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雷米拉唑对吲哚美辛诱导的兔胃黏膜细胞损伤的细胞保护作用。

The cytoprotective effect of leminoprazole on indomethacin-induced damage to rabbit gastric mucosal cells.

作者信息

Takahashi S, Okabe S

机构信息

Department of Applied Pharmacology, Kyoto Pharmaceutical University, Japan.

出版信息

J Pharmacol Exp Ther. 1996 Nov;279(2):975-82.

PMID:8930207
Abstract

Leminoprazole (an acid pump inhibitor) has a mucosal protective effect against various experimental gastric lesions, but the underlying mechanism remains unknown. We examined whether leminoprazole prevents indomethacin-induced damage to cultured gastric mucosal cells. The viability of rabbit gastric mucosal cells was assessed by the 3-(4,5-dimethyl-2-thiazoyl)-2,5-diphenyl-2H-tetrazolium bromide and dye exclusion methods. [35S]Methionine-labeled proteins were detected by autoradiography after sodium dodecylsulfate-polyacrylamide gel electrophoresis. Western blot analysis was carried out using anti-heat shock protein (HSP)-70 and anti-HSP-72 antibodies. Exposure of gastric mucosal cells to indomethacin for 4 hr apparently reduced their viability in a dose-related manner. Pretreatment with leminoprazole for 4 hr significantly prevented the reduction in cell viability caused by 50 microM indomethacin, although omeprazole was not effective. However, such pretreatment did not prevent the severe damage induced by 500 microM indomethacin. 16,16-Dimethyl prostaglandin E2 significantly prevented the cell damage induced by indomethacin at both 50 and 500 microM. Leminoprazole alone did not affect cell viability. The cytoprotection by leminoprazole was expressed after a 2-hr lag period. Leminoprazole did not promote prostaglandin E2 synthesis by cells, but it apparently induced the synthesis of 83-kDa, 72-kDa, 52-kDa and 35-kDa proteins. Both the cytoprotection and the induction of such protein synthesis were abolished by cycloheximide and actinomycin D. The leminoprazole-induced 72-kDa protein did not react with the antibodies against HSP-70 and HSP-72. These results indicate that leminoprazole directly protects gastric mucosal cells against mild damage caused by indomethacin and that its cytoprotective effect might be mediated through de novo synthesized proteins. In addition, it is suggested that the leminoprazole-induced proteins might be unknown proteins related to cytoprotection, although the exact characters of the proteins are unclear.

摘要

雷米诺拉唑(一种酸泵抑制剂)对各种实验性胃损伤具有黏膜保护作用,但其潜在机制尚不清楚。我们研究了雷米诺拉唑是否能预防吲哚美辛对培养的胃黏膜细胞的损伤。通过3-(4,5-二甲基-2-噻唑基)-2,5-二苯基-2H-溴化四氮唑和染料排除法评估兔胃黏膜细胞的活力。在十二烷基硫酸钠-聚丙烯酰胺凝胶电泳后,通过放射自显影检测[35S]甲硫氨酸标记的蛋白质。使用抗热休克蛋白(HSP)-70和抗HSP-72抗体进行蛋白质印迹分析。将胃黏膜细胞暴露于吲哚美辛4小时明显以剂量相关的方式降低其活力。用雷米诺拉唑预处理4小时可显著预防50微摩尔吲哚美辛引起的细胞活力降低,尽管奥美拉唑无效。然而,这种预处理并不能预防500微摩尔吲哚美辛引起的严重损伤。16,16-二甲基前列腺素E2可显著预防50和500微摩尔吲哚美辛引起的细胞损伤。单独使用雷米诺拉唑不影响细胞活力。雷米诺拉唑的细胞保护作用在2小时的延迟期后表现出来。雷米诺拉唑不促进细胞合成前列腺素E2,但它明显诱导了83 kDa、72 kDa、52 kDa和35 kDa蛋白质的合成。环己酰亚胺和放线菌素D消除了细胞保护作用和这种蛋白质合成的诱导。雷米诺拉唑诱导的72 kDa蛋白质与抗HSP-70和抗HSP-72抗体不发生反应。这些结果表明,雷米诺拉唑直接保护胃黏膜细胞免受吲哚美辛引起的轻度损伤,其细胞保护作用可能通过从头合成的蛋白质介导。此外,尽管这些蛋白质的确切特性尚不清楚,但提示雷米诺拉唑诱导的蛋白质可能是与细胞保护相关的未知蛋白质。

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