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Keywords = asymmetric hemispherical resonator

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10 pages, 564 KiB  
Article
What Changes Occur in the Brain of Veteran? A Magnetic Resonance Imaging and Proton Magnetic Resonance Spectroscopy Study
by Andrzej Urbanik, Iwona Kucybała, Przemysław Guła, Maciej Brożyna and Wiesław Guz
Appl. Sci. 2023, 13(3), 1882; https://doi.org/10.3390/app13031882 - 1 Feb 2023
Viewed by 1606
Abstract
The aims of this study were to assess the common anomalies in the MRI examinations of the heads of soldiers as well as to compare the relative concentration of magnetic resonance spectroscopy (MRS) metabolites in the brains of soldiers with those of healthy [...] Read more.
The aims of this study were to assess the common anomalies in the MRI examinations of the heads of soldiers as well as to compare the relative concentration of magnetic resonance spectroscopy (MRS) metabolites in the brains of soldiers with those of healthy age-matched controls. Overall, 54 professional male soldiers were included in the study group and 46 healthy, age-matched males were in the control group. The relative values of N-acetylaspartate (NAA), choline (Cho), and myoinositol (mI) to creatine (Cr) were assessed. The mean relative concentrations of metabolites were compared between the study and the control group, separately for the frontal and occipital lobes, as well as between the right and left hemispheres within the study group only. The most frequent findings in the head MRI of the soldiers were: asymmetric lateral ventricles and dilated perivascular spaces, enlargement of the subarachnoid spaces, and the presence of cavum septum pellucidum and cavum vergae; the high frequency of sinus disease should also be noted. In the frontal lobes, the mI/Cr ratio was significantly higher (p = 0.005), while the NAA/Cr ratio was lower (p = 0.001), in the group of soldiers (vs. the study group). In the occipital lobes, the NAA/Cr ratio was significantly lower (p = 0.005) in the military personnel and there was a tendency to a higher mI/Cr ratio in the soldiers’ occipital lobes (p = 0.056) (vs. the study group). Comparing the metabolites between the left and right hemispheres in soldiers preferring a right shooting position, a significantly higher mI/Cr (p < 0.001) ratio was observed in the right frontal lobe (vs. the left) and a markedly lower NAA/Cr (p = 0.003) in the right occipital lobe (vs. the left). These changes are associated with astrogliosis and neuronal loss, presumably secondary to repetitive mild traumatic brain injury. Full article
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Figure 1
<p>Exemplary <sup>1</sup>HMRS spectra obtained from volumes of interest in the brains of (<b>A</b>) a healthy control and (<b>B</b>) a soldier.</p>
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8 pages, 857 KiB  
Article
Sex-Related Left-Lateralized Development of the Crus II Region of the Ansiform Lobule in Cynomolgus Monkeys
by Kazuhiko Sawada and Shigeyoshi Saito
Symmetry 2022, 14(5), 1015; https://doi.org/10.3390/sym14051015 - 16 May 2022
Cited by 2 | Viewed by 2007
Abstract
The asymmetric development of the cerebellum has been reported in several mammalian species. The current study quantitatively characterized cerebellar asymmetry and sexual dimorphism in cynomolgus macaques using magnetic resonance (MR) imaging-based volumetry. Three-dimensional T1W MR images at 7-tesla were acquired ex [...] Read more.
