Smith D V, Li C S, Davis B J
Department of Anatomy & Neurobiology, University of Maryland School of Medicine, Baltimore 21201-1509, USA.
Ann N Y Acad Sci. 1998 Nov 30;855:450-6. doi: 10.1111/j.1749-6632.1998.tb10605.x.
The rostral portion of the nucleus of the solitary tract (NST) contains second-order gustatory neurons, sends projections to the parabrachial complex and brainstem reticular formation, and receives descending projections from several nuclei of the ascending gustatory pathway. Electrophysiological responses of NST neurons can be modulated by several factors, including blood glucose and insulin levels and taste aversion conditioning. We are using extracellular electrophysiological recording in vivo, combined with local microinjection of neurotransmitter agonists and antagonists, to study the mechanisms by which taste responses of cells in the hamster NST can be modulated. Afferent fibers of the chorda tympani (CT) nerve make excitatory synaptic contact with NST neurons; this excitation is probably mediated by the excitatory amino acid glutamate. Microinjection of kynurenic acid, a nonspecific glutamate receptor antagonist, into the NST completely and reversibly blocks afferent input from the CT nerve, produced by either anodal electrical or chemical stimulation of the anterior tongue. The non-NMDA ((RS)-alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA)/kainate) receptor antagonist 6-cyano-7-nitroquinoxaline-2, 3-dione (CNQX) also completely blocks gustatory input to these cells, whereas the N-methyl-D-aspartate (NMDA) antagonist DL-2-amino-5-phosphonovalerate (APV) produces only a small effect. There are many gamma-aminobutyric acid (GABA)-containing neurons within the NST and taste-responsive NST cells are maintained under a tonic GABAergic inhibition. Microinjection of the GABAA receptor antagonist bicuculline methiodide increases the taste responsiveness of NST neurons, whereas application of GABA inhibits taste responses in these cells. Preliminary data show that GABAergic inhibition can be produced by stimulation of the gustatory cortex. There are both intrinsic substance P (SP)-containing neurons and extrinsic SP-immunoreactive fibers in the rostral NST. Microinjection of SP into the NST enhances the responses of many NST cells to gustatory stimulation; NaCl-best neurons are preferentially excited by SP.
孤束核(NST)的吻侧部分包含二级味觉神经元,向臂旁复合体和脑干网状结构发出投射,并接收来自上行味觉通路多个核团的下行投射。NST神经元的电生理反应可受多种因素调节,包括血糖和胰岛素水平以及味觉厌恶条件反射。我们正在使用体内细胞外电生理记录技术,结合局部微量注射神经递质激动剂和拮抗剂,来研究仓鼠NST中细胞味觉反应的调节机制。鼓索神经(CT)的传入纤维与NST神经元形成兴奋性突触联系;这种兴奋可能由兴奋性氨基酸谷氨酸介导。向NST微量注射非特异性谷氨酸受体拮抗剂犬尿氨酸,可完全且可逆地阻断由阳极电刺激或前舌化学刺激产生的来自CT神经的传入输入。非NMDA((RS)-α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)/海人藻酸)受体拮抗剂6-氰基-7-硝基喹喔啉-2,3-二酮(CNQX)也可完全阻断这些细胞的味觉输入,而N-甲基-D-天冬氨酸(NMDA)拮抗剂DL-2-氨基-5-磷酸戊酸(APV)仅产生微小影响。NST内有许多含γ-氨基丁酸(GABA)的神经元,味觉反应性NST细胞处于持续性GABA能抑制之下。向NST微量注射GABAA受体拮抗剂甲硫酸荷包牡丹碱可增加NST神经元的味觉反应性,而应用GABA则抑制这些细胞的味觉反应。初步数据表明,味觉皮质的刺激可产生GABA能抑制。吻侧NST既有含内源性P物质(SP)的神经元,也有外源性SP免疫反应性纤维。向NST微量注射SP可增强许多NST细胞对味觉刺激的反应;对NaCl反应最佳的神经元优先被SP兴奋。