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聚普瑞锌对佐剂诱导性关节炎大鼠慢性胃溃疡愈合受损的影响——胰岛素样生长因子(IGF)-1的作用

Effect of polaprezinc on impaired healing of chronic gastric ulcers in adjuvant-induced arthritic rats--role of insulin-like growth factors (IGF)-1.

作者信息

Kato S, Tanaka A, Ogawa Y, Kanatsu K, Seto K, Yoneda T, Takeuchi K

机构信息

Department of Pharmacology and Experimental Therapeutics, Kyoto Pharmaceutical University, Misasagi, Yamashina, Kyoto, Japan.

出版信息

Med Sci Monit. 2001 Jan-Feb;7(1):20-5.

Abstract

Polaprezinc, N-(3-aminopropionyl)-L-histidinatozinc, has been shown to stimulate the production of insulin-like growth factor-1 (IGF-1) in mesenchymal cells, the polypeptide playing a role in the gastric epithelial wound repair. The present study was performed to examine the effect of polaprezinc on the impaired healing of chronic gastric ulcers in adjuvant-induced arthritic rats, in relation to IGF-1. Arthritis was induced in male Dark Agouti (DA) rats by a single injection of Freund's complete adjuvant (FCA), and the gastric ulcers were induced by thermal cauterization (70 degrees C for 30 sec) 7 days after FCA injection. Omeprazole (30 mg/kg) was administered p.o. once daily, while recombinant human IGF-1 (rhIGF-1) (30 micrograms/kg, s.c.) or polaprezinc (3-10 mg/kg, p.o.) was administered twice daily, starting from 3 days after ulceration for 14 days. The healing of gastric ulcers was significantly delayed in arthritic rats as compared to normal rats on day 10 and 17 following ulceration. The expression of IGF-1 mRNA was markedly increased in the ulcerated mucosa, but this response was apparently attenuated in arthritic rats. Repeated administration of polaprezinc accelerated the healing of gastric ulcers in both normal and arthritic rats, in a dose-dependent manner, and this effect was more pronounced in arthritic rats. Likewise, treatment with omeprazole also significantly promoted the healing of gastric ulcers in both normal and arthritic rats. On the other hand, rhIGF-1 significantly promoted the gastric ulcer healing in arthritic rats without any effect on that in normal rats. These results suggest that the impaired healing of chronic gastric ulcers in arthritic rats is, at least partly, accounted for by less expression of IGF-1, and the polaprezinc improves the delayed healing of gastric ulcers in arthritic rats, probably through an increase in IGF-1 production.

摘要

聚普瑞锌,即N-(3-氨丙酰基)-L-组氨酸锌,已被证明可刺激间充质细胞中胰岛素样生长因子-1(IGF-1)的产生,该多肽在胃上皮伤口修复中发挥作用。本研究旨在探讨聚普瑞锌对佐剂性关节炎大鼠慢性胃溃疡愈合受损的影响,并与IGF-1相关联。通过单次注射弗氏完全佐剂(FCA)诱导雄性暗褐大鼠(DA)患关节炎,并在FCA注射7天后通过热烧灼(70℃,30秒)诱导胃溃疡。奥美拉唑(30mg/kg)口服给药,每日一次,而重组人IGF-1(rhIGF-1)(30μg/kg,皮下注射)或聚普瑞锌(3-10mg/kg,口服)每日给药两次,从溃疡形成后3天开始,持续14天。与正常大鼠相比,关节炎大鼠在溃疡形成后第10天和第17天胃溃疡的愈合明显延迟。IGF-1 mRNA在溃疡黏膜中的表达明显增加,但这种反应在关节炎大鼠中明显减弱。重复给予聚普瑞锌可加速正常和关节炎大鼠胃溃疡的愈合,且呈剂量依赖性,这种作用在关节炎大鼠中更明显。同样,用奥美拉唑治疗也显著促进了正常和关节炎大鼠胃溃疡的愈合。另一方面,rhIGF-1显著促进了关节炎大鼠胃溃疡的愈合,而对正常大鼠没有任何影响。这些结果表明,关节炎大鼠慢性胃溃疡愈合受损至少部分是由于IGF-1表达减少所致,聚普瑞锌可能通过增加IGF-1的产生来改善关节炎大鼠胃溃疡的延迟愈合。

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