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痛敏肽(孤啡肽FQ),一种QRL1(阿片受体样1)受体的内源性配体;调节由兴奋性氨基酸和体感刺激诱发的三叉神经神经元反应。

Nociceptin (orphanin FQ), an endogenous ligand for the QRL1 (opioid-receptor-like1) receptor; modulates responses of trigeminal neurons evoked by excitatory amino acids and somatosensory stimuli.

作者信息

Wang X M, Zhang K M, Mokha S S

机构信息

Department of Physiology, Meharry Medical College, Nashville, Tennessee 37208, USA.

出版信息

J Neurophysiol. 1996 Nov;76(5):3568-72. doi: 10.1152/jn.1996.76.5.3568.

Abstract
  1. This is the first in vivo electrophysiological evidence demonstrating the effects of Phe-Gly-Gly-Phe-Thr-Gly-Ala-Arg-Lys-Ser-Ala-Arg-Lys-Leu-Ala-Asn-Gln (nociceptin or orphanin FQ), an endogenous ligand for the orphan ORL1 receptor, on nociceptive neurons in the CNS. The effects of nociceptin were tested on the responses of neurons recorded in the superficial and deeper dorsal horn of the medulla (trigeminal nucleus caudalis) in the rat. 2. Nociceptin applied microiontophoretically produced a predominantly long-lasting (5-30 min) inhibitory modulation of the N-methyl-D-aspartic acid (NMDA)-evoked responses of 24 of 31 nociceptive and 12 of 12 nonnociceptive neurons. Excitatory or biphasic effects of nociceptin were also observed in 6 of 43 neurons. Responses evoked by (+/-)-alpha-amino-3-hydroxy-5-methylisox-azole-4-propionic acid (AMPA) were reduced in eight of nine nociceptive and nonnociceptive neurons. 3. The inhibitory effect of nociceptin was not modality specific; responses to both noxious and nonnoxious stimuli were reduced. 4. Although naloxone applied iontophoretically blocked or reduced the peak inhibitory effect of [D-Ala2,N-Me-Phe4, Gly5-ol]-Enkephalin (DAMGO) or trans-(+/-)-3,4-dicholoro-N-methyl-N-(2-1-pyrrolidinyl-cyclo hexyl)-benzene acetamide (U50, 488H), it did not produce a significant alteration in the peak inhibitory effect of nociceptin. 5. Nociceptin administered intracerebroventricularly produced a long-lasting (20-35 min) reduction in the NMDA-evoked responses of three of three nociceptive neurons. 6. Nociceptin produces a predominantly antinociceptive action in the trigeminal system.
摘要
  1. 这是首个体内电生理学证据,证明孤啡肽(Phe-Gly-Gly-Phe-Thr-Gly-Ala-Arg-Lys-Ser-Ala-Arg-Lys-Leu-Ala-Asn-Gln),即孤儿ORL1受体的内源性配体,对中枢神经系统伤害性神经元的作用。在大鼠延髓(三叉神经尾侧核)浅部和深部背角记录的神经元反应上测试了孤啡肽的作用。2. 微离子导入法施加孤啡肽对31个伤害性神经元中的24个以及12个非伤害性神经元中12个的N-甲基-D-天冬氨酸(NMDA)诱发反应产生了主要为持久的(5 - 30分钟)抑制性调制。在43个神经元中的6个中也观察到了孤啡肽的兴奋性或双相性作用。在9个伤害性和非伤害性神经元中的8个中,(±)-α-氨基-3-羟基-5-甲基异恶唑-4-丙酸(AMPA)诱发的反应减弱。3. 孤啡肽的抑制作用并非模式特异性;对有害和无害刺激的反应均减弱。4. 虽然离子导入法施加的纳洛酮阻断或降低了[D-丙氨酸2,N-甲基苯丙氨酸4,甘氨酸5-醇]-脑啡肽(DAMGO)或反式-(±)-3,4-二氯-N-甲基-N-(2-1-吡咯烷基-环己基)-苯乙酰胺(U50,488H)的峰值抑制作用,但它并未使孤啡肽的峰值抑制作用产生显著改变。5. 脑室内给予孤啡肽使3个伤害性神经元中的3个的NMDA诱发反应产生了持久的(20 - 35分钟)降低。6. 孤啡肽在三叉神经系统中主要产生抗伤害感受作用。

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