Scarpignato C, Tramacere R, Zappia L, Del Soldato P
Pharmacology. 1987;34(5):264-8. doi: 10.1159/000138278.
The effects of adenosine and its metabolically stable derivative L-phenylisopropyladenosine (L-PIA), acting mainly on A1 receptors, on gastric acid secretion were studied in the rat. Although inactive by intraduodenal route, subcutaneous adenosine significantly inhibited acid secretion. This inhibition, however, was not dose-dependent. On the contrary, L-PIA was able to decrease dose-dependently acid output by both subcutaneous and intraduodenal route, its ED50 being 0.11 mg/kg subcutaneously and 0.24 mg/kg intraduodenally. The inhibitory effect of L-PIA was reduced by prior administration of theophylline. These results suggest that activation of A1-receptors inhibits acid secretion in the rat.
在大鼠中研究了主要作用于A1受体的腺苷及其代谢稳定衍生物L-苯异丙基腺苷(L-PIA)对胃酸分泌的影响。尽管十二指肠内给药时无活性,但皮下注射腺苷可显著抑制胃酸分泌。然而,这种抑制作用不呈剂量依赖性。相反,L-PIA能够通过皮下和十二指肠内途径剂量依赖性地降低胃酸分泌量,其皮下注射的半数有效剂量(ED50)为0.11mg/kg,十二指肠内给药为0.24mg/kg。预先给予茶碱可降低L-PIA的抑制作用。这些结果表明,激活A1受体可抑制大鼠胃酸分泌。