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Keywords = Andrographis Herba

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17 pages, 4035 KiB  
Article
Exploring the Active Constituents of Andrographis paniculata in Protecting the Skin Barrier and the Synergistic Effects with Collagen XVII
by Heng Xu, Shiying Lan, Simin Lin, Anjing Wang, Yuanlin Luo, Jing Wang and Zhenzhong Yang
Antioxidants 2025, 14(1), 118; https://doi.org/10.3390/antiox14010118 - 20 Jan 2025
Viewed by 868
Abstract
Andrographis paniculata is mainly used to treat skin inflammations, wounds, and infections. In this study, Andrographis Herba, the aerial part of the plant, was proven to increase the viability of UVB-damaged HaCat cells and reduce reactive oxygen species levels. The chemical composition of [...] Read more.
Andrographis paniculata is mainly used to treat skin inflammations, wounds, and infections. In this study, Andrographis Herba, the aerial part of the plant, was proven to increase the viability of UVB-damaged HaCat cells and reduce reactive oxygen species levels. The chemical composition of Andrographis Herba extract (AHE) was analyzed using UPLC-Q-TOF-MS, and diterpene lactones were identified as its primary constituents. Then, the fraction of diterpene lactones was prepared and exhibited similar effects to AHE. AHE, its diterpene lactones component, and its representative constituent andrographolide all decreased the expression of IL-1β, IL-6, and CDKN1A. Furthermore, the protective effects of AHE and its active ingredients on UVB-damaged epidermal stem cells were investigated. Notably, the combined treatment with andrographolide and collagen XVII enhanced the viability of UVB-damaged epidermal stem cells, increased the expression of stemness markers integrin β1 and p63, and decreased the expression of the differentiation marker keratin 10. This combination demonstrated significant synergy in maintaining skin homeostasis, which provides evidences for the development of skin-protective products. Full article
(This article belongs to the Special Issue Antioxidant and Protective Effects of Plant Extracts—2nd Edition)
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Graphical abstract

Graphical abstract
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<p>The protective effects of AHE on UVB-damaged HaCat cells. (<b>A</b>) The cells were incubated with AHE. Cell viability was measured by CCK-8 assay. (<b>B</b>) The cells were preincubated with AHE and irradiated with UVB (510 mJ/cm<sup>2</sup>). Cell viability was measured by CCK-8 assay. (<b>C</b>) The intracellular ROS in HaCat cells were assessed by DCFH-DA. The appearance of green fluorescence represents the intensity of the generated ROS. (<b>D</b>) The fluorescence intensity was quantified. The mRNA expression levels of (<b>E</b>) IL-1β, (<b>F</b>) IL-6, and (<b>G</b>) CDKN1A in HaCat cells were measured by RT-qPCR. <sup>#</sup> <span class="html-italic">p</span> &lt; 0.05, <sup>##</sup> <span class="html-italic">p</span> &lt; 0.01 vs. Ctrl group; * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01 vs. UVB-damaged group.</p>
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<p>The base peak chromatograms of AHE obtained by UPLC-Q-TOF-MS in negative (<b>A</b>) and positive (<b>B</b>) ion modes.</p>
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<p>(<b>A</b>) The chromatograms of the AHE (blue) and AHDL (green) at 203 nm. (<b>B</b>) Representative diterpene lactone constituents in AHDL.</p>
