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Effect of exenatide on the cardiac expression of adiponectin receptor 1 and NADPH oxidase subunits and heart function in streptozotocin-induced diabetic rats

机译:艾塞那肽对链脲佐菌素致糖尿病大鼠心脏脂联素受体1和NADPH氧化酶亚基心脏表达及心脏功能的影响

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Background This study investigated the effect of exenatide on the cardiac expression of adiponectin receptor 1 and nicotinamide adenine dinucleotide phosphate (NADPH) oxidase subunits and heart function in streptozotocin-induced diabetic rats. Methods Male Sprague–Dawley rats were randomly divided into four groups, i.e. control group, diabetic group, diabetic treated with low doses of exenatide (2 μg?·?kg?1.d?1) and diabetic treated with high doses of exenatide (10 μg?·?kg?1.d?1). Diabetes was induced by intraperitoneal injection of streptozotocin (65 mg/kg body weight). At the termination after exenatide treatment for eight weeks, following anesthesia of the rats, a catheter was inserted into the left ventricle through the right common carotid artery for measurement of left ventricular pressure, which included left ventricular systolic pressure (LVSP), left ventricular end-diastolic pressure (LVEDP) and the maximal rate of rise and decline of ventricular pressure (±dp/dt[max]). Plasma and myocardial adiponectin levels, and the expressions of myocardial adiponectin receptor 1, p22phox, NADPH oxidase 4 (NOX4), glucose transporter type 4 (Glut4), AMPK-α, phosphorylated-AMPK-α, connective tissue growth factor (CTGF) and copper zinc superoxide dismutase (Cu-Zn-SOD) were assayed. Results Heart function, plasma adiponectin levels, the protein expression of myocardial phosphorylated-AMPK-α, the mRNA expression of myocardial Glut4, and the positive expression of myocardial Cu-Zn-SOD were significantly decreased in diabetic. The protein expression of myocardial adiponectin receptor 1, the mRNA expression of myocardial p22phox and NOX4, and the positive expression of myocardial CTGF were significantly increased in diabetic. Low and high doses of exenatide treatment significantly attenuated these changes in diabetic rats. Conclusions These results suggest that exenatide may contribute to the improvement of the heart function in diabetic rats by down-regulating the expression of myocardial adiponectin receptor 1, p22phox and NOX4, and up-regulating plasma adiponectin level and the expression of myocardial AMPK-α, Glut4 and Cu-Zn-SOD.
机译:背景本研究调查了艾塞那肽对链脲佐菌素诱导的糖尿病大鼠脂联素受体1和烟酰胺腺嘌呤二核苷酸磷酸(NADPH)氧化酶亚基心脏表达的影响以及心脏功能的影响。方法将雄性Sprague–Dawley大鼠随机分为四组,即对照组,糖尿病组,低剂量艾塞那肽(2μg··kg·kg·1.d?1)和高剂量艾塞那肽(2mg / kg·kg·1·d?1)。 10μg··kg·kg·1·d·1)。腹膜内注射链脲佐菌素(65 mg / kg体重)可诱发糖尿病。在艾塞那肽治疗八周后的终点处,在麻醉后,将导管通过右颈总动脉插入左心室以测量左心室压力,其中包括左心室收缩压(LVSP),左心室末端舒张压(LVEDP)和心室压的最大上升和下降速率(±dp / dt [max])。血浆和心肌脂联素水平,心肌脂联素受体1,p22phox,NADPH氧化酶4(NOX4),葡萄糖转运蛋白4型(Glut4),AMPK-α,磷酸化AMPK-α,结缔组织生长因子(CTGF)和测定铜锌超氧化物歧化酶(Cu-Zn-SOD)。结果糖尿病患者的心脏功能,血浆脂联素水平,心肌磷酸化AMPK-α蛋白表达,心肌Glut4 mRNA表达以及心肌Cu-Zn-SOD阳性表达均明显降低。糖尿病患者心肌脂联素受体1的蛋白表达,心肌p22phox和NOX4的mRNA表达以及心肌CTGF的阳性表达明显增加。低剂量和高剂量的艾塞那肽治疗显着减弱了糖尿病大鼠的这些变化。结论这些结果表明,艾塞那肽可能通过下调心肌脂联素受体1,p22phox和NOX4的表达,以及上调血浆脂联素水平和心肌AMPK-α的表达,从而改善糖尿病大鼠的心脏功能。 Glut4和Cu-Zn-SOD。

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