4.6 Article

Enduring prevention and transient reduction of postoperative pain by intrathecal resolvin D1

期刊

PAIN
卷 152, 期 3, 页码 557-565

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1016/j.pain.2010.11.021

关键词

Postoperative pain; Inflammation; Glia; Intrathecal; MAP kinases

资金

  1. BWH Anesthesia Foundation for Education and Research
  2. National Institutes of Health [GM38765, NS67686]

向作者/读者索取更多资源

Postoperative pain slows surgical recovery, impacting the return of normal function for weeks, months, or longer. Here we report the antihyperalgesic actions of a new compound, resolvin D1 (RvD1), known to reduce inflammation and to suppress pain after peripheral nerve injury, on the acute pain occurring after paw incision and the prolonged pain after skin-muscle retraction. Injection of RvD1 (20-40 ng) into the L5-L6 intrathecal space 30 minutes before surgery reduces the postincisional primary mechanical hypersensitivity, lowering the peak change by approximately 70% (with 40 ng) and reducing the area under the curve (AUC) for the entire 10-day postincisional course by approximately 60%. Intrathecal injection of RvD1 on postoperative day (POD) 1 reduces the hyperalgesia to the same level as that from preoperative injection within a few hours, an effect that persists for the remaining PODs. Tactile allodynia and hyperalgesia following the skin/muscle incision retraction procedure, measured at the maximum values 12 to 14 days, is totally prevented by intrathecal RvD1 (40 ng) given at POD 2. However, delaying the injection until POD 9 or POD 17 results in RvD1 causing only transient and incomplete reversal of hyperalgesia, lasting for <1 day. These findings demonstrate the potent, effective reduction of postoperative pain by intrathecal RvD1 given before or shortly after surgery. The much more limited effect of this compound on retraction-induced pain, when given 1 to 2 weeks later, suggests that the receptors or pathways for resolvins are more important in the early than the later stages of postoperative pain. (C) 2010 International Association for the Study of Pain. Published by Elsevier B. V. All rights reserved.

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