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槟榔成分槟榔次碱和去甲槟榔次碱对猫中枢神经系统中γ-氨基丁酸作用的影响。

Effects of the Areca nut constituents arecaidine and guvacine on the action of GABA in the cat central nervous system.

作者信息

Lodge D, Johnston G A, Curtis D R, Brand S J

出版信息

Brain Res. 1977 Nov 18;136(3):513-22. doi: 10.1016/0006-8993(77)90075-0.

Abstract

Arecaidine and guvacine, constituents of the nut of Areca catechu, inhibited the uptake of GABA and beta-alanine, but not that of glycine, by slices of cat spinal cord. In cats anesthetised with pentobarbitone, electrophoretic arecaidine enhanced the inhibitory actions of GABA and beta-alanine, but not those of glycine or taurine, on the firing of spinal neurones. Similarly, electrophoretic guvacine enhanced the inhibition of spinal neurones by GABA but not that by glycine. The uptake of GABA by slices of cat cerebellum was inhibited by arecaidine, and the effect of electrophoretic GABA on the firing of cerebellar Purkinje cells was enhanced by electrophoretic arecaidine. When administered intravenously arecaidine failed to affect synaptic inhibitions considered to be mediated by GABA. Intravenous arecaidine had no effect on either spinal prolonged (presynaptic) inhibition (20mg/kg), dorsal root potentials (20mg/kg) or basket cell inhibition of Purkinje cells (250 mg/kg), although topical arecaidine (6.6-10 x 10(-3) M) blocked this latter inhibition. Large doses of arecaidine (1 g/kg subcutaneous) marginally reduced the lethal effects of bicuculline in mice but appeared to have little or no anticonvulsant activity.

摘要

槟榔次碱和去甲槟榔次碱是槟榔坚果的成分,它们能抑制猫脊髓切片对γ-氨基丁酸(GABA)和β-丙氨酸的摄取,但不影响对甘氨酸的摄取。在用戊巴比妥麻醉的猫中,电泳施加的槟榔次碱增强了GABA和β-丙氨酸对脊髓神经元放电的抑制作用,但不增强甘氨酸或牛磺酸的抑制作用。同样,电泳施加的去甲槟榔次碱增强了GABA对脊髓神经元的抑制作用,但不增强甘氨酸的抑制作用。槟榔次碱抑制了猫小脑切片对GABA的摄取,并且电泳施加的槟榔次碱增强了电泳施加的GABA对小脑浦肯野细胞放电的影响。静脉注射槟榔次碱未能影响被认为由GABA介导的突触抑制。静脉注射槟榔次碱对脊髓长时间(突触前)抑制(20mg/kg)、背根电位(20mg/kg)或浦肯野细胞的篮状细胞抑制(250mg/kg)均无影响,尽管局部应用槟榔次碱(6.6 - 10×10⁻³M)可阻断后者的抑制作用。大剂量的槟榔次碱(1g/kg皮下注射)略微降低了荷包牡丹碱对小鼠的致死作用,但似乎几乎没有或没有抗惊厥活性。

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