Amomum villosum Lour. Fruit extract mitigates hyperlipidemia through SREBP-2/LDLR/HMGCR signaling in high-cholesterol diet-fed mice

辛伐他汀 高脂血症 低密度脂蛋白受体 胆固醇 化学 内分泌学 内科学 HMG-CoA还原酶 甾醇 还原酶 生物 医学 生物化学 脂蛋白 糖尿病
作者
Ye-Seul Kim,Ha-Rim Kim,Paulrayer Antonisamy,Young‐Rae Lee,Guemsan Lee,Hyun-Jong Jung,Kang‐Beom Kwon
出处
期刊:Journal of King Saud University - Science [Elsevier BV]
卷期号:34 (7): 102230-102230 被引量:5
标识
DOI:10.1016/j.jksus.2022.102230
摘要

Amomum villosum Lour. (Zingiberaceae) is an herbal medicine used in Asian countries for various ailments. In the current experiment, the effect of AV water extract (AVE) on cholesterol-lowering capabilities along with its essential bio-molecular mechanisms have been examined. The efficiency of AVE against high-cholesterol diet (HCD)-generated hyperlipidemia was investigated using C57BL/6 mice. Mice have been divided to six categories: control group (normal diet), high-cholesterol diet (HCD), and HCD treated with AVE at 100, 200, and 500 mg/kg, or simvastatin 40 mg/kg for four weeks. AVE treated animal groups (100, 200, 500 mg/kg) had markedly lessened body mass increase ( p < 0.01) and also had reduced liver and epididymal fat weights ( p < 0.05) related to HCD alone batch. Hepatic TG levels in AVE 100 mg/kg, 200 mg/kg, and 500 mg/kg treated groups were meaningfully reduced by 13.32%, 14.61%, and 21.78%, respectively; and serum TG decreased by 25.65%, 31.97%, and 32.22%, respectively, compared to the HCD alone group. Serum TC was reduced by 11.17%, 12.48%, and 26.85% with AVE at 100, 200, and 500 mg/kg, respectively; and serum LDL-C declined by 10.08%, 18.50%, and 30.90% ( p < 0.05) with AVE at 100, 200, and 500 mg/kg, respectively. Levels of mRNA expression including LDL receptor (LDLR), sterol regulatory element-binding protein 2 (SREBP2), and HMG-CoA reductase (HMGCR) were noticeably amplified by AVE (500 mg/kg) treatment. Similarly, AVE treatment significantly increased Hmgcr protein expression levels in a dose related fashion. These outcomes show that AVE displays a hypolipidemic effect and might function as a novel hypolipidemic therapy, further; they suggest a mechanism of action for this effect.
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