Lipolytic responsiveness to epinephrine in nondiabetic and diabetic humans

GD Divertie, MD Jensen, PE Cryer… - American Journal of …, 1997 - journals.physiology.org
GD Divertie, MD Jensen, PE Cryer, JM Miles
American Journal of Physiology-Endocrinology and Metabolism, 1997journals.physiology.org
To determine whether the sensitivity of adipose tissue lipolysis to catecholamines is
increased in poorly controlled insulin-dependent diabetes, the lipolytic response to
epinephrine was measured in seven nondiabetic volunteers and seven poorly controlled
diabetic subjects with use of [1-(14) C] palmitate as a tracer. Subjects received sequential 1-
h infusions of epinephrine, which produced epinephrine concentrations of approximately
1,000, approximately 1,750, approximately 3,500, and approximately 6,000 pmol/l. A …
To determine whether the sensitivity of adipose tissue lipolysis to catecholamines is increased in poorly controlled insulin-dependent diabetes, the lipolytic response to epinephrine was measured in seven nondiabetic volunteers and seven poorly controlled diabetic subjects with use of [1-(14)C]palmitate as a tracer. Subjects received sequential 1-h infusions of epinephrine, which produced epinephrine concentrations of approximately 1,000, approximately 1,750, approximately 3,500, and approximately 6,000 pmol/l. A pancreatic clamp was used to maintain constant plasma hormone levels. Concentration-response curves were constructed for each subject from the integrated lipolytic response during each epinephrine infusion. There was no difference in maximal lipolytic response (117 +/- 19 vs. 152 +/- 11 mumol.kg-1.h-1) or in maximally effective (3,171 +/- 267 vs. 3,357 +/- 349 pmol/l) or half-maximally effective (1,081 +/- 109 vs. 1,015 +/- 120 pmol/l) epinephrine concentrations between nondiabetic and diabetic subjects, respectively (all P = NS). In control subjects, maximum beta-hydroxybutyrate concentrations were achieved at lower epinephrine concentrations than those required for a maximum lipolytic effect. Thus, under pancreatic clamp conditions, the lipolytic response to epinephrine in nondiabetic and diabetic subjects was similar.
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