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<p>The protective effects of AHDL on UVB-damaged HaCat cells. (<b>A</b>) The cells were incubated with AHDL. (<b>B</b>) The cells were preincubated with AHDL and irradiated with UVB (510 mJ/cm<sup>2</sup>). (<b>C</b>) The intracellular ROS in HaCat cells was assessed by DCFH-DA. The appearance of green fluorescence represents the intensity of the generated ROS. (<b>D</b>) The fluorescence intensity was quantified. The mRNA expression levels of (<b>E</b>) IL-β, (<b>F</b>) IL-6, and (<b>G</b>) CDKN1A in HaCat cells were measured by RT-qPCR. <sup>##</sup> <span class="html-italic">p</span> &lt; 0.01 vs. Ctrl group; * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01 vs. UVB-damaged group.</p>
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<p>The protective effects of AG on UVB-damaged HaCat cells. (<b>A</b>) The cells were incubated with AG. (<b>B</b>) The cells were preincubated with AG and irradiated with UVB (510 mJ/cm<sup>2</sup>). (<b>C</b>) The intracellular ROS in HaCat cells was assessed by DCFH-DA. The appearance of green fluorescence represents the intensity of the generated ROS. (<b>D</b>) The fluorescence intensity was quantified. The mRNA expression levels of (<b>E</b>) IL-β, (<b>F</b>) IL-6, and (<b>G</b>) CDKN1A in HaCat cells were measured by RT-qPCR. <sup>#</sup> <span class="html-italic">p</span> &lt; 0.05, <sup>##</sup> <span class="html-italic">p</span> &lt; 0.01 vs. Ctrl group; * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01 vs. UVB-damaged group.</p>
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<p>Identification of ESCs.</p>
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<p>The protective effects of AHE, AHDL, AG, and COL XVII on UVB-damaged ESCs. The cells were preincubated with different treatments and irradiated with UVB (450 mJ/cm²). (<b>A</b>) AHE, (<b>B</b>) AHDL, (<b>C</b>) AG, (<b>D</b>) COL XVII, (<b>E</b>) Combination of AG and COL XVII. <sup>##</sup> <span class="html-italic">p</span> &lt; 0.01 vs. Ctrl group; * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01 vs. UVB-damaged group.</p>
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<p>Changes in the expression of ESC markers of UVB-damaged ESCs after combined treatment with AG and COL XVII and the exploration of the combination index (CI). The protein expression levels of integrin β1 (<b>A</b>,<b>D</b>), p63 (<b>B</b>,<b>E</b>), and keratin 10 (<b>C</b>,<b>F</b>) were measured by western blotting. Comparison of the observed effects and additive effects of AG and COL XVII on integrin β1 (<b>G</b>), p63 (<b>H</b>), and keratin 10 (<b>I</b>). <sup>#</sup> <span class="html-italic">p</span> &lt; 0.05, <sup>##</sup> <span class="html-italic">p</span> &lt; 0.01 vs. Ctrl group; * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01 vs. UVB-damaged group.</p>
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13 pages, 2910 KiB  
Article
Determination of Bitterness of Andrographis Herba Based on Electronic Tongue Technology and Discovery of the Key Compounds of Bitter Substances
by Xiao Zhang, Hongwei Wu, Xiankuo Yu, Hanyan Luo, Yaqi Lu, Hongjun Yang, Xin Li, Zhiyong Li, Liying Tang and Zhuju Wang
Molecules 2018, 23(12), 3362; https://doi.org/10.3390/molecules23123362 - 19 Dec 2018
Cited by 27 | Viewed by 4973
Abstract
Andrographis Herba (AH), the dry aerial segments of Andrographis paniculata (Burm.f.) Nees, is a common herbal remedy with bitter properties in traditional Chinese medicine (TCM) theory. Although bitterness is one of the features representing Chinese medicine, it has not been implemented as an [...] Read more.
