Peskar B M
Scand J Gastroenterol Suppl. 1980;65:109-14.
Carbenoxolone in a dose dependent manner inhibits the activity of the prostaglandin (PG) metabolizing enzymes 15-hydroxy-PG-dehydrogenase and delta 13-PG-reductase in vitro, while this drug in the same dose range does not influence gastric mucosal PG synthesis by a microsomal cell fraction. Using a radioimmunoassay for carbenoxolone determination, we could show that during absorption high levels of the drug are reached within the gastric mucosa of human volunteers and gastric ulcer patients. From the tissue levels reached it seems possible that carbenoxolone inhibits PG inactivating enzymes of gastric mucosa in vivo as it does in vitro. Thus, decreased inactivation cytoprotective PG synthesized within the gastric mucosa, might contribute to the ulcer healing effect of carbenoxolone.
甘草次酸在体外以剂量依赖性方式抑制前列腺素(PG)代谢酶15-羟基-PG-脱氢酶和δ13-PG-还原酶的活性,而在相同剂量范围内该药物不影响微粒体细胞组分对胃黏膜PG的合成。通过放射免疫分析法测定甘草次酸,我们发现人类志愿者和胃溃疡患者的胃黏膜在吸收过程中会达到较高的药物水平。从所达到的组织水平来看,甘草次酸在体内似乎有可能像在体外一样抑制胃黏膜的PG失活酶。因此,胃黏膜内合成的具有细胞保护作用的PG失活减少,可能有助于甘草次酸的溃疡愈合作用。