4.6 Article

Relative potency of epidural to intrathecal clonidine differs between acute thermal pain and capsaicin-induced allodynia

期刊

PAIN
卷 84, 期 1, 页码 57-64

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/S0304-3959(99)00181-5

关键词

clonidine; capsaicin; hyperalgesia; allodynia

资金

  1. NATIONAL CENTER FOR RESEARCH RESOURCES [M01RR007122] Funding Source: NIH RePORTER
  2. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM048085, R37GM048085] Funding Source: NIH RePORTER
  3. NCRR NIH HHS [MO1 RR07122] Funding Source: Medline
  4. NIGMS NIH HHS [GM48085] Funding Source: Medline

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Clonidine is approved in the US for epidural administration in the treatment of intractable neuropathic cancer pain, but is also administered intrathecally for this indication and both epidurally and intrathecally in the treatment of acute, postoperative pain. The purpose of the current study was to estimate the relative potency of clonidine by epidural and intrathecal routes in the treatment of capsaicin-induced hyperalgesia and allodynia as a model of central hypersensitivity and of noxious heat as a model of acute pain. Twenty-four healthy volunteers were randomized to receive either intrathecal clonidine (75, 150, or 300 mu g) or epidural clonidine (150, 300, or 600 mu g) and rated pain from a Peltier-controlled thermode at a lumbar, thoracic, and cervical dermatomal site before and after drug administration. In addition, they rated pain from intradermal capsaicin injections at a lumbar dermatome before and 60 min after clonidine injection and described areas of hyperalgesia and allodynia to mechanical stimuli. Clonidine's effect differed with route of administration and modality of sensory testing. For acute thermal pain, intrathecal clonidine produced a dose-dependent analgesia with a lumbar > thoracic > cervical gradient, whereas only one dose of epidural clonidine reduced thermal pain and this was at the thoracic testing site. In contrast, the potency of clonidine to reduce capsaicin-induced allodynia was similar between the two routes of injection, and, for hyperalgesia, clonidine was only slightly more potent after intrathecal than epidural injection. These data support clinical studies from non-comparative trials and suggest there is a > 6-fold potency ratio of intrathecal: epidural administration of clonidine for acute pain, but a < 2-fold potency ratio for these routes for mechanical hypersensitivity. (C) 2000 International Association for the Study of Pain. Published by Elsevier Science B.V.

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