Diurnal fluctuations in triglyceride, free fatty acids, and insulin during sucrose consumption and insulin infusion in man.

Serial changes in circulating triglyceride, free fatty acids (FFA), insulin, and glucose have been measured in human subjects fed sucrose as the sole source of calories for 2- or 3-day periods. The sucrose was given either during the day with overnight fasting (19 subjects) or as continual 3-hour meals during the day and night (seven subjects). Insulin was infused overnight in five additional subjects on the day-feeding regimen to determine the effect on triglyceride concentration. The concentration of triglyceride increased during the study in all subjects, but there was a clear diurnal pattern in the response which was present even in the continual feeding studies. The rise in triglyceride occurred mainly overnight, and during the day there was frequently a fall in the concentration. The overnight increase was significantly less when insulin was infused. There were also diurnal fluctuations in FFA and insulin in both daytime and continual feeding regimens. The plasma FFA, like triglyceride, rose during the night and fell during the day while the insulin rose during the day and fell overnight. Separate statistical analysis of the daytime and overnight changes revealed that the changes in triglyceride were significantly but negatively correlated with changes in insulin during both periods. The changes in triglyceride and FFA were positively correlated during the day but not significantly related during the night. The data show that when sucrose is eaten for 2 or 3 days, there is a general increase in triglyceride concentration upon which are superimposed major diurnal fluctuations in the concentrations of triglyceride, insulin, and FFA. It is suggested that the highly significant inverse relationship between changes in triglyceride and insulin may be mediated through an effect of insulin on triglyceride removal.

[1]  R. Fuller,et al.  Diurnal variation of liver glycogen and plasma free fatty acids in rats fed ad libitum or single daily meal. , 1970, Metabolism: clinical and experimental.

[2]  F. Pi‐Sunyer,et al.  Insulin and Ketone Responses to Ingestion of Medium and Long-chain Triglycerides in Man , 1969, Diabetes.

[3]  T. Skillman,et al.  Interrelationships of Hyperinsulinism and Hypertriglyceridemia in Young Patients with Coronary Heart Disease , 1968, Circulation.

[4]  P. Nestel,et al.  The effect of glucose and insulin in vitro on the uptake of triglyceride and on lipoprotein lipase activity in fat pads from normal, fed rats. , 1968, Biochimica et biophysica acta.

[5]  H. Knowles,et al.  Interactions of obesity, and glucose and insulin levels in hypertriglyceridemia. , 1968, The American journal of clinical nutrition.

[6]  D. Kipnis,et al.  Growth hormone secretion during sleep. , 1968, The Journal of clinical investigation.

[7]  R. Goldrick,et al.  A SIMPLIFIED METHOD FOR ESTIMATING PLASMA TRIGLYCERIDES: THEIR STABILITY DURING COLD STORAGE , 1968, The Medical journal of Australia.

[8]  M. Schotz,et al.  Hepatic triglyceride secretion in relation to lipogenesis and free fatty acid mobilization in fasted and glucose-refed rats. , 1968, Journal of lipid research.

[9]  P. Nestel Relationship between FFA flux and TGFA influx in plasma before and during the infusion of insulin. , 1967, Metabolism: clinical and experimental.

[10]  G. Reaven,et al.  Role of insulin in endogenous hypertriglyceridemia. , 1967, The Journal of clinical investigation.

[11]  D. Schwartz,et al.  Les triglycérides sanguins dans un groupe professionnel , 1967 .

[12]  T. O. Brown,et al.  Hepatic lipid metabolism in experimental diabetes: II. Incorporation of [1-14C]palmitate into lipids of the liver and of the d < 1.020 perfusate lipoproteins , 1967 .

[13]  D. Porte,et al.  Diabetic lipemia. A form of acquired fat-induced lipemia. , 1967, The New England journal of medicine.

[14]  R. Lees,et al.  Fat transport in lipoproteins--an integrated approach to mechanisms and disorders. , 1967, The New England journal of medicine.

[15]  G. Reaven,et al.  Glucose, insulin, and triglyceride responses to high and low carbohydrate diets in man. , 1966, The Journal of clinical investigation.

[16]  P. Nestel Carbohydrate-induced hypertriglyceridemia and glucose utilization in ischemic heart disease. , 1966, Metabolism: clinical and experimental.

[17]  G. Reaven,et al.  Effect of Insulin Pretreatment on Glucose and Lipid Metabolism of Liver Slices from Normal Rats.∗ , 1966, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

[18]  D. P. Jones,et al.  Effects of insulin on triglyceride and free fatty acid metabolism in man. , 1965, Metabolism: clinical and experimental.

[19]  G. Eagle,et al.  The ability of actinomycin D to increase the clearing-factor lipase activity of rat adipose tissue. , 1964, The Biochemical journal.

[20]  W. Connell,et al.  THE EFFECT OF THE TYPE AND AMOUNT OF DIETARY FAT ON THE LEVEL OF PLASMA TRIGLYCERIDES IN HUMAN SUBJECTS IN THE POSTABSORPTIVE STATE. , 1964, Canadian journal of biochemistry.

[21]  A. Lazarow,et al.  Immunoassay of Insulin: Two Antibody System: Plasma Insulin Levels of Normal, Subdiabetic and Diabetic Rats , 1963, Diabetes.

[22]  J. Farquhar,et al.  Carbohydrate-induced and fat-induced lipemia. , 1961, Transactions of the Association of American Physicians.

[23]  V. Dole,et al.  Microdetermination of long-chain fatty acids in plasma and tissues. , 1960, The Journal of biological chemistry.

[24]  R. Havel Early effects of fasting and of carbohydrate ingestion on lipids and lipoproteins of serum in man. , 1957, The Journal of clinical investigation.

[25]  F. H. Tyler,et al.  The diurnal variation of plasma levels and urinary excretion on 17-hydroxycorticosteroids in normal subjects, night workers and blind subjects. , 1956, The Journal of clinical endocrinology and metabolism.