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猫脊髓中功能确定的背角神经元感觉输入的兴奋性氨基酸受体介导

Excitatory amino acid receptor mediation of sensory inputs to functionally identified dorsal horn neurons in cat spinal cord.

作者信息

Radhakrishnan V, Henry J L

机构信息

Department of Psychiatry, McGill University, Montreal, Quebec, Canada.

出版信息

Neuroscience. 1993 Jul;55(2):531-44. doi: 10.1016/0306-4522(93)90522-h.

DOI:10.1016/0306-4522(93)90522-h
PMID:7690912
Abstract

As excitatory amino acid receptors have been implicated in nociceptive sensory transmission, the principal objective of the present study was to investigate the effects of various excitatory amino acid antagonists on naturally evoked responses in spinal dorsal horn neurons. Extracellular single unit activity was recorded from functionally identified, spinal dorsal horn neurons in unanesthetized, decerebrated cats and in alpha-chloralose-anesthetized cats. The tests included iontophoretic application of the N-methyl-D-aspartate (NMDA) receptor antagonist 2-amino-5-phosphonovaleric acid (APV), the non-N-methyl-D-aspartate receptor antagonists 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX) and kynurenate, and also the intravenous administration of the N-methyl-D-aspartate receptor antagonist, ketamine. In addition, attempts were made to determine the effects on these neurons of iontophoretic application of the excitatory amino acid agonists, L-glutamate, N-methyl-D-aspartate, quisqualate, (RS)-alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionate (AMPA) and domoate. Marked differences were noted in the actions of agonists and antagonists between the responses observed in the unanesthetized, decerebrated and the anesthetized animals. In decerebrated cats, responses to hair afferent stimulation were blocked by kynurenate, 6-cyano-7-nitroquinoxaline-2,3-dione and 2-amino-5-phosphonovaleric acid. Responses to noxious thermal stimulation were attenuated by 2-amino-5-phosphonovaleric acid and in one unit also by ketamine. Neither 6-cyano-7-nitroquinoxaline-2,3-dione nor kynurenate affected the responses to noxious thermal stimulation. The proportion of cells responding to the agonists were: N-methyl-D-aspartate 24/27 (89%), quisqualate 12/13 (92%) and domoate 6/7 (86%). In chloralose-anesthetized cats, responses to hair afferent stimulation were blocked by 6-cyano-7-nitroquinoxaline-2,3-dione and kynurenate but not by 2-amino-5-phosphonovaleric acid. Responses to noxious thermal stimulation were not affected by any of these antagonists, while the response to non-noxious thermal stimulation was blocked by 2-amino-5-phosphonovaleric acid, ketamine and kynurenate in the one neuron studied. The proportion of cells excited by the agonists differed from those observed in decerebrated cats: N-methyl-D-aspartate 9/32 (28%), quisqualate 50/54 (93%), (RS)-alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionate 19/23 (83%) and domoate 17/38 (45%). Application of the putative endogenous excitatory amino acid precursor N-acetyl-aspartyl-glutamate (NAAG) did not elicit a response in any of the neurons studied.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

由于兴奋性氨基酸受体与伤害性感觉传递有关,本研究的主要目的是探讨各种兴奋性氨基酸拮抗剂对脊髓背角神经元自然诱发反应的影响。在未麻醉、去大脑的猫以及α-氯醛糖麻醉的猫中,对功能鉴定的脊髓背角神经元进行细胞外单单位活动记录。测试包括离子导入N-甲基-D-天冬氨酸(NMDA)受体拮抗剂2-氨基-5-磷酸戊酸(APV)、非N-甲基-D-天冬氨酸受体拮抗剂6-氰基-7-硝基喹喔啉-2,3-二酮(CNQX)和犬尿烯酸,以及静脉注射N-甲基-D-天冬氨酸受体拮抗剂氯胺酮。此外,还尝试确定离子导入兴奋性氨基酸激动剂L-谷氨酸、N-甲基-D-天冬氨酸、quisqualate、(RS)-α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)和软骨藻酸对这些神经元的影响。在未麻醉、去大脑的动物和麻醉动物中观察到的激动剂和拮抗剂的作用存在明显差异。在去大脑的猫中,犬尿烯酸、6-氰基-7-硝基喹喔啉-2,3-二酮和2-氨基-5-磷酸戊酸可阻断对毛发传入刺激的反应。2-氨基-5-磷酸戊酸可减弱对有害热刺激的反应,在一个单位中氯胺酮也有此作用。6-氰基-7-硝基喹喔啉-2,3-二酮和犬尿烯酸均不影响对有害热刺激的反应。对激动剂有反应的细胞比例分别为:N-甲基-D-天冬氨酸24/27(89%)、quisqualate 12/13(92%)和软骨藻酸6/7(86%)。在氯醛糖麻醉的猫中,6-氰基-7-硝基喹喔啉-2,3-二酮和犬尿烯酸可阻断对毛发传入刺激的反应,但2-氨基-5-磷酸戊酸无此作用。这些拮抗剂均不影响对有害热刺激的反应,而在所研究的一个神经元中,2-氨基-5-磷酸戊酸、氯胺酮和犬尿烯酸可阻断对非有害热刺激的反应。被激动剂兴奋的细胞比例与在去大脑猫中观察到的不同:N-甲基-D-天冬氨酸9/32(28%)、quisqualate 50/54(93%)、(RS)-α-氨基-3-羟基-5-甲基-4-异恶唑丙酸19/23(83%)和软骨藻酸17/38(45%)。应用假定的内源性兴奋性氨基酸前体N-乙酰天冬氨酰谷氨酸(NAAG)在所研究的任何神经元中均未引发反应。(摘要截断于400字)

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