (AMPs) provide a promising alternative due to their rapid, broad-spectrum activity, low AMR risk, and additional bioactivities, including immunomodulatory, anticancer, and antifouling properties. AMPs derived from aquatic invertebrates, particularly marine-derived, are well-suited for aquaculture, offering enhanced stability in high-salinity environments. This study compiles and analyzes data from AMP databases and over 200 scientific sources, identifying approximately 350 AMPs derived from aquatic invertebrates, mostly cationic and α-helical, across 65 protein families. While in vitro assays highlight their potential, limited in vivo studies hinder practical application. These AMPs could serve as feed additives, therapeutic agents, or in genetic engineering approaches like CRISPR/Cas9-mediated transgenesis to enhance resilience of farmed species. Despite challenges such as stability, ecological impacts, and regulatory hurdles, advancements in peptidomimetics and genetic engineering hold significant promise. Future research should emphasize refining AMP enhancement techniques, expanding their diversity and bioactivity profiles, and prioritizing comprehensive in vivo evaluations. Harnessing the potential of AMPs represents a significant step forward on the path to aquaculture sustainability, reducing antibiotic dependency, and combating AMR, ultimately safeguarding public health and ecosystem resilience. Full article
(This article belongs to the Special Issue Host–Bacteria Interactions in Aquaculture Systems, 2nd Edition)
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Figure 1
<p>Distribution of antimicrobial activities of aquatic invertebrate AMPs against various pathogens. The chart categorizes microorganisms into Gram-positive bacteria, Gram-negative bacteria, fungi, viruses, and parasites, showing their pathogenic (red) and non-pathogenic (blue) statuses. Each taxonomic group (<span class="html-italic">Ann</span>: <span class="html-italic">Annelida</span>, <span class="html-italic">Art</span>: <span class="html-italic">Arthropoda</span>, <span class="html-italic">Cho</span>: <span class="html-italic">Chordata</span>, <span class="html-italic">Cni</span>: <span class="html-italic">Cnidaria</span>, <span class="html-italic">Ech</span>: <span class="html-italic">Echinodermata</span>, <span class="html-italic">Mol</span>: <span class="html-italic">Mollusca</span>, <span class="html-italic">Others</span>: <span class="html-italic">Nematoda</span>, <span class="html-italic">Placozoa</span>, <span class="html-italic">Platyhelminthes</span>, <span class="html-italic">Porifera</span>) highlights the diversity and potential antimicrobial targets of AMPs, emphasizing their relevance to aquaculture pathogens.</p>
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<p>Phylogenetic distribution of currently known AMPs from aquatic invertebrates by phylum and subphylum/class.</p>
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<p>Examples of AMPs from aquatic invertebrate phyla.</p>
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<p>Key categories of “non-classical” AMPs.</p>
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30 pages, 6831 KiB  
Review
Recent Advances in Natural Products Derived from Marine Echinoderms and Endophytic Microbes: Chemical Insights and Therapeutic Potential
by Shuangyu Li, Yan Xiao, Qiang Li, Mingzhi Su, Yuewei Guo and Xin Jin
Mar. Drugs 2025, 23(1), 33; https://doi.org/10.3390/md23010033 - 10 Jan 2025
Viewed by 790
Abstract
Echinoderms, a diverse group of marine invertebrates including starfish, sea urchins, and sea cucumbers, have been recognized as prolific sources of structurally diverse natural products. In the past five years, remarkable progress has been made in the isolation, structural elucidation, and pharmacological assessment [...] Read more.
Echinoderms, a diverse group of marine invertebrates including starfish, sea urchins, and sea cucumbers, have been recognized as prolific sources of structurally diverse natural products. In the past five years, remarkable progress has been made in the isolation, structural elucidation, and pharmacological assessment of these bioactive compounds. These metabolites, including polysaccharides, triterpenoids, steroids, and peptides, demonstrate potent bioactivities such as anticancer, anti-inflammatory, antiviral, and antimicrobial effects, providing valuable insights and scaffolds for drug discovery. This review highlights the structural diversity and biological activities of natural products derived from echinoderms over the last five years, with a particular focus on their structure–activity relationships and therapeutic potential. It also outlines the prospects and challenges for future research, aiming to stimulate further exploration in marine drug discovery. Full article
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Figure 1
<p>The structure of gymnochrome G (<b>1</b>) and strychnine (<b>2</b>).</p>
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<p>The structure of compound <b>3</b>.</p>
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<p>The structure of 6-BHP.</p>
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<p>The structure of penicilloneines A (<b>5</b>) and B (<b>6</b>).</p>
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<p>The structure of catalindoles A–C (<b>7</b>–<b>9</b>).</p>
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<p>The structure of coloquadranoside A (<b>10</b>).</p>
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<p>The structure of quadrangularisoside A (<b>11</b>), quadrangularisoside A<sub>1</sub> (<b>12</b>), quadrangularisoside B (<b>13</b>), quadrangularisoside B1 (<b>14</b>), quadrangularisoside B2 (<b>15</b>), quadrangularisoside C (<b>16</b>), quadrangularisoside C1 (<b>17</b>), quadrangularisoside D (<b>18</b>), quadrangularisoside D1 (<b>19</b>), quadrangularisoside D2 (<b>20</b>), quadrangularisoside D3 (<b>21</b>), quadrangularisoside D4 (<b>22</b>), and quadrangularisoside E (<b>23</b>).</p>
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<p>The structure of chitonoidosides A (<b>24</b>), A<sub>1</sub> (<b>25</b>), B (<b>26</b>), C (<b>27</b>), D (<b>28</b>), E (<b>29</b>), E<sub>1</sub> (<b>30</b>), F (<b>31</b>), G (<b>32</b>), H (<b>33</b>), I (<b>34</b>), J (<b>35</b>), K (<b>36</b>), K<sub>1</sub> (<b>37</b>), and L (<b>38</b>).</p>
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<p>The structure of chilensosides A (<b>39</b>), A<sub>1</sub> (<b>40</b>), B (<b>41</b>), C (<b>42</b>), D (<b>43</b>), E (<b>44</b>), F (<b>45</b>), and G (<b>46</b>).</p>
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<p>The structure of triterpene glycosides: djakonoviosides A (<b>47</b>), A<sub>1</sub> (<b>48</b>), A<sub>2</sub> (<b>49</b>), B<sub>1</sub> (<b>50</b>), B<sub>2</sub> (<b>51</b>), B<sub>3</sub> (<b>52</b>), B<sub>4</sub> (<b>53</b>), C<sub>1</sub> (<b>54</b>), D<sub>1</sub> (<b>55</b>), E<sub>1</sub> (<b>56</b>), and F<sub>1</sub> (<b>57</b>).</p>
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<p>The structure of peronioside A (<b>58</b>).</p>
