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자료유형
학술저널
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Wu, Liu-Qing (Department of Anesthesiology, Wenzhou Central Hospital) Li, Yu (Department of Anesthesiology, Wenzhou Central Hospital) Li, Yuan-Yan (Department of Anesthesiology, Wenzhou Central Hospital) Xu, Shi-hao (Department of Anesthesiology, Wenzhou Central Hospital) Yang, Zong-Yong (Department of Anesthesiology, Wenzhou Central Hospital) Lin, Zheng (Department of Anesthesiology, Wenzhou Central Hospital) Li, Jun (Department of Anesthesiology, Second Affiliated Hospital of Wenzhou Medical University)
저널정보
한국응용약물학회 Biomolecules & Therapeutics(구 응용약물학회지) Biomolecules & therapeutics 제24권 제4호
발행연도
2016.1
수록면
418 - 425 (8page)

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We measured anti-nociceptive activity of prim-o-glucosylcimifugin (POG), a molecule from Saposhnikovia divaricate (Turcz) Schischk. Anti-nociceptive or anti-inflammatory effects of POG on a formalin-induced tonic nociceptive response and a complete Freund's adjuvant (CFA) inoculation-induced rat arthritis pain model were studied. Single subcutaneous injections of POG produced potent anti-nociception in both models that was comparable to indomethacin analgesia. Anti-nociceptive activity of POG was dose-dependent, maximally reducing pain 56.6% with an $ED_{50}$ of 1.6 mg. Rats given POG over time did not develop tolerance. POG also time-dependently reduced serum TNF${\alpha}$, IL-$1{\beta}$ and IL-6 in arthritic rats and both POG and indomethacin reduced spinal prostaglandin E2 ($PGE_2$). Like indomethacin which inhibits cyclooxygenase-2 (COX-2) activity, POG dose-dependently decreased spinal COX-2 content in arthritic rats. Additionally, POG, and its metabolite cimifugin, downregulated COX-2 expression in vitro. Thus, POG produced potent anti-nociception by downregulating spinal COX-2 expression.

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