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新型β-肾上腺素能阻滞剂茚萘洛尔(YB-2)及其右旋异构体对小鼠和家兔中枢神经系统的作用。

Effects of indenolol (YB-2), a new beta-adrenergic blocking agent, and its dextro isomer on the central nervous system of mice and rabbits.

作者信息

Tachikawa S, Takenaka T, Maeno H

出版信息

Arch Int Pharmacodyn Ther. 1978 Jul;234(1):74-87.

PMID:30422
Abstract

Central depressant actions of a new beta-adrenergic blocking agent, indenolol (YB-2), and its dextro isomer were studied in mice and rabbits. d-Indenolol was less active than dl-indenolol in lowering of methamphetamine group toxicity and calming of fighting behavior, though muscle relaxant, hypolocomotive and anticonvulsant effects of d-indenolol were virtually equal to those of the racemate. dl-Propranolol showed a similar profile of central depressant actions to dl-indenolol, whereas dl-practolol revealed no significant central effects in mice. The dose-response relationship between beta-blocking and central effects in the same animal species suggested that both taming and anti-methamphetamine group toxicity effects of dl-indenolol s.c. do not directly relate to either the peripheral beta-blocking or the membrane stabilizing activity. Intravenous as well as intracerebroventricular administration of dl-indenolol resulted in suppression of pressor responses to the electrical stimulation of the brain stem of unanesthetized rabbits. Neither d-indenolol nor dl-practolol was effective against the pressor responses, suggesting that these two compounds acted on the CNS in a manner different from dl-indenolol even when intracerebroventricularly administered. A possible central beta-adrenergic blocking effect of dl-indenolol was discussed in the light of mechanisms of an antihypertensive action of this compound.

摘要

研究了一种新型β-肾上腺素能阻滞剂茚萘洛尔(YB-2)及其右旋异构体在小鼠和兔子体内的中枢抑制作用。在降低甲基苯丙胺组毒性和抑制争斗行为方面,d-茚萘洛尔的活性低于dl-茚萘洛尔,不过d-茚萘洛尔的肌肉松弛、运动减少和抗惊厥作用实际上与消旋体相当。dl-普萘洛尔的中枢抑制作用表现与dl-茚萘洛尔相似,而dl-普拉洛尔在小鼠中未显示出明显的中枢作用。同一动物物种中β-阻断作用与中枢作用之间的剂量-反应关系表明,dl-茚萘洛尔皮下注射的驯服作用和抗甲基苯丙胺组毒性作用均与外周β-阻断作用或膜稳定活性无直接关系。静脉注射以及脑室内注射dl-茚萘洛尔均可抑制未麻醉兔子脑干电刺激引起的升压反应。d-茚萘洛尔和dl-普拉洛尔对升压反应均无效,这表明即使脑室内给药,这两种化合物对中枢神经系统的作用方式也与dl-茚萘洛尔不同。根据该化合物的降压作用机制,讨论了dl-茚萘洛尔可能存在的中枢β-肾上腺素能阻断作用。

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