Garamszegi M, Beró T, Jávor T, Mózsik G
Acta Physiol Hung. 1984;64(3-4):349-53.
Intestinal mucosal damage was produced in rats by the s.c. administration of indomethacin (10 mg/kg). The number and severity of the small intestinal mucosal lesions was recorded. Different doses of prostacyclin (PGI2), 7-oxo-PGI2 and 17-aza-PGF2 alpha (0.25-0.5-1.00 mg/kg) were given i.p. at the time of administration of indomethacin. The effects of these compounds were studied on the number and severity of the small intestinal mucosal lesions. It was shown that (1) all tested compounds inhibited the number and severity of the intestinal mucosal lesions, however, to different extent; (2) the inhibition of the development of small intestinal mucosal damage displayed a dose-response relationship; (3) 17-aza-PGF2 alpha was found to have the most potent effect on the development of the intestinal lesions as well as on the development of gastric mucosal damage produced by ethanol.
通过皮下注射消炎痛(10毫克/千克)在大鼠中造成肠道粘膜损伤。记录小肠粘膜损伤的数量和严重程度。在给予消炎痛时,腹腔注射不同剂量的前列环素(PGI2)、7-氧代-PGI2和17-氮杂-PGF2α(0.25 - 0.5 - 1.00毫克/千克)。研究了这些化合物对小肠粘膜损伤数量和严重程度的影响。结果表明:(1)所有测试化合物均能抑制肠道粘膜损伤的数量和严重程度,但程度不同;(2)对小肠粘膜损伤发展的抑制呈现剂量反应关系;(3)发现17-氮杂-PGF2α对肠道损伤的发展以及乙醇所致胃粘膜损伤的发展具有最显著的作用。