Role of delayed gastric emptying in the pathogenesis of cysteamine-induced duodenal ulcer in the rat

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Role of delayed gastric emptying in the pathogenesis of cysteamine-induced duodenal ulcer in the rat. / Poulsen, Steen Seier.

I: Scandinavian Journal of Gastroenterology, Bind 17, Nr. 3, 04.1982, s. 325-30.

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt

Harvard

Poulsen, SS 1982, 'Role of delayed gastric emptying in the pathogenesis of cysteamine-induced duodenal ulcer in the rat', Scandinavian Journal of Gastroenterology, bind 17, nr. 3, s. 325-30.

APA

Poulsen, S. S. (1982). Role of delayed gastric emptying in the pathogenesis of cysteamine-induced duodenal ulcer in the rat. Scandinavian Journal of Gastroenterology, 17(3), 325-30.

Vancouver

Poulsen SS. Role of delayed gastric emptying in the pathogenesis of cysteamine-induced duodenal ulcer in the rat. Scandinavian Journal of Gastroenterology. 1982 apr.;17(3):325-30.

Author

Poulsen, Steen Seier. / Role of delayed gastric emptying in the pathogenesis of cysteamine-induced duodenal ulcer in the rat. I: Scandinavian Journal of Gastroenterology. 1982 ; Bind 17, Nr. 3. s. 325-30.

Bibtex

@article{6abf9402696b40da843836d85fae4c54,
title = "Role of delayed gastric emptying in the pathogenesis of cysteamine-induced duodenal ulcer in the rat",
abstract = "Cysteamine is a potent duodenal ulcerogen in rats. It has been demonstrated to inhibit gastric empyting, whose role in ulcer formation is unknown. In the present study the effect of cysteamine on gastric motility and emptying rate in rats was studied by direct fluoroscopic observation. The delayed gastric empyting was due to a pronounced relaxation of the stomach and a complete blocking of gastric peristalsis. These effects have their maximum within the first 4 h after administration of cysteamine. Thereafter peristalsis and gastric empyting slowly return. In controls contrast medium administered intragastrically was completely discharged from the stomach within 30 min. After cysteamine the first small amounts of contrast medium were discharged into the duodenum after 4 h, and contrast medium remained in the stomach for at least 12 h after administration. The size of the stomach reached a maximum after 3 h and approached normal values again after 12 h. Because of complete gastric retention the acid gastric secretions provoked by cysteamine probably accumulate in the stomach during the first 4 h after cysteamine administration, and because of the absence of peristalsis they are not mixed with gastric contents. After 4 h this pool of undiluted gastric secretions gradually is emptied into the duodenum, where the mucosal resistance is reduced by inhibition of the secretory activity of Brunner's glands, and ulceration rapidly develops. The time relationship is supported by histopathologic findings and measurements of gastric acid secretions after cysteamine. Vagotomy augmented the inhibitory effect of cysteamine on gastric motility. The relaxation was even more pronounced, and contrast medium was not discharged from the stomach within 24 h. In these rats cysteamine induced ulcerations in the stomach.",
keywords = "Animals, Cysteamine, Duodenal Ulcer, Female, Gastric Dilatation, Gastric Emptying, Gastrointestinal Motility, Rats, Stomach Ulcer, Vagotomy",
author = "Poulsen, {Steen Seier}",
year = "1982",
month = apr,
language = "English",
volume = "17",
pages = "325--30",
journal = "Scandinavian Journal of Gastroenterology",
issn = "0036-5521",
publisher = "Taylor & Francis",
number = "3",

}

RIS

TY - JOUR

T1 - Role of delayed gastric emptying in the pathogenesis of cysteamine-induced duodenal ulcer in the rat

AU - Poulsen, Steen Seier

PY - 1982/4

Y1 - 1982/4

N2 - Cysteamine is a potent duodenal ulcerogen in rats. It has been demonstrated to inhibit gastric empyting, whose role in ulcer formation is unknown. In the present study the effect of cysteamine on gastric motility and emptying rate in rats was studied by direct fluoroscopic observation. The delayed gastric empyting was due to a pronounced relaxation of the stomach and a complete blocking of gastric peristalsis. These effects have their maximum within the first 4 h after administration of cysteamine. Thereafter peristalsis and gastric empyting slowly return. In controls contrast medium administered intragastrically was completely discharged from the stomach within 30 min. After cysteamine the first small amounts of contrast medium were discharged into the duodenum after 4 h, and contrast medium remained in the stomach for at least 12 h after administration. The size of the stomach reached a maximum after 3 h and approached normal values again after 12 h. Because of complete gastric retention the acid gastric secretions provoked by cysteamine probably accumulate in the stomach during the first 4 h after cysteamine administration, and because of the absence of peristalsis they are not mixed with gastric contents. After 4 h this pool of undiluted gastric secretions gradually is emptied into the duodenum, where the mucosal resistance is reduced by inhibition of the secretory activity of Brunner's glands, and ulceration rapidly develops. The time relationship is supported by histopathologic findings and measurements of gastric acid secretions after cysteamine. Vagotomy augmented the inhibitory effect of cysteamine on gastric motility. The relaxation was even more pronounced, and contrast medium was not discharged from the stomach within 24 h. In these rats cysteamine induced ulcerations in the stomach.

AB - Cysteamine is a potent duodenal ulcerogen in rats. It has been demonstrated to inhibit gastric empyting, whose role in ulcer formation is unknown. In the present study the effect of cysteamine on gastric motility and emptying rate in rats was studied by direct fluoroscopic observation. The delayed gastric empyting was due to a pronounced relaxation of the stomach and a complete blocking of gastric peristalsis. These effects have their maximum within the first 4 h after administration of cysteamine. Thereafter peristalsis and gastric empyting slowly return. In controls contrast medium administered intragastrically was completely discharged from the stomach within 30 min. After cysteamine the first small amounts of contrast medium were discharged into the duodenum after 4 h, and contrast medium remained in the stomach for at least 12 h after administration. The size of the stomach reached a maximum after 3 h and approached normal values again after 12 h. Because of complete gastric retention the acid gastric secretions provoked by cysteamine probably accumulate in the stomach during the first 4 h after cysteamine administration, and because of the absence of peristalsis they are not mixed with gastric contents. After 4 h this pool of undiluted gastric secretions gradually is emptied into the duodenum, where the mucosal resistance is reduced by inhibition of the secretory activity of Brunner's glands, and ulceration rapidly develops. The time relationship is supported by histopathologic findings and measurements of gastric acid secretions after cysteamine. Vagotomy augmented the inhibitory effect of cysteamine on gastric motility. The relaxation was even more pronounced, and contrast medium was not discharged from the stomach within 24 h. In these rats cysteamine induced ulcerations in the stomach.

KW - Animals

KW - Cysteamine

KW - Duodenal Ulcer

KW - Female

KW - Gastric Dilatation

KW - Gastric Emptying

KW - Gastrointestinal Motility

KW - Rats

KW - Stomach Ulcer

KW - Vagotomy

M3 - Journal article

C2 - 7134859

VL - 17

SP - 325

EP - 330

JO - Scandinavian Journal of Gastroenterology

JF - Scandinavian Journal of Gastroenterology

SN - 0036-5521

IS - 3

ER -

ID: 47489886