Insulin resistance in Pima Indians. A combined effect of genetic predisposition and obesity-related skeletal muscle cell hypertrophy
- PMID: 3134799
Insulin resistance in Pima Indians. A combined effect of genetic predisposition and obesity-related skeletal muscle cell hypertrophy
Abstract
Obesity and diabetes are epidemic in the Pima Indians of Southwest United States. Recent evidence suggests that a reduced metabolic rate may predispose the obesity and, since metabolic rate appears to be familial, this may predispose to the familial dependence of obesity. Obesity is associated with an increased risk of diabetes. Insulin resistance is associated with obesity, but is also familial, independent of obesity. In this population insulin resistance is a risk factor for the development of diabetes. Diabetes occurs when insulin secretory failure is superimposed on insulin resistance. Reduced glucose storage in muscle, regulated by glycogen synthase, is important in determining insulin resistance especially at high plasma insulin concentrations and it is possible that a specific genetic defect may be the cause of this. Obesity has its major effect on insulin action at lower plasma insulin concentrations and we propose that this may in part be due to abnormalities of insulin action induced by an increased fat-free mass with a consequent enlargement of muscle cells, a reduced capillary supply, and reduced penetration of insulin into muscle in obese subjects. We propose therefore that insulin resistance may be due to a combination of a genetic defect and obesity-induced changes in the biophysical properties of skeletal muscle. These defects, by slightly increasing the plasma glucose concentration and inducing pancreatic glucose insensitivity, may in turn lead to the development of non-insulin-dependent diabetes mellitus.
Similar articles
-
Postabsorptive respiratory quotient and insulin-stimulated glucose storage rate in nondiabetic pima indians are related To glycogen synthase fractional activity in cultured myoblasts.J Clin Invest. 1998 May 15;101(10):2251-6. doi: 10.1172/JCI1778. J Clin Invest. 1998. PMID: 9593781 Free PMC article.
-
Elevated plasma nonesterified fatty acids are associated with deterioration of acute insulin response in IGT but not NGT.Am J Physiol Endocrinol Metab. 2003 Jun;284(6):E1156-61. doi: 10.1152/ajpendo.00427.2002. Epub 2003 Feb 11. Am J Physiol Endocrinol Metab. 2003. PMID: 12582008 Clinical Trial.
-
Insulin downregulates pyruvate dehydrogenase kinase (PDK) mRNA: potential mechanism contributing to increased lipid oxidation in insulin-resistant subjects.Mol Genet Metab. 1998 Oct;65(2):181-6. doi: 10.1006/mgme.1998.2748. Mol Genet Metab. 1998. PMID: 9787110
-
On the pathophysiology of late onset non-insulin dependent diabetes mellitus. Current controversies and new insights.Dan Med Bull. 1999 Jun;46(3):197-234. Dan Med Bull. 1999. PMID: 10421979 Review.
-
Insulin resistance in type II diabetes mellitus.Adv Second Messenger Phosphoprotein Res. 1990;24:511-6. Adv Second Messenger Phosphoprotein Res. 1990. PMID: 2169826 Review.
Cited by
-
Rapid formation of capillary endothelial cells in rat skeletal muscle after exposure to insulin.Diabetologia. 1996 Feb;39(2):206-11. doi: 10.1007/BF00403964. Diabetologia. 1996. PMID: 8635673
-
Skeletal muscle membrane lipid composition is related to adiposity and insulin action.J Clin Invest. 1995 Dec;96(6):2802-8. doi: 10.1172/JCI118350. J Clin Invest. 1995. PMID: 8675650 Free PMC article.
-
Glucose status and depressive symptoms: a cohort study of elderly people in northwest Finland.Scand J Prim Health Care. 2019 Jun;37(2):242-248. doi: 10.1080/02813432.2019.1608050. Epub 2019 May 17. Scand J Prim Health Care. 2019. PMID: 31099298 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Other Literature Sources
Medical