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Role of α1 adrenoceptor subtypes in renal haemodynamics in heart failure and diabetic SD rats

机译:α1肾上腺素受体亚型在心力衰竭和糖尿病SD大鼠肾血流动力学中的作用

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Diabetes has been declared as one of the major global health hazards by the WHO and it leads to renal, cardiac and nervous tissue complications. Therefore, the present study was designed to examine the specific subclass of α adrenoceptors that are involved in the regulation of renal haemodynamics in diabetes and cardiac failure induced SD rats. Diabetes was induced by a single dose of streptozotocin (55mg/kg IP). Cardiac failure was induced by the combined treatment of caffeine and isoprenaline for seven days. On day eight the animals were anaesthetized by pentobarbitone sodium and the left kidney was exposed. The renal artery was cleared and electromagnetic flow probe was placed on it for renal blood flow (RBF) measurement. The left iliac artery was cannulated for the infusion of saline and all drugs. The renal nerves were stimulated by bipolar electrodes. The reduction in RBF to electrical nerve stimulation (1-10 Hz), bolus doses of noradrenaline (25-200 ng), phenylephrine (0.25-2.0 μ/kg) and methoxamine (1-4 μ/kg were determined before and after bolus doses of amlodipine (200 and 400 μ/kg), 5- methylurapidil (5 and 10 μ/kg), chloroethylclonidine (5 and 10 μ/kg) and BMY7378 (100 and 200 μ/kg). The results obtained indicated that the renal vasoconstrictor responses in this model were attenuated mainly by amlodipine, 5 methylurapidil and BMY7378 but not by chloroethylclonidine. The findings from this study suggest that α1A and α1D - adrenoceptors mediate the adrenergically induced renal vasoconstrictor responses in cardiac failure SD rats with diabetes.
机译:世卫组织已宣布糖尿病为全球主要健康危害之一,并导致肾脏,心脏和神经组织并发症。因此,本研究旨在检查参与糖尿病和心力衰竭诱发的SD大鼠肾血流动力学调节的α肾上腺素能受体的特定亚类。单剂量链脲佐菌素(55mg / kg IP)可诱发糖尿病。咖啡因和异丙肾上腺素联合治疗7天可导致心脏衰竭。在第八天,用戊巴比妥钠麻醉动物,并暴露左肾。清除肾动脉,并在其上放置电磁流量探针以测量肾血流量(RBF)。插入左动脉以注入盐水和所有药物。双极电极刺激肾神经。推注前后测定电神经刺激(1-10 Hz)的RBF减少,去甲肾上腺素(25-200 ng),去氧肾上腺素(0.25-2.0μ/ kg)和甲氧胺(1-4μ/ kg)的推注剂量剂量的氨氯地平(200和400μ/ kg),5-甲基尿嘧啶(5和10μ/ kg),氯乙基可乐定(5和10μ/ kg)和BMY7378(100和200μ/ kg)。该模型的肾血管收缩反应主要被氨氯地平,5甲基尿嘧啶和BMY7378减弱,但不被氯乙基可乐定减弱,该研究结果表明α1A和α1D-肾上腺素能受体介导肾上腺素诱导的心衰SD糖尿病大鼠肾血管收缩反应。

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