FEBS Letters | |
Up‐regulation of cyclooxygenase‐2 mRNA in the rat spinal cord following peripheral inflammation | |
Geisslinger, Gerd1  Scheuerer, Stefan1  Brune, Kay1  Beiche, Flora1  Goppelt-Struebe, Margarete2  | |
[1] Department of Experimental and Clinical Pharmacology and Toxicology, University of Erlangen-Nürnberg, Universitätsstr. 22, D-91054 Erlangen, Germany;Department of Medicine IV, University of Erlangen-Nürnberg, Loschgestr. 8, D-91054 Erlangen, Germany | |
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; | |
DOI : 10.1016/0014-5793(96)00604-7 | |
学科分类:生物化学/生物物理 | |
来源: John Wiley & Sons Ltd. | |
【 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.
【 授权许可】
Unknown
【 预 览 】
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