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γ-氨基丁酸A(GABA(A))和γ-氨基丁酸B(GABA(B))受体可能参与林丹对小脑颗粒神经元递质释放的抑制作用。

Possible involvement of GABA(A) and GABA(B) receptors in the inhibitory action of lindane on transmitter release from cerebellar granule neurons.

作者信息

Damgaard I, Nyitrai G, Kovács I, Kardos J, Schousboe A

机构信息

NeuroScience, PharmaBiotec Center, Dept. of Pharmacology, Royal Danish School of Pharmacy, Copenhagen.

出版信息

Neurochem Res. 1999 Sep;24(9):1189-93. doi: 10.1023/a:1020724823117.

DOI:10.1023/a:1020724823117
PMID:10485591
Abstract

Cerebellar granule cells in culture express receptors for GABA belonging to the GABA(A) and GABA(B) classes. In order to characterize the ability of the insecticide lindane to interact with these receptors cells were grown in either plain culture media or media containing 150 microM THIP as this is known to influence the properties of both GABA(A) and GABA(B) receptors. It was found that lindane regardless of the culture condition inhibited evoked (40 mM K+) release of neurotransmitter ([3H]D-aspartate as label for glutamate). In naive cells both GABA(A) and GABA(B) receptor active drugs prevented the inhibitory action of lindane but in THIP treated cultures none of the GABA(A) and GABA(B) receptor active drugs had any effect on the inhibitory action of lindane. This lack of effect was not due to inability of baclofen itself to inhibit transmitter release. It is concluded that lindane dependent on the state of the GABA(A) and GABA(B) receptors is able to indirectly interfere with both GABA(A) and GABA(B) receptors. In case of the latter receptors it was shown using [3H]baclofen to label the receptors that lindane could not displace the ligand confirming that lindane is likely to exert its action at a site different from the agonist binding site.

摘要

培养的小脑颗粒细胞表达属于GABA(A)和GABA(B)类别的GABA受体。为了表征杀虫剂林丹与这些受体相互作用的能力,细胞在普通培养基或含有150微摩尔THIP的培养基中生长,因为已知THIP会影响GABA(A)和GABA(B)受体的特性。结果发现,无论培养条件如何,林丹都会抑制诱发的(40毫摩尔钾离子)神经递质(以[3H]D-天冬氨酸作为谷氨酸的标记物)释放。在未处理的细胞中,GABA(A)和GABA(B)受体活性药物都能阻止林丹的抑制作用,但在经THIP处理的培养物中,GABA(A)和GABA(B)受体活性药物对林丹的抑制作用均无任何影响。这种无效并非由于巴氯芬本身无法抑制递质释放。得出的结论是,林丹取决于GABA(A)和GABA(B)受体的状态,能够间接干扰GABA(A)和GABA(B)受体。对于后一种受体,使用[3H]巴氯芬标记受体表明,林丹不能取代配体,这证实林丹可能在与激动剂结合位点不同的位点发挥作用。

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