Andrographis Herba (AH), the dry aerial segments of Andrographis paniculata (Burm.f.) Nees, is a common herbal remedy with bitter properties in traditional Chinese medicine (TCM) theory. Although bitterness is one of the features representing Chinese medicine, it has not been implemented as an index to assess the quality and efficacy of TCM because of peoples’ subjectivity to taste. In this study, 30 batches of AH with different commercial classifications (leaves, stems, or mixtures of both) were collected. Bitterness of AH was quantified by electronic tongue technology. Meanwhile, chemical compositions were characterized through establishing high-performance liquid chromatography fingerprints. The result indicated that the radar curves of the bitterness from different AH commercial classifications displayed different taste fingerprint information. Based on six taste factors, a Principal Component Analysis (PCA) score three-dimensional (3D) plot exhibited a clear grouping trend (R2X, 0.912; Q2, 0.763) among the three different commercial classifications. Six compounds (Peaks 2, 3, 4, 6, 7, 8) with positive correlation to bitterness were discovered by a Spearman correlation analysis. Peaks 2, 6, 7, 8 were identified as andrographolide, neoandrographolide, 14-deoxyandrographolide, and dehydroandrographolide, respectively. The electronic tongue can be used to distinguish AH samples with different commercial classifications and for quality evaluation. Full article
(This article belongs to the Section Analytical Chemistry)
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Figure 1

Figure 1
<p>Radar curves of <span class="html-italic">Andrographis Herba</span> (AH) samples’ bitterness for different commercial classifications. A: Leaf samples, B: Stem/Leaf samples, C: Stem samples.</p>
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<p>The Principal Component Analysis Three-Dimensional (PCA 3D) scores plot using AH bitterness data. <span style="color:#00FF40">●</span>: Leaf, <span style="color:blue">●</span>: Stem/Leaf, <span style="color:red">●</span>: Stem.</p>
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<p>Chromatographic fingerprints of all AH samples. (L1–L5 are leaf samples; SL1–SL13 are stem and leaf mixed samples; S1–S12 are stem samples. Peaks 2,6,7,8 are andrographolide, neoandrographolide, 14-deoxyandrographolide, and dehydroandrographolide, respectively).</p>
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<p>Correlation network between bitterness (radar curve area) and the common peaks in HPLC fingerprint. Visualization of data concentrated on the correlations between chemical constituents in relation to bitterness (radar curve area). The negative correlations are indicated with dots lines, and positive correlations are indicated with solid lines; thicker lines indicate a stronger correlation. The length of each line has no meaning.</p>
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<p>Three typical AH samples with different specification. <b>A</b>: leaf sample; <b>B</b>: a mixture of leaf and stem sample; <b>C</b>: stem sample; <b>D</b>: stem; <b>E</b>: leaf.</p>
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11 pages, 2764 KiB  
Article
Screening and Identification for Immunological Active Components from Andrographis Herba Using Macrophage Biospecific Extraction Coupled with UPLC/Q-TOF-MS
by Yaqi Wang, Jiaojiao Jiao, Yuanzhen Yang, Ming Yang and Qin Zheng
Molecules 2018, 23(5), 1047; https://doi.org/10.3390/molecules23051047 - 30 Apr 2018
Cited by 17 | Viewed by 4257
Abstract
The method of cell biospecific extraction coupled with UPLC/Q-TOF-MS has been developed as a tool for the screening and identification of potential immunological active components from Andrographis Herba (AH). In our study, a macrophage cell line (RAW264.7) was used to extract cell-combining compounds [...] Read more.
