Benbouzid Malika, Gavériaux-Ruff Claire, Yalcin Ipek, Waltisperger Elisabeth, Tessier Luc-Henri, Muller André, Kieffer Brigitte L, Freund-Mercier Marie José, Barrot Michel
Institut des Neurosciences Cellulaires et Intégratives, Centre National de Recherche Scientifique/Université Louis Pasteur, Strasbourg, France.
Biol Psychiatry. 2008 Mar 15;63(6):633-6. doi: 10.1016/j.biopsych.2007.06.016. Epub 2007 Aug 13.
The therapeutic effect of antidepressant drugs against depression usually necessitates a chronic treatment. A large body of clinical evidence indicates that antidepressant drugs can also be highly effective against chronic neuropathic pain. However, the mechanism by which these drugs alleviate pain is still unclear.
We used a murine model of neuropathic pain induced by sciatic nerve constriction to study the antiallodynic properties of a chronic treatment with the tricyclic antidepressants nortriptyline and amitriptyline. Using knockout and pharmacological approaches in mice, we determined the influence of delta-opioid receptors in the therapeutic action of chronic antidepressant treatment.
In our model, a chronic treatment by tricyclic antidepressant drugs totally suppresses the mechanical allodynia in neuropathic C57Bl/6J mice. This therapeutic effect can be acutely reversed by an injection of the delta-opioid receptor antagonist naltrindole. Moreover, the antiallodynic property of antidepressant treatment is absent in mice deficient for the delta-opioid receptor gene.
The antiallodynic effect of chronic antidepressant treatment is mediated by a recruitment of the endogenous opioid system acting through delta-opioid receptors.
抗抑郁药物治疗抑郁症通常需要长期治疗。大量临床证据表明,抗抑郁药物对慢性神经性疼痛也可能具有高效性。然而,这些药物缓解疼痛的机制仍不清楚。
我们使用坐骨神经缩窄诱导的神经性疼痛小鼠模型,研究三环类抗抑郁药去甲替林和阿米替林长期治疗的抗痛觉过敏特性。通过基因敲除和药理学方法,我们确定了δ-阿片受体在慢性抗抑郁治疗的治疗作用中的影响。
在我们的模型中,三环类抗抑郁药物的长期治疗完全抑制了神经性C57Bl/6J小鼠的机械性痛觉过敏。注射δ-阿片受体拮抗剂纳曲吲哚可急性逆转这种治疗效果。此外,在缺乏δ-阿片受体基因的小鼠中,抗抑郁治疗的抗痛觉过敏特性不存在。
慢性抗抑郁治疗的抗痛觉过敏作用是通过内源性阿片系统经δ-阿片受体介导的。