Dembinski A, Konturek S J
Am J Physiol. 1985 Feb;248(2 Pt 1):G170-5. doi: 10.1152/ajpgi.1985.248.2.G170.
We investigated the effects of prostaglandins (PG) of E, F, and I series and their stable analogues on gastric acid secretion, serum gastrin level, and growth of gastroduodenal mucosa and pancreas in rats. Short-term administration (every 8 h for 48 h) of E and F series PGs and their stable analogues caused significant stimulation of DNA synthesis; prolonged PG treatment (every 8 h for 10 days) significantly increased weight and total DNA and RNA contents of the organs tested. PGs of E series were given in doses that inhibited gastric acid secretion about 50% and raised serum gastrin significantly; PGs of F series were injected in the same dose (1,000 micrograms/kg) as PGs of E series but did not affect acid secretion or serum gastrin. Short- or long-term treatment with PGI2 or its stable analogue (Hoe 892), injected in doses causing about 50% inhibition of acid secretion and significant increments in serum gastrin levels, failed to affect any of the growth-related parameters in the stomach, duodenum, or pancreas. We conclude that PGs of E and F (but not of I) series exhibit a marked stimulatory influence on growth of gastroduodenal mucosa and pancreas. These trophic effects appear to be unrelated to gastric secretion or serum gastrin release.
我们研究了E、F和I系列前列腺素(PG)及其稳定类似物对大鼠胃酸分泌、血清胃泌素水平以及胃十二指肠黏膜和胰腺生长的影响。短期给药(每8小时一次,共48小时)E和F系列PG及其稳定类似物可显著刺激DNA合成;延长PG治疗时间(每8小时一次,共10天)可显著增加受试器官的重量以及总DNA和RNA含量。给予E系列PG的剂量可抑制约50%的胃酸分泌并显著提高血清胃泌素水平;给予F系列PG的剂量与E系列PG相同(1000微克/千克),但不影响胃酸分泌或血清胃泌素。以导致约50%胃酸分泌抑制和血清胃泌素水平显著升高的剂量注射PGI2或其稳定类似物(Hoe 892)进行短期或长期治疗,均未影响胃、十二指肠或胰腺中任何与生长相关的参数。我们得出结论,E和F(而非I)系列PG对胃十二指肠黏膜和胰腺的生长具有显著的刺激作用。这些营养作用似乎与胃酸分泌或血清胃泌素释放无关。