The asymmetric development of the cerebellum has been reported in several mammalian species. The current study quantitatively characterized cerebellar asymmetry and sexual dimorphism in cynomolgus macaques using magnetic resonance (MR) imaging-based volumetry. Three-dimensional T1W MR images at 7-tesla were acquired ex vivo from fixed adult male (n = 5) and female (n = 5) monkey brains. Five transverse domains of the cerebellar cortex, known as cerebellar compartmentation defined by the zebrin II/aldolase expression pattern, were segmented on MR images, and the left and right sides of their volumes were calculated. Asymmetry quotient (AQ) analysis revealed significant left-lateralization at the population level in the central zone posterior to the cerebellar transverse domains, which included lobule VII of the vermis with the crura I and II of ansiform lobules, in males but not females. Next, the volume of the cerebellar hemispherical lobules was calculated. Population-level leftward asymmetry was revealed in the crus II regions in males using AQ analysis. The AQ values of the other hemispherical lobules showed no left/right side differences at the population level in either sex. The present findings suggest a sexually dimorphic asymmetric aspect of the cerebellum in cynomolgus macaques, characterized by a leftward lateralization of the crus II region in males, but no left/right bias in females. Full article
(This article belongs to the Special Issue Brain Asymmetry in Evolution II)
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Figure 1
<p>Three-dimensional volume-rendered images of the cerebella of young adult cynomolgus monkeys. (<b>A</b>–<b>C</b>) Anterior, dorsal, and posterior views in the male cerebellum. (<b>D</b>–<b>F</b>) Anterior, dorsal, and posterior views in the female cerebellum. The cerebellar cortex was divided into five transverse domains: the left and right sides of the anterior zone (AZ) (vermal lobules I–V), central zone anterior (CZa; vermal lobule VI and lobules simplex), central zone posterior (CZp; vermal lobule VII, and the crura I and II regions of the ansiform lobules), posterior zone (PZ; vermal lobules VIII–IXa, and paramedian lobule), and nodular zone (NZ; vermal lobules IXb–X, paraflocculus and flocculus). The left and right sides are divided at midline, which was defined by the position of the cerebral longitudinal fissure. Dot lines delineate the intercrucial fissure (icf) and paramedian sulcus (pms). CI—crus I of ansiform lobule; CII—crus II of ansiform lobule; F—flocculus; LP—paramedian lobule; LS—lobulus simplex; PF—paraflocculus; pmf—primary fissure; psf—posterior superior fissure.</p>
Full article ">Figure 2
<p>Ex vivo MR images (using a RARE sequence with a short TR and the minimum TE settings) of cerebella through the deep cerebellar nuclei in young adult cynomolgus monkeys. (<b>A</b>) Axial MR image of the male cerebellum. (<b>B</b>) Axial MR image of the female cerebellum. Abbreviations are posted at the left side. Roman numerals identify the vermal lobules. CI—crus I of ansiform lobule; CII—crus II of ansiform lobule; DCN—deep cerebellar nuclei; icf—intercrucial fissure; LP—paramedian lobule; LS—lobulus simplex; pmf—primary fissure; pms—paramedian sulcus; ppt—prepyramidal fissure; psf—posterior superior fissure.</p>
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16 pages, 35768 KiB  
Article
Implementation of Hemispherical Resonator Gyroscope with 3 × 3 Optical Interferometers for Analysis of Resonator Asymmetry
by Myeongseop Kim, Bobae Cho, Hansol Lee, Taeil Yoon and Byeongha Lee
Sensors 2022, 22(5), 1971; https://doi.org/10.3390/s22051971 - 2 Mar 2022
Cited by 5 | Viewed by 2813
Abstract
A hemispherical resonator gyroscope (HRG) has been implemented by using a consumer wineglass as the resonator and 3 × 3 optical interferometers as the detectors. The poorness of the off-the-shelf wineglass as the resonator can be overcome by the high performance of the [...] Read more.
