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诱导型一氧化氮合酶及一氧化氮修饰蛋白在幽门螺杆菌相关性萎缩性胃黏膜中的表达

Expression of inducible nitric oxide synthase and nitric oxide-modified proteins in Helicobacter pylori-associated atrophic gastric mucosa.

作者信息

Naito Yuji, Takagi Tomohisa, Okada Hitomi, Nukigi Yayoi, Uchiyama Kazuhiko, Kuroda Masaaki, Handa Osamu, Kokura Satoshi, Yagi Nobuaki, Kato Yoji, Osawa Toshihiko, Yoshikawa Toshikazu

机构信息

Medical Proteomics, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kamigyo-ku, Kyoto, Japan.

出版信息

J Gastroenterol Hepatol. 2008 Dec;23 Suppl 2:S250-7. doi: 10.1111/j.1440-1746.2008.05412.x.

Abstract

BACKGROUND AND AIM

Induction of inducible nitric oxide synthase (iNOS) may be involved in carcinogenesis of the stomach, because nitric oxide (NO) derived from iNOS can exert DNA damage and post-transcriptional modification of target proteins. In the present study, we investigated the correlation between endoscopic findings and iNOS mRNA expression/NO-modified proteins in the gastric mucosa.

METHODS

Fifty patients were prospectively selected from subjects who underwent upper gastrointestinal chromoendoscopy screening for abdominal complaints. The Helicobacter pylori (H. pylori) status of patients was determined by anti-H. pylori IgG antibody levels. We classified the mucosal area of the fundus as F0, fine small granules; F1, edematous large granules without a sulcus between granules; F2, reduced-size granules with a sulcus between granules; and F3, irregular-sized granules with extended sulcus between granules. Gastritis was graded using the visual analog scale of the Updated Sydney System. The expression of interleukin (IL)-8 and iNOS mRNA was assayed in gastric biopsy specimens by reverse transcription-polymerase chain reaction. NO-modified proteins were analyzed by Western blotting using novel monoclonal antibodies against nitrotyrosine.

RESULTS

A total of 91.7% (11/12) of the F0 group was H. pylori-negative, whereas 94.7% (36/38) of the F1-3 groups was H. pylori-positive. Spearman's analysis showed good correlation between the endoscopic grading and the score of chronic inflammation (r=0.764) and glandular atrophy (r=0.751). The expression of IL-8 mRNA was significantly increased in F1, F2, and F3 cases compared with the F0 group, with no significant differences among them. iNOS mRNA was significantly increased in the F3 group compared with the other groups, with increased nitration of tyrosine residues of proteins.

CONCLUSION

The proposed classification by chromoendoscopy is useful for screening patients for atrophic and iNOS-expressing gastric mucosa with NO-modified proteins in H. pylori-associated atrophic gastric mucosa.

摘要

背景与目的

诱导型一氧化氮合酶(iNOS)的诱导可能参与胃癌的发生,因为iNOS产生的一氧化氮(NO)可导致DNA损伤和靶蛋白的转录后修饰。在本研究中,我们调查了内镜检查结果与胃黏膜中iNOS mRNA表达/NO修饰蛋白之间的相关性。

方法

前瞻性地从因腹部不适接受上消化道染色内镜筛查的受试者中选取50例患者。通过抗幽门螺杆菌IgG抗体水平确定患者的幽门螺杆菌(H. pylori)感染状况。我们将胃底黏膜区域分为F0,细小颗粒;F1,水肿性大颗粒且颗粒间无沟;F2,颗粒尺寸减小且颗粒间有沟;F3,颗粒尺寸不规则且颗粒间沟延长。使用更新后的悉尼系统的视觉模拟量表对胃炎进行分级。通过逆转录-聚合酶链反应检测胃活检标本中白细胞介素(IL)-8和iNOS mRNA的表达。使用针对硝基酪氨酸的新型单克隆抗体通过蛋白质印迹分析NO修饰的蛋白。

结果

F0组中91.7%(11/12)的患者幽门螺杆菌阴性,而F1 - 3组中94.7%(36/38)的患者幽门螺杆菌阳性。Spearman分析显示内镜分级与慢性炎症评分(r = 0.764)和腺体萎缩评分(r = 0.751)之间具有良好的相关性。与F0组相比,F1、F2和F3组中IL - 8 mRNA的表达显著增加,它们之间无显著差异。与其他组相比,F3组中iNOS mRNA显著增加,蛋白质酪氨酸残基的硝化作用增强。

结论

所提出的染色内镜分类法有助于筛查幽门螺杆菌相关性萎缩性胃黏膜中具有NO修饰蛋白的萎缩性和iNOS表达性胃黏膜患者。

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