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Effects of antihypertensive drugs on angiotensinase activities in the testis of spontaneously hypertensive rats

机译:降压药对自发性高血压大鼠睾丸血管紧张素酶活性的影响

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Sexual dysfunction is a frequent adverse effect during antihypertensive therapy. However, the mechanisms responsible for these effects are not well understood. The renin-angiotensin system has been identified in testis where it may play a role in testicular function and be involved in the detrimental effects of antihypertensive drugs. Therefore, our objective was to compare the influence of captopril and propranolol on plasma testosterone levels and on hydrolyzing angiotensin's enzymes (angiotensinases) in the testis of spontaneously hypertensive rats (SHRs) and in control animals. Twenty-four adult male SHRs were used in this study; eight were treated with captopril in drinking water, 8 with propranolol, and 8 were controls. At the end of the 4 weeks treatment period, systolic blood pressure (SBP) was recorded, blood samples were collected, and the right testis was dissected after perfusion of the rat with saline. The soluble (Sol) and membrane-bound (MB) fractions were obtained after solubilization and ultracentrifugation. Fluorometric measurement of Sol and MB angiotensinase activities were performed using arylamide derivatives as substrates. Testosterone was measured by enzyme immunoassay. SBP decreased after captopril but did not change with propranolol treatment. Whereas captopril did not affect angiotensinase activities, highly significant reductions in Sol and MB angiotensinase activities, particularly glutamyl- and aspartyl-aminopeptidases, were observed after treatment with propranolol. Plasma testosterone decreased in captopril treated rats but propranolol had a greater effect. The present results support a general functional depression of the RAS cascade in the testis of propranolol-treated SHR, which may influence the sexual function of these animals.
机译:性功能障碍是抗高血压治疗期间的常见不良反应。但是,造成这些影响的机制还没有被很好地理解。肾素-血管紧张素系统已在睾丸中被发现,该系统可能在睾丸功能中起作用,并参与降压药的有害作用。因此,我们的目的是比较卡托普利和普萘洛尔对自发性高血压大鼠(SHRs)和对照动物的睾丸血浆睾丸激素水平和水解血管紧张素酶(血管紧张素酶)的影响。在这项研究中使用了二十四个成年男性SHR。八名患者在饮用水中接受卡托普利治疗,八名患者接受普萘洛尔治疗,而八名患者为对照组。在治疗的4周结束时,记录了收缩压(SBP),收集了血液样本,并在用盐水灌注大鼠后解剖了右睾丸。溶解和超速离心后获得可溶性(Sol)和膜结合(MB)级分。使用芳基酰胺衍生物作为底物进行Sol和MB血管紧张素酶活性的荧光测定。通过酶免疫测定法测定睾丸激素。卡托普利后SBP降低,但心得安治疗后SBP不变。尽管卡托普利不影响血管紧张素酶活性,但是在用心得安治疗后,Sol和MB血管紧张素酶活性特别是谷氨酰胺和天冬氨酰氨基肽酶的活性显着降低。在卡托普利治疗的大鼠中血浆睾丸激素降低,但普萘洛尔的作用更大。本结果支持普萘洛尔治疗的SHR的睾丸中RAS级联的一般功能降低,这可能会影响这些动物的性功能。

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