阻断肾素血管紧张素系统可增加长期高脂饮食大鼠对stz诱导的糖尿病的抵抗力。

Experimental Diabetes Research Pub Date : 2012-01-01 Epub Date: 2012-11-12 DOI:10.1155/2012/618923
Xin Li, Li Yuan, Jin Li, Hailing Li, Suosuo Cheng
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引用次数: 14

摘要

本研究旨在探讨替米沙坦阻断肾素-血管紧张素系统(RAS)是否会增加胰岛素抵抗大鼠对链脲佐菌素(STZ-)诱导的糖尿病的抵抗。选用Wistar大鼠60只,分为正常对照组(NC)、高脂饮食组(HF)、高脂饮食+ STZ注射组(HF+S)、高脂饮食+ STZ注射+替米沙坦干预组(HF+S+T)。从NC组和HF组中随机选取5只大鼠进行高胰岛素正糖钳夹。从四组中随机选取5只大鼠分别进行静脉注射胰岛素释放试验(IVIRT),另外5只大鼠胰腺标本进行胰岛细胞免疫组化染色(胰岛素、NF-κB和caspase-3染色)、胰岛细胞凋亡染色和逆转录PCR (AT1R和IL-1 β)。HF+S+T组与HF+S组明显糖尿病发生率比较,差异有统计学意义(P < 0.05)。与HF+S组相比,HF+S+T组炎症标志物和胰岛细胞凋亡均显著减少(P < 0.01或P < 0.05)。总的来说,替米沙坦治疗的大鼠发现RAS活性降低,对stz诱导的糖尿病的抵抗力增加,炎症标志物减少,胰岛细胞功能和形态改善。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Blockade of renin angiotensin system increased resistance to STZ-induced diabetes in rats with long-term high-fat diet.

This study aimed to investigate whether rennin-angiotensin system (RAS) blockade through telmisartan would increase the resistance to streptozotocin- (STZ-) induced diabetes in insulin resistance rats. There were sixty Wistar rats that were divided into four groups: normal control (NC), high-fat diet (HF), high-fat diet plus STZ injection (HF+S), and high-fat diet plus STZ injection and telmisartan intervention (HF+S+T). Five rats were chosen randomly and respectively from groups NC and HF to undergo a hyperinsulinemic euglycemic clamp. Another five rats were selected randomly from the four groups, respectively, for intravenous injection insulin releasing test (IVIRT), and the other five rats for pancreas specimens used in islet cell immunohistochemistry staining (stained for insulin, NF-κB, and caspase-3), islet cell apoptosis staining, and reverse transcription PCR (AT1R and IL-1 beta). There was a significant difference of overt diabetes incidence between groups HF+S+T and HF+S (P < 0.05). Furthermore, inflammatory markers and islet cell apoptosis were found to be significantly reduced in group HF+S+T compared with group HF+S (all P < 0.01 or P < 0.05). Overall, telmisartan-treated rats were found to have reduced RAS activity, increased resistance to STZ-induced diabetes, reduced inflammatory markers, and improvement of islet cell function and morphology.

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Experimental Diabetes Research
Experimental Diabetes Research 医学-内分泌学与代谢
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