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化合物ICI 118,551,一种β2肾上腺素能受体拮抗剂,可降低血压。

Compound ICI 118,551, a beta 2-adrenoceptor antagonist, lowers blood pressure.

作者信息

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

机构信息

Department of Internal Medicine I, University Hospital, Dijkzigt, Rotterdam, The Netherlands.

出版信息

J Hypertens Suppl. 1985 Dec;3(3):S247-9.

PMID:2908820
Abstract

Adrenaline may increase noradrenaline release and enhance sympathetic pressor effects through activation of pre-synaptic beta 2-adrenoceptors. Conversely, blockade of beta 2-receptors could lead to a fall in blood pressure. To test this hypothesis we performed a double-blind placebo controlled crossover study in nine patients with mild hypertension, comparing the effects of the beta 2-selective blocker ICI 118,551, 50 mg t.i.d. with those of propranolol, 80 mg t.i.d. Two hours after the first dose of ICI 118,551 or propranolol, plasma noradrenaline and blood pressure remained unchanged while heart rate and renin were reduced. After 1 week, blood pressure was significantly reduced by both drugs. The beta 2-selectivity of ICI 118,551 was confirmed by isoprenaline infusion studies. After 1 week of treatment ICI 118,551 had no effect on the beta 1-receptor mediated shortening of electromechanical systole (QS2I), the rise in systolic pressure and rise in renin, whereas these responses were blocked by a dose factor of eight after propranolol. ICI 118,551 and propranolol equally blocked the beta 2-receptor mediated fall in diastolic pressure and the rise in noradrenaline. We conclude that beta 2-selective blockade by ICI 118,551 lowers blood pressure. This finding is compatible with a role of pre-synaptic beta 2-receptors in blood pressure control.

摘要

肾上腺素可能通过激活突触前β2-肾上腺素能受体增加去甲肾上腺素的释放,并增强交感神经升压作用。相反,β2-受体的阻断可能导致血压下降。为了验证这一假设,我们对9例轻度高血压患者进行了一项双盲安慰剂对照交叉研究,比较了β2-选择性阻滞剂ICI 118,551(50 mg,每日3次)和普萘洛尔(80 mg,每日3次)的效果。在首次服用ICI 118,551或普萘洛尔2小时后,血浆去甲肾上腺素和血压保持不变,而心率和肾素降低。1周后,两种药物均使血压显著降低。异丙肾上腺素输注研究证实了ICI 118,551的β2-选择性。治疗1周后,ICI 118,551对β1-受体介导的机电收缩期缩短(QS2I)、收缩压升高和肾素升高均无影响,而普萘洛尔给药后这些反应被8倍剂量因子阻断。ICI 118,551和普萘洛尔同样阻断了β2-受体介导的舒张压下降和去甲肾上腺素升高。我们得出结论,ICI 118,551的β2-选择性阻断可降低血压。这一发现与突触前β2-受体在血压控制中的作用相符。

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