Literature DB >> 9521828

Levels of cyclooxygenase-1 and -2 mRNA expression at various stages of acute gastric injury induced by ischemia-reperfusion in rats.

Y Kishimoto1, K Wada, K Nakamoto, H Kawasaki, J Hasegawa.   

Abstract

Recently, the state of cyclooxygenase (COX) mRNA expression has been reported in an acetic acid-induced chronic gastric ulcer model of mice. However, the time course of COX expression during the developmental stage and the subsequent repair process of acute gastric injury is not well understood at present. In this study, we quantitatively investigated the time course of the level of COX-2 and -1 mRNA expression from the developmental stage through the healing stage in ischemia-reperfusion (I-R)-induced acute gastric damage. COX-2 mRNA was expressed at low or undetectable levels in the normal gastric tissues of control rats. The COX-2 expression between 6 and 48 h following I-R was higher than that of the control gastric tissues; the histological findings were erosion during 1-36 h and transitional appearance from erosion to ulcer at 48 h. The maximum expression of COX-2 mRNA was recorded at 24 h (approximately 200-fold elevation). The COX-2 message was very low or undetectable at 72 h (ulcer stage) and at 96 and 120 h (healing stage of ulcer) after I-R. The level of COX-1 mRNA remained stable through all stages of acute gastric damage. These results are potentially useful for understanding the role of COX and evaluating the effects of drugs on expression of COX at various stages of acute gastric injury. Copyright 1998 Academic Press.

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Year:  1998        PMID: 9521828     DOI: 10.1006/abbi.1997.0572

Source DB:  PubMed          Journal:  Arch Biochem Biophys        ISSN: 0003-9861            Impact factor:   4.013


  6 in total

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Authors:  A Tatsuguchi; C Sakamoto; K Wada; T Akamatsu; T Tsukui; K Miyake; S Futagami; T Kishida; Y Fukuda; N Yamanaka; M Kobayashi
Journal:  Gut       Date:  2000-06       Impact factor: 23.059

Review 2.  Role of cyclooxygenase isoforms in gastric mucosal defense and ulcer healing.

Authors:  Brigitta M Peskar
Journal:  Inflammopharmacology       Date:  2005       Impact factor: 4.473

3.  Selective cyclo-oxygenase-2 inhibitors aggravate ischaemia-reperfusion injury in the rat stomach.

Authors:  N Maricic; K Ehrlich; B Gretzer; R Schuligoi; M Respondek; B M Peskar
Journal:  Br J Pharmacol       Date:  1999-12       Impact factor: 8.739

Review 4.  Cyclooxygenase 2-implications on maintenance of gastric mucosal integrity and ulcer healing: controversial issues and perspectives.

Authors:  F Halter; A S Tarnawski; A Schmassmann; B M Peskar
Journal:  Gut       Date:  2001-09       Impact factor: 23.059

5.  Genetic ablation of carbonic anhydrase IX disrupts gastric barrier function via claudin-18 downregulation and acid backflux.

Authors:  T Li; X Liu; B Riederer; K Nikolovska; A K Singh; K A Mäkelä; A Seidler; Y Liu; G Gros; H Bartels; K H Herzig; U Seidler
Journal:  Acta Physiol (Oxf)       Date:  2017-10-19       Impact factor: 6.311

6.  Piceatannol Affects Gastric Ulcers Induced by Indomethacin: Association of Antioxidant, Anti-Inflammatory, and Angiogenesis Mechanisms in Rats.

Authors:  Rasheed A Shaik; Basma G Eid
Journal:  Life (Basel)       Date:  2022-02-28
  6 in total

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