The method of cell biospecific extraction coupled with UPLC/Q-TOF-MS has been developed as a tool for the screening and identification of potential immunological active components from Andrographis Herba (AH). In our study, a macrophage cell line (RAW264.7) was used to extract cell-combining compounds from the ethanol extract of AH. The cell binding system was then analyzed and identified by UPLC/Q-TOF-MS analysis. Finally, nine compounds, which could combine with macrophages, in an ethanol extract of AH were detected by comparing basic peak intensity (BPI) profiles of macrophages before and after treatment with AH. Then they were identified as Andrographidine E (1), Andrographidine D (2), Neoandrographolide (3), Dehydroandrographolide (4), 5, 7, 2′, 3′-tetramethoxyflavone (5), β-sitosterol (7), 5-hydroxy-7, 2′, 3′-trimethoxyflavone (8) and 5-hydroxy-7, 8, 2′, 3′-tetramethoxyflavone (9), which could classified into five flavonoids, three diterpene lactones, and one sterol. Their structures were recognized by their characteristic fragment ions and fragmentations pattern of diterpene lactones and flavonoids. Additionally, the activity of compounds 3, 4, and 7 was tested in vitro. Results showed that these three compounds could decrease the release of NO (p < 0.01) in macrophages remarkably. Moreover, 3, 4, and 7 showed satisfactory dose-effect relationships and their IC50 values were 9.03, 18.18, and 13.76 μg/mL, respectively. This study is the first reported work on the screening of immunological active components from AH. The potential immunological activity of flavonoids from AH has not been reported previously. Full article
(This article belongs to the Special Issue Green Analytical Chemistry)
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Figure 1
<p>The structures of compounds identified in the cell extract of Andrographis Herba (AH). (<b>1</b>. Andrographidine E, <b>2</b>. Andrographidine D, <b>3</b>. Neoandrographolide, <b>4</b>. Dehydroandrographolide, <b>5</b>. 5,7,2′,3′-tetramethoxyflavone, <b>7</b>. β-sitosterol, <b>8</b>. 5-hydroxy-7,2′,3′-trimethoxyflavone, <b>9</b>. 5-hydroxy-7,8,2′,3′-tetramethoxyflavone).</p>
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<p>Base peak intensity (BPI) profiles of: (<b>A</b>) extract of AH treated with macrophages; (<b>B</b>) extract of denatured deposited macrophages; (<b>C</b>) ethanol extract of AH.</p>
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<p>MS/MS spectra of andrographidine E (<b>1</b>).</p>
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<p>The proposed fragmentations pattern of andrographidine E (<b>1</b>).</p>
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<p>MS/MS spectra of neoandrographolide (<b>3</b>).</p>
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<p>The proposed fragmentations pattern of neoandrographolide (<b>3</b>).</p>
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1441 KiB  
Review
Hepatoprotective Effects of Chinese Medicinal Herbs: A Focus on Anti-Inflammatory and Anti-Oxidative Activities
by Puiyan Lam, Fan Cheung, Hor Yue Tan, Ning Wang, Man Fung Yuen and Yibin Feng
Int. J. Mol. Sci. 2016, 17(4), 465; https://doi.org/10.3390/ijms17040465 - 29 Mar 2016
Cited by 126 | Viewed by 14108
Abstract
The liver is intimately connected to inflammation, which is the innate defense system of the body for removing harmful stimuli and participates in the hepatic wound-healing response. Sustained inflammation and the corresponding regenerative wound-healing response can induce the development of fibrosis, cirrhosis and [...] Read more.
The liver is intimately connected to inflammation, which is the innate defense system of the body for removing harmful stimuli and participates in the hepatic wound-healing response. Sustained inflammation and the corresponding regenerative wound-healing response can induce the development of fibrosis, cirrhosis and eventually hepatocellular carcinoma. Oxidative stress is associated with the activation of inflammatory pathways, while chronic inflammation is found associated with some human cancers. Inflammation and cancer may be connected by the effect of the inflammation-fibrosis-cancer (IFC) axis. Chinese medicinal herbs display abilities in protecting the liver compared to conventional therapies, as many herbal medicines have been shown as effective anti-inflammatory and anti-oxidative agents. We review the relationship between oxidative stress and inflammation, the development of hepatic diseases, and the hepatoprotective effects of Chinese medicinal herbs via anti-inflammatory and anti-oxidative mechanisms. Moreover, several Chinese medicinal herbs and composite formulae, which have been commonly used for preventing and treating hepatic diseases, including Andrographis Herba, Glycyrrhizae Radix et Rhizoma, Ginseng Radix et Rhizoma, Lycii Fructus, Coptidis Rhizoma, curcumin, xiao-cha-hu-tang and shi-quan-da-bu-tang, were selected for reviewing their hepatoprotective effects with focus on their anti-oxidative and ant-inflammatory activities. This review aims to provide new insight into how Chinese medicinal herbs work in therapeutic strategies for liver diseases. Full article
