Poulsen S S, Kirkegaard P, Skov Olsen P, Christiansen J
Scand J Gastroenterol. 1981;16(4):459-64. doi: 10.3109/00365528109181998.
Duodenal ulcers can be produced in rats by subcutaneous administration of cysteamine-HCl. The pathogenesis of these ulcers has not been fully explained. Increased acid secretion is necessary but not sufficient for ulcer production. In the present study we have observed pronounced alterations in the histologic appearance of the duodenal glands of Brunner during ulcer formation. The secretory cells became extremely flattened without mucus content and the lumina of the acini dilated. Changes became most pronounced between 4 and 8 h after administration of cysteamine. Repeated injections of pentagastrin in a dosage inducing an acid response equivalent to the one induced by cysteamine did not produce any histologic changes in Brunner's glands or any ulcerations. When cysteamine was administered to rats with chronic gastric fistulas draining the gastric secretions, no duodenal ulcerations were produced, but Brunner's glands still became depleted of mucus. These findings suggest that the histologic changes in Brunner's glands are not secondary either to the increased acid secretion induced by cysteamine or to ulcer formation. Together with our previous demonstration of a marked reduction duodenal secretion in the first 10 h after cysteamine administration, the results of the present study suggest an inhibitory effect of cysteamine on the synthetic activity of Brunner's glands rather than an impaired release mechanism. The effect of cysteamine on Brunner's glands may be an important factor in the pathogenesis of cysteamine-induced duodenal ulceration.
通过皮下注射盐酸半胱胺可在大鼠身上诱发十二指肠溃疡。这些溃疡的发病机制尚未完全阐明。胃酸分泌增加是溃疡形成的必要条件,但并非充分条件。在本研究中,我们观察到在溃疡形成过程中,Brunner十二指肠腺的组织学外观出现了明显改变。分泌细胞变得极度扁平,不含黏液,腺泡腔扩张。在注射半胱胺后4至8小时,变化最为明显。重复注射五肽胃泌素,其剂量诱导的酸反应与半胱胺诱导的酸反应相当,但并未在Brunner腺中产生任何组织学变化或溃疡。当给有慢性胃瘘引流胃液的大鼠注射半胱胺时,未产生十二指肠溃疡,但Brunner腺仍出现黏液缺失。这些发现表明,Brunner腺的组织学变化既不是半胱胺诱导的胃酸分泌增加的继发结果,也不是溃疡形成的继发结果。结合我们之前的研究表明,在注射半胱胺后的前10小时十二指肠分泌显著减少,本研究结果提示半胱胺对Brunner腺的合成活性有抑制作用,而非释放机制受损。半胱胺对Brunner腺的作用可能是半胱胺诱导十二指肠溃疡发病机制中的一个重要因素。