Loseva L A, Degtiar' V G, Vinogradov V A, Smagin V G
Biull Eksp Biol Med. 1986 Oct;102(10):406-8.
The influence of different doses (0.01, 0.1, 1.0, 10.0, 100.0, 250.0, 1,000.0, 2,500.0 gamma/kg body weight) of testosterone, dihydrotestosterone, 5 alpha-androstane-3 alpha, 17 beta-diol, 5 alpha-androstane-3 beta, 17 beta-diall, 4-androsterone-3,17-dione, estradiol and progesterone on the formation of cysteamine-induced duodenal ulcer was studied in mature male rats. It has been shown that all the steroids, but for progesterone, bring down the ulcer index after six days of i/p administration, the effect depending on the nature and dose of a steroid. Estradiol and 4-androstene-3,17-dione proved to be the most effective in the given dose range. The results do not only confirm the role of androgens and estradiol in the pathogenesis of duodenal ulcer, but also indicate the participation of their precursors and metabolites in the ulcer induction. The prospects of using steroids in the treatment of ulcer are discussed.
研究了不同剂量(0.01、0.1、1.0、10.0、100.0、250.0、1,000.0、2,500.0微克/千克体重)的睾酮、双氢睾酮、5α-雄烷-3α,17β-二醇、5α-雄烷-3β,17β-二醇、4-雄甾酮-3,17-二酮、雌二醇和孕酮对成年雄性大鼠半胱胺诱导的十二指肠溃疡形成的影响。结果表明,除孕酮外,所有类固醇在腹腔注射六天后均可降低溃疡指数,其效果取决于类固醇的性质和剂量。在给定剂量范围内,雌二醇和4-雄烯-3,17-二酮被证明是最有效的。这些结果不仅证实了雄激素和雌二醇在十二指肠溃疡发病机制中的作用,还表明它们的前体和代谢产物参与了溃疡的诱导。文中还讨论了使用类固醇治疗溃疡的前景。