Centre National de la Recherche Scientifique, CNR2M, Unité Mixte de Recherche 6231, Université Paul Cézanne, Université de la Méditerranée, IFR Jean Roche, Faculté de Médecine, CS80011, Bd Pierre Dramard, 13344, Marseille Cx15, France.
J Physiol. 2010 Apr 1;588(Pt 7):1097-115. doi: 10.1113/jphysiol.2009.184838. Epub 2010 Feb 15.
Using combined morphological and electrophysiological approaches, we have determined the composition of inhibitory synapses of the nucleus tractus solitarii (NTS), a brainstem structure that is a gateway for many visceral sensory afferent fibres. Immunohistochemical experiments demonstrate that, in adult rat, GABA axon terminals are present throughout the NTS while mixed GABA-glycine axon terminals are strictly located to the lateral part of the NTS within subnuclei surrounding the tractus solitarius. Purely glycine axon terminals are rare in the lateral part of the NTS and hardly detected in its medial part. Electrophysiological experiments confirm the predominance of GABA inhibition throughout the NTS and demonstrate the existence of a dual inhibition involving the co-release of GABA and glycine restricted to the lateral part of NTS. Since GABA(A) and glycine receptors are co-expressed postsynaptically in virtually all the inhibitory axon terminals throughout the NTS, it suggests that the inhibition phenotype relies on the characteristics of the axon terminals. Our results also demonstrate that glycine is mostly associated with GABA within axon terminals and raise the possibility of a dynamic regulation of GABA/glycine release at the presynaptic level. Our data provide new information for understanding the mechanisms involved in the processing of visceral information by the central nervous system in adult animals.
我们采用形态学和电生理学相结合的方法,确定了孤束核(NTS)抑制性突触的组成,NTS 是许多内脏感觉传入纤维的门户。免疫组织化学实验表明,在成年大鼠中,GABA 轴突末梢存在于整个 NTS 中,而混合的 GABA-甘氨酸轴突末梢严格位于围绕孤束的 NTS 的外侧部分的亚核内。纯粹的甘氨酸轴突末梢在 NTS 的外侧部分很少见,在其内侧部分几乎检测不到。电生理学实验证实 GABA 抑制在整个 NTS 中占主导地位,并证明存在一种双重抑制,涉及 GABA 和甘氨酸的共同释放,仅限于 NTS 的外侧部分。由于 GABA(A)和甘氨酸受体在后突触几乎所有抑制性轴突末梢中共表达,这表明抑制表型依赖于轴突末梢的特征。我们的结果还表明,甘氨酸主要与轴突末梢内的 GABA 相关,并提出了在突触前水平动态调节 GABA/甘氨酸释放的可能性。我们的数据为理解成年动物中枢神经系统处理内脏信息的机制提供了新的信息。