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塞利洛尔,一种强效的心脏选择性β1肾上腺素能受体拮抗剂,具有轻度的α2肾上腺素能受体拮抗特性。

Celiprolol, a potent cardioselective beta 1-adrenoceptor antagonist with mild alpha 2-adrenoceptor antagonist properties.

作者信息

Wolf P S, Pruss T P, Rand M J, Smith R D, Mann W S, Romano D V

机构信息

Department of Pharmacology, Revlon Health Care, Research and Development Division, Tuckahoe, New York 10707.

出版信息

J Hypertens Suppl. 1985 Dec;3(3):S195-7.

PMID:2908816
Abstract

Celiprolol is a cardioselective beta-adrenoceptor antagonist, with interesting propranolol-insensitive cardiostimulatory, vasodilatory and bronchodilatory effects. Recent reports suggest that mild alpha 2-adrenoceptor antagonism may contribute to these effects. The present investigation further explored the alpha 2 effects of celiprolol. In isolated electrically-stimulated rat atria celiprolol (1.0 and 10 mumol/l) significantly increased the release of [3H]-norepinephrine, consistent with the blockade of pre-junctional alpha 2-adrenoceptors. Evidence for post-synaptic alpha 2-adrenoceptor antagonist activity was obtained in studies of the effects of celiprolol on the pressor response to clonidine and either phenylephrine or methoxamine in perfused hind-limbs of dogs (pretreated with mecamylamine and propranolol) and pithed rats. In the dog, celiprolol (10 mg/kg) significantly inhibited the vasoconstrictor response of clonidine while in the rat higher doses were required (> or = 12.5 mg/kg). Celiprolol did not affect the pressor response induced by alpha 1-agonists. We conclude that celiprolol possesses a mild alpha 2-adrenoceptor blocking action which may contribute to its unconventional profile.

摘要

塞利洛尔是一种心脏选择性β-肾上腺素能受体拮抗剂,具有有趣的对普萘洛尔不敏感的心脏刺激、血管舒张和支气管舒张作用。最近的报告表明,轻度的α2-肾上腺素能受体拮抗作用可能促成了这些效应。本研究进一步探讨了塞利洛尔的α2效应。在离体电刺激的大鼠心房中,塞利洛尔(1.0和10 μmol/l)显著增加了[3H]-去甲肾上腺素的释放,这与对突触前α2-肾上腺素能受体的阻断一致。在塞利洛尔对狗(用美加明和普萘洛尔预处理)和去脑大鼠的灌注后肢中可乐定与去氧肾上腺素或甲氧明的升压反应影响的研究中,获得了突触后α2-肾上腺素能受体拮抗活性的证据。在狗中,塞利洛尔(10 mg/kg)显著抑制了可乐定的血管收缩反应,而在大鼠中则需要更高的剂量(≥12.5 mg/kg)。塞利洛尔不影响α1-激动剂诱导的升压反应。我们得出结论,塞利洛尔具有轻度的α2-肾上腺素能受体阻断作用,这可能促成了其非传统的特性。

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