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高脂饮食联合低剂量链脲佐菌素注射可诱导猕猴发生代谢综合征。

High-fat diet combined with low-dose streptozotocin injections induces metabolic syndrome in Macaca mulatta.

作者信息

Li Linzhao, Liao Guangneng, Yang Guang, Lu Yanrong, Du Xiaojiong, Liu Jingping, Li Lan, Wang Chengshi, Li Li, Ren Yan, Zhong Zhihui, Cheng Jingqiu, Chen Younan

机构信息

Key Laboratory of Transplant Engineering and Immunology, NHFPC, Regenerative Medicine Research Center, West China Hospital, Sichuan University, No. 1, Ke yuan 4th Road, Gao Peng Street, Chengdu, 610041, Sichuan, People's Republic of China.

出版信息

Endocrine. 2015 Aug;49(3):659-68. doi: 10.1007/s12020-015-0542-9. Epub 2015 Feb 12.

Abstract

Metabolic syndrome (MetS) is associated with abdominal obesity, hyperlipidemia, insulin resistance, and type 2 diabetes mellitus, and increases the risk of cardiovascular disease. Given the complex multifactorial pathogenesis of MetS, qualified animal models are currently seriously limited for researchers. The aim of our study was to develop a MetS model in juvenile rhesus monkeys (Macaca mulatta). Rhesus monkeys (1-year-old) fed a high-fat diet (15 % fat, 2 % cholesterol) were used as the HF group (n = 6), and those on a normal diet (5 % fat) were used as the control group (n = 4). After being fed a high-fat diet for approximately 12 months, 2 monkeys (HF + STZ group) were injected with low-dose streptozotocin (STZ, 25 mg/kg) twice, with a 7 days interval, and were then fed the same diet continuously for another 24 months. After 36 months of treatment, the high-fat diet monkeys, including the HF and HF + STZ groups, had acquired increased body weights, abnormal serum lipids, and impaired glucose tolerance compared to the control group. In addition, much more marked metabolic changes were observed in the two monkeys of the HF + STZ group, particularly in terms of high-blood glucose level and insulin resistance. Morphological observation of biopsies of liver and pancreatic tissues showed decreased islet number and mass and decreased insulin staining in the monkeys of the HF + STZ group. In addition, Oil red O staining suggested remarkable accumulation of lipid droplets in the hepatocytes. Our study suggested that a long-term high-fat diet followed with a low-dose STZ was able to induce MetS in juvenile rhesus monkeys with faster pathophysiological progress compared with high-fat diet induction alone. Our primary data showed that this method may have potentials to develop MetS animal model in non-human primates.

摘要

代谢综合征(MetS)与腹型肥胖、高脂血症、胰岛素抵抗和2型糖尿病相关,并增加心血管疾病风险。鉴于MetS复杂的多因素发病机制,目前合格的动物模型严重限制了研究人员的研究。我们研究的目的是在幼年恒河猴(猕猴)中建立一个MetS模型。将喂食高脂饮食(15%脂肪,2%胆固醇)的1岁恒河猴用作高脂组(n = 6),将喂食正常饮食(5%脂肪)的恒河猴用作对照组(n = 4)。在喂食高脂饮食约12个月后,2只猴子(高脂+链脲佐菌素组)每隔7天注射两次低剂量链脲佐菌素(STZ,25 mg/kg),然后继续喂食相同饮食24个月。治疗36个月后,与对照组相比,包括高脂组和高脂+链脲佐菌素组在内的高脂饮食猴子体重增加、血脂异常且糖耐量受损。此外,在高脂+链脲佐菌素组的两只猴子中观察到更明显的代谢变化,特别是在高血糖水平和胰岛素抵抗方面。肝脏和胰腺组织活检的形态学观察显示,高脂+链脲佐菌素组猴子的胰岛数量和质量减少,胰岛素染色减弱。此外,油红O染色表明肝细胞中脂滴明显积累。我们的研究表明,与单独的高脂饮食诱导相比,长期高脂饮食后给予低剂量STZ能够在幼年恒河猴中诱导MetS,且病理生理进展更快。我们的原始数据表明,这种方法可能有潜力在非人类灵长类动物中建立MetS动物模型。

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