Menozzi A, Pozzoli C, Poli E, Dacasto M, Giantin M, Lopparelli R M, Passeri B, Zullian C, Gobbetti T, Bertini S
Dipartimento di Salute Animale, Università di Parma, 43100 Parma, Italy.
Res Vet Sci. 2009 Feb;86(1):129-35. doi: 10.1016/j.rvsc.2008.04.006. Epub 2008 Jun 18.
We investigated the effects of nonselective cyclooxygenase (COX) inhibitors (indomethacin and flunixin meglumine) and selective COX-1 (SC-560) or COX-2 (celecoxib, DUP-398 and NS-697) inhibitors on horse small bowel motility in vitro. At this purpose, samples of equine ileum were put in isolated organ baths for the motility experiments. Nonselective COX inhibitors were devoid of major effects on motility, except for an inhibition of tonic contraction shown by flunixin meglumine. SC-560, selective COX-1 inhibitor, was devoid of significant effects on ileal motility. Selective COX-2 inhibitors reduced both tonic contraction and spontaneous phasic contractions, while prostaglandin (PG) receptor antagonists were uneffective. Some of the intestinal samples were submitted to histological investigation or reverse transcription-polymerase chain reaction (RT-PCR), which revealed the presence of an inflammation reaction and the presence of both COX isoforms mRNAs. Present data support the hypothesis that the effects of COX inhibitors on horse small intestinal motility are not linked to PG depletion.
我们研究了非选择性环氧化酶(COX)抑制剂(吲哚美辛和氟尼辛葡甲胺)以及选择性COX-1(SC-560)或COX-2(塞来昔布、DUP-398和NS-697)抑制剂对马小肠体外运动的影响。为此,将马回肠样本置于离体器官浴槽中进行运动实验。非选择性COX抑制剂对运动无主要影响,但氟尼辛葡甲胺表现出对紧张性收缩的抑制作用。选择性COX-1抑制剂SC-560对回肠运动无显著影响。选择性COX-2抑制剂可同时降低紧张性收缩和自发性相性收缩,而前列腺素(PG)受体拮抗剂则无效。部分肠道样本进行了组织学研究或逆转录-聚合酶链反应(RT-PCR),结果显示存在炎症反应以及两种COX同工型mRNA。目前的数据支持以下假设:COX抑制剂对马小肠运动的影响与PG耗竭无关。