• Biochem. Soc. Trans. · Apr 2010

    Review

    The anti-allodynic alpha(2)delta ligand pregabalin inhibits the trafficking of the calcium channel alpha(2)delta-1 subunit to presynaptic terminals in vivo.

    • Claudia S Bauer, Wahida Rahman, Alexandra Tran-van-Minh, Rafael Lujan, Anthony H Dickenson, and Annette C Dolphin.
    • Department of Neuroscience, Physiology and Pharmacology, University College London, London WC1E 6BT, UK. c.bauer@ucl.ac.uk
    • Biochem. Soc. Trans. 2010 Apr 1;38(2):525-8.

    AbstractNeuropathic 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.

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