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长效生长抑素类似物(SMS 201-995)对正常受试者试餐后中间代谢及胃肠激素的影响。

The effect of a long-acting somatostatin analogue (SMS 201-995) on intermediary metabolism and gut hormones after a test meal in normal subjects.

作者信息

Fuessl H S, Burrin J M, Williams G, Adrian T E, Bloom S R

机构信息

Department of Medicine, Royal Postgraduate Medical School, London, UK.

出版信息

Aliment Pharmacol Ther. 1987 Aug;1(4):321-30. doi: 10.1111/j.1365-2036.1987.tb00632.x.

DOI:10.1111/j.1365-2036.1987.tb00632.x
PMID:2979676
Abstract

SMS 201-995 is an octapeptide analogue of somatostatin. The effect of a single subcutaneous (s.c.) injection of 50 micrograms SMS 201-995 on post-prandial intermediary metabolism was investigated in normal subjects. In spite of a long-lasting post-prandial suppression of insulin secretion, there were no significant changes in the plasma concentration of alanine, glycerol, 3-OH-butyrate or lactate. However, SMS 201-995 impairs carbohydrate tolerance, probably due to inhibition of insulin secretion. Basal and post-prandial plasma concentrations of the gut regulatory peptides pancreatic glucagon, motilin, pancreatic polypeptide, gastric inhibitory polypeptide, enteroglucagon, gastrin and peptide YY were suppressed up to 5 hours after subcutaneous administration of a single dose of SMS 201-995.

摘要

SMS 201-995是一种生长抑素的八肽类似物。在正常受试者中研究了单次皮下注射50微克SMS 201-995对餐后中间代谢的影响。尽管餐后胰岛素分泌受到长期抑制,但丙氨酸、甘油、3-羟基丁酸或乳酸的血浆浓度没有显著变化。然而,SMS 201-995损害糖耐量,可能是由于胰岛素分泌受到抑制。单次皮下注射SMS 201-995后长达5小时,肠道调节肽胰高血糖素、胃动素、胰多肽、胃抑制多肽、肠高血糖素、胃泌素和肽YY的基础和餐后血浆浓度均受到抑制。

相似文献

1
The effect of a long-acting somatostatin analogue (SMS 201-995) on intermediary metabolism and gut hormones after a test meal in normal subjects.长效生长抑素类似物(SMS 201-995)对正常受试者试餐后中间代谢及胃肠激素的影响。
Aliment Pharmacol Ther. 1987 Aug;1(4):321-30. doi: 10.1111/j.1365-2036.1987.tb00632.x.
2
Effect of long acting somatostatin-analogue, SMS 201 995, on gut hormone secretion in normal subjects.长效生长抑素类似物SMS 201 995对正常受试者肠道激素分泌的影响。
Experientia. 1985 Jun 15;41(6):738-40. doi: 10.1007/BF02012573.
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Postprandial effects of SMS 201-995 on gut hormones and glucose tolerance.SMS 201-995对肠道激素和葡萄糖耐量的餐后效应。
Scand J Gastroenterol Suppl. 1986;119:73-83. doi: 10.3109/00365528609087434.
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Reduced postprandial hyperglycemia after subcutaneous injection of a somatostatin-analogue (SMS 201-995) in insulin-dependent diabetes mellitus.胰岛素依赖型糖尿病患者皮下注射生长抑素类似物(SMS 201-995)后餐后高血糖降低。
Diabetes Care. 1985 Sep-Oct;8(5):429-35. doi: 10.2337/diacare.8.5.429.
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Effect of somatostatin analog on peptide release and tumor growth in the Zollinger-Ellison syndrome.生长抑素类似物对卓-艾综合征中肽释放及肿瘤生长的影响。
Surg Gynecol Obstet. 1990 Jun;170(6):476-84.
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Effect of somatostatin analogue (SMS 201-995, Sandostatin) on pancreatic secretion in humans.生长抑素类似物(SMS 201-995,善得定)对人体胰腺分泌的影响。
Am J Med. 1987 May 29;82(5B):49-54. doi: 10.1016/0002-9343(87)90426-8.
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Prolonged inhibition of meal-stimulated acid secretion and gastrin release following single subcutaneous administration of octreotide (SMS 201-995) in man.单次皮下注射奥曲肽(SMS 201-995)后,人体进餐刺激的胃酸分泌和胃泌素释放受到长期抑制。
Aliment Pharmacol Ther. 1989 Dec;3(6):527-38. doi: 10.1111/j.1365-2036.1989.tb00244.x.
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Effects of the somatostatin analogue SMS 201-995 (sandostatin) on mouth-to-caecum transit time and absorption of fat and carbohydrates in normal man.生长抑素类似物SMS 201-995(善得定)对正常人口腔至盲肠转运时间及脂肪和碳水化合物吸收的影响。
Clin Sci (Lond). 1988 Oct;75(4):345-50. doi: 10.1042/cs0750345.
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The effects of SMS 201-995 (sandostatin) on metabolic profiles in insulin-dependent diabetes mellitus.SMS 201-995(善得定)对胰岛素依赖型糖尿病患者代谢谱的影响。
J Clin Endocrinol Metab. 1989 Jan;68(1):63-7. doi: 10.1210/jcem-68-1-63.
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Sandostatin, a new analogue of somatostatin, reduces the metabolic changes induced by the nocturnal interruption of continuous subcutaneous insulin infusion in type 1 (insulin-dependent) diabetic patients.善得定,一种新的生长抑素类似物,可减轻1型(胰岛素依赖型)糖尿病患者因夜间中断持续皮下胰岛素输注所引起的代谢变化。
Diabetologia. 1989 Nov;32(11):801-9. doi: 10.1007/BF00264911.

引用本文的文献

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Clin Pharmacokinet. 1993 Nov;25(5):375-91. doi: 10.2165/00003088-199325050-00004.
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Somatostatin prevents the postoperative increases in plasma amino acid clearance and urea synthesis after elective cholecystectomy.
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Gut. 1995 May;36(5):766-70. doi: 10.1136/gut.36.5.766.
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Octreotide. A review of its pharmacodynamic and pharmacokinetic properties, and therapeutic potential in conditions associated with excessive peptide secretion.奥曲肽。对其药效学和药代动力学特性以及在与肽分泌过多相关病症中的治疗潜力的综述。
Drugs. 1989 Nov;38(5):658-702. doi: 10.2165/00003495-198938050-00002.