TY - JOUR
T1 - Effect of intravenous insulin treatment on in vivo whole body leucine kinetics and oxygen consumption in insulin-deprived type I diabetic patients
AU - Nair, K. Sreekumaran
AU - Ford, G. Charles
AU - Halliday, David
N1 - Funding Information:
From the Medical Research Council, Clinical Research Center, Harrow, United Kingdom. Address reprint requests to K. Sreekumaran Nair, MD, Department of Medicine, University of Rochester School of Medicine and Dentistry, Endocrinology-Metabolism Unit. Monroe Community Hospital, 435 East Henrietta Rd, Rochester NY 14603. o I987 by Grune & Stratton, Inc. 0026-0495/87/3605-0015$03.00/O
PY - 1987/5
Y1 - 1987/5
N2 - In vivo leucine metabolism was studied after an overnight fast in nine type I diabetic patients and nine healthy control subjects using l-[1-13C] leucine as a tracer. In the insulin-deprived state, leucine flux (reflecting proteolysis), leucine oxidation, and plasma leucine concentrations were higher in the diabetic patients than in the control subjects (P < .001). In 4 of the 9 insulin-deprived diabetic patients, a four-hour intravenous insulin treatment decreased plasma glucose and leucine concentrations and leucine flux, but failed to decrease leucine oxidation. In the remaining 5 of the 9 diabetic patients, uninterrupted insulin treatment prior to the study and a seven-hour intravenous insulin treatment during the study period decreased not only the concentrations of plasma glucose and leucine and leucine flux, but also leucine oxidation (P < .01). In all 9 diabetic patients the nonoxidative portion of leucine flux (reflecting protein synthesis) decreased during insulin treatment (P < .01), but this decrease was lower than that of leucine flux (reflecting proteolysis), and therefore protein was conserved during insulin treatment. We conclude that the effect of insulin on proteolysis (reflected by leucine flux) is more rapid than its effect on leucine oxidation, but on aggressive insulin treatment accelerated leucine oxidation also was decreased in type I diabetic patients.
AB - In vivo leucine metabolism was studied after an overnight fast in nine type I diabetic patients and nine healthy control subjects using l-[1-13C] leucine as a tracer. In the insulin-deprived state, leucine flux (reflecting proteolysis), leucine oxidation, and plasma leucine concentrations were higher in the diabetic patients than in the control subjects (P < .001). In 4 of the 9 insulin-deprived diabetic patients, a four-hour intravenous insulin treatment decreased plasma glucose and leucine concentrations and leucine flux, but failed to decrease leucine oxidation. In the remaining 5 of the 9 diabetic patients, uninterrupted insulin treatment prior to the study and a seven-hour intravenous insulin treatment during the study period decreased not only the concentrations of plasma glucose and leucine and leucine flux, but also leucine oxidation (P < .01). In all 9 diabetic patients the nonoxidative portion of leucine flux (reflecting protein synthesis) decreased during insulin treatment (P < .01), but this decrease was lower than that of leucine flux (reflecting proteolysis), and therefore protein was conserved during insulin treatment. We conclude that the effect of insulin on proteolysis (reflected by leucine flux) is more rapid than its effect on leucine oxidation, but on aggressive insulin treatment accelerated leucine oxidation also was decreased in type I diabetic patients.
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U2 - 10.1016/0026-0495(87)90049-7
DO - 10.1016/0026-0495(87)90049-7
M3 - Article
C2 - 3553851
AN - SCOPUS:0023235606
SN - 0026-0495
VL - 36
SP - 491
EP - 495
JO - Metabolism: Clinical and Experimental
JF - Metabolism: Clinical and Experimental
IS - 5
ER -