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<p>The structure of triterpene glycoside echinoside B 12-O-methyl ether (<b>59</b>).</p>
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<p>The structure of triterpene glycosides: desholothurin B (<b>60</b>) and 12-epi-desholothurin B (<b>61</b>).</p>
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<p>The structure of kurilosides A<sub>1</sub> (<b>62</b>), A<sub>2</sub> (<b>63</b>), A<sub>3</sub> (<b>64</b>), C<sub>1</sub> (<b>65</b>), D (<b>66</b>), D<sub>1</sub> (<b>67</b>), E (<b>68</b>), F (<b>69</b>), G (<b>70</b>), H (<b>71</b>), I (<b>72</b>), I<sub>1</sub> (<b>73</b>), J (<b>74</b>), K (<b>75</b>), and K<sub>1</sub> (<b>76</b>).</p>
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<p>The structure of pacificusosides A–Q: A (<b>77</b>), B (<b>78</b>), C (<b>79</b>), D (<b>80</b>), E (<b>81</b>), F (<b>82</b>), G (<b>83</b>), H (<b>84</b>), I (<b>85</b>), J (<b>86</b>), K (<b>87</b>), L (<b>88</b>), M (<b>89</b>), N (<b>90</b>), O (<b>91</b>), P (<b>92</b>), and Q (<b>93</b>).</p>
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<p>The structure of bivittoside E (<b>94</b>).</p>
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<p>The structure of apostichoposide A (<b>95</b>) and apostichoposide B (<b>96</b>).</p>
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<p>The structures of compounds <b>97</b> and <b>98</b>.</p>
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<p>The structure of microdiscusoside A (<b>99</b>) and microdiscusol G (<b>100</b>).</p>
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<p>The structures of compounds <b>101</b>–<b>104</b>.</p>
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<p>The structure of spiculiferosides A-D (<b>105</b>–<b>108</b>).</p>
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<p>The structure of compounds <b>109</b>–<b>112</b>.</p>
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<p>The structure of compounds <b>113</b>–<b>116</b>.</p>
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<p>The structure of compounds <b>117</b>–<b>120</b>.</p>
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<p>The structure of comatulins A−E (<b>121</b>–<b>125</b>).</p>
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<p>The structure of delicapyrons A-E (<b>126</b>–<b>130</b>).</p>
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<p>The structure of salmachroman (<b>131</b>).</p>
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<p>The structure of compound <b>132</b>.</p>
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<p>The structure of sajaroketides A (<b>133</b>) and B (<b>134</b>).</p>
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<p>The structure of compounds <b>135</b>–<b>139</b>.</p>
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<p>The structure of compounds <b>140</b>–<b>142</b>.</p>
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<p>The structure of spiniferosides A-C (<b>143</b>–<b>145</b>).</p>
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<p>The structure of salmacembrane A (<b>146</b>) and B (<b>147</b>).</p>
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<p>The structure of aspergillolide (<b>148</b>).</p>
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<p>The structure of holospiniferoside (<b>149</b>).</p>
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<p>The structure of O-7 (<b>150</b>) and O-8 (<b>151</b>).</p>
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<p>The structure of compounds <b>152</b>–<b>157</b>.</p>
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<p>The structure of herrmananes A and B (<b>158</b> and <b>159</b>).</p>
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<p>The structure of compound <b>160</b>.</p>
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7 pages, 1225 KiB  
Communication
The Interspecific Abundance–Occupancy Relationship in Invertebrate Metacommunities Associated with Intertidal Mussel Patches
by Ricardo A. Scrosati
Ecologies 2025, 6(1), 4; https://doi.org/10.3390/ecologies6010004 - 3 Jan 2025
Viewed by 626
Abstract
To explain the distribution and abundance of species, ecology searches for general models. A pattern often encountered in nature is the interspecific abundance–occupancy relationship (AOR), which describes how the mean local abundance of species relates to the proportion of local sites that each [...] Read more.
To explain the distribution and abundance of species, ecology searches for general models. A pattern often encountered in nature is the interspecific abundance–occupancy relationship (AOR), which describes how the mean local abundance of species relates to the proportion of local sites that each species occupies. Both are central variables in ecology and are often positively correlated, although exceptions have been found. As most AOR research has been conducted with terrestrial systems, recent studies are testing for its occurrence in marine systems. This contribution tests the AOR for invertebrate metacommunities associated with intertidal mussel patches. Using data from six coastal locations in Nova Scotia (Canada), this study shows that the negative binomial model properly describes the relationship between abundance and occupancy for these systems. The degree of wave exposure (wave-sheltered versus wave-exposed habitats) had some influence on the shape of the AOR. Overall, these findings extend the applicability of the AOR to intertidal invertebrate metacommunities. The raw data are included as part of this article to help future syntheses on the AOR, which will need data for a variety of terrestrial and aquatic environments. Full article
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Figure 1
<p>Map of Nova Scotia indicating the six surveyed intertidal locations.</p>
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<p>Abundance–occupancy relationship (with a 95% confidence band) for each of the six surveyed locations (invertebrate metacommunities). Each dot represents a single invertebrate species. For each species, abundance (<span class="html-italic">µ</span>) represents the mean number of individuals per mussel patch (per dm<sup>2</sup>) averaged over the 15 patches surveyed at each location, while occupancy (<span class="html-italic">P</span>) represents the proportion of the 15 surveyed mussel patches where the invertebrate species in question was present.</p>
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12 pages, 3607 KiB  
Perspective
Regeneration, Regengrow and Tissue Repair in Animals: Evolution Indicates That No Regeneration Occurs in Terrestrial Environments but Only Recovery Healing
by Lorenzo Alibardi
J. Dev. Biol. 2025, 13(1), 2; https://doi.org/10.3390/jdb13010002 - 30 Dec 2024
Viewed by 526
Abstract
The present, brief review paper summarizes previous studies on a new interpretation of the presence and absence of regeneration in invertebrates and vertebrates. Broad regeneration is considered exclusive of aquatic or amphibious animals with larval stages and metamorphosis, where also a patterning process [...] Read more.
