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血管紧张素转化酶抑制作用可增加急性束缚应激时葡萄糖诱导的胰岛素分泌。

Angiotensin-converting enzyme inhibition increases glucose-induced insulin secretion in response to acute restraint.

机构信息

Laboratory of Endocrinology, Department of Internal Medicine, Belo Horizonte, Minas Gerais, Brazil.

出版信息

Clin Exp Pharmacol Physiol. 2012 Dec;39(12):1034-7. doi: 10.1111/1440-1681.12021.

Abstract

There is increasing evidence suggesting involvement of the renin-angiotensin system (RAS) in carbohydrate metabolism and its response to stress. Thus, the aim of the present study was to evaluate the effects of chronic inhibition of the RAS on glucose and insulin levels during acute restraint stress. Male Holtzman rats were treated with 10 mg/kg per day enalapril solution or vehicle for 14 days. After 14 days, rats were divided into three experimental groups: enalapril + restraint (ER), vehicle + restraint (VR) and enalapril + saline (ES). Rats in the restraint groups were subjected to 30 min restraint stress, whereas rats in the ES groups were given saline infusion instead. Blood samples were collected at baseline and after 5, 10, 20 and 30 min restraint stress or saline infusion. After restraint, a hyperglycaemic response was observed in the ER and VR groups that peaked at 20 and 10 min, respectively (P < 0.05 compared with baseline). The area under the glucose curve was markedly increased in the ER and VR groups compared with that in the ES group (P < 0.05 for both). Importantly, restraint induced a marked increase in insulin secretion in the ER group compared with only a mild elevation in the VR group; insulin secretion in both groups peaked at 20 min (P < 0.05 compared with baseline). Analysis of the area under the insulin curve confirmed an increase in insulin secretion in the ER compared with the VR and ES groups (P < 0.05 for both). The results of the present study reinforce that the RAS is involved in modulating responses to stress and suggest that RAS inhibition with enalapril may increase glucose-induced insulin secretion in response to acute restraint.

摘要

有越来越多的证据表明肾素-血管紧张素系统(RAS)参与碳水化合物代谢及其对应激的反应。因此,本研究旨在评估慢性抑制 RAS 对急性束缚应激时血糖和胰岛素水平的影响。雄性霍茨曼大鼠每天用 10mg/kg 的依那普利溶液或载体处理 14 天。14 天后,大鼠分为三组:依那普利+束缚(ER)、载体+束缚(VR)和依那普利+盐水(ES)。束缚组大鼠接受 30 分钟束缚应激,而 ES 组大鼠给予盐水输注。在基线和束缚或盐水输注后 5、10、20 和 30 分钟采集血样。束缚后,ER 和 VR 组大鼠出现高血糖反应,分别在 20 和 10 分钟达到峰值(与基线相比,P<0.05)。ER 和 VR 组的血糖曲线下面积明显大于 ES 组(均 P<0.05)。重要的是,与 VR 组相比,束缚应激诱导 ER 组胰岛素分泌明显增加,而 VR 组仅轻度升高;两组胰岛素分泌均在 20 分钟达到峰值(与基线相比,P<0.05)。胰岛素曲线下面积分析证实,与 VR 和 ES 组相比,ER 组胰岛素分泌增加(均 P<0.05)。本研究结果进一步证实 RAS 参与调节对应激的反应,并表明依那普利抑制 RAS 可能增加急性束缚应激时葡萄糖诱导的胰岛素分泌。

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