Gardiner S M, Compton A M, Bennett T
Department of Physiology and Pharmacology, Medical School, Queen's Medical Centre, Nottingham, United Kingdom.
Am J Physiol. 1990 Apr;258(4 Pt 2):R912-7. doi: 10.1152/ajpregu.1990.258.4.R912.
Regional hemodynamic responses to bolus doses (4 and 40 pmol) and 60-min infusions (12 and 120 pmol/h) of endothelin-2 (ET-2) and sarafotoxin-S6b (S6b) were measured in conscious Long-Evans and Brattleboro rats chronically instrumented with pulsed Doppler flow probes. In both strains of rat the two bolus doses of ET-2 and S6b peptides caused an initial fall in mean blood pressure (MBP). At the higher dose S6b caused a greater fall in MBP than ET-2. In Long-Evans rats the fall in MBP after S6b was associated with renal, mesenteric, and hindquarters vasodilatations; in Brattleboro rats there was no renal or mesenteric vasodilatation with S6b. The high dose of ET-2 caused early mesenteric vasoconstriction in both strains. After the initial fall in MBP there were dose-dependent increases in MBP together with renal and mesenteric vasoconstrictions. These effects were generally greater after S6b than after ET-2 and no less marked in Brattleboro than in Long-Evans rats, indicating that release of endogenous vasopressin was not an indispensable component of the response. Infusions of the higher dose of ET-2 or S6b caused increases in MBP only, associated with renal, mesenteric, and hindquarters vasoconstrictions. The results indicate that S6b is a more potent stimulus than ET-2 of vasodilator mechanisms in vivo; despite this, S6b also exerts more marked vasoconstrictor effects than ET-2.
在长期植入脉冲多普勒血流探头的清醒朗-埃文斯大鼠和布拉特洛伯大鼠中,测量了给予大剂量(4和40皮摩尔)和60分钟输注(12和120皮摩尔/小时)内皮素-2(ET-2)和蛙皮毒素-S6b(S6b)后的局部血流动力学反应。在两种品系的大鼠中,两种大剂量的ET-2和S6b肽均引起平均血压(MBP)的初始下降。在较高剂量时,S6b导致的MBP下降幅度大于ET-2。在朗-埃文斯大鼠中,S6b给药后MBP的下降与肾、肠系膜和后肢血管舒张有关;在布拉特洛伯大鼠中,S6b给药后未出现肾或肠系膜血管舒张。高剂量的ET-2在两种品系中均引起早期肠系膜血管收缩。在MBP初始下降后,MBP出现剂量依赖性升高,同时伴有肾和肠系膜血管收缩。这些效应通常S6b给药后比ET-2给药后更明显,在布拉特洛伯大鼠中与在朗-埃文斯大鼠中一样显著,表明内源性血管加压素的释放不是该反应必不可少的组成部分。输注较高剂量的ET-2或S6b仅引起MBP升高,伴有肾、肠系膜和后肢血管收缩。结果表明,在体内,S6b比ET-2是更有效的血管舒张机制刺激物;尽管如此,S6b也比ET-2发挥更明显的血管收缩作用。