Team Pain, INSERM UMRS 975, CNRS UMR 7225, Paris, France.
Neuropharmacology. 2011 Sep;61(4):551-7. doi: 10.1016/j.neuropharm.2011.04.020. Epub 2011 May 6.
Gabapentin is a structural analogue of gamma-amino-butyric acid with anticonvulsant activity. Recently, indications for its use were extended to the management of acute pain in the postoperative period. The effects of pre-administration of gabapentin on the depressive action of intravenous morphine were studied on the C-fibre reflex elicited by a wide range of stimulus intensities. The reflex was elicited by electrical stimulation of the sural nerve and recorded from the ipsilateral biceps femoris muscle in halothane anaesthetized rats with either an intact neuraxis or a brainstem previously transected at the level of the obex. As previously reported, 6 mg/kg intravenous morphine both increased the threshold and decreased the slope of the stimulus-response recruitment curve. The C-fibre reflex was not modified following intravenous gabapentin. Gabapentin pre-treatment at lower doses (0.01-7.5 mg/kg) not only antagonized the depressive effect of morphine, but caused facilitation of the reflex. At higher doses (10-50 mg/kg), gabapentin pre-treatment potentiated the depressive effect of morphine. In obex-transected rats, the facilitation of the C-fibre reflex, seen following 1 mg/kg gabapentin and 6 mg/kg morphine, disappeared and was replaced by a strong reinforcement of the depressive effect of morphine. It is concluded that a strong synergy between the effects of gabapentin and morphine can be seen at the spinal level. However, radically opposite effects with supraspinal origins thwart this mechanism. From the clinical standpoint, these results incite cautiousness in the use of combinations of gabapentin and opioids.
加巴喷丁是一种γ-氨基丁酸的结构类似物,具有抗惊厥活性。最近,其用途的适应证已扩展到管理术后期间的急性疼痛。在广泛的刺激强度下,研究了加巴喷丁给药前对静脉注射吗啡的抑制作用。在氟烷麻醉的大鼠中,通过刺激腓肠神经来引发 C 纤维反射,并从对侧股二头肌肌肉记录反射,此时神经轴完整或脑干在延髓水平之前被横切。如前所述,6 mg/kg 静脉注射吗啡既增加了阈值,又降低了刺激-反应募集曲线的斜率。静脉注射加巴喷丁后,C 纤维反射没有改变。较低剂量(0.01-7.5 mg/kg)的加巴喷丁预处理不仅拮抗了吗啡的抑制作用,而且还引起了反射的易化。在较高剂量(10-50 mg/kg)时,加巴喷丁预处理增强了吗啡的抑制作用。在延髓横切大鼠中,1 mg/kg 加巴喷丁和 6 mg/kg 吗啡引起的 C 纤维反射易化消失,被吗啡抑制作用的强烈增强所取代。结论是,在脊髓水平可以看到加巴喷丁和吗啡之间的强烈协同作用。然而,来自于脊髓以上的根本相反的影响却挫败了这种机制。从临床角度来看,这些结果促使在使用加巴喷丁和阿片类药物的组合时要谨慎。