Pentacyclic triterpenes: New tools to fight metabolic syndrome

代谢综合征 胰岛素抵抗 脂肪生成 熊果酸 脂肪生成 曲格列酮 氧化应激 药理学 内分泌学 内科学 医学 化学 生物化学 胰岛素 糖尿病 脂质代谢 脂肪组织 过氧化物酶体增殖物激活受体 受体 色谱法
作者
Munish Garg,Pushpander Kumar,Rahul Deshmukh,Anupam Bishayee,Sunil Kumar
出处
期刊:Phytomedicine [Elsevier]
卷期号:50: 166-177 被引量:85
标识
DOI:10.1016/j.phymed.2018.09.011
摘要

Metabolic syndrome is a combination of dysregulated cardiometabolic risk factors characterized by dyslipidemia, impaired glucose tolerance, insulin resistance, inflammation, obesity as well as hypertension. These factors are tied to the increased risk for type-II diabetes and cardiovascular diseases including myocardial infarction in patients with metabolic syndrome.To review the proposed molecular mechanisms of pentacyclic triterpenes for their potential use in the metabolic syndrome.PubMed, Science Direct, and Google Scholar database were searched from commencement to April 2018. Following keywords were searched in the databases with varying combinations: "metabolic syndrome", "pentacyclic triterpenes", "transcription factors", "protein kinase", "lipogenesis", "adipogenesis", "lipolysis", "fatty acids", "gluconeogenesis", "cardiovascular", "mitochondria", "oxidative stress", "pancreas", "hepatic cells", "skeletal muscle", "3T3-L1", "C2C12", "obesity", "inflammation", "insulin resistance", "glucose uptake", "clinical studies" and "bioavailability".Pentacyclic triterpenes, such as asiatic acid, ursolic acid, oleanolic acid, 18β-glycyrrhetinic acid, α,β-amyrin, celastrol, carbenoxolone, corosolic acid, maslinic acid, bardoxolone methyl and lupeol downregulate several metabolic syndrome components by regulating transcription factors, protein kinases and enzyme involved in the adipogenesis, lipolysis, fatty acid oxidation, insulin resistance, mitochondria biogenesis, gluconeogenesis, oxidative stress and inflammation.In vitro and in vivo studies suggests that pentacyclic triterpenes effectively downregulate various factors related to metabolic syndrome. These phytochemicals may serve as promising candidates for clinical trials for the management of metabolic syndrome.
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