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Figure 1 in Potential Hepatoprotective Effect of Cheatomorpha gracilis extract against High Fat Diet (HFD)-Induced Liver Damage, and its characterization by HPLC
Figure 1. Phenolic compounds of Cheatomorpha gracilis extract by chemical High Performance Liquid Chromatography (HPLC) analysis (gallic acid, Rutin, quercetin, Apegenin, kaempferol and Naringenin).
Figure 4 in Potential Hepatoprotective Effect of Cheatomorpha gracilis extract against High Fat Diet (HFD)-Induced Liver Damage, and its characterization by HPLC
Figure 4. Effects of C.gracilis aqueous extract (AEC) on TBARS and protein carbonyls products (PCO) in HFD-treated mice. TBARS: thiobarbituric acid reactive substance. Data are presented as mean ± SD, n =8. *P≤ 0.05, **P≤ 0.01 compared with the control group. +P ≤0.05, ++P ≤0.01 as compared with HFD- treated mice.
Validation of a standardized MRI method for liver fat and T2* quantification
<p><strong>Dataset description:</strong> These data have been uploaded and shared as part of the manuscript <em>“Validation of a standardized MRI method for liver fat and T2* quantification, Chloe Hutton, Michael L. Gyngell, Matteo Milanesi, Alexandre Bagur, and Michael Brady, Perspectum Diagnostics, Oxford, United Kingdom", which was submitted for publication to PLOS ONE on August 27th 2018.</em></p> <p><strong>Details:</strong> The LMSIDEAL_Results.zip file extracts into 28 MATLAB files (MATLAB R2017b) corresponding to LMS IDEAL PDFF results calculated as described in the above manuscript for 28 sets of publicly-available phantom data available from another repository. The original phantom data can be accessed from (<a href="http://dx.doi.org/10.5281/zenodo.48266)">http://dx.doi.org/10.5281/zenodo.48266)</a> and are described in detail in [Hernando et al., Magn Reson Med. 2017;77:1516-1524. doi: 10.1002/mrm.26228. Epub 2016 Apr 15.].</p> <p>To summarise, the original phantom data were acquired using one phantom at six sites, covering: 3 vendors (GE Healthcare, Siemens and Philips); 2 field strengths (1.5T and 3T); and 2 protocols. One of the six sites had two sets of data (one at the beginning of the phantom study and one at the end), to give (6+1)x2x2=28 sets of data in total. The phantom consisted of 11 vials with oil/water concentrations: 0%, 2.6%, 5.3%, 7.9%, 10.5%, 15.7%, 20.9%, 31.2%, 41.3%, 51.4%, 100%. The data from each system, and for each protocol, involved 6 echoes of complex-valued multi-echo gradient echo MR images.</p> <p>Each of the 28 LMSIDEAL_Results_* MATLAB files contains 3 MAT files:</p> <p>LMSIDEAL_PDFF - contains PDFF maps (sized X x Y x 3 slices)</p> <p>ROI - contains x,y coordinates for each ROI (sized 2 x 11) (circular ROI with diameter approximately = 19.5mm)</p> <p>MEAN - contains mean for each slice and each ROI (sized 3 x 11)</p> <p> </p> <p> </p> <p> </p> <p> </p> <p> </p>
FIGURE 5 in Linalool chemotype essential oil from Lippia alba in the anesthesia of fat snook (Centropomus parallelus): ventilatory rate, biochemical, antioxidant, and oxidative status parameters
FIGURE 5 | Antioxidant and oxidative stress parameters in the liver after transferring to recovery aquariums of fat snook (Centropomus parallelus) anesthetized with the essential oil from Lippia alba (EOLA). A = GST (glutathione S-transferase). B = SOD (superoxide dismutase). C = CAT (catalase). D = LPO (lipid peroxidation). Data are presented as the mean ± SEM (n = 5 fish per treatment each time). Capital letters indicate significant differences between time points within the same treatment. Lowercase letters indicate significant differences between treatments at the same time point. Two-way ANOVA and Tukey's tests were used to determine statistical significance (P <0.05).
