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乙唑酯(SQ20009):培养皮层神经元中的电生理学及对[3H]氟硝西泮结合的影响

Etazolate (SQ20009): electrophysiology and effects on [3H]flunitrazepam binding in cultured cortical neurons.

作者信息

Barnes D M, White W F, Dichter M A

出版信息

J Neurosci. 1983 Apr;3(4):762-72. doi: 10.1523/JNEUROSCI.03-04-00762.1983.

Abstract

The actions of etazolate (SQ20009) on cultured cortical neurons have been examined in electrophysiological experiments and in receptor binding studies. Etazolate (0.3 to 100 microM) prolongs the duration of spontaneously occurring IPSPs. Higher concentrations of etazolate produce an increase in membrane chloride conductance, an effect which is picrotoxinin and bicuculline sensitive. Etazolate potentiates the response to exogenously applied GABA and acts synergistically with diazepam to enhance GABA-mediated conductance. Etazolate does not increase glycine-mediated conductance changes. Etazolate increases [3H]flunitrazepam binding and stimulates the GABA enhancement of [3H]flunitrazepam binding. In addition, GABA stimulates the etazolate enhancement of [3H]flunitrazepam binding. The etazolate-mediated increases in binding are Cl- dependent and picrotoxinin and bicuculline sensitive. The dose response relationships for etazolate-mediated effects are similar in physiological experiments and in binding studies. These data suggest that etazolate interacts with the postsynaptic GABA receptor complex at a site distinct from either the GABA recognition site or the benzodiazepine binding site to enhance GABA-mediated inhibition and to increase benzodiazepine binding.

摘要

已通过电生理实验和受体结合研究考察了乙唑酯(SQ20009)对培养的皮质神经元的作用。乙唑酯(0.3至100微摩尔)可延长自发出现的抑制性突触后电位(IPSP)的持续时间。较高浓度的乙唑酯可使膜氯化物电导增加,此效应受匹鲁卡品和荷包牡丹碱影响。乙唑酯可增强对外源性施加的γ-氨基丁酸(GABA)的反应,并与地西泮协同作用以增强GABA介导的电导。乙唑酯不会增加甘氨酸介导的电导变化。乙唑酯可增加[3H]氟硝西泮结合,并刺激GABA对[3H]氟硝西泮结合的增强作用。此外,GABA可刺激乙唑酯对[3H]氟硝西泮结合的增强作用。乙唑酯介导的结合增加依赖于氯离子,且受匹鲁卡品和荷包牡丹碱影响。在生理实验和结合研究中,乙唑酯介导效应的剂量反应关系相似。这些数据表明,乙唑酯与突触后GABA受体复合物在一个不同于GABA识别位点或苯二氮䓬结合位点的部位相互作用,以增强GABA介导的抑制作用并增加苯二氮䓬结合。

相似文献

7
Molecular interactions of etazolate with benzodiazepine and picrotoxinin binding sites.
J Neurochem. 1982 Apr;38(4):1180-2. doi: 10.1111/j.1471-4159.1982.tb05370.x.

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