(This article belongs to the Section Biochemistry)
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Graphical abstract
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<p>Schematic diagram of major pathways of alcoholic fatty liver (ALD) and potential molecular targets of herbal medicine for the protection of ALD. The arrows indicate the potential molecular targets involved in the development of ALD and regulated by herbal medicines. ACC: Acetyl-CoA carboxylase; AMPK: AMP-activated protein kinase; CD14: cluster of differentiation 14 COX-2: Cyclooxygenase-2; CPT-1: Carnitine palmitoyltransferase-1; CYP2E1: Cytochrome P450 2E; FAS: Fatty acid synthase; IL-6: Interleukin 6; MCP-1: Monocyte chemotactic protein-1; MyD88: Myeloid differentiation factor 88; NF-κB: Nuclear factor-κB; PGC-1α: Peroxisome proliferator-activated receptor g coactivator α; PPARα: Peroxisome proliferator activated receptor RNS Reactive nitrogen species; ROS: Reactive oxygen species; SCD-1: Stearyl CoA desaturase-1; SIRT1: Sirtuin 1; SREBP-1c: Sterol regulatory element-binding protein-1c; STAT-3: signal transducer and activator of transcription-3; TLR: Toll-like receptor 4; TRIF: TIR-domain-containing adapter-inducing interferon-b; TNF-α: Tumor necrosis factor-α.</p>
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<p>Pathophysiology of nonalcoholic fatty liver disease (NAFLD). The pathogenesis can be explained by the “two hit” hypothesis, and the different grades of severity are indicated by the white arrow. Various factors are involved in the development of NAFLD and represented by the red arrows.</p>
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568 KiB  
Article
Chemical Compositions, Chromatographic Fingerprints and Antioxidant Activities of Andrographis Herba
by Yang Zhao, Chun-Pin Kao, Kun-Chang Wu, Chi-Ren Liao, Yu-Ling Ho and Yuan-Shiun Chang
Molecules 2014, 19(11), 18332-18350; https://doi.org/10.3390/molecules191118332 - 10 Nov 2014
Cited by 28 | Viewed by 7178
Abstract
This paper describes the development of an HPLC-UV-MS method for quantitative determination of andrographolide and dehydroandrographolide in Andrographis Herba and establishment of its chromatographic fingerprint. The method was validated for linearity, limit of detection and quantification, inter- and intra-day precisions, repeatability, stability and [...] Read more.
This paper describes the development of an HPLC-UV-MS method for quantitative determination of andrographolide and dehydroandrographolide in Andrographis Herba and establishment of its chromatographic fingerprint. The method was validated for linearity, limit of detection and quantification, inter- and intra-day precisions, repeatability, stability and recovery. All the validation results of quantitative determination and fingerprinting methods were satisfactory. The developed method was then applied to assay the contents of andrographolide and dehydroandrographolide and to acquire the fingerprints of all the collected Andrographis Herba samples. Furthermore, similarity analysis and principal component analysis were used to reveal the similarities and differences between the samples on the basis of the characteristic peaks. More importantly, the DPPH free radical-scavenging and ferric reducing capacities of the Andrographis Herba samples were assayed. By bivariate correlation analysis, we found that six compounds are positively correlated to DPPH free radical scavenging and ferric reducing capacities, and four compounds are negatively correlated to DPPH free radical scavenging and ferric reducing capacities. Full article
(This article belongs to the Section Natural Products Chemistry)
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<p>Overlapped chromatograms of AH samples detected at 225 nm.</p>
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<p>PCA scores plot of AH samples.</p>
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<p>DPPH radical scavenging capacity of AH samples. The values are expressed as μmol BHT equivalents per gram dried AH sample (mean ± SD). Values that share the same letter are not significantly different (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>EC<sub>50</sub> values of BHT and AH samples. Values that share the same letter are not significantly different (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Ferric reducing capacity of AH samples. The values are expressed as μmol Fe<sup>2+</sup> equivalents per gram of dried AH sample (mean ± SD). Values that share the same letter are not significantly different (<span class="html-italic">p</span> &lt; 0.05).</p>
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