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大鼠背角I层和III - V层区域中不同阿片受体介导的不同抗伤害感受作用。

Distinct antinociceptive actions mediated by different opioid receptors in the region of lamina I and laminae III-V of the dorsal horn of the rat.

作者信息

Hope P J, Fleetwood-Walker S M, Mitchell R

机构信息

Department of Preclinical Veterinary Sciences, University of Edinburgh.

出版信息

Br J Pharmacol. 1990 Oct;101(2):477-83. doi: 10.1111/j.1476-5381.1990.tb12733.x.

Abstract
  1. In view of the presence of mu, delta and kappa opioid receptors in the spinal dorsal horn and their apparent involvement in behavioural analgesia, the present experiments addressed the action of selective agonists ionophoresed in the vicinity of rat dorsal horn neurones which were located either in lamina I or in laminae III-V. 2. In laminae III-V, kappa agonists (U50488H and dynorphin A) caused a selective inhibition of the nociceptive responses of multireceptive cells, whilst mu and delta agonists [( D-Ala2, MePhe4, Gly-ol]enkephalin and [D-Pen2, D-Pen5]enkephalin respectively) failed to alter either the spontaneous activity or the response to noxious and innocuous cutaneous stimuli and to D,L-homocysteic acid or glutamate. Nocispecific neurones were encountered too rarely in laminae III-V to study their properties. 3. In lamina I, agonists had no effects on either nocispecific or multireceptive neurones. In contrast, the mu agonist [D-Ala2, MePhe4, Gly-ol]enkephalin consistently inhibited nociceptive responses of both multireceptive and nocispecific lamina I cells. The delta agonist [D-Pen2, D-Pen5]enkephalin consistently caused selective inhibition of the nociceptive responses of multireceptive cells but had a mixed profile of action on nocispecific cells. 4. These results suggest that mu, delta and kappa opioid receptors mediate different antinociceptive actions in both laminae III-V and lamina I. The study reveals a distinct physiological role for delta receptors in modulating nociceptive inputs to lamina I neurones. In contrast to mu and kappa receptor actions, delta receptors heterogeneously influence subpopulations of neurones.
摘要
  1. 鉴于脊髓背角中存在μ、δ和κ阿片受体,且它们明显参与行为性镇痛,本实验研究了选择性激动剂在位于I层或III - V层的大鼠背角神经元附近进行离子导入时的作用。2. 在III - V层,κ激动剂(U50488H和强啡肽A)对多感受性细胞的伤害性反应产生选择性抑制,而μ和δ激动剂(分别为[D - Ala2,MePhe4,Gly - ol]脑啡肽和[D - Pen2,D - Pen5]脑啡肽)未能改变自发活动,也未改变对有害和无害皮肤刺激以及对D,L - 高半胱氨酸或谷氨酸的反应。在III - V层中遇到的伤害特异性神经元太少,无法研究其特性。3. 在I层,激动剂对伤害特异性或多感受性神经元均无影响。相反,μ激动剂[D - Ala2,MePhe4,Gly - ol]脑啡肽持续抑制I层多感受性和伤害特异性细胞的伤害性反应。δ激动剂[D - Pen2,D - Pen5]脑啡肽持续对多感受性细胞的伤害性反应产生选择性抑制,但对伤害特异性细胞的作用具有混合特征。4. 这些结果表明,μ、δ和κ阿片受体在III - V层和I层中介导不同的抗伤害作用。该研究揭示了δ受体在调节向I层神经元的伤害性输入方面具有独特的生理作用。与μ和κ受体的作用不同,δ受体对神经元亚群有不同的影响。

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