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四种二氢异喹啉衍生物的筛选药理学研究

Screening pharmacological studies of four dihydroisoquinoline derivatives.

作者信息

Stoychev T, Koleva M, Orahovats A, Trifonov L

出版信息

Acta Physiol Pharmacol Bulg. 1979;5(3):82-90.

PMID:539451
Abstract

Screening studies are carried out of the pharmacological activity of 3,4-dihydropapaverine (DHP) and three of its newly-synthesized derivatives: 6'-iodo-DHP, 6'-bromo-DHP and 6'-iodu-DHP methiodide. All compounds studied manifest central depressive action which is manifested in general depression, potentiation of hexobarbital anaesthesia, without inducing sleep when independently applied, as well as inhibition of the spontaneous and amphetamine-induced motor activity of mice. 6'-Iodo-DHP and its methiodide manifest analgesic effect. All four compounds studied reduce the blood pressure of urethane-anaesthesized cats, but they do not change the noradrenaline and the acetylcholine effects. The hypotensive effect of the compounds is preserved even after atropinization of the cats. The compounds studied manifest no antitussive effect. DHP-derivatives eliminate the spasms in guinea-pig colon, induced by BaCl2 and nicotine, while DHP has no effect on them. 6'-Iodo-DHP methoiodide inhibits the hypertensive nicotine effect on cats. DHP and 6'-iodo-DHP methoiodide manifest vasoconstricting action upon perfusion of the blood vessels of isolated rat hind legs.

摘要

对3,4-二氢罂粟碱(DHP)及其新合成的三种衍生物:6'-碘-DHP、6'-溴-DHP和6'-碘-DHP甲碘化物进行了药理活性筛选研究。所有研究的化合物均表现出中枢抑制作用,表现为全身抑郁、增强己巴比妥麻醉作用,单独应用时不诱导睡眠,以及抑制小鼠的自发运动和苯丙胺诱导的运动活动。6'-碘-DHP及其甲碘化物表现出镇痛作用。所有四种研究的化合物均可降低乌拉坦麻醉猫的血压,但它们不会改变去甲肾上腺素和乙酰胆碱的作用。即使在猫阿托品化后,这些化合物的降压作用仍然存在。研究的化合物没有镇咳作用。DHP衍生物可消除由BaCl2和尼古丁诱导的豚鼠结肠痉挛,而DHP对其没有影响。6'-碘-DHP甲碘化物可抑制尼古丁对猫的升压作用。DHP和6'-碘-DHP甲碘化物在灌注离体大鼠后腿血管时表现出血管收缩作用。

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