Soto C, Martín-Cora F, Leiras R, Velo P, Canedo A
Department of Physiology, Faculty of Medicine, 15705 Santiago de Compostela, Spain.
Neuroscience. 2006 Feb;137(3):1015-30. doi: 10.1016/j.neuroscience.2005.09.026. Epub 2005 Nov 17.
This study examined the modulatory influence exerted by GABA(B) receptors on the transmission of cutaneous afferent input to cuneate nucleus neurons in anesthetized cats. Electrical stimulation at the center of a receptive field activated cuneate nucleus cells at latencies of < or = 7 ms whereas stimulation at neighboring sites (receptive field edge) increased the response latency. Extracellular recording combined with microiontophoresis demonstrated that GABA(B) receptors are tonically active. Blockade of GABA(B) receptors prolonged sensory-evoked response durations and decreased times of occurrence of successive bursts whereas the agonist baclofen suppressed both these effects. Ejection of baclofen delayed the evoked response from the receptive field edge with respect to the receptive field center response and inhibited responses from the receptive field edge more effectively than responses from the receptive field center. From these results it is concluded that activation of GABA(B) receptors precludes cuneate cells from reaching firing threshold when afferent inputs are weak, spatially modulate cuneate nucleus excitability, play a major role in temporal pattern of discharges, and shape cutaneous receptive fields.
本研究检测了γ-氨基丁酸B(GABA(B))受体对麻醉猫皮肤传入输入至楔束核神经元传递的调节作用。在感受野中心进行电刺激,能在潜伏期≤7毫秒时激活楔束核细胞,而在相邻部位(感受野边缘)进行刺激则会增加反应潜伏期。细胞外记录结合微离子电泳表明,GABA(B)受体具有紧张性活动。阻断GABA(B)受体可延长感觉诱发反应的持续时间,并减少连续爆发的发生次数,而激动剂巴氯芬则可抑制这两种效应。与感受野中心反应相比,巴氯芬的注入延迟了感受野边缘的诱发反应,并更有效地抑制了感受野边缘的反应。从这些结果可以得出结论,当传入输入较弱时,GABA(B)受体的激活可阻止楔束核细胞达到放电阈值,在空间上调节楔束核的兴奋性,在放电的时间模式中起主要作用,并塑造皮肤感受野。