Beales I L, Post L, Calam J, Yamada T, Delvalle J
Department of Medicine, Royal Postgraduate Medical School, Hammersmith Hospital, London, UK.
Eur J Clin Invest. 1996 Jul;26(7):609-11. doi: 10.1046/j.1365-2362.1996.2040517.x.
There is evidence that gastric Helicobacter pylori (Hp) infection promotes duodenal ulceration by releasing gastrin. We therefore asked how Hp releases gastrin. Tumour necrosis factor alpha (TNF-alpha) is up-regulated in Hp gastritis and stimulates hormone release from pituitary cells, so we tested its effect on primary cultures of canine antral G cells and human antral fragments. TNF-alpha pretreatment (100 ng mL-1) of canine G cells significantly increased both basal (by 89%: P < 0.01) and bombesin-stimulated (by 39% P < 0.05) gastrin release. A similar pattern of increase was seen following TNF-alpha (20 ng mL-1) pretreatment of human antral fragments: basal gastrin release was increased by 38% (P < 0.05) and bombesin-stimulated by 26% (P < 0.05). This effect persisted during immunoblockade with anti-somatostatin antibody S6. We propose that TNF-alpha provides the link between Hp infection and gastrin release and thus contributes to duodenal ulceration.
有证据表明,胃幽门螺杆菌(Hp)感染通过释放胃泌素促进十二指肠溃疡形成。因此,我们探究了Hp如何释放胃泌素。肿瘤坏死因子α(TNF-α)在Hp胃炎中上调,并刺激垂体细胞释放激素,所以我们测试了其对犬胃窦G细胞原代培养物和人胃窦组织块的作用。用TNF-α(100 ng/mL)预处理犬G细胞,显著增加了基础胃泌素释放(增加89%:P<0.01)和蛙皮素刺激的胃泌素释放(增加39%,P<0.05)。用人胃窦组织块进行TNF-α(20 ng/mL)预处理后,也出现了类似的增加模式:基础胃泌素释放增加38%(P<0.05),蛙皮素刺激的胃泌素释放增加26%(P<0.05)。在用抗生长抑素抗体S6进行免疫阻断期间,这种作用持续存在。我们认为,TNF-α是Hp感染与胃泌素释放之间的联系,因此促成了十二指肠溃疡的形成。