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内皮素3对经硝苯地平预处理前后的脊髓横断的Sprague-Dawley大鼠、Wistar Kyoto大鼠和自发性高血压大鼠舒张压的影响。

Effects of endothelin 3 on diastolic blood pressure of pithed Sprague-Dawley, Wistar Kyoto, and spontaneously hypertensive rats before and after pretreatment with nifedipine.

作者信息

Tabrizchi R, Triggle C R

机构信息

Division of Basic Medical Sciences, Faculty of Medicine, Memorial University of Newfoundland, St. John's, Canada.

出版信息

Can J Physiol Pharmacol. 1991 Apr;69(4):531-5. doi: 10.1139/y91-080.

Abstract

Pressor actions of endothelin 3 (ET3) were examined in pithed Sprague-Dawley (SD), Wistar-Kyoto (WKY), and spontaneously hypertensive (SH) rats before and after the administration of the calcium channel antagonist, nifedipine. Systolic and diastolic blood pressures were recorded via an intra-arterial catheter from sodium pentobarbital anaesthized rats prior to pithing. The systolic and diastolic blood pressures recorded from SH rats were significantly greater than those of SD and WKY rats; however, after pithing there were no significant differences between the diastolic blood pressures among the various strains. Administration of nifedipine significantly reduced the diastolic blood pressure of pithed rats to an equal extent in all three strains. The infusion of ET3 produced a dose-dependent increase in diastolic blood pressure of SD, WKY, and SH rats, but neither vascular sensitivity nor reactivity to ET3 was altered in SH rats. Nifedipine was more effective at inhibiting the vasoactive actions of ET3 in SD and WKY than in SH rats. It was therefore concluded that the pressor actions of ET3 in SH rats may be less dependent on the influx of calcium through a dihydropyridine-sensitive calcium channel as compared with WKY and SD rats.

摘要

在给予钙通道拮抗剂硝苯地平之前和之后,在脊髓横断的斯普拉格-道利(SD)大鼠、Wistar-Kyoto(WKY)大鼠和自发性高血压(SH)大鼠中检测了内皮素3(ET3)的升压作用。在脊髓横断前,通过动脉内导管从戊巴比妥钠麻醉的大鼠记录收缩压和舒张压。SH大鼠记录的收缩压和舒张压显著高于SD和WKY大鼠;然而,脊髓横断后,各品系间舒张压无显著差异。硝苯地平的给药在所有三个品系中均同等程度地显著降低了脊髓横断大鼠的舒张压。ET3的输注使SD、WKY和SH大鼠的舒张压呈剂量依赖性升高,但SH大鼠对ET3的血管敏感性和反应性均未改变。硝苯地平在抑制SD和WKY大鼠中ET3的血管活性作用方面比在SH大鼠中更有效。因此得出结论,与WKY和SD大鼠相比,ET3在SH大鼠中的升压作用可能较少依赖于通过二氢吡啶敏感性钙通道的钙内流。

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