Xia Chen, Lin Zou, Yingxuan Li, Li Peng, Xing Wang, Qian Xi, Fei Sun, Junhua Ma
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引用次数: 0
摘要
褐色脂肪组织(BAT)是治疗肥胖的理想靶器官。Resinacein S从灵芝中提取,可提高细胞解偶联蛋白1 (Uncoupling protein 1, UCP1)水平,但在动物水平上的相关作用尚不清楚。采用高脂饲料建立肥胖模型,并用树脂蛋白酶s处理小鼠,测定空腹血糖和胰岛素浓度。通过注射葡萄糖和胰岛素记录血糖变化,并记录冷刺激时的体温变化。对BAT称重,HE染色。采用试剂盒检测血脂代谢指标,检测UCP1水平。树脂蛋白酶S能改善小鼠肥胖,降低体重、脂肪重量、脂肪细胞直径和大小,降低空腹血糖,改善血脂异常、高胰岛素血症和胰岛素抵抗,增强对冷刺激的耐受性。敲除UCP1后,小鼠体重和血糖升高,血脂紊乱加重,产热和BAT活性降低,而树脂蛋白酶S上调UCP1水平,激活BAT活性。Resinacein S可以通过上调UCP1表达激活BAT活性来改善小鼠肥胖。
Resinacein S ameliorates the obesity in mice via activating the brown adipose tissue.
Brown adipose tissue (BAT) is an ideal target organ for obesity treatment. Resinacein S is extracted from Ganoderma lucidum and can elevate Uncoupling protein 1 (UCP1) in cells, but its related effects at the animal level are not clear. The mice were fed with high-fat diet to construct obesity models and treated with Resinacein S. Fasting blood glucose and insulin concentrations were measured. The blood glucose changes were recorded by injection of glucose and insulin and the body temperature during cold stimulation were recorded. BAT was weighed and stained with HE. The blood lipid metabolism indexes were detected by kits and the UCP1 level was tested. Resinacein S could improve the obesity of mice, lower the body weight, fat weight, fat cell diameter and size, reduce fasting blood glucose, improve dyslipidemia, hyperinsulinemia and insulin resistance, enhance the tolerance to cold stimulation. After UCP1 knocking out, the body weight and blood glucose levels were raised, the blood lipid disorder was aggravated and the heat production and BAT activity of mice were decreased, while Resinacein S up-regulated UCP1 level and activate BAT activity. Resinacein S can improve obesity in mice by up-regulating UCP1 expression to activate BAT activity.
期刊介绍:
Pakistan Journal of Pharmaceutical Sciences (PJPS) is a peer reviewed multi-disciplinary pharmaceutical sciences journal. The PJPS had its origin in 1988 from the Faculty of Pharmacy, University of Karachi as a biannual journal, frequency converted as quarterly in 2005, and now PJPS is being published as bi-monthly from January 2013.
PJPS covers Biological, Pharmaceutical and Medicinal Research (Drug Delivery, Pharmacy Management, Molecular Biology, Biochemical, Pharmacology, Pharmacokinetics, Phytochemical, Bio-analytical, Therapeutics, Biotechnology and research on nano particles.