Values reported for basal hepatic glucose production and glucose utilization do not reflect metabolic changes occurring during sleep. To determine the effect of sleep with its associated lowered metabolic rate and thermogenesis on glucose kinetics and gluconeogenic substrate availability, 11 normal volunteers underwent an overnight study in which [3-3H]glucose was infused. Despite decreased insulin secretion, a fall in hepatic glucose output was observed with sleep that was synchronous with a reduction in glucose utilization and lipolysis (decreased plasma glycerol and free fatty acids). When activity was increased, these parameters rose toward previously reported basal levels. Prevention of sleep in 6 additional subjects attenuated the fall in glucose utilization and production as well as the fall in glycerol and free fatty acids despite similar insulin and counterregulatory hormone profiles. We suggest that sleep-associated metabolic changes produce a peripheral signal(s) that modulates hepatic glucose production in humans.
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March 01 1989
Sleep-Associated Fall in Glucose Disposal and Hepatic Glucose Output in Normal Humans: Putative Signaling Mechanism Linking Peripheral and Hepatic Events
John N clore;
John N clore
Division of Endocrinology and Metabolism, Medical College of Virginia
Richmond, Virginia
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John E Nestler;
John E Nestler
Division of Endocrinology and Metabolism, Medical College of Virginia
Richmond, Virginia
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William G Blackard
William G Blackard
Division of Endocrinology and Metabolism, Medical College of Virginia
Richmond, Virginia
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Address correspondence and reprint requests to J.N. Clore, MD, Box 155 MCV Station, Richmond, VA 23298.
Diabetes 1989;38(3):285–290
Article history
Received:
July 05 1988
Revision Received:
October 03 1988
Accepted:
October 03 1988
PubMed:
2645186
Citation
John N clore, John E Nestler, William G Blackard; Sleep-Associated Fall in Glucose Disposal and Hepatic Glucose Output in Normal Humans: Putative Signaling Mechanism Linking Peripheral and Hepatic Events. Diabetes 1 March 1989; 38 (3): 285–290. https://doi.org/10.2337/diab.38.3.285
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