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Up‐regulation of cyclooxygenase‐2 mRNA in the rat spinal cord following peripheral inflammation
[摘要]

Prostaglandins (PG) have been described as mediators in spinal nociceptive processing after peripheral inflammation. Enzymes essential for PG biosynthesis, cyclooxygenase isozymes COX-1 and COX-2, have not yet been investigated in the spinal cord. In two studies on rats with adjuvant-induced peripheral inflammation levels of mRNA expression of both COX isoforms were analyzed in the lumbar section of the spinal cord using reverse transcription-polymerase chain reaction (RT-PCR) technique. We could show that mRNA of both COX isoforms is expressed constitutively in the spinal cord with COX-2 as the predominant isoform. Six hours after induction of peripheral inflammation, levels of COX-2 mRNA expression were raised significantly in respect to untreated control rats and returned to baseline within 3 days after induction of inflammation. COX-2 might therefore be regarded as the COX isozyme responsible for spinal PG release in nociceptive processing under a peripheral inflammatory stimulus.

[发布日期]  [发布机构] 
[效力级别]  [学科分类] 生物化学/生物物理
[关键词] Cyclooxygenase-2;Inflammation;Spinal cord;RT-PCR;bp;basepair;CFA;complete Freund's adjuvant;CNS;central nervous system;COX;cyclooxygenase;GAPDH;glyceraldehyde-3-phosphate dehydrogenase;kb;kilobase;MOPS;4-morpholinepropanesulfonic acid;NSAIDs;non-steroidal anti-inflammatory drugs;PG;prostaglandin;RT-PCR;reverse transcription-polymerase chain reaction;SSC;saline sodium citrate [时效性] 
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