Balint G A
Department of Neurology and Psychiatry, Albert Szent-Györgyi Medical University, Szeged, Hungary.
Acta Med Hung. 1991;48(3-4):197-201.
The 6-keto-prostaglandin-F1 alpha content (as the stable break-down product of prostacyclin) of rat antral and fundic gastric, as well as of duodenal mucosa, significantly increases after 1, 5 and 10 mg/kg orally administered colloidal bismuth subcitrate treatment. The results indicate that (i) colloidal bismuth subcitrate-induced stimulation of endogenous prostacyclin content ("adaptive cytoprotection") of rat gastroduodenal mucosa may contribute to its therapeutic effect; (ii) the effect of colloidal bismuth subcitrate is not due exclusively to the bismuth content of the molecule, but seems to be connected with the structure of colloidal bismuth subcitrate itself; (iii) the effect seems to be dose-dependent, showing a dose-response relationship.
大鼠胃窦、胃底以及十二指肠黏膜中6-酮-前列腺素F1α的含量(作为前列环素的稳定分解产物),在口服1、5和10mg/kg枸橼酸铋胶体治疗后显著增加。结果表明:(i)枸橼酸铋胶体诱导大鼠胃十二指肠黏膜内源性前列环素含量增加(“适应性细胞保护作用”)可能有助于其治疗效果;(ii)枸橼酸铋胶体的作用并非完全归因于该分子中的铋含量,而似乎与枸橼酸铋胶体本身的结构有关;(iii)该作用似乎具有剂量依赖性,呈现剂量-反应关系。