The present, brief review paper summarizes previous studies on a new interpretation of the presence and absence of regeneration in invertebrates and vertebrates. Broad regeneration is considered exclusive of aquatic or amphibious animals with larval stages and metamorphosis, where also a patterning process is activated for whole-body regeneration or for epimorphosis. In contrast, terrestrial invertebrates and vertebrates can only repair injury or the loss of body parts through a variable “recovery healing” of tissues, regengrow or scarring. This loss of regeneration likely derives from the change in genomes during land adaptation, which included the elimination of larval stages and intense metamorphosis. The terrestrial conditions are incompatible with the formation of embryonic organs that are necessary for broad regeneration. In fact, no embryonic organ can survive desiccation, intense UV or ROS exposition on land, and rapid reparative processes without embryonic patterning, such as recovery healing and scarring, have replaced broad regeneration in terrestrial species. The loss of regeneration in land animals likely depends on the alteration of developmental gene pathways sustaining regeneration that occurred in progenitor marine animals. Terrestrial larval stages, like those present in insects among arthropods, only metamorphose using small body regions indicated as imaginal disks, a terrestrial adaptation, not from a large restructuring process like in aquatic-related animals. These invertebrates can reform body appendages only during molting, a process indicated as regengrow, not regeneration. Most amniotes only repair injuries through scarring or a variable recovery healing, occasionally through regengrow, the contemporaneous healing in conjunction with somatic growth, forming sometimes new heteromorphic organs. Full article
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Figure 1
<p>Summarizing image reporting the distribution of regenerative abilities among extant aquatic (light-blue background) and terrestrial (pale-brown background) animals. The colored bars associated with the different animal phyla represent the progressive phases of their main life cycles (embryo phase in pale blue, larval phase in green, metamorphic phase in vermillion, juvenile and growing phase in brown, adult phase in deep blue, and aging phase in grey). Phyla including metamorphosis (vermillion color segment inside their life cycle bars) also show large regenerative ability and are generally marine. Among arthropods, one or more metamorphic transitions occur in insects, but these are mainly body growths through molting in heterometabolous insects and large changes derived from localized imaginal disks in holometabolous insects (see text for further explanation). In minor phyla (Tardigrada, Onychophora, Priapulida but also Phoronida, Ectoprocta and Rotifera), no or insufficient information on regeneration is available.</p>
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<p>Schematic drawing showing the indicative evolution of the main phyla of animals, from a primitive planula and/or aceloid progenitor in the marine environment (light-blue background) to a marine or a terrestrial environment (light-brown background). Dots along the evolutionary lines indicate elapsed time (millions of years) to evolve new animals. Each representative animal form is associated with an idealized simple genome network of different extension, according to the animal complexity (small in simple invertebrates and larger in more complex marine or terrestrial invertebrates and vertebrates). The final genome network of extant animals is invariant and includes developmental genes (or groups of genes), some of which can be re-activated in adult animals after injury, promoting regeneration. All terrestrial animals (light-brown background) lost a larval phase or evolved a terrestrial adapted larva (insects) and also lost metamorphosis and broad regenerative ability. Terrestrial restrictions imposed the evolution of a rapid healing process, generally through scarring.</p>
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<p>Schematic drawing for vertebrate evolution in relation to regeneration. From a basic embryonic form at the base of the tree, different embryos were derived and gave rise to cyclostomes and different types of fish (light-blue background), then amphibians (green background), and finally terrestrial vertebrates, reptiles, birds and mammals (pale-brown background). Each embryo or adult form is associated with an idealized gene network of different complexity. Dots along the evolutionary lines indicate elapsed time (millions of years) to evolve new animals. Numerous fish and amphibians possess one or more larval phases with one or more metamorphic transitions and, after an injury as adults, can often broadly regenerate. This is not the case for amniotes (terrestrial vertebrates) that lost a larval form and related metamorphosis during land adaptation and also do not regenerate after injury or have limited healing recovery, regengrow or heteromorphic regeneration in rare cases and generally scar.</p>
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<p>Schematic drawing illustrating few examples of <span class="html-italic">regengrow</span> or of recovery healing after loss (small arrows) of appendages in terrestrial animals (myriapods, insects and arachnids), eyed-peduncles in the head (gastropod mollusks), or posterior sections of the body (earthworms). Within the associated gene networks for each animal, in light-blue colored areas, are indicated the idealized region of the genome utilized for the development of the specific appendages (left) or regions of the body that are later lost (small arrows) and regenerated (large arrows and genomes on the right). Regenerated organs are colored in red. Note that in these simple examples, the light-blue areas of the genome utilized for regeneration (on the right) are smaller than those utilized for the development of the same organs (on the left). This ideally indicates that not all developmental genes can be re-activated for regenerating the lost organs, but they are, however, sufficient to restitute all or most of the lost organ (see text and Alibardi, 2023 a–c, for more explanation).</p>
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<p>Schematic drawing featuring a few examples of different healing abilities among amphibians (light-blue background) and amniotes (light-brown background). The light-blue areas within the gene networks for each embryo or adult animals ideally represent genes utilized for development (on the left) and for recovery healing after injury or loss of the same organs (arrows on the right). The regenerated organs are colored in red. Ample regeneration is present in freshwater anuran tadpoles, but regeneration is lost at metamorphosis, and, rarely, heteromorphic appendages (arms or digits) are regenerated/regengrown. The light-blue area present in the gene network associated to tadpoles ideally indicates genes utilized during development that, in combination with genes utilized for metamorphosis, also determine regeneration. Heteromorphic but large regeneration occurs in lizard tail and, occasionally, in growing crocodilians (<span class="html-italic">regengrow</span>). In mammals, aside from the prevalent scarring outcome and physiological tissue regeneration, three examples of “recovery healing” are shown: cyclical bony regeneration in deer or reindeers after drop of antlers in previous cycles, ear hole recovering in hares, and digit tips <span class="html-italic">regengrow</span> in rodents (see text for further explanation). Within the gene networks associated with each animal, the light-blue areas ideally indicate those sections of the genome utilized for developing the specific organ or appendage (on the left) and those re-activated for healing or regenerate the same organ (arrows on the right). Note the smaller light-blue areas utilized for healing or regeneration in each idealized gene network, in comparison to those utilized for development (on the left), an indication of limited re-activation of the same or closely related genes.</p>
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11 pages, 606 KiB  
Article
A Novel Sesterterpenoid, Petrosaspongin and γ-Lactone Sesterterpenoids with Leishmanicidal Activity from Okinawan Marine Invertebrates
by Takahiro Jomori, Nanami Higa, Shogo Hokama, Trianda Ayuning Tyas, Natsuki Matsuura, Yudai Ueda, Ryo Kimura, Sei Arizono, Nicole Joy de Voogd, Yasuhiro Hayashi, Mina Yasumoto-Hirose, Junichi Tanaka and Kanami Mori-Yasumoto
Mar. Drugs 2025, 23(1), 16; https://doi.org/10.3390/md23010016 - 30 Dec 2024
Viewed by 830
Abstract
Leishmaniasis is a major public health problem, especially affecting vulnerable populations in tropical and subtropical regions. The disease is endemic in 90 countries, and with millions of people at risk, it is seen as one of the ten most neglected tropical diseases. Current [...] Read more.
