The effects of glutamate, N-methyl-D-aspartate (NMDA), and NMDA receptor antagonists, D-alpha-aminoadipate (D alpha AA) and 2-amino-5-phosphonovalerate (APV), microionophoretically applied onto neurons in the caudal divisions (posteroventral and dorsal subnuclei) of the cochlear nuclear complex (CN), were investigated during postnatal development in kittens with the use of extracellular techniques. From birth through postnatal day 7, microionophoretically applied glutamate elevated the acoustically evoked discharge rates of nearly 80% of neurons studied. Although fewer neurons were studied with the use of NMDA, approximately 65% of these responded to this glutamatergic agonist, and no developmental changes in the percentage of responsive neurons were observed. The actions of NMDA antagonists were studied in a relatively small number of neurons, and results support the supposition that glutamate, or a glutamate-like substance, acts as a CN neurotransmitter throughout postnatal life. 2. Approximately 64% of CN neurons encountered among neonatal animals were unresponsive to acoustic stimulation, even at the highest output levels available (> 120 dB SPL). That percentage declined monotonically during the next three postnatal days, such that approximately 23% of neurons encountered were unresponsive to acoustic stimulation on the third day. Essentially all encountered neurons were responsive to acoustic stimulation by the middle of the second postnatal week. Under conditions of simultaneous glutamate and acoustic stimulation, neurons in this general class of "acoustically unresponsive" neurons segregated into two groups. Glutamate increased spontaneous discharge rate in 45% of the neurons studied, however, these units remained acoustically unresponsive during combined sound and excitatory amino acid stimulation (group A1). In the second group (A2), 55% of the neurons that were acoustically unresponsive under control (sound alone) conditions responded to the acoustic component of the combined acoustic and glutamate stimulation (the experimental condition) in a frequency-dependent manner. A2 neurons exhibited temporal firing patterns characteristic of acoustically responsive neurons of corresponding age, suggesting that these neurons are functionally connected to the auditory periphery, whereas A1 neurons are not. 3. Dose-response curves were either sigmoidal or linear over the range that measurements were made, and maximum discharge rates evoked by high doses of glutamate in the youngest animals studied tended to be lower than those produced by acoustic stimulation alone in older animals. These results suggest that intrinsic properties contribute to the mechanism(s) that limits neuronal responsiveness. Average dose-response curve slopes were higher for neurons recorded from older animals, also indicating that intrinsic properties regulating dynamic response range are acquired postnatally in the kitten CN.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
利用细胞外记录技术,研究了在新生小猫出生后发育期间,微量离子电泳施加于蜗神经核复合体(CN)尾侧部分(后腹侧和背侧亚核)神经元上的谷氨酸、N-甲基-D-天冬氨酸(NMDA)以及NMDA受体拮抗剂D-α-氨基己二酸(DαAA)和2-氨基-5-磷酸戊酸(APV)的作用。从出生到出生后第7天,微量离子电泳施加的谷氨酸使近80%被研究神经元的声诱发放电率升高。虽然使用NMDA研究的神经元较少,但其中约65%的神经元对这种谷氨酸能激动剂有反应,且未观察到反应性神经元百分比的发育变化。在相对较少数量的神经元中研究了NMDA拮抗剂的作用,结果支持谷氨酸或类似谷氨酸的物质在出生后整个生命过程中作为CN神经递质起作用的假设。2. 在新生动物中遇到的CN神经元中,约64%即使在最高可用输出水平(>120 dB SPL)下也对声刺激无反应。在接下来的出生后三天中,该百分比单调下降,以至于在出生后第三天遇到的神经元中约23%对声刺激无反应。到出生后第二周中期,基本上所有遇到的神经元都对声刺激有反应。在谷氨酸和声刺激同时存在的条件下,这类“声无反应”神经元大致分为两组。谷氨酸使45%被研究神经元的自发放电率增加,然而,在声音和兴奋性氨基酸联合刺激期间,这些单位仍对声音无反应(A1组)。在第二组(A2组)中,在对照(仅声音)条件下对声音无反应的神经元中有55%对声音和谷氨酸联合刺激(实验条件)的声音成分以频率依赖方式有反应。A2神经元表现出相应年龄的声反应性神经元特有的时间放电模式,表明这些神经元在功能上与听觉外周相连,而A1神经元则不然。3. 在进行测量的范围内,剂量-反应曲线呈S形或线性,在最年幼动物中高剂量谷氨酸诱发的最大放电率往往低于年长动物中单独声刺激产生的最大放电率。这些结果表明内在特性有助于限制神经元反应性的机制。从年长动物记录的神经元的平均剂量-反应曲线斜率更高,这也表明调节动态反应范围的内在特性是小猫CN在出生后获得的。(摘要截断于400字)