Ye J M, Colquhoun E Q
Division of Biochemistry, School of Medicine, University of Tasmania, Hobart, Tasmania, Australia 7001.
J Pharmacol Exp Ther. 1998 Aug;286(2):599-606.
Norepinephrine (NE) induces a sigmoidal dose-response curve for perfusion pressure and a bell-shaped curve for oxygen consumption (VO2) in the constant-flow perfused hindlimb of Wistar rats. These effects are now described in spontaneously hypertensive rats (SHR) and age-matched Wistar-Kyoto rats (WKY). In SHR, the pressure curve was shifted left- and upward whereas the VO2 curve was shifted left- but downward, when compared with WKY. In the presence of 10 microM propranolol, prazosin (2.5 nM) shifted the pressure and VO2 curves much more than yohimbine (0.1 microM) to the right in both strains and its effects were greater in SHR, suggesting that these effects were mediated largely by alpha-1 receptors, particularly in SHR. In the presence of propranolol plus yohimbine, the pressure curve was markedly shifted to the right by both the selective alpha-1A-antagonist 5-methylurapidil (3.3 nM), and by the alpha-1D antagonist BMY 7378 (0.1 microM) or SK&F 105854 (2 microM) in SHR but not in WKY. With respect to the VO2 curve, 5-methylurapidil attenuated the descending limb without affecting the ascending limb. Similar effects were also obtained with another alpha-1A antagonist 1 nM KMD-3213 in both SHR and WKY. In contrast, BMY and SK&F markedly inhibited the ascending limb of the VO2 curve. These results indicate that both alpha-1A- and alpha-1D subtypes are functionally up-regulated in SHR muscle vascular bed where the ascending limb of VO2 is predominantly mediated by the alpha-1D at a much lower concentration for NE than the descending limb which is predominantly mediated by the alpha-1A subtype.
去甲肾上腺素(NE)在Wistar大鼠恒流灌注的后肢中,可诱导灌注压力呈S形剂量反应曲线,耗氧量(VO2)呈钟形曲线。现在对自发性高血压大鼠(SHR)和年龄匹配的Wistar-Kyoto大鼠(WKY)进行了这些效应的研究。与WKY相比,SHR的压力曲线向左上方移动,而VO2曲线向左下方移动。在存在10微摩尔普萘洛尔的情况下,哌唑嗪(2.5纳摩尔)使两种品系的压力和VO2曲线向右移动的幅度比育亨宾(0.1微摩尔)大得多,且在SHR中的作用更大,这表明这些效应主要由α-1受体介导,尤其是在SHR中。在普萘洛尔加育亨宾存在的情况下,选择性α-1A拮抗剂5-甲基乌拉地尔(3.3纳摩尔)、α-1D拮抗剂BMY 7378(0.1微摩尔)或SK&F 105854(2微摩尔)可使SHR的压力曲线明显向右移动,但对WKY无效。关于VO2曲线,5-甲基乌拉地尔减弱了下降支,而不影响上升支。在SHR和WKY中,另一种α-1A拮抗剂1纳摩尔KMD-3213也得到了类似的结果。相比之下,BMY和SK&F明显抑制了VO2曲线的上升支。这些结果表明,α-1A和α-1D亚型在SHR肌肉血管床中功能上调,其中VO2的上升支主要由α-1D介导,所需NE浓度远低于主要由α-1A亚型介导的下降支。