Leishmaniasis is a major public health problem, especially affecting vulnerable populations in tropical and subtropical regions. The disease is endemic in 90 countries, and with millions of people at risk, it is seen as one of the ten most neglected tropical diseases. Current treatments face challenges such as high toxicity, side effects, cost, and growing drug resistance. There is an urgent need for safer, affordable treatments, especially for cutaneous leishmaniasis (CL), the most common form. Marine invertebrates have long been resources for discovering bioactive compounds such as sesterterpenoids. Using bioassay-guided fractionations against cutaneous-type leishmaniasis promastigotes, we identified a novel furanosesterterpenoid, petrosaspongin from Okinawan marine sponges and a nudibranch, along with eight known sesterterpenoids, hippospongins and manoalides. The elucidated structure of petrosaspongin features a β-substituted furane ring, a tetronic acid, and a conjugated triene. The sesterterpenoids with a γ-butenolide group exhibited leishmanicidal activity against Leishmania major promastigotes, with IC50 values ranging from 0.69 to 53 μM. The structure–activity relationship and molecular docking simulation suggest that γ-lactone is a key functional group for leishmanicidal activity. These findings contribute to the ongoing search for more effective treatments against CL. Full article
(This article belongs to the Special Issue Marine-Derived Bioactive Substances and Their Mechanisms of Action)
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<p>The structures of compounds (<b>1</b>–<b>9</b>).</p>
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<p>Key 2D NMR correlations for petrosaspongin (<b>1</b>). (<b>a</b>) <sup>1</sup>H-<sup>1</sup>H COSY and key HMBC correlations. (<b>b</b>) Key NOESY correlations.</p>
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19 pages, 1810 KiB  
Article
Chemical Changes Under Heat Stress and Identification of Dendrillolactone, a New Diterpene Derivative with a Rare Rearranged Spongiane Skeleton from the Antarctic Marine Sponge Dendrilla antarctica
by Andrea Prófumo, Conxita Avila and Adele Cutignano
Mar. Drugs 2025, 23(1), 10; https://doi.org/10.3390/md23010010 - 28 Dec 2024
Viewed by 857
Abstract
The waters around the western Antarctic Peninsula are experiencing fast warming due to global change, being among the most affected regions on the planet. This polar area is home to a large and rich community of benthic marine invertebrates, such as sponges, tunicates, [...] Read more.
The waters around the western Antarctic Peninsula are experiencing fast warming due to global change, being among the most affected regions on the planet. This polar area is home to a large and rich community of benthic marine invertebrates, such as sponges, tunicates, corals, and many other animals. Among the sponges, the bright yellow Dendrilla antarctica is commonly known for using secondary diterpenoids as a defensive mechanism against local potential predators. From the dichloromethane extract of sponge samples from Deception Island collected in January 2023, we isolated a novel derivative with an unusual β-lactone diterpene skeleton here named dendrillolactone (1), along with seven previously described diterpenes, including deceptionin (2), a gracilane norditerpene (3), cadlinolide C (4), a glaciolane norditerpene (5), membranolide (6), aplysulphurin (7), and tetrahydroaplysulphurine-1 (8). Here, we also report our studies on the changes in the chemical arsenal of this sponge by slow temperature increase in aquaria experiments. Despite being a species capable of inhabiting volcanically active areas, with frequent water temperature fluctuations due to the existing fumaroles, the results show that diterpenes such as deceptionin, cadlinolide C, membranolide, and tetrahydroaplysulphurin-1 seem to be susceptible to the temperature increase, resulting in a trend to higher concentrations. However, temperatures above 4 °C severely affected sponge metabolism, causing its death much earlier than expected. Further research on the roles of these natural products in D. antarctica and their relationship to the sponge’s resilience to environmental changes should help to better understand the defensive mechanisms of Antarctic marine benthos in the context of global change. Full article
(This article belongs to the Section Marine Chemoecology for Drug Discovery)
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<p>Representative GC-MS chemical profile of <span class="html-italic">D. antarctica</span> extracts: internal standard (IS). DDL—dendrillolactone (<b>1</b>); DCP—deceptionin (<b>2</b>); GRN—the gracilane norditerpene <b>3</b>; CLC—cadlinolide C (<b>4</b>); GLN—the glaciolane norditerpene <b>5</b>; MBN—membranolide (<b>6</b>); APS—aplysulphurin (<b>7</b>); and TTS—tetrahydroaplysulphurin-1 (<b>8</b>).</p>
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<p>Diterpene metabolites <b>1</b>–<b>8</b> of <span class="html-italic">D. antarctica</span> from Deception Island (Antarctica).</p>
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<p>Quantification of main diterpenes in the control and treatment groups. The values of all the molecules are reported as the mean μg/mg of dry sponge weight (DW) ± SD (n = 5). EC—environmental control; AT—aquarium temperature control; and HS—heat stress treatment. DDL—dendrillolactone (<b>1</b>); DCP—deceptionin (<b>2</b>); GRN—the gracilane norditerpene <b>3</b>; CLC—cadlinolide C (<b>4</b>); GLN—the glaciolane norditerpene <b>5</b>; MBN—membranolide (<b>6</b>); APS—aplysulphurin (<b>7</b>); and TTS—tetrahydroaplysulphurin-1 (<b>8</b>).</p>
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<p>Maps of the sampling area: (<b>A</b>) an overview of the WAP and South Shetland Islands (SSIs), (<b>B</b>) a close-up of the SSIs, and (<b>C</b>) a detailed map of Deception Island and the specific sampling area (Cormoran Town, Whalers Bay).</p>
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11 pages, 2811 KiB  
Article
Isopods in the Bioremediation of Invasive Seaweeds? First Experience with the Seaweed Rugulopteryx okamurae Mass Dumped on Beaches
by Daniel Patón and José Carlos García-Gómez
J. Mar. Sci. Eng. 2025, 13(1), 12; https://doi.org/10.3390/jmse13010012 - 26 Dec 2024
Viewed by 427
Abstract
Since 2015, the invasive seaweed Rugulopteryx okamurae has triggered the most serious marine macrophyte invasion in Europe. Its huge coastal biomass dumped on beaches generates health problems, strong odors, impacts on tourism, and high clean-up costs, but it also constitutes a new potential [...] Read more.
