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Isoliquiritigenin Inhibits Atherosclerosis by Blocking TRPC5 Channel Expression
Jie Qi1, Jianguo Cui1, Baobin Mi1
1Department of Geriatrics, Binzhou Medical University Hospital, No. #661 Yellow River Road No. 2, Binzhou, Shandong 256603, China.
Isoliquiritigenin (ISL), a licorice flavonoid, shows potential in preventing atherosclerosis. It reduced arterial plaque and improved lipid levels in mice by inhibiting TRPC5 expression.
Area of Science:
- Pharmacology
- Cardiovascular Science
- Natural Products
Background:
- Isoliquiritigenin (ISL) is a flavonoid from licorice with known anticancer, anti-inflammatory, antioxidant, and antidiabetic properties.
- The therapeutic potential of ISL in treating atherosclerosis remains largely unexplored.
- Atherosclerosis is a chronic inflammatory disease characterized by plaque buildup in arteries.
Purpose of the Study:
- To investigate the pharmacological effects of ISL on atherosclerosis.
- To elucidate the mechanism by which ISL inhibits atherosclerosis progression.
- To evaluate ISL's impact on vascular smooth muscle cell proliferation and related molecular pathways.
Main Methods:
- Utilized apolipoprotein E (ApoE) knockout mouse model for in vivo studies.
- Employed angiotensin II (Ang II)-stimulated vascular smooth muscle cells (VSMCs) for in vitro experiments.
- Assessed atherosclerotic lesion size, serum lipid profiles, and expression of TRPC5 and PCNA.
Main Results:
- ISL treatment attenuated atherosclerotic lesions and reduced serum lipid levels in ApoE knockout mice.
- ISL inhibited Ang II-induced proliferation of VSMCs in a dose-dependent manner.
- ISL suppressed Ang II-induced expression of TRPC5 and PCNA in VSMCs.
Conclusions:
- ISL demonstrates significant inhibitory effects against atherosclerosis.
- ISL's mechanism involves the inhibition of TRPC5 expression and VSMC proliferation.
- ISL holds promise as a therapeutic agent for cardiovascular protection against atherosclerosis.
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