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通过GABAB受体调节海马体过度兴奋。

Regulating hippocampal hyperexcitability through GABAB Receptors.

作者信息

Lang Min, Moradi-Chameh Homeira, Zahid Tariq, Gane Jonathan, Wu Chiping, Valiante Taufik, Zhang Liang

机构信息

Toronto Western Research Institute, University Health Network, Toronto, Ontario, Canada.

出版信息

Physiol Rep. 2014 Apr 22;2(4):e00278. doi: 10.14814/phy2.278. Print 2014.

Abstract

Abstract Disturbances of GABAergic inhibition are a major cause of epileptic seizures. GABA exerts its actions via ionotropic GABAA receptors and metabotropic G protein-coupled GABAB receptors. Malfunction of GABAA inhibition has long been recognized in seizure genesis but the role of GABAB receptors in controlling seizure activity is still not well understood. Here, we examined the anticonvulsive, or inhibitory effects, of GABAB receptors in a mouse model of hippocampal kindling as well as mouse hippocampal slices through the use of GS 39783, a positive allosteric GABAB receptor modulator, and CGP 55845, a selective GABAB receptor antagonist. When administered via intraperitoneal injections in kindled mice, GS 39783 (5 mg/kg) did not attenuate hippocampal EEG discharges, but did reduce aberrant hippocampal spikes, whereas CGP 55845 (10 mg/kg) prolonged hippocampal discharges and increased spike incidences. When examined in hippocampal slices, neither GS 39783 at 5 μmol/L nor the GABAB receptor agonist baclofen at 0.1 μmol/L alone significantly altered repetitive excitatory field potentials, but GS 39783 and baclofen together reversibly abolished these field potentials. In contrast, CGP 55845 at 1 μmol/L facilitated induction and incidence of these field potentials. In addition, CGP 55845 attenuated the paired pulse depression of CA3 population spikes and increased the frequency of EPSCs in individual CA3 pyramidal neurons. Collectively, these data suggest that GABABB receptors regulate hippocampal hyperexcitability by inhibiting CA3 glutamatergic synapses. We postulate that positive allosteric modulation of GABAB receptors may be effective in reducing seizure-related hyperexcitability.

摘要

摘要 GABA能抑制紊乱是癫痫发作的主要原因。GABA通过离子型GABAA受体和代谢型G蛋白偶联GABAB受体发挥作用。GABAA抑制功能障碍在癫痫发作起源中早已得到认识,但GABAB受体在控制癫痫活动中的作用仍未完全明确。在此,我们通过使用正性变构GABAB受体调节剂GS 39783和选择性GABAB受体拮抗剂CGP 55845,研究了GABAB受体在海马点燃小鼠模型以及小鼠海马切片中的抗惊厥或抑制作用。当通过腹腔注射给予点燃小鼠时,GS 39783(5毫克/千克)并未减弱海马脑电图放电,但确实减少了异常海马棘波,而CGP 55845(10毫克/千克)延长了海马放电并增加了棘波发生率。在海马切片中进行检测时,单独使用5微摩尔/升的GS 39783或0.1微摩尔/升的GABAB受体激动剂巴氯芬均未显著改变重复性兴奋性场电位,但GS 39783和巴氯芬共同作用可使这些场电位可逆性消失。相比之下,1微摩尔/升的CGP 55845促进了这些场电位的诱导和发生率。此外,CGP 55845减弱了CA3群体峰电位的双脉冲抑制,并增加了单个CA3锥体神经元中兴奋性突触后电流的频率。总体而言,这些数据表明GABAB受体通过抑制CA3谷氨酸能突触来调节海马的过度兴奋性。我们推测GABAB受体的正性变构调节可能对降低癫痫相关的过度兴奋性有效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a400/4001873/0518f668cd68/phy2-2-e00278-g1.jpg

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