A hemispherical resonator gyroscope (HRG) has been implemented by using a consumer wineglass as the resonator and 3 × 3 optical interferometers as the detectors. The poorness of the off-the-shelf wineglass as the resonator can be overcome by the high performance of the optical interferometer. The effects of asymmetries in stiffness and absorption of the resonator are analyzed theoretically and confirmed experimentally. We prove that the trace of the amplitude ratio of two n = 2 fundamental resonant modes of the resonator follows a straight line in a complex plane. By utilizing the straightness of the ratio and the high performance of the optical interferometer, we extract four real constant parameters characterizing the HRG system. Experimentally, by using a resonator having an average resonance frequency of 444 Hz and Q value of 1477.2, it was possible to measure the Coriolis force at the level of industrial grade. The bias stability was measured as small as 2.093°/h. Full article
(This article belongs to the Section Optical Sensors)
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Figure 1
<p>Schematic of a 3 × 3 optical interferometer system. The lights reflected at the sample and the reference arms make interference at the coupler, which is then measured by two detectors simultaneously.</p>
Full article ">Figure 2
<p>Lumped element models of hemispherical resonators; (<b>a</b>) ideal symmetric resonator model, and (<b>b</b>) general resonator model having asymmetry in stiffness and damping. <span class="html-italic">M</span>: mass, <span class="html-italic">c</span>: damping constant, Δ<span class="html-italic">c</span>: damping constant difference, <math display="inline"><semantics> <mrow> <msub> <mi>θ</mi> <mi>τ</mi> </msub> </mrow> </semantics></math>: damping axis angle, <span class="html-italic">k</span>: spring constant, Δ<span class="html-italic">k</span>: spring constant difference, <math display="inline"><semantics> <mrow> <msub> <mi>θ</mi> <mi>ω</mi> </msub> </mrow> </semantics></math>: spring axis angle, <math display="inline"><semantics> <mrow> <msub> <mi>F</mi> <mi>x</mi> </msub> </mrow> </semantics></math>: driving force in <span class="html-italic">x</span> direction, <math display="inline"><semantics> <mrow> <msub> <mi>F</mi> <mi>y</mi> </msub> </mrow> </semantics></math>: driving force in <span class="html-italic">y</span> direction.</p>
Full article ">Figure 3
<p>The trace of the ratio <span class="html-italic">y/x</span> in Equation (16) simulated with various resonator parameters and drawn in a complex plane. The trace is plotted when <span class="html-italic">B</span>, <math display="inline"><semantics> <mi>θ</mi> </semantics></math>, <span class="html-italic">a</span>, and <span class="html-italic">b</span> are (<b>a</b>) 1, 0°, 0, and 0; (<b>b</b>) 1, 0°, 10, and 5; (<b>c</b>) 2, 0°, 10, and 5; (<b>d</b>) 2, 60°, 10, and 5, respectively. The trace is always on a straight line and the line is determined by the four real constants <span class="html-italic">B</span>, <math display="inline"><semantics> <mi>θ</mi> </semantics></math>, <span class="html-italic">a</span>, and <span class="html-italic">b</span> of Equation (16). The dotted line is the trace made with just the previous conditions.</p>
Full article ">Figure 4
<p>Analysis of the <span class="html-italic">y/x</span> trace for an asymmetric resonator. The <span class="html-italic">y/x</span> ratios collected with various angular rates form a straight line in a complex plane. The plot shows that the distance from the origin to the nearest point on the line is <span class="html-italic">Bb</span>, and the angular rate giving the nearest point is −<span class="html-italic">a</span>, and the distance from the nearest point to the <math display="inline"><semantics> <mrow> <msub> <mi mathvariant="sans-serif">Ω</mi> <mi mathvariant="normal">z</mi> </msub> <mo>=</mo> <mn>0</mn> </mrow> </semantics></math> point, along the line, is <span class="html-italic">Ba</span>.</p>
Full article ">Figure 5
<p>The photographs of (<b>a</b>) the hemispherical resonator and (<b>b</b>) the rotating part of the implemented HRG system. A general consumer wineglass was used as the resonator. A sheet of thin gold foil was attached and used as the electrode for activating the resonator.</p>
Full article ">Figure 6
<p>The HRG system implemented with 3 × 3 optical interferometers. The system operates in the non-feedback open-loop (NFOL) mode. RM: reference mirror, SA: sample arm, PC: polarization controller, HR: hemispherical resonator, E: electrode, FC: fiber coupler, OC: optical circulator, FG: function generator, AMP: amplifier, C: collimator, L: lens.</p>
Full article ">Figure 7
