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[厄贝沙坦对糖尿病大鼠心肌中血管紧张素转换酶2表达的影响]

[Effect of irbesartan on ACE2 expression in diabetic rat myocardium].

作者信息

Hu Yuan-yuan, Shen Jie, Zhu Yan, Tang Jie-long, Liu Shuai

机构信息

Department of Endocrinology and Metabolism, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.

出版信息

Nan Fang Yi Ke Da Xue Xue Bao. 2010 Jun;30(6):1336-8.

Abstract

OBJECTIVE

To explore the effect of irbesartan on angiotensin-converting enzyme 2 (ACE2) mRNA expression in diabetic rat myocardium.

METHODS

Thirty 8-week-old male Wistar rats were randomly divided into control group (n=7), diabetic model group (n=14) and irbesartan group (n=9). Diabetes was induced by a single intraperitoneal injection of STZ (55 mg/kg), a blood glucose>16.7 mmol/L 72 h after the injection indicated successful establishment of diabetes. Four weeks after the modeling, the rats in irbesartan group were given 50 mg/kg irbesartan. ELISA was used to measure myocardial AngII content in the rats, and myocardial ACE2 mRNA expression was determined by real-time PCR.

RESULTS

Myocardial AngII level in the diabetic model group was significantly higher than that in the control group (P<0.001). Irbesartan administration significantly lowered cardiac AngII levels in the diabetic rats (P<0.001). The rats in irbesartan group showed significantly increased myocardial ACE2 mRNA expression compared with those in the control and diabetic rat groups (P<0.05).

CONCLUSION

Irbesartan can increase ACE2 mRNA expression in the myocardium, which might be one of the mechanisms underlying its effect in improving the cardiac function in diabetic rats.

摘要

目的

探讨厄贝沙坦对糖尿病大鼠心肌中血管紧张素转换酶2(ACE2)mRNA表达的影响。

方法

将30只8周龄雄性Wistar大鼠随机分为对照组(n = 7)、糖尿病模型组(n = 14)和厄贝沙坦组(n = 9)。通过单次腹腔注射链脲佐菌素(STZ,55 mg/kg)诱导糖尿病,注射后72小时血糖>16.7 mmol/L表明糖尿病模型建立成功。建模4周后,给厄贝沙坦组大鼠给予50 mg/kg厄贝沙坦。采用酶联免疫吸附测定法(ELISA)检测大鼠心肌血管紧张素II(AngII)含量,通过实时聚合酶链反应(real-time PCR)测定心肌ACE2 mRNA表达。

结果

糖尿病模型组心肌AngII水平显著高于对照组(P<0.001)。给予厄贝沙坦显著降低了糖尿病大鼠心脏AngII水平(P<0.001)。与对照组和糖尿病大鼠组相比,厄贝沙坦组大鼠心肌ACE2 mRNA表达显著增加(P<0.05)。

结论

厄贝沙坦可增加心肌中ACE2 mRNA表达,这可能是其改善糖尿病大鼠心脏功能作用的机制之一。

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