AI Article Synopsis
- The study aimed to evaluate how a specific extract protects against mitochondrial damage in mice with atherosclerosis, focusing on its chemical composition and efficacy using advanced analytical techniques.
- Results showed that the extract significantly boosted heart and mesenteric microcirculation, lowered harmful lipid levels, and enhanced ATP levels, indicating improved mitochondrial function and lipid metabolism.
- The mechanism behind these effects involves the PGC-1α/Sirt3/Epac1 signaling pathway, with the extract increasing beneficial protein markers while reducing those associated with cell death.
Article Abstract
Objective: To investigate the protective effect of the of extract on mitochondrial injury in AS mice and the underlying mechanism.
Methods: Firstly, Ultra-High performance liquid chromatography-quadrupole time-of-flight mass spectrometer (UPLC / Q-TOF-MS) was proposed to explore the chemical composition of extract. ApoE-/- mice were employed for in vivo experiments. The efficacy of extract was detected by B-ultrasound, Biochemical, Oil Red O staining, HE staining and Masson staining analysis. The molecular mechanism of extract in regulating mitochondrial energy metabolism for the treatment of atherosclerosis was elucidated after Monitoring System of Vascular Microcirculation and transmission electron microscopy. Use the corresponding reagent kit to detect ACTH level, CHRNα1 level and ATP level, and measure the expression levels of PGC-1α, Sirt3, Epac1, Caspase-3, and Caspase-9 through real-time qPCR, and Western blot.
Results: A total of 29 metabolites were newly discovered from KYXC using UPLC-MS. The drug had a significant positive effect on the growth of atherosclerotic plaque in mice. It also improved the microcirculation of the heart and mesentery, reduced the levels of CHOL, TG, and VLDL in the serum, and increased the levels of HDL-C to maintain normal lipid metabolism in the body. Additionally, it increased the levels of ATP, improved the ultrastructure of mitochondria to maintain mitochondrial energy metabolism, and increased the levels of T-SOD to combat oxidative stress of the organism. Furthermore, the drug significantly increased the mRNA and protein expression of PGC-1α and Sirt3 in aortic tissue, while decreasing the mRNA and protein expression of Epac1, Caspase-3, and Caspase-9.
Conclusion: This study has verified that the extract of is highly effective in enhancing atherosclerosis disease. The mechanism is suggested through the PGC-1α/Sirt3/Epac1 signaling pathway, which improves mitochondrial energy metabolism.
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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11611558 | PMC |
| http://dx.doi.org/10.3389/fphar.2024.1483518 | DOI Listing |
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