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两种甲基化前列腺素E2类似物对人体胃十二指肠压力的影响。

Effect of two methylated prostaglandin E2 analogs on gastroduodenal pressure in man.

作者信息

Nylander B, Andersson S

出版信息

Scand J Gastroenterol. 1975;10(1):91-5.

PMID:1124344
Abstract

The effect of two methylated analogs of prostaglandin E2 (PGE2), namely 16, 16-dimethyl PGE2 and 15 (S)-15-methyl PGE2 methyl ester, on gastroduodenal motility has been studied in healthy male volunteers. Oral administration of 140 mug of the 16-alkylated analog produced a significant decrease in motor activity in both the gastric antrum and the duodenum. 80 mug had no detectable effect on pressure. However, 80 mug of the 15-methylated analog administered directly into the duodenum caused an almost immidiated inhibition of the duodenal motor activity. In view of previous findings on the inhibitory action of these two analogs on gastric acid secretion, it seems as if the gastrointestinal smooth muscles are less sensitive to the action of the analogs than are the oxyntic glands.

摘要

在健康男性志愿者中研究了前列腺素E2(PGE2)的两种甲基化类似物,即16,16 - 二甲基PGE2和15(S)-15 - 甲基PGE2甲酯对胃十二指肠运动的影响。口服140微克的16 - 烷基化类似物可使胃窦和十二指肠的运动活性显著降低。80微克对压力没有可检测到的影响。然而,将80微克的15 - 甲基化类似物直接注入十二指肠会立即引起十二指肠运动活性的几乎完全抑制。鉴于先前关于这两种类似物对胃酸分泌的抑制作用的研究结果,似乎胃肠道平滑肌对类似物作用的敏感性低于泌酸腺。

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