<p>The displacements induced by the vibrations of two fundamental modes of a hemispherical resonator derived by a single actuator. The system was rotated by a constant rate of <math display="inline"><semantics> <mrow> <msub> <mi mathvariant="sans-serif">Ω</mi> <mi mathvariant="normal">z</mi> </msub> <mo>=</mo> <mo>−</mo> <mn>4.19</mn> <mo>°</mo> <mo>/</mo> <mi mathvariant="normal">s</mi> </mrow> </semantics></math>. A phase difference of 61.8° between two modes was measured.</p>
Full article ">Figure 8
<p>The experimental results: (<b>a</b>) the plot of amplitude ratios <span class="html-italic">y/x</span> of Equation (20) measured with various angular rates, and (<b>b</b>) the fitted straight line characterizing the resonator. From the fitting with a straight line, the 4 real constants characterizing the resonator are extracted as <span class="html-italic">B</span> = 0.318, <math display="inline"><semantics> <mi>θ</mi> </semantics></math> = −22.84°, <span class="html-italic">a</span> = 1.033°/s, and <span class="html-italic">b</span> = 3.944°/s.</p>
Full article ">Figure 9
<p>The comparison of the applied angular rate and the measured angular rate. They are well matched with the coefficient of determination of <math display="inline"><semantics> <mrow> <msup> <mi mathvariant="normal">R</mi> <mn>2</mn> </msup> </mrow> </semantics></math> = 0.9994.</p>
Full article ">Figure 10
<p>The plot of Allan deviations made with the implemented HRG. The measurements have been made for 2 h at room temperature without temperature control. The bias stability was 2.093°/h, which corresponds to an industrial-grade gyroscope.</p>
Full article ">Figure 11
<p>The amplitude ratio <span class="html-italic">y/x</span> measured at several angular rates: (<b>a</b>) the magnitude and (<b>b</b>) the phase of the ratio. The magnitude variation is not linear to the applied angular rate, and does not vanish at any rate. The phase varies with the angular rate but the sign of the phase is not changed exactly at the zero rate.</p>
Full article ">
492 KiB  
Review
Review of Computational Methods on Brain Symmetric and Asymmetric Analysis from Neuroimaging Techniques
by P. Kalavathi, M. Senthamilselvi and V. B. Surya Prasath
Technologies 2017, 5(2), 16; https://doi.org/10.3390/technologies5020016 - 18 Apr 2017
Cited by 15 | Viewed by 14072
Abstract
The brain is the most complex organ in the human body and it is divided into two hemispheres—left and right. The left hemisphere is responsible for control of the right side of our body, whereas the right hemisphere is responsible for control of [...] Read more.
The brain is the most complex organ in the human body and it is divided into two hemispheres—left and right. The left hemisphere is responsible for control of the right side of our body, whereas the right hemisphere is responsible for control of the left side of our body. Brain image segmentation from different neuroimaging modalities is one of the important parts of clinical diagnostic tools. Neuroimaging based digital imagery generally contain noise, inhomogeneity, aliasing artifacts, and orientational deviations. Therefore, accurate segmentation of brain images is a very difficult task. However, the development of accurate segmentation of brain images is very important and crucial for a correct diagnosis of any brain related diseases. One of the fundamental segmentation tasks is to identify and segment inter-hemispheric fissure/mid-sagittal planes, which separate the two hemispheres of the brain. Moreover, the symmetric/asymmetric analyses of left and right hemispheres of brain structures are important for radiologists to analyze diseases such as Alzheimer’s, autism, schizophrenia, lesions and epilepsy. Therefore, in this paper, we have analyzed the existing computational techniques used to find brain symmetric/asymmetric analysis in different neuroimaging techniques such as the magnetic resonance (MR), computed tomography (CT), positron emission tomography (PET), single-photon emission computed tomography (SPECT), which are utilized for detecting various brain related disorders. Full article
(This article belongs to the Special Issue Medical Imaging & Image Processing Ⅱ)
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Figure 1
<p>(<b>a</b>) inter-hemispheric fissure in a normal human brain; and (<b>b</b>) different brain anatomical structures from sagittal cross-section in a magnetic resonance (MR) image (courtesy of [<a href="#B5-technologies-05-00016" class="html-bibr">5</a>]).</p>
Full article ">Figure 2
<p>Classification of brain symmetric/asymmetric analysis methods and approaches.</p>
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