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新型口服及透皮长效抗高血压药物dl-15-脱氧-16-羟基-16(α/β)-乙烯基前列腺素E2甲酯(CL 115,347)的抗高血压活性

Antihypertensive activity of dl-15-deoxy-16-hydroxy-16(alpha/beta)-vinyl prostaglandin E2 methyl ester (CL 115,347), a new orally and transdermally long-acting antihypertensive agent.

作者信息

Chan P S, Cervoni P, Ronsberg M A, Accomando R C, Quirk G J, Scully P A, Lipchuck L M

出版信息

J Pharmacol Exp Ther. 1983 Sep;226(3):726-32.

PMID:6887009
Abstract

CL 115,347 [dl-15-deoxy-16-hydroxy-16(alpha/beta)-vinyl prostaglandin E2 methyl ester] has a broad spectrum of antihypertensive activity in many animal hypertension models in every species tested. In conscious spontaneously hypertensive rats, CL 115,347 at 0.25 to 10 mg/kg orally produced 31 to 53 mm Hg lowering of the mean arterial blood pressure (MABP) with a duration of action of 1 to greater than 8 hr. When applied transdermally, CL 115,347 was more potent and longer acting than by the oral route. At 0.03 to 1 mg/kg, topically applied CL 115,347 lowered MABP of spontaneously hypertensive rats 27 to 46 mm Hg. Duration of action was greater than 6 to greater than 24 hr. CL 115,347 was also active in conscious normotensive rats (-27 mm Hg), deoxycorticosterone-salt-induced hypertensive rats (-51 mm Hg) and aorta-coarcted hypertensive rats (-52 mm Hg) when tested at 1 mg/kg orally. At 3 mg/kg orally, CL 115,347 lowered MABP of Dahl "S" salt-sensitive rats 55 mm Hg. CL 115,347 orally and s.c. lowered MABP in two-kidney, one-clip Goldblatt renal hypertensive dogs and was accompanied by tachycardia. CL 115,347, at 0.1 and 0.2 mg/kg orally, maximally lowered the systolic blood pressure of conscious rhesus monkeys 33 to 63 mm Hg with only a slight increase in heart rate. Therefore, CL 115,347 was antihypertensive in animals with low, normal and high plasma renin activity. The present findings suggest that CL 115,347 may be useful for the treatment of human hypertension.

摘要

CL 115,347[dl-15-脱氧-16-羟基-16(α/β)-乙烯基前列腺素E2甲酯]在所有受试物种的多种动物高血压模型中均具有广泛的降压活性。在清醒的自发性高血压大鼠中,口服0.25至10mg/kg的CL 115,347可使平均动脉血压(MABP)降低31至53mmHg,作用持续时间为1至超过8小时。经皮给药时,CL 115,347比口服途径更有效且作用时间更长。局部应用0.03至1mg/kg的CL 115,347可使自发性高血压大鼠的MABP降低27至46mmHg。作用持续时间大于6至大于24小时。当以1mg/kg口服测试时,CL 115,347在清醒的正常血压大鼠(-27mmHg)、脱氧皮质酮盐诱导的高血压大鼠(-51mmHg)和主动脉缩窄性高血压大鼠(-52mmHg)中也具有活性。口服3mg/kg时,CL 115,347可使Dahl“S”盐敏感大鼠的MABP降低55mmHg。CL 115,347口服和皮下注射可降低两肾一夹Goldblatt肾性高血压犬的MABP,并伴有心动过速。口服0.1和0.2mg/kg的CL 115,347可使清醒恒河猴的收缩压最大降低33至63mmHg,心率仅略有增加。因此,CL 115,347对血浆肾素活性低、正常和高的动物均有降压作用。目前的研究结果表明,CL 115,347可能对治疗人类高血压有用。

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