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[2-甲基-3-氨基苯丙酮衍生物的中枢肌肉松弛活性]

[Central muscle relaxant activities of 2-methyl-3-aminopropiophenone derivatives].

作者信息

Kontani H, Mano A, Koshiura R, Yamazaki M, Shimada Y, Oshita M, Morikawa K, Kato H, Ito Y

出版信息

Nihon Yakurigaku Zasshi. 1987 Feb;89(2):91-101. doi: 10.1254/fpj.89.91.

Abstract

In this experiment, we synthetized new 2-methyl-3-aminopropiophenone (MP) derivatives, whose structure is known to have central muscle relaxant activities, and quinolizidine and indan . tetralin derivatives derived from MP by cyclization, and we investigated the central muscle relaxant activity. Among the quinolizidine derivatives, there was a very strong central depressant agent, trans (3H, 9aH)-3-(p-chloro) benzoyl-quinolizidine (HSR-740), and among the indan . tetralin derivatives, there was an excitant agents, trans (1H, 2H)-5-methoxy-3, 3-dimethyl-2-piperidinomethyl indan-1-ol (HSR-719). From the results, these derivatives were not considered to be adequate for central muscle relaxant. Among the MP derivatives, (4'-chloro-2'-methoxy-3-piperidino) propiophenone HCl (HSR-733) and (4'-ethyl-2-methyl-3-pyrrolidino) propiophenone HCl (HSR-770) strongly inhibited the cooperative movement in the rotating rod method using mice, and it exerted almost the same depressant activity on the cross extensor reflex using alpha-chloralose anesthetized rats. However, the inhibitory effects of HSR-733 on the anemic decerebrate rigidity and the rigidity induced by intracollicular decerebration in rats were weaker than those of HSR-770 and eperisone. In spinal cats, at a low dose (5 mg/kg, i.v.), HSR-733 depressed monosynaptic and dorsal root reflex potentials as compared with polysynaptic reflex potentials, and inhibitory effects of HSR-733 on these three reflex potentials were more potent than those of eperisone and HSR-770. Although HSR-770 acts on the spinal cord and supraspinal level on which eperisone has been reported to act, HSR-733 may mainly act on the spinal cord. These results indicate that the MP derivative with a 2-methyl group may be suitable as a central muscle relaxant. HSR-770, which has equipotent muscle relaxant activity to eperisone, exerted strong inhibitory effects on oxotremorine-induced tremor and weak inhibitory effects on spontaneous motor activity in the Animex method using mice, as compared with eperisone.

摘要

在本实验中,我们合成了新的2-甲基-3-氨基苯丙酮(MP)衍生物,已知其结构具有中枢性肌肉松弛活性,以及通过环化从MP衍生而来的喹嗪烷和茚满。四氢萘衍生物,并研究了其中枢性肌肉松弛活性。在喹嗪烷衍生物中,有一种非常强的中枢抑制剂,反式(3H,9aH)-3-(对氯)苯甲酰基喹嗪烷(HSR-740),在茚满。四氢萘衍生物中,有一种兴奋剂,反式(1H,2H)-5-甲氧基-3,3-二甲基-2-哌啶基甲基茚满-1-醇(HSR-719)。从结果来看,这些衍生物被认为不适合作为中枢性肌肉松弛剂。在MP衍生物中,(4'-氯-2'-甲氧基-3-哌啶基)苯丙酮盐酸盐(HSR-733)和(4'-乙基-2-甲基-3-吡咯烷基)苯丙酮盐酸盐(HSR-770)在使用小鼠的转棒法中强烈抑制协同运动,并且在使用α-氯醛糖麻醉的大鼠的交叉伸肌反射中发挥几乎相同的抑制活性。然而,HSR-733对大鼠贫血去大脑强直和中脑内去大脑引起的强直的抑制作用比HSR-770和乙哌立松弱。在脊髓猫中,低剂量(5mg/kg,静脉注射)时,与多突触反射电位相比,HSR-733抑制单突触和背根反射电位,并且HSR-733对这三种反射电位的抑制作用比乙哌立松和HSR-770更强。虽然HSR-770作用于据报道乙哌立松作用的脊髓和脊髓上水平,但HSR-733可能主要作用于脊髓。这些结果表明具有2-甲基的MP衍生物可能适合作为中枢性肌肉松弛剂。与乙哌立松相比,具有与乙哌立松等效肌肉松弛活性的HSR-770在使用小鼠的Animex法中对奥氮平诱导的震颤具有强烈抑制作用,对自发运动活性具有弱抑制作用。

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