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NMDA和非NMDA受体参与介导猫脊髓内脏作害性信息传递
引用本文:宋学军 赵志奇. NMDA和非NMDA受体参与介导猫脊髓内脏作害性信息传递[J]. 中国药理学报, 1999, 20(4): 308-312
作者姓名:宋学军 赵志奇
摘    要:

关 键 词:天冬氨酸受体 NMDA 脊髓 内脏传入

Involvement of NMDA and non-NMDA receptors in transmission of spinal visceral nociception in cat.
X J Song,Z Q Zhao. Involvement of NMDA and non-NMDA receptors in transmission of spinal visceral nociception in cat.[J]. Acta Pharmacologica Sinica, 1999, 20(4): 308-312
Authors:X J Song  Z Q Zhao
Affiliation:Shanghai Brain Research Institute, Chinese Academy of Sciences, China.
Abstract:AIM: To study the role of N-methyl-D-aspartic acid (NMDA) and non-NMDA receptors in processing nociceptive visceral information in the spinal cord. METHODS: The firing of spinal dorsal horn neurons to colorectal distension (3-15 kPa, 20 s) by inflation with air of latex balloon was recorded in 25 anesthetized cats. RESULTS: 1) According to the patterns of responses to colorectal distension, the neurons with increase and decrease in firing were classified as excitatory and inhibitory, respectively. The former consisted of 17 short-latency abrupt (SLA) neurons, 11 short-latency sustained (SLS) neurons, 9 long-latency (LL) neurons. The 15 inhibited (Inh) neurons were recorded. 2) Microelectrophoretic administration of NMDA, quisqualic acid (QA), and kainic acid (KA) activated 67.6%, 78.4%, and 59.5% of the colorectal distension-excited neurons tested. Also, 60%, 86.7%, and 53.3% of Inh neurons were activated by these 3 amino acids. 3) Colorectal distension-induced excitatory responses were reduced by 35% +/- 10% and 65% +/- 14% by a selective NMDA receptor antagonist d,l-2-amino-5-phosphonovalerate (APV) and a selective non-NMDA receptor antagonist 6,7-dinitro-quinoxaline-2,3-dione (DNQX), respectively. Such DNQX-induced inhibition was significantly more potent than that by APV (P < 0.05). Colorectal distension-induced inhibitory responses were partially relieved by 30%-50% in 3/7 Inh neurons by DNQX, but not APV. CONCLUSION: Both NMDA and non-NMDA receptors are involved in transmission and/or modulation of spinal visceral nociceptive information and non-NMDA receptors may play more important role than NMDA receptors.
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