Comparison of the suppressive effects of elevated plasma glucose and free fatty acid levels on glucagon secretion in normal and insulin-dependent diabetic subjects. Evidence for selective alpha-cell insensitivity to glucose in diabetes mellitus.
Open Access
- 1 August 1976
- journal article
- research article
- Published by American Society for Clinical Investigation in Journal of Clinical Investigation
- Vol. 58 (2) , 320-325
- https://doi.org/10.1172/jci108475
Abstract
To examine whether abnormal pancreatic alpha-cell function found in human diabetes mellitus may represent a selective insensitivity to glucose, plasma glucagon responses to hyperglycemia and elevation of plasma free fatty acid levels (both known suppressors of glucagon secretion) were compared in juvenile-onset, insulin-requiring diabetic subjects, and in normal nondiabetic subjects. In the latter, both elevation of plasma free fatty acid levels induced by heparin administration of hyperglycemia produced by intravenous infusion of glucose resulted in a comparable 30--40% suppression of circulating glucagon levels (P less than 0.01). In the diabetic subjects, glucagon suppression by hyperglycemia (less than 20%) was less than that occurring in normal subjects (P less than 0.01), even when accompanied by infusion of supraphysiologic amounts of insulin. However, suppression of glucagon levels by elevation of plasma free fatty acids in the diabetic group was similar to that found in normal subjects and of comparable magnitude to that due to hyperglycemia in the normal subjects. These results thus demonstrate a selective impairment of the diabetic alpha-cell response to glucose and provide further evidence for the presence of an abnormal alpha-cell glucoreceptor in human diabetes mellitus.Keywords
This publication has 29 references indexed in Scilit:
- Plasma glucagon levels in normal women during pregnancyDiabetologia, 1975
- Effect of insulin-glucose infusions on plasma glucagon levels in fasting diabetics and nondiabetics.Journal of Clinical Investigation, 1975
- IS DIABETES MELLITUS A DISORDER OF THE GLUCORECEPTOR?The Lancet, 1975
- ROLE OF GLUCAGON AND OTHER HORMONES IN DEVELOPMENT OF DIABETIC KETOACIDOSISThe Lancet, 1975
- Insulin and glucose as modulators of the amino acid-induced glucagon release in the isolated pancreas of alloxan and streptozotocin diabetic rats.Journal of Clinical Investigation, 1975
- Anomeric Specificity of Glucose-Stimulated Insulin Release: Evidence for a Glucoreceptor?Science, 1974
- The Effect of Insulin on the Alpha-Cell Response to Hyperglycemia in Long-Standing Alloxan DiabetesJournal of Clinical Investigation, 1974
- Operation of the “Glucose‐Fatty Acid Cycle” during Experimental Elevations of Plasma Free Fatty Acid Levels in ManEuropean Journal of Clinical Investigation, 1974
- Lack of Glucagon Response to Hypoglycemia in Diabetes: Evidence for an Intrinsic Pancreatic Alpha Cell DefectScience, 1973
- ABNORMALITIES OF GLUCAGON METABOLISM IN UNTREATED DIABETES MELLITUSThe Lancet, 1972