Effect of endurance training on adrenergic control of lipolysis in adipose tissue of obese women
Language English Country United States Media print
Document type Clinical Trial, Journal Article, Research Support, Non-U.S. Gov't
- MeSH
- Epinephrine administration & dosage blood MeSH
- Adrenergic Agonists administration & dosage blood MeSH
- Receptors, Adrenergic, alpha-2 genetics metabolism MeSH
- Receptors, Adrenergic, beta genetics metabolism MeSH
- Abdomen MeSH
- Adult MeSH
- Gene Expression physiology MeSH
- Physical Endurance physiology MeSH
- Glycerol blood MeSH
- Body Mass Index MeSH
- Insulin blood MeSH
- Blood Glucose MeSH
- Fatty Acids, Nonesterified blood MeSH
- Humans MeSH
- Lipolysis drug effects physiology MeSH
- RNA, Messenger analysis MeSH
- Norepinephrine blood MeSH
- Obesity physiopathology MeSH
- Rest physiology MeSH
- Reverse Transcriptase Polymerase Chain Reaction MeSH
- Oxygen Consumption physiology MeSH
- Adipose Tissue physiology MeSH
- Check Tag
- Adult MeSH
- Humans MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Clinical Trial MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Epinephrine MeSH
- Adrenergic Agonists MeSH
- Receptors, Adrenergic, alpha-2 MeSH
- Receptors, Adrenergic, beta MeSH
- Glycerol MeSH
- Insulin MeSH
- Blood Glucose MeSH
- Fatty Acids, Nonesterified MeSH
- RNA, Messenger MeSH
- Norepinephrine MeSH
The effect of a 12-wk training program on sc abdominal adipose tissue (SCAAT) was studied in 11 obese women. Before and after the training, biopsies of SCAAT were performed for mRNA levels determination. Using the microdialysis method, involvement of alpha(2)- and beta-adrenergic receptor (ARs) in the control of lipolysis in SCAAT was studied using local perfusion of epinephrine alone or supplemented with phentolamine, an alpha(2)-AR antagonist. In addition, the variation in dialysate glycerol concentrations during exercise (50% peak oxygen consumption at 40 min) in a probe perfused with Ringer's solution was compared with that obtained in a probe perfused with Ringer's solution plus phentolamine. Training did not promote changes in the expression of key genes of the lipolytic pathway. The epinephrine-induced rise in the dialysate glycerol concentration was identical before and after training and was similarly potentiated by phentolamine. During exercise, the potentiating effect of phentolamine on the glycerol response was apparent before, but not after, training. The exercise-induced increase in plasma norepinephrine was lower after training (P = 0.04). In conclusion, training did not modify either the expression of genes involved in the control of lipolysis or alpha(2)- and beta-ARs in situ sensitivity to epinephrine in SCAAT. Training reduced the antilipolytic action of catecholamines mediated by alpha(2)-ARs during exercise, probably due to a reduction of exercise-induced catecholamine increase.
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