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外周γ-氨基丁酸A型受体:外周初级传入神经去极化的证据

Peripheral GABA(A) receptors: evidence for peripheral primary afferent depolarization.

作者信息

Carlton S M, Zhou S, Coggeshall R E

机构信息

Department of Anatomy and Neuroscience, Marine Biomedical Institute, University of Texas Medical Branch, Galveston 77555-1069, USA.

出版信息

Neuroscience. 1999;93(2):713-22. doi: 10.1016/s0306-4522(99)00101-3.

Abstract

We propose that the primary afferent depolarization that follows GABA(A) receptor activation in the spinal cord also occurs in the periphery. As evidence, the present study localizes beta2/beta3 and alpha1 subunits of the GABA(A) receptor on 10-14% of the unmyelinated primary afferents axons in the glabrous skin of the cat paw. Behavioral studies demonstrate that local peripheral injection of the GABA(A) agonist muscimol at a low concentration (2.0 microM) attenuates, and at a high concentration (1 mM) enhances, formalin-induced nociceptive behaviors. Intraplantar injection of muscimol alone at a high dose evokes thermal hyperalgesia. Bicuculline, a GABA(A) antagonist, prevents these muscimol-induced changes in behavior. The muscimol-induced effects are due to local rather than systemic or central activation of GABA(A) receptors, as such effects are not observed in the contralateral paw. We interpret these findings to indicate that activation of GABA(A) receptors by low concentrations of muscimol depolarizes peripheral primary afferent terminals, a phenomenon we call peripheral primary afferent depolarization, in turn reducing the size of the peripheral action potentials and concomitantly reducing the amount of algogenic substances released from the peripheral terminals of these fibers. This sequence of events presumably results in a reduction in nociceptor activation. Higher concentrations of muscimol further depolarize GABA(A) receptor-containing terminals, which then initiates action potentials in nociceptors analogous to the appearance of dorsal root reflexes that arise following activation of GABA(A) receptors on central primary afferent terminals. These latter events reverse the analgesic effects of GABA(A) ligands and lead to potentiation of nociceptive input. Thus, the present study provides anatomical and behavioral evidence supporting a bimodal role for GABA(A) receptors in the modulation of peripheral nociceptive transmission.

摘要

我们提出,脊髓中γ-氨基丁酸A(GABA(A))受体激活后出现的初级传入去极化现象在外周也会发生。作为证据,本研究在猫爪无毛皮肤中,将GABA(A)受体的β2/β3和α1亚基定位在10%-14%的无髓初级传入轴突上。行为学研究表明,在外周局部注射低浓度(2.0微摩尔)的GABA(A)激动剂蝇蕈醇会减弱福尔马林诱导的伤害性反应行为,而高浓度(1毫摩尔)则会增强该反应。足底注射高剂量的蝇蕈醇会引发热痛觉过敏。GABA(A)拮抗剂荷包牡丹碱可阻止这些蝇蕈醇诱导的行为变化。蝇蕈醇诱导的效应是由于外周局部而非全身或中枢的GABA(A)受体激活所致,因为在对侧爪未观察到此类效应。我们将这些发现解释为,低浓度蝇蕈醇激活GABA(A)受体会使外周初级传入终末去极化,我们将这一现象称为外周初级传入去极化,进而减小外周动作电位的幅度,并相应减少这些纤维外周终末释放的致痛物质的量。这一系列事件可能导致伤害感受器激活减少。更高浓度的蝇蕈醇会使含有GABA(A)受体的终末进一步去极化,进而在伤害感受器中引发动作电位,类似于中枢初级传入终末上GABA(A)受体激活后出现的背根反射。后一种情况会逆转GABA(A)配体的镇痛作用,并导致伤害性输入增强。因此,本研究提供了解剖学和行为学证据,支持GABA(A)受体在外周伤害性传递调制中具有双相作用。

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