Since 2015, the invasive seaweed Rugulopteryx okamurae has triggered the most serious marine macrophyte invasion in Europe. Its huge coastal biomass dumped on beaches generates health problems, strong odors, impacts on tourism, and high clean-up costs, but it also constitutes a new potential marine resource that offers significant prospects for exploitation. In this sense, as a circular economy strategy, seaweed bioremediation with isopods (Isopoda, Crustacea, Arthropoda) was experimented on for the first time. Specimens of Porcellio laevis (native terrestrial isopod) were obtained from urban parks and kept in terrariums with adequate humidity and temperature control. A sample of 150 adult specimens was divided into six batches of 25 animals. Three batches were fed with 100 g of mulch of Quercus pyrenaica leaves (control) and three with a diet composed of 100 g of mulch of algae (treatment). P. laevis consumed up to 1.5 times their weight per day on the algae diet, with little or no weight loss and adequate reproduction rates. The weight of the isopods averaged 1.6 g in the seaweed group and 2.5 g in the control group. However, high mortality was observed in both mancas and adults in the treatment group. In this sense, the average number of mancas per cm2 was 0 in the algae group and 325 in the control group. Despite this, the results are promising, and consequently, we propose to encourage research with isopods due to their high voracity, high prolificacy, and resistance to invasive algal recycling. Future work should explore what percentage of R. okamurae prevents diterpene mortality of isopods and other invertebrates. This is a preliminary step towards the massive bioremediation of spring and summer blooms of R. okamurae. This work contributes to highlighting this abundant marine resource. Full article
(This article belongs to the Section Marine Pollution)
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<p>Massive <span class="html-italic">Rugulopteryx okamurae</span> biomass dumped on the beaches of the coast of Tarifa (Strait of Gibraltar) in June 2023. In the lower right photo, note the accumulated volume of algae, above the knees, of those collecting samples for this study.</p>
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<p>The counting of <span class="html-italic">Porcellio laevis</span> mancas (right) on the substrate using ImageJ’s particle counting tool.</p>
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<p>The decrease in the biomass in percent after consumption by <span class="html-italic">Porcellio laevis</span> in both types of mulch.</p>
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<p>Decrease in percentage of blatticompost substrate over time for both types of mulch (with and without algae).</p>
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<p>Box plots of feed conversion rate (FCR) for both types of mulch.</p>
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<p>Differences in isopod weight for both types of mulching.</p>
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<p>The survival of <span class="html-italic">Porcellio laevis</span> adults throughout the study period for both types of mulches.</p>
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<p>The effect of the mulch type on mancae production per square centimeter in the isopod <span class="html-italic">Porcellio laevis</span>.</p>
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37 pages, 9405 KiB  
Review
Structure Diversity and Properties of Some Bola-like Natural Products
by Valentin A. Stonik, Tatyana N. Makarieva, Larisa K. Shubina, Alla G. Guzii and Natalia V. Ivanchina
Mar. Drugs 2025, 23(1), 3; https://doi.org/10.3390/md23010003 - 24 Dec 2024
Viewed by 552
Abstract
In their shapes, molecules of some bipolar metabolites resemble the so-called bola, a hunting weapon of the South American inhabitants, consisting of two heavy balls connected to each other by a long flexible cord. Herein, we discuss the structures and properties of these [...] Read more.
In their shapes, molecules of some bipolar metabolites resemble the so-called bola, a hunting weapon of the South American inhabitants, consisting of two heavy balls connected to each other by a long flexible cord. Herein, we discuss the structures and properties of these natural products (bola-like compounds or bolaamphiphiles), containing two polar terminal fragments and a non-polar chain (or chains) between them, from archaea, bacteria, and marine invertebrates. Additional modifications of core compounds of this class, for example, interchain and intrachain cyclization, hydroxylation, methylation, etc., expand the number of known metabolites of this type, providing their great structural variety. Isolation of such complex compounds individually is problematic, since they usually exist as mixtures of regioisomers and stereoisomers, that are very difficult to be separated. The main approaches to the study of their structures combine various methods of HPLC/MS or GC/MS, 2D-NMR experiments and organic synthesis. The recent identification of new enzymes, taking part in their biosynthesis and metabolism, made it possible to understand molecular aspects of their origination and some features of evolution during geological times. The promising properties of these metabolites, such as their ability to self-assemble and stabilize biological or artificial membranes, and biological activities, attract additional attention to them. Full article
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<p>Schematic representation of polar and bipolar natural compounds.</p>
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<p>1,2-Di-<span class="html-italic">O</span>-palmitoyl-<span class="html-italic">sn</span>-glycerol (<b>1</b>) of bacteria and eukarya, diether (<b>2</b>), and tetraether (<b>3</b>, <b>4</b>) lipids of archaea.</p>
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<p>GDGTs <b>5a</b>–<b>12a</b> and glycerol-calditol bipolar lipids <b>5b</b>–<b>12b</b> and calditol (<b>13</b>).</p>
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<p>Crenarchaeol (<b>14</b>) and crenarchaeol isomer (<b>15</b>); both structures are shown for parallel conformations.</p>
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<p>The structure of H-shaped caldarchaeol (<b>16</b>) and its chemical transformations.</p>
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<p>The structures of some other H-shaped bipolar lipids <b>24</b>–<b>27</b>.</p>
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<p>The structures of butanetriol (<b>28</b>), pentanetriol (<b>29</b>), and some hydroxylated (<b>30</b>–<b>33</b>) archaeal core lipids.</p>
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<p>Some intact lipids from <span class="html-italic">Methanobacterium thermoautotrophicum</span> (<b>34</b>), from the <span class="html-italic">Sulfolobus</span> genus (<b>35</b>, <b>36</b>), and from <span class="html-italic">Pyrococcus furiosus</span> (<b>37</b>).</p>
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<p>Some branched FAs (<b>38</b>, <b>39</b>), diabolic acid (<b>40</b>), brGDGTs based on diabolic acid (<b>41a</b>–<b>f</b>), and <span class="html-italic">iso-</span>diabolic acid (<b>42</b>).</p>
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<p>Sponge natural products <b>72</b>–<b>77</b>, related to rhizochalin.</p>
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<p>Structures of oceanapiside (<b>78</b>) and calyxoside (<b>79</b>).</p>
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<p>Structures of leucettamols A (<b>93</b>) and B (<b>94</b>) and some derivatives of <b>93</b>.</p>
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<p>Oceanalins A (<b>97</b>) and B (<b>102</b>) and some derivatives of oceanalin A (<b>98–101</b>).</p>
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<p>Sagittamides A–F (<b>103</b>–<b>108</b>).</p>
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<p>Structures of α,ω-bifunctionalized bola-like metabolites <b>110</b>–<b>120</b> from some sponges.</p>
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<p>A simplified scheme of biosynthesis of brGDGTs in thermophilic bacteria, adopted from [<a href="#B93-marinedrugs-23-00003" class="html-bibr">93</a>].</p>
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<p>Determination of a keto group position in rhizochalin (<b>57</b>).</p>
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<p>A hypothetic pathway of biosynthesis of terminal fragments in rhizochalin and related compounds.</p>
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<p>Synthesis of model compounds for determination of absolute configurations in rhizochalin.</p>
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<p>Chemical transformations of calyxoside B (<b>81</b>) [<a href="#B112-marinedrugs-23-00003" class="html-bibr">112</a>].</p>
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<p>Hypothetical biosynthetic pathway to hexa-<span class="html-italic">O</span>-acetylated fragment (<b>109</b>) in sagittamides (adopted from [<a href="#B124-marinedrugs-23-00003" class="html-bibr">124</a>]).</p>
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25 pages, 10534 KiB  
Review
How Significant Are Marine Invertebrate Collagens? Exploring Trends in Research and Innovation
by Mariana Almeida, Tiago Silva, Runar Gjerp Solstad, Ana I. Lillebø, Ricardo Calado and Helena Vieira
Mar. Drugs 2025, 23(1), 2; https://doi.org/10.3390/md23010002 - 24 Dec 2024
Viewed by 788
Abstract
This review is focused on the research, innovation and technological breakthroughs on marine invertebrate collagens and their applications. The findings reveal that research dates back to the 1970s, and after a period of reduced activity, interest in collagens from several marine invertebrate groups [...] Read more.
