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中缝大核刺激诱导的猫抗伤害感受与腰段背角中氨基酸以及5-羟色胺的释放有关。

Raphe magnus stimulation-induced antinociception in the cat is associated with release of amino acids as well as serotonin in the lumbar dorsal horn.

作者信息

Sorkin L S, McAdoo D J, Willis W D

机构信息

Marine Biomedical Institute, University of Texas Medical Branch, Galveston 77555-0843.

出版信息

Brain Res. 1993 Jul 30;618(1):95-108. doi: 10.1016/0006-8993(93)90433-n.

DOI:10.1016/0006-8993(93)90433-n
PMID:8402183
Abstract

Stimulation in the nucleus raphe magnus (NRM) inhibits transmission of nociceptive information within the spinal cord through activation of bulbospinal pathways. This study used microdialysis in combination with high pressure liquid chromatography to measure the release of serotonin (5HT) and several amino acids, including glutamate, aspartate and glycine, from the lumbar dorsal horn during electrical stimulation within the NRM in the alpha-chloralose anesthetized cat. Observed release of putative neurotransmitters was correlated with inhibition of nociceptive projection neurons recorded from sites within 800 microns rostral or caudal to the dialysis fiber. NRM stimulus parameters considered to preferentially activate myelinated fibers caused inhibition of nociceptive evoked activity, and increased the release of excitatory amino acids and glycine within the spinal cord, with no detectable release of 5HT. When pulse widths were lengthened and unmyelinated fibers were also activated, increases in 5HT in the spinal dialysate were observed as well. Strychnine administered through the dialysis fiber (0.02-1 mM) antagonized NRM-induced inhibition when 5HT release was not detected. Inhibition produced by stimulation that increased 5HT concentrations was relatively strychnine resistant. These results point to a raphe-spinal inhibitory pathway that is not dependent on 5HT, the activation of which results in the spinal release of glycine.

摘要

中缝大核(NRM)的刺激通过激活延髓脊髓通路抑制脊髓内伤害性信息的传递。本研究采用微透析结合高压液相色谱法,在α-氯醛糖麻醉的猫中,测量在NRM电刺激期间腰段背角中5-羟色胺(5HT)以及包括谷氨酸、天冬氨酸和甘氨酸在内的几种氨基酸的释放。观察到的假定神经递质的释放与从透析纤维头端或尾端800微米范围内记录的伤害性投射神经元的抑制相关。被认为优先激活有髓纤维的NRM刺激参数可抑制伤害性诱发活动,并增加脊髓内兴奋性氨基酸和甘氨酸的释放,而未检测到5HT的释放。当脉冲宽度延长且无髓纤维也被激活时,脊髓透析液中的5HT也会增加。当未检测到5HT释放时,通过透析纤维给予士的宁(0.02-1 mM)可拮抗NRM诱导的抑制作用。由增加5HT浓度的刺激产生的抑制作用相对抗士的宁。这些结果表明存在一条不依赖5HT的中缝脊髓抑制通路,其激活导致脊髓释放甘氨酸。

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