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Submitted on January 31, 2007
Accepted on April 18, 2007
Franz-Volhard Clinical Research Center, Medical Faculty of the Charité and Helios Klinikum, Berlin, Germany
* To whom correspondence should be addressed. E-mail: jens.jordan{at}charite.de.
Context: Nitric oxide synthase (NOS) expression in adipose tissue is increased in obese subjects. The functional relevance is not known.
Objective: To compare adipose tissue metabolism between obese men with greater or lower adipose eNOS or iNOS expression.
Design: Prospective, open-label.
Setting: Academic clinical research center.
Patients: 14 obese (32±0.6 kg/m2) and 8 normal weight (23±2 kg/m2) healthy men.
Intervention: Perfusion of microdialysis catheters in abdominal subcutaneous adipose tissue and in vastus lateralis muscle with L-NAME or with D-NAME. Addition of incremental isoproterenol concentrations to the perfusate.
Main outcome measures: Microdialysate glycerol.
Results: Tissue perfusion and microdialysate glycerol concentrations at baseline and during isoproterenol stimulation were similar in obese men with high or with low eNOS or iNOS expression, both, during L-NAME and during D-NAME. During D-NAME, basal and maximal isoproterenol stimulated glycerol were similar in lean and in obese men. However, in lean men, the dose-response relationship between isoproterenol and glycerol was shifted towards the left (p<0.0001). NOS inhibition with L-NAME had no effect on basal or isoproterenol stimulated glycerol in the obese group in skeletal muscle or in adipose tissue. In contrast, L-NAME augmented the lipolytic response in lean subjects in both tissues.
Conclusions: Differences in eNOS and iNOS mRNA expression at the adipose tissue level may have a limited effect on lipolysis and tissue perfusion. The lower resting lipolysis in adipose tissue of obese, compared to nonobese subjects cannot be explained by a tonic NO effect.
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