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糖尿病高血压大鼠内皮素-1 的肾和全身效应。

Renal and systemic effects of endothelin-1 in diabetic-hypertensive rats.

机构信息

Hypertension Research Unit, Department of Physiology and Pharmacology, Sackler School of Medicine, Tel Aviv University, Israel.

出版信息

Clin Exp Hypertens. 2011;33(7):444-54. doi: 10.3109/10641963.2010.549270. Epub 2011 Sep 20.

Abstract

The Cohen-Rosenthal Diabetic Hypertensive rat (CRDH) is a unique animal model in which genetic hypertension and diabetes developed after crossbreeding of Cohen diabetic rats sensitive substrain (CDR) and spontaneously hypertensive rats (SHR). The present study examined: 1) The acute effects of ET-1 on the systemic and renal hemodynamics in CRDH rats, CDR, and SHR; 2) The expression of ET-1 and its receptors in the renal tissue of CRDH rats. Intravenous injection of ET-1 (1.0 nmol/kg) into anesthetized SHR rats resulted in a significant immediate depressor response (mean arterial pressure (MAP) decreased from 165 ± 3 to 124 ± 12 mmHg, p < 0.0001) followed by a minor hypertensive phase (MAP increased to 170 ± 2 mmHg). Simultaneously, the administration of ET-1 caused a significant decrease in renal blood flow (RBF) from 5.8 ± 0.9 ml/min to 3.2 ± 0.5 ml/min (p = 0.026). These responses were blunted in CRDH rats and CDR. Analysis of intra-renal blood flow by laser-Doppler in CRDH rats revealed that ET-1 injection caused a decrease in cortical blood flow (Δ = -12 ± 2.9%). However, in contrast to its well-known renal medullary vasodilatory effect, ET-1 produced a significant decline in the medulla blood flow (Δ = -17.5 ± 3.4%) (p = 0.0125). These findings suggest that CDR and CRDH rats have reduced sensitivity to vascular and renal action of ET-1. Furthermore, in the CRDH rats, the expected ET-1-induced medullary vasodilatation was abolished and even reversed into prolonged vasoconstriction.

摘要

科恩-罗森塔尔糖尿病高血压大鼠(CRDH)是一种独特的动物模型,通过将糖尿病敏感亚系的科恩大鼠(CDR)和自发性高血压大鼠(SHR)杂交,导致遗传高血压和糖尿病的发展。本研究检查了:1)ET-1 对 CRDH 大鼠、CDR 和 SHR 全身和肾脏血液动力学的急性影响;2)CRDH 大鼠肾脏组织中 ET-1 及其受体的表达。静脉注射 ET-1(1.0 nmol/kg)到麻醉的 SHR 大鼠中,导致显著的即时降压反应(平均动脉压(MAP)从 165±3 降至 124±12 mmHg,p<0.0001),随后出现轻度高血压阶段(MAP 增加到 170±2 mmHg)。同时,ET-1 的给药导致肾血流量(RBF)从 5.8±0.9 ml/min 显著下降至 3.2±0.5 ml/min(p=0.026)。这些反应在 CRDH 大鼠和 CDR 中被减弱。在 CRDH 大鼠中通过激光多普勒分析肾内血流,发现 ET-1 注射导致皮质血流减少(Δ=-12±2.9%)。然而,与它众所周知的肾髓质血管扩张作用相反,ET-1 导致髓质血流显著下降(Δ=-17.5±3.4%)(p=0.0125)。这些发现表明 CDR 和 CRDH 大鼠对 ET-1 的血管和肾脏作用的敏感性降低。此外,在 CRDH 大鼠中,预期的 ET-1 诱导的髓质血管扩张被消除,甚至逆转成长期的血管收缩。

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