The influence of agonists of GABA(A) and GABA(B) receptors on the formation of the defensive and inhibitory conditioned reflexes.

作者信息

Shul'gina G I, Zyablitseva E A, Kositsyn N S

机构信息

Institute for Higher Nervous Activity and Neurophysiology, Russian Academy of Sciences, ul. Butlerova 5a, Moscow 117485, Russia.

出版信息

Dokl Biol Sci. 2009 Nov-Dec;429:497-9. doi: 10.1134/s0012496609060040.

DOI:10.1134/s0012496609060040

PMID:20170055

Abstract

摘要

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The influence of agonists of GABA(A) and GABA(B) receptors on the formation of the defensive and inhibitory conditioned reflexes.

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本文引用的文献

GABA(A) receptor channel pharmacology.γ-氨基丁酸A型（GABA(A)）受体通道药理学

Curr Pharm Des. 2005;11(15):1867-85. doi: 10.2174/1381612054021024.

The neurophysiological validation of the hyperpolarization theory of internal inhibition.内抑制超极化理论的神经生理学验证

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GABA(A) agonists and partial agonists: THIP (Gaboxadol) as a non-opioid analgesic and a novel type of hypnotic.γ-氨基丁酸A（GABA(A)）受体激动剂和部分激动剂：噻吡咯烷酮（加波沙朵）作为一种非阿片类镇痛药和新型催眠药。

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Gaboxadol. Lundbeck/Merck.加波沙朵。灵北/默克公司。

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Pharmacology of GABA(A) receptors exhibiting different levels of spontaneous activity.表现出不同自发活动水平的γ-氨基丁酸A（GABA(A)）受体的药理学

Eur J Pharmacol. 2003 Aug 22;476(1-2):17-24. doi: 10.1016/s0014-2999(03)02125-3.

Pharmacological characterization of a novel cell line expressing human alpha(4)beta(3)delta GABA(A) receptors.一种表达人α(4)β(3)δ GABA(A)受体的新型细胞系的药理学特性

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gamma-aminobutyric Acid(A) (GABA(A)) agonist 4,5,6, 7-tetrahydroisoxazolo[4,5-c]pyridin-3-ol persistently increases sleep maintenance and intensity during chronic administration to rats.γ-氨基丁酸(A)(GABA(A))激动剂4,5,6,7-四氢异恶唑并[4,5-c]吡啶-3-醇在长期给予大鼠期间持续增加睡眠维持时间和睡眠强度。

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[GABAergic theory of epilepsy].

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[Use of fenibut in psychiatry and neurology and its place among other psychotropic drugs (review of the literature)].[芬乙脲在精神病学和神经病学中的应用及其在其他精神药物中的地位（文献综述）]

Zh Nevropatol Psikhiatr Im S S Korsakova. 1989;89(4):142-51.

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