FIGURE 1 in Linalool chemotype essential oil from Lippia alba in the anesthesia of fat snook (Centropomus parallelus): ventilatory rate, biochemical, antioxidant, and oxidative status parameters
FIGURE 1 | Time (s) required for mild and deep anesthesia and recovery in fat snook angelfish (Centropomus parallelus) with increasingly essential oil from Lippia alba (EOLA) concentrations. Data are presented as the mean ± SEM (n = 10 fish per treatment). Different letters indicate significant differences between treatments. One-way ANOVA and Tukey's tests were used to determine statistical significance (P <0.05). Mild and deep anesthesia times showed regression.
FIGURE 4 in Linalool chemotype essential oil from Lippia alba in the anesthesia of fat snook (Centropomus parallelus): ventilatory rate, biochemical, antioxidant, and oxidative status parameters
FIGURE 4 | Blood glucose (A) and whole-body cortisol (B) levels after transferring to recovery aquariums of anesthetized fat snook (Centropomus parallelus) with essential oil from Lippia alba (EOLA). Data are presented as the mean ± SEM (n = 5 fish per treatment each time). Capital letters indicate significant differences between time points within the same treatment. Lowercase letters indicate significant differences between treatments at the same time point. Two-way ANOVA and Tukey's tests were used to determine statistical significance (P <0.05).
FIGURE 2 in Linalool chemotype essential oil from Lippia alba in the anesthesia of fat snook (Centropomus parallelus): ventilatory rate, biochemical, antioxidant, and oxidative status parameters
FIGURE 2 | Time (s) required for mild and deep anesthesia and recovery in fat snook (Centropomus parallelus) exposed to essential oil from Lippia alba (180 µL L−1). Smaller fish = 6.03 ± 0.09 g; 9.30 ± 0.05 cm. Larger fish = 38.49 ± 2.07 g; 16.55 ± 0.26 cm. Data are presented as the mean ± SEM (n = 10 fish per treatment). Different letters indicate significant differences between fish body size classes. One-way ANOVA and Tukey's tests were used to determine statistical significance (P <0.05).
FIGURE 3 in Linalool chemotype essential oil from Lippia alba in the anesthesia of fat snook (Centropomus parallelus): ventilatory rate, biochemical, antioxidant, and oxidative status parameters
FIGURE 3 | Ventilatory rate (VR) of fat snook (Centropomus parallelus) during exposure to the essential oil from Lippia alba (EOLA). Data are presented as the mean ± SEM (n = 8 fish per treatment). Capital letters indicate significant differences between time points within the same treatment. Lowercase letters indicate significant differences between treatments at the same time point. Two-way ANOVA and Tukey's tests were used to determine statistical significance (P <0.05).
Figures 13-18. Phyllocnistis citrella pupae. 13 in Histology and histochemistry of Phyllocnistis citrella Stainton (Lepidoptera: Gracillariidae) fat body during the post embrionary development
Figures 13-18. Phyllocnistis citrella pupae. 13. Sagittal and frontal section pupae. Hematoxilin- Eosin technique (HE). 14. Fat body (FB). Anterior abdominal region with spherical trophocytes (t) and cytoplasm filled with intensely acidophilic granules. (HE). 15. Fat body (FB). Median region with numerous intensely acidophilic granules and numerous strongly basophillous plasmatocytes (p). Oenocytes (o). (HE). 16. Fat body (FB). Median region with PAS-positive granules and big intensely basophillous plasmatocytes (p). Periodic Acid-Schiff technique- Hematoxilin (PAS-H). 17. Fat body (FB). Median region with Sudan III-positive lipidic droplets. Sudan III technique (SIII). 18. Fat body (FB). Median region with increase in the lipidic acid concentration related to neutral lipids. (NB).
