Guo Jin-Sheng, Cho Chi-Hin, Wang Wei-Ping, Shen Xi-Zhong, Cheng Chuen-Lung, Koo Marcel Wing Leung
Department of Pharmacology, Faculty of Medicine, University of Hong Kong, Pokfulam, Hong Kong.
World J Gastroenterol. 2003 Aug;9(8):1767-71. doi: 10.3748/wjg.v9.i8.1767.
To explore the roles of nitric oxide synthase (NOS), heme oxygenase (HO) and cyclooxygenase (COX) in gastric ulceration and to investigate the relationships of the expression and activities of these enzymes at different stages of gastric ulceration.
Gastric ulcers (kissing ulcers) were induced by luminal application of acetic acid. Gastric tissue samples were obtained from the ulcer base, ulcer margin, and non-ulcerated area around the ulcer margin at different time intervals after ulcer induction. The mRNA expression and protein levels of inducible and constitutive isoforms of NOS, HO and COX were analyzed with RT-PCR and Western blotting methods. The activities of the total NOS, inducible NOS (iNOS), HO, and COX were also determined.
Differential expression of inducible iNOS, HO-1 and COX-2 and enzyme activities of NOS, HO and COX were found in the gastric ulcer base. High iNOS expression and activity were observed on day 1 to day 3 in severely inflamed ulcer tissues. Maximum expressions of HO-1 and COX-2 and enzyme activities of HO and COX lagged behind that of iNOS, and remained at high levels during the healing phase.
The expression and activities of inducible NOS, HO-1 and COX-2 are found to be correlated to different stages of gastric ulceration. Inducible NOS may contribute to ulcer formation while HO-1 and COX-2 may promote ulcer healing.
探讨一氧化氮合酶(NOS)、血红素加氧酶(HO)和环氧化酶(COX)在胃溃疡形成中的作用,并研究这些酶在胃溃疡不同阶段的表达及活性之间的关系。
通过向胃腔内注射乙酸诱导胃溃疡(吻合性溃疡)。在诱导溃疡后的不同时间间隔,从溃疡底部、溃疡边缘以及溃疡边缘周围的非溃疡区域获取胃组织样本。采用逆转录聚合酶链反应(RT-PCR)和蛋白质免疫印迹法分析NOS、HO和COX诱导型及组成型同工型的mRNA表达和蛋白质水平。同时测定总NOS、诱导型NOS(iNOS)、HO和COX的活性。
在胃溃疡底部发现诱导型iNOS、HO-1和COX-2的表达差异以及NOS、HO和COX的酶活性差异。在严重炎症的溃疡组织中,第1天至第3天观察到iNOS高表达和高活性。HO-1和COX-2的最大表达以及HO和COX的酶活性滞后于iNOS,并在愈合阶段保持在高水平。
诱导型NOS、HO-1和COX-2的表达及活性与胃溃疡的不同阶段相关。诱导型NOS可能促成溃疡形成,而HO-1和COX-2可能促进溃疡愈合。