Jiang Z G, Shen E, Dun N J
Department of Pharmacology, Loyola University Stritch School of Medicine, Maywood, IL 60153.
Brain Res. 1990 Dec 3;535(1):110-8. doi: 10.1016/0006-8993(90)91829-6.
Intracellular recordings were made from antidromically identified motoneurons in neonate (12-22 days) rat transverse spinal cord slices and the transmitters and receptors probably involved in initiating the excitatory (EPSP) and inhibitory (IPSP) postsynaptic potentials were investigated. Stimulation of dorsal roots elicited in motoneurons an EPSP, an IPSP, or an EPSP followed by an IPSP. EPSPs in 70% of motoneurons had a short latency (less than or equal to 1 ms) and in the remaining cells a latency longer than 1 ms. The IPSPs had a long latency (greater than or equal to 1 ms). Short- and long-latency EPSPs were enhanced by the acidic amino acid uptake inhibitor L-aspartic acid-beta-hydroxamate (AAH) and depressed by the non-selective glutamate receptor antagonists gamma-D-glutamylglycine (DGG) and kynurenic acid. Short-latency EPSPs were suppressed by the quisqualate/kainate (QA/KA) receptor antagonist 6,7-dinitroquinoxaline-2,3-dione (DNQX) but not by the N-methyl-D-aspartate (NMDA) receptor antagonists D-(-)-2-amino-5-phosphonovaleric acid (APV) and ketamine. Long-latency EPSPs were reduced by DNQX as well as by APV and ketamine. Superfusion of the slices with a Mg-free solution increased the EPSPs and unmasked a late, APV-sensitive component. The IPSP was reduced by the glycine antagonist strychnine as well as by APV and ketamine but resistant to DNQX. The results indicate that stimulation of dorsal roots elicited in motoneurons a monosynaptic EPSP mediated by glutamate/aspartate acting predominantly on the QA/KA subtype of glutamate receptors; an NMDA component can be unveiled in Mg-free solution.(ABSTRACT TRUNCATED AT 250 WORDS)
在新生(12 - 22天)大鼠横断脊髓切片中,对经逆向冲动鉴定的运动神经元进行细胞内记录,并研究了可能参与引发兴奋性(EPSP)和抑制性(IPSP)突触后电位的递质和受体。刺激背根在运动神经元中引发一个EPSP、一个IPSP或一个先出现EPSP随后出现IPSP的情况。70%的运动神经元中的EPSP潜伏期较短(小于或等于1毫秒),其余细胞中的潜伏期长于1毫秒。IPSP潜伏期较长(大于或等于1毫秒)。酸性氨基酸摄取抑制剂L - 天冬氨酸 - β - 羟肟酸(AAH)增强了短潜伏期和长潜伏期的EPSP,而非选择性谷氨酸受体拮抗剂γ - D - 谷氨酰甘氨酸(DGG)和犬尿氨酸则使其降低。quisqualate/kainate(QA/KA)受体拮抗剂6,7 - 二硝基喹喔啉 - 2,3 - 二酮(DNQX)抑制短潜伏期EPSP,但N - 甲基 - D - 天冬氨酸(NMDA)受体拮抗剂D - ( - ) - 2 - 氨基 - 5 - 磷酸戊酸(APV)和氯胺酮则无此作用。DNQX以及APV和氯胺酮均可降低长潜伏期EPSP。用无镁溶液灌流切片可增强EPSP并揭示出一个晚期的、对APV敏感的成分。甘氨酸拮抗剂士的宁以及APV和氯胺酮可降低IPSP,但IPSP对DNQX有抗性。结果表明,刺激背根在运动神经元中引发一个由谷氨酸/天冬氨酸介导的单突触EPSP,其主要作用于谷氨酸受体的QA/KA亚型;在无镁溶液中可揭示出一个NMDA成分。(摘要截短于250词)