Playford R J, Marchbank T, Mandir N, Higham A, Meeran K, Ghatei M A, Bloom S R, Goodlad R A
Department of Medicine and Therapeutics, University of Leicester, U.K.
J Pathol. 1998 Mar;184(3):316-22. doi: 10.1002/(SICI)1096-9896(199803)184:3<316::AID-PATH3>3.0.CO;2-#.
Keratinocyte growth factor (KGF) is a mitogen found throughout the gastrointestinal tract, but its role in gastrointestinal pathophysiology is unclear. The effect of recombinant KGF on gut growth and repair has been examined using a variety of in vivo models. Rats receiving total parenteral nutrition had co-infusions of KGF or control for 6 days. Changes in gut growth (wet weight and vincristine-induced metaphase arrest) were then assessed. The effects of KGF on gastric repair and acid secretion in rats were determined using an indomethacin (20 mg/kg)/restraint model and animals fitted with chronic gastric fistulae. KGF at 0.1, 1, and 3 mg/kg increased gut growth as assessed by wet weight throughout the gastrointestinal tract and increased vincristine-induced accumulation of metaphases in the stomach and small intestine but not in the colon. Plasma gastrin, peptide YY, enteroglucagon, and glucagon-like peptide-1 were all increased, whereas insulin was lowered by KGF (all P < 0.01). KGF was ineffective in reducing indomethacin-induced gastric damage but caused a reduction in basal acid secretion of about 35 and 50 per cent when administered at 0.2 or 5 mg/kg (P < 0.05). These studies support the idea that KGF is involved in the control of proliferation of the gastrointestinal tract. They do not provide evidence, however, for a role in the early reparative process invoked during short-term models of gastrointestinal injury.
角质形成细胞生长因子(KGF)是一种在整个胃肠道中发现的促分裂原,但其在胃肠道病理生理学中的作用尚不清楚。已经使用多种体内模型研究了重组KGF对肠道生长和修复的影响。接受全胃肠外营养的大鼠连续6天同时输注KGF或对照物。然后评估肠道生长的变化(湿重和长春新碱诱导的中期阻滞)。使用吲哚美辛(20mg/kg)/束缚模型和装有慢性胃瘘的动物,确定KGF对大鼠胃修复和胃酸分泌的影响。0.1、1和3mg/kg的KGF通过整个胃肠道的湿重评估增加了肠道生长,并增加了长春新碱诱导的胃和小肠中期积累,但在结肠中没有增加。血浆胃泌素、肽YY、肠高血糖素和胰高血糖素样肽-1均增加,而KGF使胰岛素降低(所有P<0.01)。KGF在减少吲哚美辛诱导的胃损伤方面无效,但在以0.2或5mg/kg给药时,可使基础胃酸分泌减少约35%和50%(P<0.05)。这些研究支持KGF参与胃肠道增殖控制的观点。然而,它们没有提供证据证明KGF在胃肠道损伤短期模型中引发的早期修复过程中起作用。