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Berberine inhibited carotid atherosclerosis through PI3K/AKTmTOR signaling pathway
1Department of Neurology, Affiliated Hospital of Shandong University of Traditional Chinese Medicine, Jinan City, Shandong Province, China.
Insights
Berberine (BBR) effectively reduces atherosclerosis in ApoE knockout mice by lowering lipids and improving vascular health. This natural compound may offer a new therapeutic option for preventing and treating atherosclerosis.
Area of Science:
- Cardiovascular Research
- Pharmacology
- Molecular Biology
Background:
- Atherosclerosis is a complex vascular disease driven by lipid disorders and inflammation.
- Current treatments for atherosclerosis have limitations, necessitating novel therapeutic agents.
- Berberine (BBR), a natural product, shows promise for anti-atherosclerosis effects, but its mechanism remains unclear.
Purpose of the Study:
- To investigate the mechanism by which Berberine (BBR) ameliorates carotid atherosclerosis in apolipoprotein E knockout (ApoE-/-) mice.
- To elucidate BBR's effects on lipid metabolism, vascular remodeling, and cellular processes in atherosclerosis.
Main Methods:
- ApoE-/- mice were fed a high-fat diet for 12 weeks to induce atherosclerosis.
- Mice were treated with Berberine (BBR) to evaluate its therapeutic effects.
- Serum lipid levels, intimal hyperplasia, and carotid lipid accumulation were assessed.
- The PI3K/AKT/mTOR signaling pathway, autophagy, cell proliferation, and apoptosis were analyzed.
Main Results:
- BBR treatment significantly reduced serum lipid levels in ApoE-/- mice.
- BBR improved intimal hyperplasia and reduced lipid accumulation in the carotid arteries.
- BBR modulated the PI3K/AKT/mTOR pathway, regulated autophagy, promoted cell proliferation, and inhibited apoptosis.
Conclusions:
- Berberine (BBR) effectively ameliorates carotid atherosclerosis in a mouse model.
- BBR exerts its protective effects by regulating lipid metabolism, vascular inflammation, and cellular signaling pathways.
- Berberine (BBR) represents a potential therapeutic candidate for atherosclerosis treatment.
Abstract:
Atherosclerosis, a multifactorial vascular disease resulting from lipid metabolism disorders, features chronic inflammatory damage resulting from endothelial dysfunction, which usually affects multiple arteries. The carotid artery is a common site for clinical atherosclerosis evaluation. The aortic root is the standard site for quantifying atherosclerosis in mice. Due to the adverse reactions of first-line drugs, it is necessary to discover new drugs to prevent and treat atherosclerosis. Berberine (BBR) is one of the most promising natural products derived from herbal medicine Coptidis Rhizoma (Huanglian) that features significant anti-atherosclerosis properties. However, overall BBR mechanism against carotid atherosclerosis has not been clearly discovered. Our work aimed to investigate potential BBR mechanism in improving carotid atherosclerosis in ApoE knockout mice. Here, we proved that in ApoE -/- mice receiving high-fat diet for 12 weeks, BBR can reduce serum lipid levels, improve intimal hyperplasia, and antagonize carotid lipid accumulation, which may be achieved through regulating the PI3K/AKT/mTOR signaling pathway, regulating autophagy, promoting cell proliferation and inhibiting cell apoptosis. In summary, these data indicate that BBR can ameliorate carotid atherosclerosis. Therefore, it could be a promisingly therapeutic alternative for atherosclerosis.
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