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COX-2 inhibitor prevents the development of hyperalgesia induced by intrathecal NMDA or AMPA.

作者信息

Yamamoto T, Sakashita Y

机构信息

Department of Anesthesiology, School of Medicine, Chiba University, Japan.

出版信息

Neuroreport. 1998 Dec 1;9(17):3869-73. doi: 10.1097/00001756-199812010-00019.

DOI:10.1097/00001756-199812010-00019
PMID:9875720
Abstract

Cyclooxygenase (COX)-2 is constitutively expressed in the superficial dorsal horn of the spinal cord, but its role in the spinal cord is still unclear. We examined the effect of intrathecally administered NS398, a selective COX-2 inhibitor and indomethacin, an non-selective COX-1 and COX-2 inhibitor, on the development of thermal hyperalgesia induced by the activation of NMDA or AMPA receptors. Intrathecal injection of either NS398 or indomethacin equally blocked the development of thermal hyperalgesia induced by intrathecal injection of either NMDA or AMPA in a dose-dependent manner. These data suggest that COX-2 plays an important role in spinal thermal nociceptive transmission when neurons in the spinal cord are facilitated by NMDA or AMPA.

摘要

相似文献

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2
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The acute antihyperalgesic action of nonsteroidal, anti-inflammatory drugs and release of spinal prostaglandin E2 is mediated by the inhibition of constitutive spinal cyclooxygenase-2 (COX-2) but not COX-1.非甾体抗炎药的急性抗痛觉过敏作用以及脊髓前列腺素E2的释放是由对组成型脊髓环氧化酶-2(COX-2)而非COX-1的抑制介导的。
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