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Journal: Heliyon
Article Title: Obesity alters adipose tissue response to fasting and refeeding in women: A study on lipolytic and endocrine dynamics and acute insulin resistance
doi: 10.1016/j.heliyon.2024.e37875
Figure Lengend Snippet: Key resources table
Article Snippet:
Techniques: Recombinant, Enzyme-linked Immunosorbent Assay, Software
Journal: Frontiers in Cardiovascular Medicine
Article Title: CTRP3 attenuates myocardial lipotoxicity via suppression of lipid accumulation, inflammation, apoptosis, and mitochondrial oxidative stress
doi: 10.3389/fcvm.2025.1575929
Figure Lengend Snippet: (A,B) Compared to the high-fat diet (HFD) group, supplementation with CTRP3 significantly improves cardiac function in mice, as evidenced by enhanced left ventricular ejection fraction. (C,D) Histological examination of myocardial tissue reveals substantial lipid droplet accumulation in the HFD group. However, CTRP3 supplementation reduces lipid droplet accumulation, improves myocardial tissue structure, and alleviates the degree of fibrosis. (E–M) Immunofluorescence results indicate that CTRP3 supplementation mitigates myocardial inflammation, apoptosis, and oxidative stress in mice. (N–Q) Serum ELISA assays demonstrate that levels of triglycerides (TG), total cholesterol (TCHO), inflammatory markers, apoptotic factors, and oxidative stress indicators are significantly improved in the CTRP3 group compared to the HFD group ( n ≥ 3, p < 0.05).
Article Snippet: The
Techniques: Immunofluorescence, Enzyme-linked Immunosorbent Assay
Journal: Frontiers in Cardiovascular Medicine
Article Title: CTRP3 attenuates myocardial lipotoxicity via suppression of lipid accumulation, inflammation, apoptosis, and mitochondrial oxidative stress
doi: 10.3389/fcvm.2025.1575929
Figure Lengend Snippet: (A–F) Lipid testing results demonstrate that palmitic acid (PA) induces lipid accumulation in myocardial cells, while CTRP3 supplementation significantly reduces lipid droplet accumulation. (G) CTRP3 intervention improves the expression of genes related to fatty acid uptake, fatty acid oxidation, and lipid efflux in myocardial cells ( n ≥ 3, p < 0.05). (H) Quantitative PCR (q-PCR) results indicate that CTRP3 mitigates inflammation, apoptosis, and oxidative stress in myocardial cells stimulated by PA ( n ≥ 3, p < 0.05).
Article Snippet: The
Techniques: Expressing, Real-time Polymerase Chain Reaction
Journal: Frontiers in Cardiovascular Medicine
Article Title: CTRP3 attenuates myocardial lipotoxicity via suppression of lipid accumulation, inflammation, apoptosis, and mitochondrial oxidative stress
doi: 10.3389/fcvm.2025.1575929
Figure Lengend Snippet: (A–E) RNA sequencing analysis of myocardial tissue from the control group, HFD group, and CTRP3 group indicates that CTRP3 likely exerts its effects within myocardial mitochondria, playing a role in the metabolic regulation of myocardial lipotoxicity.
Article Snippet: The
Techniques: RNA Sequencing, Control
Journal: Frontiers in Cardiovascular Medicine
Article Title: CTRP3 attenuates myocardial lipotoxicity via suppression of lipid accumulation, inflammation, apoptosis, and mitochondrial oxidative stress
doi: 10.3389/fcvm.2025.1575929
Figure Lengend Snippet: (A,B) JC-1 staining results demonstrate a decrease in mitochondrial membrane potential in myocardial cells of the PA group. (C,D) Mito-Tracker staining results show a reduction in mitochondrial number in the PA group. (E) PA intervention in myocardial cells leads to decreased ATP production, while CTRP3 intervention improves ATP generation. (F) Transmission electron microscopy reveals increased mitochondrial damage and autophagy in myocardial cells following PA intervention. CTRP3 can mitigate mitochondrial damage and autophagy in myocardial cells.
Article Snippet: The
Techniques: Staining, Membrane, Transmission Assay, Electron Microscopy
Journal: Heliyon
Article Title: Bezafibrate alleviates diabetes-induced spermatogenesis dysfunction by inhibiting inflammation and oxidative stress
doi: 10.1016/j.heliyon.2024.e28284
Figure Lengend Snippet: Adipokines variation of DM mice after bezafibrate treatment . (A) The body weight of the mice in the indicated groups (n = 6). (B) Plasma TG levels (n = 6). (C) Plasma NEFA levels (n = 6). (D) Blood glucose levels (n = 6). (E) Percentage of HbA1C (n = 6). (F) Blood insulin levels (n = 6). (G) Plasma and testis leptin levels (n = 6). (H) Plasma and testis adiponectin levels (n = 6). (I) Plasma and testis irisin levels (n = 6). (J) Plasma and testis CTRP3 levels (n = 6). Data are presented as the mean ± SD. For A to D, the statistical analysis was carried out by one-way ANOVA. * P < 0.05 vs the matched control.
Article Snippet: The
Techniques: Clinical Proteomics, Control