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大鼠应激性溃疡自愈过程中环氧合酶表达的变化 被引量:3

Changes in cyclooxygenase gene expression during spontaneaus recovery from stress ulcer in rats
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摘要 目的研究大鼠应激性溃疡自愈过程中环氧合酶的表达;探讨环氧合酶在应激性溃疡自愈过程的作用机制。方法应用免疫组织化学和RT.PCR方法检测大鼠应激性溃疡自愈过程中环氧合酶蛋白和mRNA的表达变化。结果对照组的大鼠胃粘膜COX-2表达极低,而在溃疡自愈过程中其表达显著增加(P<0.05),并随自愈时间而减弱;COX-1在应激性溃疡自愈各组和对照组中均表达,自愈各组与对照组相比没有明显差异(P>0.05)。结论大鼠应激性溃疡自愈过程中COX-1和COX-2均有表达。参与了应激性溃疡的自愈过程,其作用可能主要与COX介导分泌的前列腺素有关。 Objective To observe the changes in gene expression of cyclooxygenase (COX) during spontaneaus recovery from stress ulcer in rats exposed to water immersion and restraint stress (WRS). Methods A rat model of stress ulcer was established by means of WRS, in which the changes in COX expression were detected with immunohistochemistry and reverse transcription (RT)-PCR. Results Very low levels of COX-2 expression were detected in the gastric mucosa of the control rats, and the expression increased significantly during the healing process of the stress ulcer (P〈0.05). COX-1 expression in the gastric mucosa showed no significant difference between the control group and the stress ulcer groups during healing (P〉0.05). Conclusion COX-1 and COX-2 expressions in rat gastric mucosa during the recovery from stress ulcer participate in the recovery of the damaged mucosa possibly by mediating prostaglandin secretion.
出处 《南方医科大学学报》 CAS CSCD 北大核心 2006年第1期91-93,97,共4页 Journal of Southern Medical University
基金 广东省自然科学基金(010578)
关键词 应激性溃疡 环氧合酶 stress ulcer cyclooxygenase
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参考文献17

  • 1[1]Tomasz Brzozowski,Peter CH,Konturek,et al.Expression of COX-1 and COX-2 in adaptive cytoprotection induced by mild stress[J].J Physiol,2000,94:83-91.
  • 2[2]Tanaka A,Hase S,Miyazawa T,et al.Role of cyclooxygenase (COX)-1 and COX-2 inhibition in nonsteroidal anti-inflammatory drug-in duced intestinal damage in rats:relation to various pathogenicevents[J].J Pharmacol Exp Ther,2002,303(3):1248-54.
  • 3[3]Tanaka A,Araki H,Komoike Y,et al.Inhibition of both COX-1 and COX-2 is required for development of gastric damage in response to nonsteroidal antiinflammatory drugs [J].J Physiol Paris,2001,95 (1-6):21-7.
  • 4[4]Peskar BM,Maricic N,Gretzera B,et al.Role ofcyclooxygenase-2 in gastric mucosal defense [J].Life Sci,2001,69(25-26):2993-3003.
  • 5[5]Shaftel SS,Olschowka JA,Hurley SD,et al.COX-3:a splice variant of cyclooxygenase-1 in mouse neural tissue and cells[J].Brain Res Mol Brain Res,2003,119(2):213-5.
  • 6[6]Brzozowski T,Konturek PC,Konturek S J,et al.Expression of COX-1 and COX-2 in adaptive cytoprotection induced by mild stress[J].J Physiol (Paris),2000,94(2):83-91.
  • 7[7]Tanaka A,Araki H,Hase S,et al.Up-regulation of COX-2 by inhibition of COX-1 in the rat:a key to NSAID-induced gastric injury[J].Aliment Pharmacol Ther,2002,16 (Suppl 2):90-101.
  • 8[8]Takeeda M,Yamato M,Kato S,et al.Cyclooxygenase isozymes involved in adaptive functional responses in rat stomach after barrier disruption[J].J Pharmacol Exp Ther,2003,307(2):713-19.
  • 9[9]Leung WK,To KF,Go MY,et al.Cyclooxygenase-2 upregulates vascular endothelial growth factor expression and angiogenesis in human gastric carcinoma[J].Int J Oncol,2003,23(5):1317-22.
  • 10[10]Kanellis J,Watanabe S,Li JH,et al.Uric acid stimulates monocyte chemoattractant protein-1 production in vascular smooth muscle cells via mitogen-activated protein kinase and cyclooxygenase-2[J].Hypertension,2003,41(6):1287-93.

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