Figures 1-6. Phyllocnistis citrella larvae. 1. Sagittal and frontal section larval instar I, II in Histology and histochemistry of Phyllocnistis citrella Stainton (Lepidoptera: Gracillariidae) fat body during the post embrionary development
Figures 1-6. Phyllocnistis citrella larvae. 1. Sagittal and frontal section larval instar I, II, III. Hematoxilin- Eosin technique (HE). 2. Larva I: Parietal fat body (PFB) with trophocytes (t) showing irregular shape and basophilic cytoplasm with few droplets. (HE). 3. Larva II: Parietal fat body (PFB) made up of masses of trophocytes (t) with abundant cytoplasmic droplets. (HE). 4. Larva III: Spongy visceral fat body (VFB) in contact with the silk glands (SG). (HE). 5. Larva III: Fat body (FB) with big cumuli of Sudan Black positive lipidic droplets. Sudan Black technique (SB). 6. Larva III: Fat body (FB) with high concentration of neutral lipidic droplets surrounded by acid lipid granules of different sizes. Nile Blue technique (NB).
Dataset related to: Sirtuin 3 Deficiency Aggravates Kidney Disease in Response to High-Fat Diet through Lipotoxicity-Induced Mitochondrial Damage
<p>The files contain all the dataset included in the manuscript divided by figures.</p> <p> </p> <p>Abstract: Sirtuin 3 (SIRT3) is the primary mitochondrial deacetylase that controls the antioxidant<br>pathway and energy metabolism. We previously found that renal Sirt3 expression and activity were<br>reduced in mice with type 2 diabetic nephropathy associated with oxidative stress and mitochondrial<br>abnormalities and that a specific SIRT3 activator improved renal damage. SIRT3 is modulated by<br>diet, and to assess whether Sirt3 deficiency aggravates mitochondrial damage and accelerates kidney<br>disease in response to nutrient overloads, wild-type (WT) and Sirt3-/- mice were fed a high-fat-diet<br>(HFD) or standard diet for 8 months. Sirt3-/- mice on HFD exhibited earlier and more severe<br>albuminuria compared to WT mice, accompanied by podocyte dysfunction and glomerular capillary<br>rarefaction. Mesangial matrix expansion, tubular vacuolization and inflammation, associated with<br>enhanced lipid accumulation, were more evident in Sirt3-/- mice. After HFD, kidneys from Sirt3-/-<br>mice showed more oxidative stress than WT mice, mitochondria ultrastructural damage in tubular<br>cells, and a reduction in mitochondrial mass and energy production. Our data demonstrate that Sirt3<br>deficiency renders mice more prone to developing oxidative stress and mitochondrial abnormalities<br>in response to HFD, resulting in more severe kidney diseases, and this suggests that mitochondria<br>protection may be a method to prevent HFD-induced renal injury.</p>
Fats test parasitoids
<p>Data base of fast test parasitoids</p>
Manipulation of photoperiod induces fat storage, but not fat mobilization in the migratory songbird, Dumetella carolinensis (Gray Catbird) 1.
<p>Datasets for "Manipulation of photoperiod induces fat storage, but not fat mobilization in the migratory songbird, Dumetella carolinensis (Gray Catbird)" publication in the Journal of Comparative Physiology B.</p>
Structural Fat Grafting for Craniofacial Trauma Using Manual Technique for Processing Fat Graft Material
ClinicalTrials.gov study NCT02267187. IPD Sharing: YES. Countries: 1. Publications: 1.
Study to Explore the Effect of Secukinumab, Compared to Placebo, on Fat Tissue and Skin in Plaque Psoriasis Patients
ClinicalTrials.gov study NCT03055494. IPD Sharing: UNDECIDED. Countries: 1. Publications: 0.
Liver and Fat Regulation in Overweight Adolescent Girls
ClinicalTrials.gov study NCT02157974. IPD Sharing: NO. Countries: 1. Publications: 2.
Clinical Effectiveness of Body Fat Distribution Imaging in Real-World Practice: The BODY-REAL Study
ClinicalTrials.gov study NCT04763772. IPD Sharing: YES. Countries: 1. Publications: 1.
Infection-nutrition feedbacks: fat supports pathogen clearance but pathogens reduce fat in a wild mammal
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Fat storage influences fasting endurance more than body size in an ungulate
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Data from: Spatial sorting caused by downstream dispersal: Implication for morphological evolution in isolated populations of fat minnow inhabiting small streams flowing through terraced rice paddies
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Allen Brain Atlas
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International Brain Laboratory public data
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