Effect of aging and diabetes on the enteroinsular axis

被引:39
作者
Korosi, J
McIntosh, CHS
Pederson, RA
Demuth, HU
Habener, JF
Gingerich, R
Egan, JM
Elahi, D
Meneilly, GS
机构
[1] Univ British Columbia, Dept Med, Vancouver, BC, Canada
[2] Univ British Columbia, Dept Physiol, Vancouver, BC, Canada
[3] Hans Kneoll Inst Nat Prod Res, Halle Saale, Germany
[4] Harvard Univ, Dept Med, Boston, MA 02115 USA
[5] Linco Res Inc, St Charles, MO USA
[6] NIA, Lab Clin Physiol, Gerontol Res Ctr, NIH, Baltimore, MD 21224 USA
来源
JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES | 2001年 / 56卷 / 09期
关键词
D O I
10.1093/gerona/56.9.M575
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Background. The current studies were designed to examine the effect of aging and diabetes on the enteroinsular axis. Methods. Healthy young control subjects (n = 10 young, age 23 +/- 1 years; body mass index [BMI] 24 +/- 1 kg/m(2)), healthy elderly subjects (n = 10; age 80 +/- 2 years; BMI 26 +/- 1 kg/m(2)), and elderly patients with type 2 diabetes (n = 10, age 76 +/- 2 years; BMI 26 +/- 2 kg/m(2)) underwent a 3-hour oral glucose tolerance test (glucose dose 40 gm/m(2)). Results. Insulin responses were not different between young controls and elderly patients with diabetes but were significantly lower in elderly patients with diabetes and young controls than in elderly controls (young control: 178 +/- 27 pM: elderly control: 355 +/- 57 pM elderly diabetes: 177 +/- 30 pM; p < .05 elderly control vs young control and elderly diabetes). Total glucagon-like peptide 1 (GLP-1) responses were not significantly different between young and elderly control, and patients with diabetes (young control: 15 +/- 2 pM; old control: 8 +/- 2 pM; elderly diabetes: 12 +/- 3 pM; p = ns). Active GLP-1 responses were also not different between young and elderly controls and patients with diabetes (young control: 5 +/- 1 pM; old control: 6 +/- 1 pM; elderly diabetes: 7 +/- 1 pM; p = ns). However, the difference between total and active GLP levels was significantly greater in the young controls (young control: 10 +/- 2 pM: old control: 2 +/- 2 pM elderly diabetes: 4 +/- 2 pM; p < .05, young vs elderly). Glucose-dependent insulinotropic polypeptide responses were not different between young and elderly controls and between elderly controls and patients witl diabetes but were significantly higher in elderly patients with diabetes than in young controls (young control: 97 +/- 12 pM; elderly control: 121 +/- 16 pM; elderly diabetes: 173 +/- 27 pM; p < .05, young vs elderly diabetes). Glucagon responses were reduced in elderly controls but were similar in young controls and elderly patients with diabetes (young control: 15 +/- 1 pM; elderly control: 9 +/- 1 pK elderly diabetes: 16 +/- 1 pM: p < .01 elderly control vs young control and elderly diabetes). Dipeptidyl peptidase IV levels were lower in both elderly controls and patients with diabetes when compared with young controls (young control: 0.17 +/- 0.01 elderly control: 0.15 +/- 0.01; elderly diabetes 0.15 +/- 0.01 Delta OD/20 minutes; p < .05, elderly vs young). Conclusions. We conclude that normal aging and diabetes are associated with multiple changes in the enteroinsular axis.
引用
收藏
页码:M575 / M579
页数:5
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