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Effects of aging on glucose-mediated glucose disposal and glucose transport.衰老对葡萄糖介导的葡萄糖处置及葡萄糖转运的影响。
J Clin Invest. 1986 Jun;77(6):2034-41. doi: 10.1172/JCI112533.
2
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本文引用的文献

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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.
2
Evidence that translocation of the glucose transport activity is the major mechanism of insulin action on glucose transport in fat cells.葡萄糖转运活性的转位是胰岛素作用于脂肪细胞葡萄糖转运的主要机制的证据。
J Biol Chem. 1982 Sep 25;257(18):10942-7.
3
Potential mechanism of insulin action on glucose transport in the isolated rat adipose cell. Apparent translocation of intracellular transport systems to the plasma membrane.胰岛素对分离的大鼠脂肪细胞葡萄糖转运作用的潜在机制。细胞内转运系统向质膜的明显易位。
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4
Influence of plasma glucose and insulin concentration on plasma glucose clearance in man.血浆葡萄糖和胰岛素浓度对人体血浆葡萄糖清除率的影响。
Diabetes. 1982 Aug;31(8 Pt 1):683-8. doi: 10.2337/diab.31.8.683.
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Does insulin removal rate from plasma decline with age?
Diabetes. 1982 Aug;31(8 Pt 1):670-3. doi: 10.2337/diab.31.8.670.
6
Effect of variations in basal plasma glucose concentration on glucose utilization (M) and metabolic clearance (MCR) rates during insulin clamp studies in patients with non-insulin-dependent diabetes mellitus.在非胰岛素依赖型糖尿病患者的胰岛素钳夹研究中,基础血浆葡萄糖浓度变化对葡萄糖利用率(M)和代谢清除率(MCR)的影响。
Diabetes. 1982 May;31(5 Pt 1):396-400. doi: 10.2337/diab.31.5.396.
7
Impaired in vivo insulin clearance in patients with severe target-cell resistance to insulin.严重胰岛素靶细胞抵抗患者体内胰岛素清除受损。
Diabetes. 1982 Feb;31(2):132-5. doi: 10.2337/diab.31.2.132.
8
Insulin increases the maximum velocity for glucose uptake without altering the Michaelis constant in man. Evidence that insulin increases glucose uptake merely by providing additional transport sites.胰岛素可提高人体葡萄糖摄取的最大速度,而不改变米氏常数。有证据表明,胰岛素仅通过提供额外的转运位点来增加葡萄糖摄取。
J Clin Invest. 1982 Dec;70(6):1310-4. doi: 10.1172/jci110731.
9
Influence of ageing on glucose homeostasis.
J Clin Endocrinol Metab. 1982 Nov;55(5):840-8. doi: 10.1210/jcem-55-5-840.
10
The role of the glucose transport system in the postreceptor defect in insulin action associated with human aging.
J Clin Endocrinol Metab. 1984 Apr;58(4):721-5. doi: 10.1210/jcem-58-4-721.

衰老对葡萄糖介导的葡萄糖处置及葡萄糖转运的影响。

Effects of aging on glucose-mediated glucose disposal and glucose transport.

作者信息

Fink R I, Wallace P, Olefsky J M

出版信息

J Clin Invest. 1986 Jun;77(6):2034-41. doi: 10.1172/JCI112533.

DOI:10.1172/JCI112533
PMID:3519685
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC370565/
Abstract

To assess the effects of aging on glucose-mediated glucose disposal and glucose transport, glucose disposal rates were measured in 10 nonelderly (32 +/- 4 yr) and 11 elderly (64 +/- 4 yr) subjects at five different plasma glucose concentrations. Glucose disposal was decreased by 30-35% in the elderly at each level of glycemia (100-350 mg/dl) in the presence of similar levels of hyperinsulinemia (approximately 100 microU/ml), and the 50% effective concentration (EC50) was similar in both the nonelderly (100 +/- 9) and elderly (103 +/- 5 mg/dl). The Michaelis constant (Km) of 3-O-methyl glucose transport in adipocytes was unchanged with aging (3.8 +/- 0.5 vs. 3.2 +/- 0.2 mM) while the maximum velocity of insulin stimulated transport was reduced by 34% in the elderly (8.3 +/- 1.3 vs. 12.6 +/- 1.5 pmol/5 X 10(4) cells per s, P less than 0.05). The insulin resistance of aging is therefore due to a reduction in the capacity of the glucose uptake system, while the affinity of glucose utilization (EC50 and Km) is unchanged. This supports the hypothesis that a reduction in the number of glucose transport and metabolic units occurs with aging, but that each unit functions normally.

摘要

为评估衰老对葡萄糖介导的葡萄糖处置及葡萄糖转运的影响,在10名非老年受试者(32±4岁)和11名老年受试者(64±4岁)中,于5种不同血浆葡萄糖浓度下测量葡萄糖处置率。在相似的高胰岛素血症水平(约100微单位/毫升)下,老年受试者在每个血糖水平(100 - 350毫克/分升)时的葡萄糖处置均降低了30 - 35%,且非老年组(100±9)和老年组(103±5毫克/分升)的50%有效浓度(EC50)相似。脂肪细胞中3 - O - 甲基葡萄糖转运的米氏常数(Km)不随衰老而改变(3.8±0.5对3.2±0.2毫摩尔),而老年组中胰岛素刺激转运的最大速度降低了34%(8.3±1.3对12.6±1.5皮摩尔/5×10⁴细胞每秒,P<0.05)。因此,衰老导致的胰岛素抵抗是由于葡萄糖摄取系统能力的降低,而葡萄糖利用的亲和力(EC50和Km)未改变。这支持了以下假说:随着衰老,葡萄糖转运和代谢单位的数量减少,但每个单位功能正常。