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IL-1β Stimulates COX-2 Dependent PGE2 Synthesis and CGRP Release in Rat Trigeminal Ganglia Cells

机译:IL-1β刺激大鼠三叉神经节细胞中COX-2依赖的PGE2合成和CGRP释放

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摘要

ObjectivePro-inflammatory cytokines like Interleukin-1 beta (IL-1β) have been implicated in the pathophysiology of migraine and inflammatory pain. The trigeminal ganglion and calcitonin gene-related peptide (CGRP) are crucial components in the pathophysiology of primary headaches. 5-HT1B/D receptor agonists, which reduce CGRP release, and cyclooxygenase (COX) inhibitors can abort trigeminally mediated pain. However, the cellular source of COX and the interplay between COX and CGRP within the trigeminal ganglion have not been clearly identified.
机译:诸如白细胞介素-1β(IL-1β)等促炎细胞因子已被证实与偏头痛和炎性疼痛的病理生理有关。三叉神经节和降钙素基因相关肽(CGRP)是原发性头痛的病理生理学的关键组成部分。减少CGRP释放的5-HT1B / D受体激动剂和环氧合酶(COX)抑制剂可以中止三叉神经介导的疼痛。但是,尚不清楚三叉神经节内COX的细胞来源以及COX与CGRP之间的相互作用。

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