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恩前列素对人体十二指肠-空肠运动的影响。

The effect of enprostil on duodeno-jejunal motility in man.

作者信息

Ducrotte P, Parent B, Masliah C, Joubert M, Colin R, Denis P

机构信息

Groupe de Biochimie et de Physiopathologie Digestive et Nutritionnelle, Hôpital Charles Nicolle, Rouen, France.

出版信息

Aliment Pharmacol Ther. 1990 Feb;4(1):73-81. doi: 10.1111/j.1365-2036.1990.tb00451.x.

DOI:10.1111/j.1365-2036.1990.tb00451.x
PMID:2129489
Abstract

Motor changes could be involved in the pathogenesis of diarrhoea that complicates the treatment of ulcer disease by prostaglandins. Our aim was to assess the effect of enprostil, a synthetic analogue of PGE2, on duodeno-jejunal motility. During this randomized double-blind crossover study, two manometric recordings, each lasting 20 h (12.00-08.00 hours), were carried out during dosing with 35 micrograms enprostil b.d. or placebo (eight volunteers: part 1), or during dosing with 35 or 70 micrograms enprostil b.d. (nine volunteers: part 2). Subjects were only allowed a standard dinner at 18.00 hours. During fasting, in part 1, the number of phase 3 activity patterns (PIIIs) was higher with enprostil than with placebo (P less than 0.01), without any difference in their characteristics; the overall duration of phase 1 activity was longer with enprostil than with placebo (P less than 0.01). In part 2, during fasting the number and characteristics of the PIIIs were not different, but there was a dose-related increase in PI, and decrease in PII activity. Fed motor patterns did not differ between the two doses of enprostil.

摘要

运动变化可能参与了前列腺素治疗溃疡病时并发腹泻的发病机制。我们的目的是评估前列腺素E2的合成类似物恩前列素对十二指肠-空肠运动的影响。在这项随机双盲交叉研究中,在每日两次服用35微克恩前列素或安慰剂期间(8名志愿者:第1部分),或在每日两次服用35或70微克恩前列素期间(9名志愿者:第2部分),进行了两次测压记录,每次持续20小时(12:00 - 08:00)。受试者仅允许在18:00吃一顿标准晚餐。在禁食期间,第1部分中,恩前列素组的3期活动模式(PIIIs)数量高于安慰剂组(P < 0.01),但其特征无差异;恩前列素组的1期活动总持续时间长于安慰剂组(P < 0.01)。在第2部分中,禁食期间PIIIs的数量和特征无差异,但PI有剂量相关增加,PII活动减少。两种剂量的恩前列素之间的进食运动模式无差异。

相似文献

1
The effect of enprostil on duodeno-jejunal motility in man.恩前列素对人体十二指肠-空肠运动的影响。
Aliment Pharmacol Ther. 1990 Feb;4(1):73-81. doi: 10.1111/j.1365-2036.1990.tb00451.x.
2
A synthetic prostaglandin E2 analogue, enprostil, hastens gastric emptying of solids in patients with an active duodenal ulcer.
Scand J Gastroenterol. 1990 Nov;25(11):1118-22. doi: 10.3109/00365529008998543.
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Oral prostaglandin E analogues induce intestinal migrating motor complexes after a meal in dogs. Evidence for a central mechanism.口服前列腺素E类似物可在犬进食后诱导肠道移行性运动复合波。存在中枢机制的证据。
Gastroenterology. 1990 Apr;98(4):888-93. doi: 10.1016/0016-5085(90)90012-p.
4
[Effect of lipid intake in meals on the duodenojejunal and sigmoid motor responses in healthy volunteers].[餐中脂质摄入对健康志愿者十二指肠空肠和乙状结肠运动反应的影响]
Gastroenterol Clin Biol. 1996 Feb;20(1):2-7.
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Sustained enhancement of gastric HCO3 secretion in humans by enprostil.恩前列素对人体胃碳酸氢盐分泌的持续增强作用。
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6
Reduction of serum lipoproteins in man by the oral administration of a prostaglandin analogue (enprostil).通过口服前列腺素类似物(恩前列素)降低人体血清脂蛋白水平。
Atherosclerosis. 1988 May;71(1):9-16. doi: 10.1016/0021-9150(88)90297-3.
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Duodenojejunal motility after oral and enteral nutrition in humans: a comparative study.人体口服和肠内营养后的十二指肠空肠运动:一项对比研究。
JPEN J Parenter Enteral Nutr. 1996 Mar-Apr;20(2):150-5. doi: 10.1177/0148607196020002150.
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Protection against aspirin-induced antral and duodenal damage with enprostil. A double-blind endoscopic study.恩前列素预防阿司匹林所致胃窦和十二指肠损伤的双盲内镜研究。
Gastroenterology. 1985 Jan;88(1 Pt 2):382-6. doi: 10.1016/s0016-5085(85)80193-1.
9
Inhibitory action of enprostil (4,5-dehydro-16-phenoxy-17,18,19,20-tetranor-PGE2) on tetra-gastrin stimulated acid secretion in human subjects.恩前列素(4,5-脱氢-16-苯氧基-17,18,19,20-四去甲-PGE2)对人体四肽胃泌素刺激的胃酸分泌的抑制作用。
Gastroenterol Jpn. 1989 Apr;24(2):115-9. doi: 10.1007/BF02774184.
10
Specificity of PGE2 analogs interaction between food intake and antisecretory effect.PGE2类似物在食物摄入与抗分泌作用之间相互作用的特异性。
Prostaglandins Leukot Med. 1986 Oct;24(2-3):219-25. doi: 10.1016/0262-1746(86)90129-0.