首页> 外文OA文献 >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.
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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.

机译:在大鼠背角的层I和层III-V区域中,不同的阿片受体介导的不同的镇痛作用。

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摘要

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.
机译:1.鉴于在脊髓背角中存在mu,delta和kappa类阿片受体,并且它们明显参与行为镇痛,本实验研究了在大鼠背角神经元附近电离选择的选择性激动剂的作用。在层I或层III-V中。 2.在薄片III-V中,κ激动剂(U50488H和强啡肽A)选择性抑制多受体细胞的伤害感受反应,而mu和δ激动剂[(D-Ala2,MePhe4,Gly-ol]脑啡肽和[D- Pen2,D-Pen5]脑啡肽均不能改变自发活性或对有害和无害的皮肤刺激以及对D,L-同型半胱氨酸或谷氨酸的反应。在III-V层中很少遇到伤害特异性神经元,无法研究其特性。 3.在层I中,激动剂对伤害特异性神经元或多受体神经元均无影响。相反,mu激动剂[D-Ala2,MePhe4,Gly-ol]脑啡肽始终抑制多感受性和伤害特异性层板I细胞的伤害感受性反应。 δ激动剂[D-Pen2,D-Pen5]脑啡肽始终引起多受体细胞伤害感受性反应的选择性抑制,但对伤害特异性细胞的作用却呈混合状态。 4.这些结果表明,μ,δ和κ阿片样物质受体在III-V层和层I中介导不同的镇痛作用。该研究揭示了δ受体在调节层I神经元的伤害感受输入中的独特生理作用。与mu和kappa受体的作用相反,δ受体异质地影响神经元的亚群。

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