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Departments of Medicine (V.Q., E.H.-T., E.M., P.A., J.B.) and Vascular Surgery (S.E.), Karolinska University HospitalHuddinge, Karolinska Institutet, SE-141 86 Stockholm, Sweden
Address all correspondence and requests for reprints to: Jan Bolinder, M.D., Ph.D., Professor, Department of Medicine, M54 Karolinska University Hospital Huddinge, SE-141 86 Stockholm, Sweden. E-mail: jan.bolinder{at}medhs.ki.se.
Context: Triglyceride (TG) deposits in skeletal muscle (SM) are an important energy reservoir, and increased im TG content is associated with muscle insulin resistance.
Objective: The objective of the study was to investigate the effect of endogenous catecholamines on TG lipolysis in human SM in vivo. Adipose tissue (AT) was studied for comparison.
Design and Main Outcome Measures: Glycerol levels (index of lipolysis) were measured using microdialysis in the gastrocnemius muscle and abdominal sc adipose tissue during a hyperinsulinemic, hypoglycemic clamp (n = 13) and in response to in situ perfusion of epinephrine and norepinephrine (1010 to 105 M) (n = 12). Local tissue blood flow was monitored with the ethanol perfusion technique.
Setting: This was an experimental study.
Participants: The study population consisted of healthy subjects.
Results: Plasma epinephrine increased 10-fold and plasma norepinephrine 2-fold in response to insulin-induced hypoglycemia. In parallel, the fractional glycerol release (difference between tissue and arterial glycerol) increased 2-fold in both tissues (P < 0.0001). No changes in AT and SM blood flow were registered. When the catecholamines were perfused in situ, tissue glycerol increased significantly at 107 M of either epinephrine and norepinephrine (P < 0.0001) in AT. The maximum stimulation was seen at 106 M norepinephrine (2-fold increase) and 105 M epinephrine (3-fold increase). In SM, tissue glycerol increased at 107 M epinephrine and 106 M norepinephrine, respectively (P < 0.0001); the maximum increase of glycerol values (at 106 M) was 2.5 times for epinephrine and 1.6 times for norepinephrine, respectively (P < 0.01).
Conclusions: The lipolytic activity of SM is increased by endogenous catecholamines in vivo and appears to be more responsive to epinephrine than norepinephrine stimulation.
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