This review is focused on the research, innovation and technological breakthroughs on marine invertebrate collagens and their applications. The findings reveal that research dates back to the 1970s, and after a period of reduced activity, interest in collagens from several marine invertebrate groups was renewed around 2008, likely driven by the increased commercial interest in these biomolecules of marine origin. Research and development are predominantly reported from China and Japan, highlighting significant research interest in cnidarians (jellyfish), echinoderms (sea cucumbers, sea urchins and starfish), molluscs (squid and cuttlefish) and sponges. Co-word analysis of the literature highlights applications in regenerative medicine, the properties of hydrolysates, and biology and biochemistry studies. Innovation and the technological landscape, however, focus on fewer taxonomic groups, possibly reflecting the challenge of sustainably sourcing raw materials, with a higher number of patents coming from Asia. Globally, jellyfish collagen is the most prominent marine invertebrate source, while Asia also emphasizes the use of collagens derived from molluscs and sea cucumbers. Europe, despite fewer patents, explores a broader range of taxonomic groups. Globally, key applications registered are mostly in medical, dental and toiletry areas, with peptide preparations spanning multiple animal groups. The food domain is notably relevant for molluscs and sea cucumbers. Market trends show a strong presence of cosmetic and supplement products, aligning with market reports that predict a growing demand for marine collagens in cosmetics and personalized nutrition, particularly in targeted health supplements. Full article
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<p>Schematic representation of a phylogenetic tree showing relationships of selected phyla analysed in the present study.</p>
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<p>Representative marine invertebrate animals (genus or species level) from the phylum studied. Porifera ((<b>A</b>): <span class="html-italic">Ircinia</span>; (<b>B</b>): <span class="html-italic">Chondrosia reniformis</span>). Cnidaria ((<b>C</b>): jellyfish <span class="html-italic">Rhizostoma pulmo</span>; (<b>F</b>): coral <span class="html-italic">Sarcophyton</span>). Mollusca: ((<b>D</b>): squid <span class="html-italic">Loligo;</span> (<b>E</b>): cuttlefish <span class="html-italic">Sepia</span>). Echinodermata: (<b>G</b>): sea-cucumber <span class="html-italic">Stichopus</span>; (<b>H</b>): starfish <span class="html-italic">Asterias amurensis</span>; (<b>I</b>): sea-urchin <span class="html-italic">Paracentrotus lividus</span>. Images sourced from iNaturalist contributors under CC BY 4.0. Modifications include cropping and resizing. For license details, see <a href="https://creativecommons.org/licenses/by/4.0/" target="_blank">https://creativecommons.org/licenses/by/4.0/</a> (accessed on 27 November 2024).</p>
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<p>Geographical distribution of scientific publications addressing collagens in marine invertebrates.</p>
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<p>Distribution of scientific publications by year and taxonomic group addressing collagens in marine invertebrates.</p>
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<p>Bibliometric network visualization of the keywords associated to the scientific publications related to marine invertebrate collagen, generated using VOSviewer. Each node represents a keyword, with node size indicating the frequency of occurrence in the analysed literature. The colours correspond to clusters of closely related keywords, highlighting main areas of research. For example, “jellyfish collagen” is clustered with keywords such as “regenerative medicine” and “biomaterials”, reflecting its relevance in these fields, while “sea cucumber” is associated with “structure” and “physicochemical properties” reflecting its connection with these more fundamental studies. The edges (connecting lines) indicate co-occurrences of keywords, with the thickness of the edges representing the strength of the association.</p>
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<p>Distribution of patent publications addressing collagens by taxonomic group of marine invertebrates (<b>A</b>) and jurisdiction (<b>B</b>).</p>
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<p>Distribution of patent publications addressing the uses of collagens by technological areas.</p>
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<p>(<b>A</b>) Patents applicants by type of entity; (<b>B</b>) legal status of patents addressing collagens by taxonomic group of marine invertebrates (for simplification, please note that taxonomic groups are either phyla, in case of sponges and molluscs, or families within a phylum, in case of jellyfish, starfish and sea cucumbers).</p>
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<p>Databases and sources used for the scientific literature review, patent analysis, and market analysis to assess the significance of collagens from marine invertebrates in research, innovation, and market applications.</p>
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15 pages, 2264 KiB  
Article
Insights into the Molecular Mechanisms of Purine Compounds Synergistically Inducing Larval Settlement in Mytilopsis sallei Using Multi-Group Comparative Transcriptomic Analysis
by Jian He, Huanhuan Hao, Huakang Pan, Shanshan Yao, Yiran Zhao, Shifeng Guo, Jianfang Huang and Danqing Feng
Biology 2024, 13(12), 1067; https://doi.org/10.3390/biology13121067 - 20 Dec 2024
Viewed by 590
Abstract
Most benthic marine invertebrates exhibit a characteristic biphasic life cycle, consisting of a planktonic larval stage followed by a benthic adult stage [...] Full article
(This article belongs to the Section Marine Biology)
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<p>Effects of various concentrations of purines on larval settlement and metamorphosis of <span class="html-italic">M. sallei</span>. (<b>A</b>) Percentage of larval settlement and metamorphosis in response to 0.25 μM of purine mixtures. (<b>B</b>) Percentage of larval settlement and metamorphosis in response to 1.25 μM of purine mixtures. (<b>C</b>) Percentage of larval settlement and metamorphosis in response to 6.25 μM of purine mixtures. 0.25 μM Mix, 1.25 μM Mix, 6.25 μM Mix: the sum of concentrations of the mixtures were 0.25 μM, 1.25 μM and 6.25 μM, respectively. Asterisks denote a significant difference compared with the control (* <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001, Dunnett’s test).</p>
