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[大鼠缰核刺激导致纳洛酮可逆性镇痛]

[Naloxone-reversible analgesia as a result of stimulation of the habenula in the rat].

作者信息

Mahieux G, Benabid A L

出版信息

Neurochirurgie. 1986;32(4):360-4.

PMID:3035396
Abstract

Electrical stimulation of rat habenular complex induces analgesia, evaluated by the tail-flick test, dependent on intensity of stimulation with a long post-effect, that is reversible by naloxone and without behavior effects at less that 400 mA. Bilateral destruction of habenula fails to provoke hyperesthesia but causes more marked long-term tolerance effects than in controls. Anatomy suggests that the habenula activates an inhibitory descending system in the spinal cord with a probable relay in the dorsal raphe and involving an endogenous opioid-dependent stage.

摘要

通过甩尾试验评估,对大鼠缰核复合体进行电刺激可诱导镇痛作用,该作用取决于刺激强度,具有较长的后效应,可被纳洛酮逆转,且在刺激强度低于400毫安时无行为效应。双侧损毁缰核不会引发感觉过敏,但与对照组相比,会导致更明显的长期耐受效应。解剖学表明,缰核激活脊髓中的抑制性下行系统,可能在中缝背核存在中继,且涉及内源性阿片依赖阶段。

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