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β1受体拮抗作用对于β受体阻滞剂的降压作用是否至关重要?

Is beta 1-antagonism essential for the antihypertensive action of beta-blockers?

作者信息

Vincent H H, Man in 't Veld A J, Boomsma F, Derkx F H, Schalekamp M A

出版信息

Hypertension. 1987 Feb;9(2):198-203. doi: 10.1161/01.hyp.9.2.198.

Abstract

Both nonselective beta-blockers and beta 1-selective blockers are effective antihypertensive agents. beta 1-Blockade generally is considered to be responsible for their antihypertensive action, whereas beta 2-blockade is regarded as undesirable. These common assumptions notwithstanding, the mechanism by which beta-blockers lower blood pressure remains unknown. To examine the possibility that beta 2-blockade may contribute to the antihypertensive action of beta-blocker therapy, we studied the cardiovascular effects of compound ICI 118551, a beta 2-selective blocker. First, we showed that 50 mg t.i.d. orally is a beta 2-selective dose. In contrast to propranolol, 80 mg t.i.d., or atenolol, 100 mg once a day, 50 mg of ICI 118551 t.i.d. failed to block beta 1-mediated inotropic stimulation and stimulation of renin by isoproterenol. We then performed a double-blind, placebo-controlled trial in patients with mild essential hypertension to compare this compound with propranolol, 80 mg t.i.d., and showed that ICI 118551 significantly decreased systolic and diastolic blood pressure. This antihypertensive effect was demonstrated by direct as well as by indirect blood pressure measurements. Thus, contrary to prevailing thought, beta 2-blockade has an antihypertensive effect independent of, and distinct from, beta 1-blockade.

摘要

非选择性β受体阻滞剂和β1选择性阻滞剂都是有效的抗高血压药物。一般认为β1受体阻滞是其抗高血压作用的原因,而β2受体阻滞则被认为是不理想的。尽管有这些普遍的假设,但β受体阻滞剂降低血压的机制仍然未知。为了研究β2受体阻滞可能有助于β受体阻滞剂治疗的抗高血压作用的可能性,我们研究了β2选择性阻滞剂化合物ICI 118551的心血管效应。首先,我们表明口服50毫克,每日三次是β2选择性剂量。与普萘洛尔(每日三次,每次80毫克)或阿替洛尔(每日一次,每次100毫克)不同,每日三次给予50毫克的ICI 118551未能阻断异丙肾上腺素介导的β1正性肌力刺激和肾素刺激。然后,我们对轻度原发性高血压患者进行了一项双盲、安慰剂对照试验,以比较该化合物与每日三次80毫克普萘洛尔的效果,结果表明ICI 118551显著降低了收缩压和舒张压。这种抗高血压作用通过直接和间接血压测量得到证实。因此,与普遍观点相反,β2受体阻滞具有独立于β1受体阻滞且与之不同的抗高血压作用。

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