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<p>Identification and enrichment analysis of differentially expressed genes. (<b>A</b>) The samples collected for transcriptome analysis. Ado: adenosine; AS: adenosine-induced settled larvae; Ino: inosine; IS: inosine-induced settled larvae; HS: hypoxanthine-induced settled larvae; Hyp: hypoxanthine; MS: mixture-induced settled larvae; NS: naturally settled larvae; P: pediveliger larvae. (<b>B</b>) Number of differentially expressed genes between settled larvae and pediveliger larvae. (<b>C</b>) Volcano plots of differentially expressed genes between mixture-induced settled larvae and pediveliger larvae. Red and green spots indicate the upregulated expressed genes and the downregulated expressed genes between settled larvae and pediveliger larvae, respectively. Blue spots indicate genes that were not differentially expressed. (<b>D</b>) Bubble plots of GO enrichment analysis of the differentially expressed genes between mixture-induced settled larvae and pediveliger larvae. (<b>E</b>) Bubble plots of KEGG enrichment analysis of the differentially expressed genes between mixture-induced settled larvae and pediveliger larvae.</p>
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<p>Expression analysis of key genes in the AMPK-FoxO signaling pathway. (<b>A</b>) FoxO signaling pathway constructed based on KEGG pathway analysis for mixture-induced settled larvae vs. pediveliger larvae. Red and green boxes represent the genes that were upregulated and downregulated, respectively. Genes shown in boxes lined with both red and green are annotated by different contigs, which may be either upregulated (red) or downregulated (green). (<b>B</b>) Expression levels of key genes from the ADK-AMPK-FoxO signaling pathway. AS: adenosine-induced settled larvae; IS: inosine-induced settled larvae; HS: hypoxanthine-induced settled larvae; MS: mixture-induced settled larvae; NS: naturally settled larvae; P: pediveliger larvae. Asterisks denote a significant difference compared with the pediveliger larvae (* <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001).</p>
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<p>mRNA relative expression levels of key genes from AMPK-FoxO signaling pathway analyzed by qRT-PCR. AS: adenosine-induced settled larvae; IS: inosine-induced settled larvae; HS: hypoxanthine-induced settled larvae; MS: mixture-induced settled larvae; NS: naturally settled larvae; P: pediveliger larvae. Asterisks denote a significant difference compared with the pediveliger larvae (* <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001).</p>
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<p>Expression analysis of genes related to byssus secretion proteins. AS: adenosine-induced settled larvae; IS: inosine-induced settled larvae; HS: hypoxanthine-induced settled larvae; MS: mixture-induced settled larvae; NS: naturally settled larvae; P: pediveliger larvae. Asterisks denote a significant difference compared with the pediveliger larvae (* <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001).</p>
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25 pages, 29385 KiB  
Article
Porifera Associated with Deep-Water Stylasterids (Cnidaria, Hydrozoa): New Species and Records from the Ross Sea (Antarctica)
by Barbara Calcinai, Teo Marrocco, Camilla Roveta, Stefania Puce, Paolo Montagna, Claudio Mazzoli, Simonepietro Canese, Carlo Vultaggio and Marco Bertolino
J. Mar. Sci. Eng. 2024, 12(12), 2317; https://doi.org/10.3390/jmse12122317 - 17 Dec 2024
Viewed by 568
Abstract
Stylasterid corals are known to be fundamental habitat-formers in both deep and shallow waters. Their tridimensional structure enhances habitat complexity by creating refuges for a variety of organisms and by acting as basibionts for many other invertebrates, including sponges. Porifera represent crucial components [...] Read more.
Stylasterid corals are known to be fundamental habitat-formers in both deep and shallow waters. Their tridimensional structure enhances habitat complexity by creating refuges for a variety of organisms and by acting as basibionts for many other invertebrates, including sponges. Porifera represent crucial components of marine benthic assemblages and, in Antarctica, they often dominate benthic communities. Here, we explore the sponge community associated with thanatocoenosis, mostly composed of dead stylasterid skeletons, collected along the Western and Northern edges of the Ross Sea continental shelf. Overall, 37 sponge species were identified from 278 fragments of the stylasterid Inferiolabiata labiata, of which 7 are first records for the Ross Sea, 1 is first record for Antarctic waters and 2 are proposed as new species. Despite the high biodiversity recorded in this and previous studies on Antarctic deep-sea communities, we are still far from capturing the true richness of Antarctic benthic assemblages. Long-term research programs designed to improve the knowledge of the deep-sea fauna inhabiting Antarctic waters are needed to support successful management and conservation plans, especially in this area, considered one of the main marine diversity hotspots worldwide. Full article
(This article belongs to the Section Marine Biology)
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<p>Map of the location of the sampling stations in the Ross Sea continental shelf.</p>
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<p>(<b>A</b>) Bar plots representing the total number of specimens for sponge species with more than 2 samples. (<b>B</b>) Donut charts showing the percentage of sponge species and specimens with an encrusting (Ec) or massive erect (ME) habit, or both (ME/Ec).</p>
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<p>Some sponge specimens with larger sizes: (<b>A</b>) <span class="html-italic">Acanthascus</span> (<span class="html-italic">Rhabdocalyptus</span>) <span class="html-italic">australis</span> (MNA 16005, GCR-02-223 D), (<b>B</b>) <span class="html-italic">Iophon unicorne</span> (MNA 16007, GRC-08-023 DC), (<b>C</b>) <span class="html-italic">Haliclona</span> (<span class="html-italic">Gellius</span>) <span class="html-italic">rudis</span> (MNA 16006, GRC-08-023 DE).</p>
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<p>Bar plots showing (<b>A</b>) the total number of specimens in relation to the area covered on the stylasterid <span class="html-italic">Inferiolabiata labiata</span> and (<b>B</b>) the sponge species with the highest percentage cover on <span class="html-italic">I. labiata</span> (expressed as average ± standard deviation).</p>
