首页> 美国卫生研究院文献>Journal of Clinical Biochemistry and Nutrition >Accelerated Ulcer Healing and Resistance to Ulcer Recurrence with Gastroprotectants in Rat Model of Acetic Acid-induced Gastric Ulcer
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Accelerated Ulcer Healing and Resistance to Ulcer Recurrence with Gastroprotectants in Rat Model of Acetic Acid-induced Gastric Ulcer

机译:乙酸诱导的胃溃疡大鼠模型中溃疡愈合的加速性及胃保护剂对溃疡复发的抵抗

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摘要

Quality of ulcer healing (QOUH) is defined as ideal ulcer healing featuring with the fine granular ulcer scar, high functional restoration and the resistance to recurrence. This study was designed to compare the rates of QOUH achievement in rat gastric ulcer model between acid suppressant treated group and gastroprotectant treated group accompanied with elucidations of molecular mechanisms. Serosal injection of acetic acids for generating gastric ulcer and intraperitoneal (ip) injection of recombinant interleukin 1-beta (IL-1β) for recurring healed ulcer was done in SD rats. The 72 rats were divided into three groups according to treatment as follows; Group I, no further treatment, Group II, 8 weeks treatment of omeprazole, and Group III, 8 weeks of gastroprotectant treatment. IL-1β was administered for ulcer recurrence after 28 weeks of acetic acid injection. At four weeks after gastric ulcerogenesis, 58.3% (7/12) of active gastric ulcer were converted to healing stage in Group III, but 16.7% (2/12) in Group II and none in Group I, for which significant levels of epidermal growth factor, mucin, and pS2/trefoil peptide1 were contributive to these accelerated healings of Group III. ip injections of rIL-1β (200 µg/kg) at 28 weeks after acetic acid injection led to 100% of ulcer recurrence in Group I and 75.0% in Group II, but only 16.7% of Group III rats showed ulcer recurrence. Significantly attenuated levels of inflammatory cytokines including IL-2, transforming growth factor-alpha (TNF-α), cyclooxygenase-2 (COX-2), nitrotyrosine were responsible for the resistance to ulcer recurrence in Group III. Conclusively, gastroprotectant might be prerequisite in order to achieve ideal QOUH through significant inductions of remodeling.
机译:溃疡愈合的质量(QOUH)被定义为理想的溃疡愈合,其特征是细颗粒的溃疡疤痕,高功能恢复性和抗复发性。本研究旨在比较酸抑制剂治疗组和胃保护剂治疗组在大鼠胃溃疡模型中QOUH达成率,并阐明其分子机制。在SD大鼠中进行乙酸的血清注射以产生胃溃疡,并通过腹膜内(ip)注射重组白介素1-β(IL-1β)来复发性溃疡。将72只大鼠按以下治疗方法分为三组:第一组,无进一步治疗,第二组,奥美拉唑治疗8周,第三组,胃保护剂治疗8周。注射乙酸28周后给予IL-1β溃疡复发。胃溃疡发生后的第4周,III组中有58.3%(7/12)的活动性胃溃疡转化为愈合阶段,II组中有16.7%(2/12)转变为愈合期,而I组则没有,这些情况下表皮水平明显升高生长因子,粘蛋白和pS2 /三叶肽1促进了III组的这些加速愈合。注射乙酸后28周腹腔注射rIL-1β(200 µg / kg)导致I组溃疡复发100%,II组溃疡复发75.0%,但III组大鼠只有16.7%溃疡复发。炎症细胞因子(包括IL-2,转化生长因子-α(TNF-α),环氧合酶-2(COX-2),硝基酪氨酸)的显着减弱是第三组对溃疡复发的抵抗力。结论是,胃保护剂可能是通过显着诱导重塑达到理想QOUH的先决条件。

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