Effects of {beta}-adrenergic receptor stimulation and blockade on substrate metabolism during submaximal exercise
1 The Human Performance Laboratory, Department of Kinesiology and Health Education, University of Texas at Austin, Austin, Texas 78712; 2 University of Castilla-la Mancha at Toledo, Toledo 45071, Spain; and 3 Pennington Biomedical Research Center, Baton Rouge, Louisiana 70808 We used -adrenergic...
Saved in:
Published in | American journal of physiology: endocrinology and metabolism Vol. 280; no. 5; p. E752 |
---|---|
Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
01.05.2001
|
Online Access | Get full text |
Cover
Loading…
Summary: | 1 The Human Performance Laboratory, Department of
Kinesiology and Health Education, University of Texas at Austin,
Austin, Texas 78712; 2 University of Castilla-la Mancha at
Toledo, Toledo 45071, Spain; and 3 Pennington Biomedical
Research Center, Baton Rouge, Louisiana 70808
We used
-adrenergic receptor stimulation and blockade as a tool to study
substrate metabolism during exercise. Eight moderately trained subjects
cycled for 60 min at 45% of O 2 peak 1 ) during a control trial (CON); 2 ) while
epinephrine was intravenously infused at 0.015 µg · kg 1 · min 1
( -STIM); 3 ) after ingesting 80 mg of propranolol
( -BLOCK); and 4 ) combining -BLOCK with intravenous
infusion of Intralipid-heparin to restore plasma fatty acid (FFA)
levels ( -BLOCK+LIPID). -BLOCK suppressed lipolysis (i.e.,
glycerol rate of appearance) and fat oxidation while elevating
carbohydrate oxidation above CON (135 ± 11 vs. 113 ± 10 µmol · kg 1 · min 1 ;
P < 0.05) primarily by increasing rate of
disappearance (R d ) of glucose (36 ± 2 vs. 22 ± 2 µmol · kg 1 · min 1 ;
P < 0.05). Plasma FFA restoration ( -BLOCK+LIPID)
attenuated the increase in R d glucose by more than one-half
(28 ± 3 µmol · kg 1 · min 1 ;
P < 0.05), suggesting that part of the compensatory
increase in muscle glucose uptake is due to reduced energy from fatty
acids. On the other hand, -STIM markedly increased glycogen
oxidation and reduced glucose clearance and fat oxidation despite
elevating plasma FFA. Therefore, reduced plasma FFA availability with
-BLOCK increased R d glucose, whereas -STIM increased
glycogen oxidation, which reduced fat oxidation and glucose clearance.
In summary, compared with control exercise at 45%
O 2 peak (CON), both -BLOCK and
-STIM reduced fat and increased carbohydrate oxidation, albeit
through different mechanisms.
lipid; glucose; propranolol; epinephrine; stable isotopes |
---|---|
ISSN: | 0193-1849 1522-1555 |