Swayne G T, Owen D A, Taylor E M, Eden R J, Slater R A, Howson W
Department of Medicinal Chemistry, Smith Kline & French Research Limited, Welwyn, Hertfordshire, England.
Arch Int Pharmacodyn Ther. 1987 Oct;289(2):251-66.
The pharmacological properties of a novel vasodilator/beta-adrenoceptor antagonist, SK & F 95018 6-[4-[3-(3-[4-(2-Cyclopropylmethoxyethyl)phenoxy]-2- hydroxypropylamino)propionamido]phenyl]-4,5-dihydro-5-met hylpyridazin- 3(2H)-one methanesulphonate] are described. SK & F 95018 lowered blood pressure and increased hindquarters blood flow in anaesthetised rats over the same dose range 1-5 mumol kg-1. Over a similar dose range SK & F 95018 inhibited isoprenaline-induced tachycardia in ganglion-blocked, anaesthetized cats. SK & F 95018 had minimal effect on bronchial beta 2-adrenoceptors, while simultaneously antagonizing cardiac beta 1-adrenoceptors in anaesthetized guinea-pigs. SK & F 95018 was demonstrated to be a potent antihypertensive agent in conscious spontaneously hypertensive rats over the dose range of 1.6-13 mumol kg-1 i.v. and 13-103 mumol kg-1 p.o. A marked and persistent hypotension was observed in conscious cats at a dose of 7.5 mumol kg-1 i.v. and 19 mumol kg-1 p.o., without reflex tachycardia. In anaesthetized cats, the hypotensive response to the compound was found to be via a reduction in total peripheral resistance with a maintained cardiac output. Vasodilatation and beta-adrenoceptor antagonism have been demonstrated in the same molecule (SK & F 95018) in a combination which would be suitable for effective treatment of hypertension.
本文描述了一种新型血管扩张剂/β-肾上腺素能受体拮抗剂SK&F 95018(6-[4-[3-(3-[4-(2-环丙基甲氧基乙基)苯氧基]-2-羟基丙基氨基)丙酰胺基]苯基]-4,5-二氢-5-甲基哒嗪-3(2H)-酮甲磺酸盐)的药理特性。在1-5 μmol·kg⁻¹的相同剂量范围内,SK&F 95018可降低麻醉大鼠的血压并增加后肢血流量。在类似剂量范围内,SK&F 95018可抑制神经节阻断的麻醉猫中异丙肾上腺素诱导的心动过速。SK&F 95018对麻醉豚鼠的支气管β₂-肾上腺素能受体影响极小,同时拮抗心脏β₁-肾上腺素能受体。在清醒的自发性高血压大鼠中,静脉注射剂量范围为1.6-13 μmol·kg⁻¹,口服剂量范围为13-103 μmol·kg⁻¹时,SK&F 95018被证明是一种有效的抗高血压药物。静脉注射剂量为7.5 μmol·kg⁻¹和口服剂量为19 μmol·kg⁻¹时,清醒猫出现明显且持续的低血压,无反射性心动过速。在麻醉猫中,发现该化合物的降压反应是通过降低总外周阻力并维持心输出量实现的。在同一分子(SK&F 95018)中已证明血管扩张和β-肾上腺素能受体拮抗作用同时存在,这种组合适合有效治疗高血压。