Department of Neuroscience, Physiology and Pharmacology, University College London, London WC1E 6BT, UK.
Biochem Soc Trans. 2010 Apr;38(2):525-8. doi: 10.1042/BST0380525.
Neuropathic pain is caused by lesion or dysfunction of the peripheral sensory nervous system. Up-regulation of the voltage-gated Ca(2+) channel subunit alpha(2)delta-1 in DRG (dorsal root ganglion) neurons and the spinal cord correlates with the onset of neuropathic pain symptoms such as allodynia in several animal models of neuropathic pain. The clinically important anti-allodynic drugs gabapentin and pregabalin are alpha(2)delta-1 ligands, but how these drugs alleviate neuropathic pain is poorly understood. In the present paper, we review recent advances in our understanding of their molecular mechanisms.
神经病理性疼痛是由外周感觉神经系统的损伤或功能障碍引起的。在几种神经病理性疼痛动物模型中,背根神经节 (DRG) 神经元和脊髓中电压门控钙 (Ca(2+)) 通道亚基 α(2)δ-1 的上调与痛觉过敏等神经病理性疼痛症状的发生相关。临床上重要的抗痛觉过敏药物加巴喷丁和普瑞巴林是 α(2)δ-1 配体,但这些药物如何缓解神经病理性疼痛尚不清楚。在本文中,我们综述了对其分子机制的理解的最新进展。