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抗 TNF-α 剂罗望子 Kunitz 胰蛋白酶抑制剂可改善表现出血脂异常和饮食诱导肥胖的 Wistar 大鼠的脂质谱,而与 PPAR-γ 诱导无关。

Anti-TNF-α Agent Tamarind Kunitz Trypsin Inhibitor Improves Lipid Profile of Wistar Rats Presenting Dyslipidemia and Diet-induced Obesity Regardless of PPAR-γ Induction.

机构信息

Biochemistry Postgraduate Program, Biosciences Center, Federal University of Rio Grande do Norte, Natal, RN 59078-970, Brazil.

Nutrition Postgraduate Program, Center for Health Sciences, Federal University of Rio Grande do Norte, Natal, RN 59078-970, Brazil.

出版信息

Nutrients. 2019 Feb 27;11(3):512. doi: 10.3390/nu11030512.

DOI:10.3390/nu11030512
PMID:30818882
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6470745/
Abstract

The increasing prevalence of obesity and, consequently, chronic inflammation and its complications has increased the search for new treatment methods. The effect of the purified tamarind seed trypsin inhibitor (TTIp) on metabolic alterations in Wistar rats with obesity and dyslipidemia was evaluated. Three groups of animals with obesity and dyslipidemia were formed, consuming a high glycemic index and glycemic load (HGLI) diet, for 10 days: Obese/HGLI diet; Obese/standard diet; Obese/HGLI diet + TTIp (730 μg/kg); and one eutrophic group of animals was fed a standard diet. Rats were evaluated daily for food intake and weight gain. On the 11th day, animals were anesthetized and sacrificed for blood and visceral adipose tissue collection. TTIp treated animals presented significantly lower food intake than the untreated group (p = 0.0065), TG (76.20 ± 18.73 mg/dL) and VLDL-C (15.24 ± 3.75 mg/dL). Plasma concentrations and TNF-α mRNA expression in visceral adipose tissue also decreased in obese animals treated with TTIp (p < 0.05 and p = 0.025, respectively) with a negative immunostaining. We conclude that TTIp presented anti-TNF-α activity and an improved lipid profile of Wistar rats with dyslipidemia and obesity induced by a high glycemic index and load diet regardless of induction.

摘要

肥胖症的患病率不断上升,随之而来的慢性炎症及其并发症也有所增加,这促使人们寻求新的治疗方法。本研究评估了纯化罗望子种子胰蛋白酶抑制剂(TTIp)对高血糖指数和高血糖负荷(HGLI)饮食诱导肥胖和血脂异常 Wistar 大鼠代谢改变的影响。将三组肥胖和血脂异常的动物分为以下几类:食用高血糖指数和高血糖负荷饮食(HGLI) 10 天的肥胖/HGLI 饮食组、肥胖/标准饮食组、肥胖/HGLI 饮食+TTIp(730 μg/kg)组;以及一组食用标准饮食的正常营养状态的动物作为对照组。每天评估大鼠的食物摄入量和体重增加情况。第 11 天,麻醉并处死动物以收集血液和内脏脂肪组织。与未治疗组相比,TTIp 治疗组的动物食物摄入量显著降低(p = 0.0065),甘油三酯(TG)(76.20 ± 18.73 mg/dL)和极低密度脂蛋白胆固醇(VLDL-C)(15.24 ± 3.75 mg/dL)也有所降低。经 TTiP 治疗的肥胖动物的血浆浓度和内脏脂肪组织中 TNF-α mRNA 表达也降低(p < 0.05 和 p = 0.025),且免疫组织化学染色呈阴性。我们的结论是,TTiP 具有抗 TNF-α 活性,并能改善高血糖指数和负荷饮食诱导的肥胖和血脂异常 Wistar 大鼠的血脂谱,而与诱导因素无关。

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J Enzyme Inhib Med Chem. 2019 Dec;34(1):405-419. doi: 10.1080/14756366.2018.1542387.
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Obes Facts. 2018;11(6):440-453. doi: 10.1159/000492733. Epub 2018 Dec 11.
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Microvascular Endothelial Dysfunction in Human Obesity: Role of TNF-α.
炎症介质在肥胖发病机制中的作用。
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Effect of dipeptidyl peptidase-4 inhibitors on tumor necrosis factor alpha levels in patients with type 2 diabetes mellitus.二肽基肽酶-4 抑制剂对 2 型糖尿病患者肿瘤坏死因子-α水平的影响。
Eur J Med Res. 2024 Jul 12;29(1):363. doi: 10.1186/s40001-024-01955-9.
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