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The effects of carbohydrate-enriched meals on glucose turnover and metabolic clearance rates of glucose in type 2 diabetic patients.

作者信息

Osei K, Falko J M, Fields P G, Bossetti B, O'Dorisio T M

出版信息

Diabetologia. 1986 Feb;29(2):100-5. doi: 10.1007/BF00456118.

DOI:10.1007/BF00456118
PMID:3516764
Abstract

The addition of fructose to natural meals elicits lower serum glucose and immunoreactive insulin responses when compared with that of sucrose and starch meals. Differences in rates of splanchnic glucose appearance and peripheral glucose disposal may be partly responsible. To evaluate the role of both parameters after different carbohydrate-enriched meals, we measured the arterialized venous blood glucose, immunoreactive insulin and gastric inhibitory polypeptide concentrations in seven Type 2 diabetic patients after ingestion of isocaloric test meals. Measurements were made in a random manner on three separate occasions. Fructose, sucrose, and bread supplementation constituted 68% of the total carbohydrate content of each meal. Rates of total glucose appearance, glucose utilization and metabolic clearance rates of glucose were determined by the D3-H-3 glucose prime-continuous infusion technique. The mean fasting glucose levels were similar in the three groups. Mean peak glucose concentrations and integrated incremental areas were significantly lower (p less than 0.02) after the fructose-enriched meals compared with that of either sucrose or bread. The basal arterialized venous blood glucose levels were similar in all three groups. The mean incremental integrated arterialized venous blood glucose area was significantly lower in the fructose group when compared with the sucrose (p less than 0.05) and bread (p less than 0.02) groups. The mean fasting gastric inhibitory polypeptide levels were similar in the three groups. However, the mean incremental integrated gastric inhibitory polypeptide areas were significantly lower in the fructose group compared with the sucrose and bread groups (p less than 0.01 and p less than 0.05 respectively). Basal hepatic glucose outputs were not significantly different in the three groups.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

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本文引用的文献

1
Glucose and fructose absorption in the unanesthetized dog.未麻醉犬体内葡萄糖和果糖的吸收
Gastroenterology. 1963 May;44:654-63.
2
Digestion and absorption of disaccharides in man.人类对双糖的消化与吸收
Biochem J. 1961 Nov;81(2):411-8. doi: 10.1042/bj0810411.
3
Measurement of size and turnover rate of body glucose pool by the isotope dilution method.用同位素稀释法测定机体葡萄糖池的大小和周转率。
Am J Physiol. 1956 Sep;187(1):15-24. doi: 10.1152/ajplegacy.1956.187.1.15.
4
Effects of plasma glucose concentration on glucose utilization and glucose clearance in normal man.血浆葡萄糖浓度对正常人体葡萄糖利用及清除的影响。
Diabetes. 1981 Jun;30(6):535-7. doi: 10.2337/diab.30.6.535.
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Effect of physical form of carbohydrate on the postprandial glucose, insulin, and gastric inhibitory polypeptide responses in type 2 diabetes.碳水化合物的物理形态对2型糖尿病患者餐后血糖、胰岛素及胃抑肽反应的影响
Am J Clin Nutr. 1982 Jul;36(1):10-4. doi: 10.1093/ajcn/36.1.10.
6
Modifications of glucose storage and oxidation in nonobese diabetics, measured by continuous indirect calorimetry.通过连续间接量热法测量非肥胖型糖尿病患者葡萄糖储存和氧化的变化。
Diabetes. 1980 Sep;29(9):752-6. doi: 10.2337/diab.29.9.752.
7
A comparison of carbohydrate metabolism after sucrose, sorbitol, and fructose meals in normal and diabetic subjects.正常人和糖尿病患者进食蔗糖、山梨醇和果糖后碳水化合物代谢的比较。
Diabetes Care. 1980 Sep-Oct;3(5):582-5. doi: 10.2337/diacare.3.5.582.
8
Effects of oral fructose in normal, diabetic, and impaired glucose tolerance subjects.口服果糖对正常、糖尿病及糖耐量受损受试者的影响。
Diabetes Care. 1980 Sep-Oct;3(5):575-82. doi: 10.2337/diacare.3.5.575.
9
Effects of growth hormone on insulin action in man. Mechanisms of insulin resistance, impaired suppression of glucose production, and impaired stimulation of glucose utilization.生长激素对人体胰岛素作用的影响。胰岛素抵抗、葡萄糖生成抑制受损及葡萄糖利用刺激受损的机制。
Diabetes. 1982 Aug;31(8 Pt 1):663-9. doi: 10.2337/diab.31.8.663.
10
The role of gastric inhibitory polypeptide in the augmented insulin response to sucrose.胃抑制性多肽在蔗糖增强胰岛素反应中的作用。
Diabetes Care. 1982 Jul-Aug;5(4):379-85. doi: 10.2337/diacare.5.4.379.