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<p>(<b>A</b>) <span class="html-italic">Lissodendoryx</span> (<span class="html-italic">Lissodendoryx</span>) <span class="html-italic">stylosa</span> sp. nov. (holotype MNA 15959, GRC-02-223 O1); (<b>B</b>) <span class="html-italic">L.</span> (<span class="html-italic">L.</span>) <span class="html-italic">styloderma</span> (MNA 13340, GRC-02-223 (1) sp. 3); (<b>C</b>) <span class="html-italic">Crella</span> (<span class="html-italic">Crella</span>) <span class="html-italic">tubifex</span> (MNA 15968, GRC-02-223 BO1); (<b>D</b>) <span class="html-italic">Esperiopsis flagellata</span> sp. nov. (holotype MNA 15962, GRC-02-223 (8) sp. 6); (<b>E</b>) <span class="html-italic">Artemisina plumosa</span> (MNA 15989, GRC-02-223 AN2); (<b>F</b>) <span class="html-italic">Mycale</span> (<span class="html-italic">Anomomycale</span>) cf. <span class="html-italic">titubans</span> (MNA 15994, GRC-02-223 AH1); (<b>G</b>) <span class="html-italic">Tetilla coronida</span> (MNA 15999, GRC-TR17-007 CP1); (<b>H</b>) <span class="html-italic">Poecillastra antarctica</span> comb. nov. (MNA 13302, GRC-02-223 (26) sp. 1). White arrows indicate the position of the sponge specimens on <span class="html-italic">Inferiolabiata labiata</span> fragments.</p>
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<p>SEM pictures of <span class="html-italic">Lissodendoryx</span> (<span class="html-italic">Lissodendoryx</span>) <span class="html-italic">stylosa</span> sp. nov.: (<b>A</b>) style I; (<b>B</b>) style II; (<b>C</b>) arcuate isochelae; (<b>D</b>) sigmas.</p>
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<p>SEM pictures of <span class="html-italic">Lissodendoryx</span> (<span class="html-italic">Lissodendoryx</span>) <span class="html-italic">styloderma</span>: (<b>A</b>) subtylostyle; (<b>B</b>) magnification of the head and the pointed tip of a subtylostyle; (<b>C</b>) tornotes; (<b>D</b>) magnification of a pointed end of a tornote; (<b>E</b>) arcuate isochelae.</p>
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<p>SEM pictures of <span class="html-italic">Crella</span> (<span class="html-italic">Crella</span>) <span class="html-italic">tubifex</span>: (<b>A</b>) acanthostyle; (<b>B</b>) anisostrongyle; (<b>C</b>) acanthostrongyle; (<b>D</b>) magnification of the central portion and extremities of an acanthostrongyle.</p>
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<p>Optical microscope pictures of <span class="html-italic">Esperiopsis flagellata</span> sp. nov.: (<b>A</b>) style; (<b>B</b>) end of a style; (<b>C</b>) isochelae I; (<b>D</b>) isochelae II; (<b>E</b>) C-shaped sigma; (<b>F</b>) flagellated sigma.</p>
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<p>SEM pictures of <span class="html-italic">Artemisina plumosa</span>: (<b>A</b>) style I; (<b>B</b>) style II; (<b>C</b>) tylote; (<b>D</b>) magnification of the spined head of a tylote; (<b>E</b>) isochelae; (<b>F</b>) toxas.</p>
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<p>SEM pictures of <span class="html-italic">Mycale</span> (<span class="html-italic">Anomomycale</span>) cf. <span class="html-italic">titubans</span>: (<b>A</b>) large mycalostyle; (<b>B</b>) thin mycalostyle; (<b>C</b>) anomochelae; (<b>D</b>) sigmas.</p>
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<p><span class="html-italic">Hymeniacidon fragilis</span> (Koltun, 1964) comb. nov.: (<b>A</b>) massively encrusting specimen MNA 13377 (GRC-02-223 (22) sp. 1); (<b>B</b>) laminar specimen MNA 16004 (GRC-02-223 (37) D); (<b>C</b>,<b>D</b>) choanosomal skeleton; (<b>E</b>) ectosomal skeleton; (<b>F</b>) spicules. White arrows indicate the position of the sponge attachment to the stylasterid.</p>
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<p>SEM pictures of <span class="html-italic">Tetilla coronida</span>: (<b>A</b>) oxeas; (<b>B</b>) extremity of a protriaene; (<b>C</b>) extremities of anatrienes; (<b>D</b>) extremities of anamonaenes; (<b>E</b>) sigmaspires.</p>
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<p>Optical microscope pictures of <span class="html-italic">Poecillastra antarctica</span>: (<b>A</b>) oxeas; (<b>B</b>) calthrops and orthotrianes; (<b>C</b>) plesiasters; (<b>D</b>) amphiasters; (<b>E</b>) spirasters.</p>
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30 pages, 3834 KiB  
Review
Preparation and Efficacy Evaluation of Antihyperuricemic Peptides from Marine Sources
by Kun Qiao, Qiongmei Huang, Tongtong Sun, Bei Chen, Wenmei Huang, Yongchang Su, Hetong Lin and Zhiyu Liu
Nutrients 2024, 16(24), 4301; https://doi.org/10.3390/nu16244301 - 12 Dec 2024
Viewed by 788
Abstract
Marine-derived foods, often called blue foods, are promising sustainable alternatives to conventional food sources owing to their abundant amino acids and high protein content. Current treatments for hyperuricemia, a chronic condition attributed to purine metabolism disorders, are associated with various side effects. Novel [...] Read more.
Marine-derived foods, often called blue foods, are promising sustainable alternatives to conventional food sources owing to their abundant amino acids and high protein content. Current treatments for hyperuricemia, a chronic condition attributed to purine metabolism disorders, are associated with various side effects. Novel peptide xanthine oxidase inhibitors have been discovered in the hydrolyzed products of marine fish and invertebrate proteins, which have demonstrated promising therapeutic potential by reducing uric acid levels in vitro and in vivo. This review explores the potential therapeutic effects of xanthine oxidase inhibitors derived from marine fish and invertebrates, summarizes the methods for extracting bioactive peptides from marine organisms, and emphasizes the impact of different proteases on the structure–activity relationship of bioactive peptides. The hypouricemic effects of these bioactive peptides warrant further verification. There is consensus on the in vitro chemical methods used to verify the xanthine oxidase inhibitory effects of these peptides. Considering several cell and animal model development strategies, this review summarizes several highly recognized modeling methods, proposes strategies to improve the bioavailability of bioactive peptides, and advocates for a diversified evaluation system. Although the screening and evaluation methods for antihyperuricemic peptides have been shown to be feasible across numerous studies, they are not optimal. This review examines the deficiencies in bioavailability, synthesis efficiency, and evaluation mechanisms in terms of their future development and proposes potential solutions to address these issues. This review provides a novel perspective for the exploration and application of marine-derived hypouricemic bioactive peptides. Full article
(This article belongs to the Section Nutrition and Metabolism)
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<p>Main causes and complications of hyperuricemia.</p>
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<p>Schematic illustration of uric acid synthesis and transport.</p>
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<p>Schematic diagram of FBPs antihyperuricemia mechanism.</p>
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