• Brain Res Rev · Jun 2011

    Review

    Cellular and molecular insights into neuropathy-induced pain hypersensitivity for mechanism-based treatment approaches.

    • Julie V Berger, Liesbeth Knaepen, Sofie P M Janssen, Robby J P Jaken, Marco A E Marcus, Elbert A J Joosten, and Ronald Deumens.
    • Department of Anesthesiology, Maastricht University Medical Centre, Maastricht, The Netherlands.
    • Brain Res Rev. 2011 Jun 24; 67 (1-2): 282-310.

    AbstractNeuropathic pain is currently being treated by a range of therapeutic interventions that above all act to lower neuronal activity in the somatosensory system (e.g. using local anesthetics, calcium channel blockers, and opioids). The present review highlights novel and often still largely experimental treatment approaches based on insights into pathological mechanisms, which impact on the spinal nociceptive network, thereby opening the 'gate' to higher brain centers involved in the perception of pain. Cellular and molecular mechanisms such as ectopia, sensitization of nociceptors, phenotypic switching, structural plasticity, disinhibition, and neuroinflammation are discussed in relation to their involvement in pain hypersensitivity following either peripheral neuropathies or spinal cord injury. A mechanism-based treatment approach may prove to be successful in effective treatment of neuropathic pain, but requires more detailed insights into the persistence of cellular and molecular pain mechanisms which renders neuropathic pain unremitting. Subsequently, identification of the therapeutic window-of-opportunities for each specific intervention in the particular peripheral and/or central neuropathy is essential for successful clinical trials. Most of the cellular and molecular pain mechanisms described in the present review suggest pharmacological interference for neuropathic pain management. However, also more invasive treatment approaches belong to current and/or future options such as neuromodulatory interventions (including spinal cord stimulation) and cell or gene therapies, respectively.Copyright © 2011 Elsevier B.V. All rights reserved.

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