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Published on: October 22, 2013
The ageing entero-insular axis
L Ranganath1, I Sedgwick, L Morgan
1Epsom General Hospital, Surrey, UK.
Aging impairs glucose tolerance by affecting insulin secretion. Older adults show increased glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1) responses, suggesting a compensatory mechanism for age-related changes in the entero-insular axis.
Area of Science:
- Endocrinology
- Gerontology
- Metabolic Health
Background:
- Aging is a significant risk factor for glucose intolerance and Type II diabetes.
- While reduced insulin secretion is noted in aging, age-related changes in key insulinotropic hormones like GIP and GLP-1 remain unclear.
Purpose of the Study:
- To investigate the entero-insular axis in young versus older women.
- To assess age-related differences in the secretion of glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1) after oral carbohydrate intake.
Main Methods:
- Comparative analysis of oral carbohydrate challenge in 6 young premenopausal and 6 older postmenopausal women.
- Measurement of integrated insulin, glucose, GIP, and GLP-1 responses.
Main Results:
- Similar integrated insulin and glucose responses were observed between the younger and older groups.
- Older subjects exhibited significantly greater total integrated responses for both GIP and GLP-1.
- Positive correlations were found between age and integrated glucose response (r=0.65) and GLP-1 response (r=0.85).
Conclusions:
- Age-related impairment in insulin secretion in response to GIP and GLP-1 may contribute to reduced glucose tolerance in older adults.
- The heightened compensatory increase in GIP and GLP-1 secretion underscores the importance of the entero-insular axis in regulating insulin secretion and highlights feedback mechanisms.
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