Chen D, Destrée M, Håkanson R, Willems G
Department of Pharmacology, University of Lund, Sweden.
Eur J Gastroenterol Hepatol. 1998 Apr;10(4):293-9. doi: 10.1097/00042737-199804000-00004.
BACKGROUND/OBJECTIVE: Gastrin is trophic for the mucosa of the acid-producing part of the rat stomach, notably the histamine-producing ECL cells. Gastrin is said to stimulate growth also of colonic mucosa and colon cancer. The purpose of the present study was to examine whether endogenous hypergastrinaemia had trophic effects on normal colonic mucosa and transplanted colon adenocarcinoma in rats.
Rats were subjected to fundectomy (surgical removal of the acid-producing part of the stomach) or treatments known to induce endogenous hypergastrinaemia. The treatments included refeeding after 48 h of food deprivation or administration of omeprazole (400 micromol/kg/day, orally). Other operations included colostomy and sham operation. A K12-cell line, originally established from a 1,2-dimethylhydrazine-induced colon adenocarcinoma, was used for transplantation. The rates of cell proliferation were determined in the oxyntic and colonic mucosa and in the tumour by measuring the proportion of the cells that accumulated bromodeoxyuridine in their nuclei, i.e. the labelling index (LI). The thickness of the oxyntic mucosa and the activity of histidine decarboxylase (HDC), the histamine-forming enzyme of the ECL cells, were measured. In addition, the thickness of the colonic mucosa and the weight and volume of the tumour were measured.
Refeeding or treatment with a single dose of omeprazole in fasted rats raised the serum gastrin concentration and the LI and HDC activity in the oxyntic mucosa; refeeding but not omeprazole raised the LI in the colonic mucosa. In fed rats, hypergastrinaemia induced by fundectomy or treatment with omeprazole (for 10 days) failed to affect either the LI or the thickness of the mucosa of the proximal colon and the excluded distal colon of the colostomized rats. Fundectomy failed to stimulate the growth of the tumour transplants.
Endogenous hypergastrinaemia did not induce trophic effects on rat colonic mucosa and did not promote growth of a transplanted colon adenocarcinoma in the rat.
背景/目的:胃泌素对大鼠胃产酸部位的黏膜具有营养作用,尤其是对产生组胺的肠嗜铬样(ECL)细胞。据说胃泌素还能刺激结肠黏膜和结肠癌的生长。本研究的目的是检验内源性高胃泌素血症对大鼠正常结肠黏膜和移植的结肠腺癌是否具有营养作用。
对大鼠进行胃底切除术(手术切除胃的产酸部位)或采用已知可诱导内源性高胃泌素血症的处理方法。这些处理方法包括禁食48小时后再喂食或给予奥美拉唑(400微摩尔/千克/天,口服)。其他手术包括结肠造口术和假手术。使用最初从1,2 - 二甲基肼诱导的结肠腺癌建立的K12细胞系进行移植。通过测量细胞核中积累溴脱氧尿苷的细胞比例,即标记指数(LI),来确定胃黏膜和结肠黏膜以及肿瘤中的细胞增殖率。测量胃黏膜厚度和ECL细胞的组胺形成酶组氨酸脱羧酶(HDC)的活性。此外,测量结肠黏膜厚度以及肿瘤的重量和体积。
禁食大鼠再喂食或用单剂量奥美拉唑处理可提高血清胃泌素浓度以及胃黏膜中的LI和HDC活性;再喂食而非奥美拉唑可提高结肠黏膜中的LI。在喂食的大鼠中,胃底切除术或用奥美拉唑处理(10天)诱导的高胃泌素血症未能影响结肠造口大鼠近端结肠和排除的远端结肠黏膜的LI或厚度。胃底切除术未能刺激肿瘤移植的生长。
内源性高胃泌素血症未对大鼠结肠黏膜产生营养作用,也未促进大鼠移植的结肠腺癌生长。