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成纤维细胞生长因子在胃保护和溃疡愈合中的作用:与硫糖铝的相互作用

Fibroblast growth factor in gastroprotection and ulcer healing: interaction with sucralfate.

作者信息

Konturek S J, Brzozowski T, Majka J, Szlachcic A, Bielanski W, Stachura J, Otto W

机构信息

Institute of Physiology, University Medical School, Krakow, Poland.

出版信息

Gut. 1993 Jul;34(7):881-7. doi: 10.1136/gut.34.7.881.

Abstract

The study was designed to determine the gastroprotective and ulcer healing efficacy of basic transforming growth factor (bFGF) and to assess whether this peptide contributes to the action of sucralfate on the rat stomach. Application of human recombinant bFGF (1-100 micrograms/kg/hour subcutaneously) failed to affect the formation of acute gastric lesions induced by 100% ethanol and acidified aspirin but reduced the stress induced by gastric lesions. Sucralfate (100-200 mg/kg given orally) protected gastric mucosa against the ethanol, aspirin, and stress induced acute gastric lesions but the addition of bFGF (100 micrograms/kg subcutaneously or intragastrically) failed to affect sucralfate induced protection against ethanol or aspirin but increased that against stress. Administration of bFGF (3-300 micrograms/kg/day) by an intragastric or an intraperitoneal route or sucralfate (400 mg/kg/day) orally to rats with acetic acid induced gastric ulcers, enhanced the healing rate of these ulcers during seven day treatment in a dose dependent manner. This was accompanied by a pronounced increase in the number of capillaries and myofibroblasts and in DNA synthesis and DNA and RNA concentrations in the granulation tissue in the ulcer area. [125I]bFGF (1 microCi) applied subcutaneously or intragastrically accumulated in two to threefold higher amounts in the ulcer area than in the intact mucosa, particularly in rats treated with sucralfate. Concurrent treatment with indomethacin (2 mg/kg intraperitoneally) delayed ulcer healing and reduced the binding of labelled bFGF to the ulcer area, angiogenesis, and DNA synthesis by sucralfate. Addition of [125I]bFGF to sucralfate at various pHs resulted in the coprecipitation of bFGF by sucralfate in a pH dependent manner from about 10% at pH 7.0 to 90% at pH 1.5. Thus bFGF shows little protective activity and is not essential for gastroprotection afforded by sucralfate but plays an important part in healing of gastric ulcers possibly due to its growth promoting and angiogenic actions.

摘要

本研究旨在确定碱性转化生长因子(bFGF)的胃保护和溃疡愈合功效,并评估该肽是否有助于硫糖铝对大鼠胃的作用。皮下注射人重组bFGF(1 - 100微克/千克/小时)未能影响100%乙醇和酸化阿司匹林诱导的急性胃损伤的形成,但减轻了胃损伤诱导的应激。硫糖铝(口服100 - 200毫克/千克)可保护胃黏膜免受乙醇、阿司匹林和应激诱导的急性胃损伤,但添加bFGF(皮下或胃内注射100微克/千克)未能影响硫糖铝对乙醇或阿司匹林诱导损伤的保护作用,但增强了对应激的保护作用。对乙酸诱导的胃溃疡大鼠经胃内或腹腔内给予bFGF(3 - 300微克/千克/天)或口服硫糖铝(400毫克/千克/天),在为期7天的治疗中以剂量依赖方式提高了这些溃疡的愈合率。这伴随着溃疡区域肉芽组织中毛细血管和成肌纤维细胞数量的显著增加以及DNA合成、DNA和RNA浓度的增加。皮下或胃内注射[125I]bFGF(1微居里)在溃疡区域的蓄积量比完整黏膜高两到三倍,尤其是在接受硫糖铝治疗的大鼠中。同时给予吲哚美辛(腹腔内注射2毫克/千克)会延迟溃疡愈合,并减少硫糖铝标记的bFGF与溃疡区域的结合、血管生成和DNA合成。在不同pH值下将[125I]bFGF添加到硫糖铝中,会导致硫糖铝以pH依赖方式共沉淀bFGF,从pH 7.0时的约10%到pH 1.5时的90%。因此,bFGF显示出很小的保护活性,对硫糖铝提供的胃保护不是必需的,但可能由于其生长促进和血管生成作用在胃溃疡愈合中起重要作用。

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Mechanisms of action of sucralfate.硫糖铝的作用机制。
J Clin Gastroenterol. 1981;3(Suppl 2):117-27.

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