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两种新型β-肾上腺素能受体阻断药物的降压及心脏效应

Antihypertensive and cardiac effects of two novel beta-adrenoceptor blocking drugs.

作者信息

Scriabine A, Ludden C T, Morgan G, Baldwin J J

出版信息

Experientia. 1979 Dec 15;35(12):1634-7. doi: 10.1007/BF01953238.

Abstract

Two new beta-adrenoceptor blocking drugs with acute antihypertensive and positive inotropic effects are described: Compound A (2-[4-(3-tert.butylamino-2-hydroxypropoxy)phenyl]-4-trifluoromethylimidazole) and MK-761 (2-(3-tert.butylamine-2-hydroxypropoxy)-3-cyanopyridine hydrochloride). In SH rats both compounds, given orally, lowered arterial pressure and were more potent than hydralazine. The antihypertensive effect of compound A but not of MK-761 was antagonized by timolol. Both compounds had positive inotropic activity on cat heart papillary muscles; these effects were antagonized by timolol. The pretreatment of animals with reserpine greatly reduced the positive inotropic effect of MK-761 but not of compound A. The acute antihypertensive and positive inotropic effects of compound A are like to be at least partially due to stimulation of beta-adrenoceptors, e.g. intrinsic sympathomimetic activity. The effects of MK-761 on the same parameters appear to be mediated by different mechanisms.

摘要

本文描述了两种具有急性降压和正性肌力作用的新型β-肾上腺素受体阻滞剂:化合物A(2-[4-(3-叔丁氨基-2-羟基丙氧基)phenyl]-4-三氟甲基咪唑)和MK-761(2-(3-叔丁胺-2-羟基丙氧基)-3-氰基吡啶盐酸盐)。在SH大鼠中,口服这两种化合物均可降低动脉血压,且比肼屈嗪更有效。噻吗洛尔可拮抗化合物A的降压作用,但不能拮抗MK-761的降压作用。两种化合物对猫心脏乳头肌均有正性肌力活性;这些作用可被噻吗洛尔拮抗。用利血平预处理动物可大大降低MK-761的正性肌力作用,但不能降低化合物A的正性肌力作用。化合物A的急性降压和正性肌力作用可能至少部分归因于β-肾上腺素受体的刺激,例如内在拟交感活性。MK-761对相同参数的作用似乎是由不同机制介导的。

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