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Simulated microgravity increases beta-adrenergic lipolysis in human adipose tissue
P Barbe1, J Galitzky, I De Glisezinski
1Institut National de la Santé et de la Recherche Médicale U-317, Laboratoire de Pharmacologie Médicale et Clinique, Toulouse, France.
The Journal of Clinical Endocrinology and Metabolism
|February 19, 1998
Summary
Reduced sympathetic nervous activity from head-down bed rest (HDBR) enhances beta-adrenergic lipolysis in adipose tissue. This hypersensitivity is linked to postreceptor events, not beta-adrenoceptor changes.
Area of Science:
- Physiology
- Endocrinology
- Metabolism
Background:
- Sympathetic nervous system activity influences adipose tissue lipolysis.
- Head-down bed rest (HDBR) is known to decrease sympathetic nervous activity.
- Understanding the impact of reduced sympathetic activity on fat metabolism is crucial.
Purpose of the Study:
- To investigate the effect of sustained sympathoinhibition via HDBR on beta-adrenergic lipolytic activity in subcutaneous adipose tissue.
- To determine if changes in beta-adrenoceptor sensitivity or postreceptor events mediate altered lipolysis.
Main Methods:
- Utilized 5-day head-down bed rest (HDBR) in eight healthy men.
- Employed microdialysis for in situ assessment of beta-adrenoceptor (AR) sensitivity in adipose tissue.
- Performed in vitro studies on isolated adipocytes to evaluate adrenergic sensitivity and lipolytic responses.
Main Results:
- HDBR increased beta-AR sensitivity to lipolysis and vascular tone.
- Basal and stimulated lipolysis in isolated adipocytes were enhanced post-HDBR.
- When normalized for postreceptor events, lipolytic responses to beta-AR agonists remained unchanged, suggesting postreceptor mediation.
Conclusions:
- Sustained sympathoinhibition through HDBR enhances the lipolytic beta-adrenergic response in adipose tissue.
- This hypersensitization appears to be primarily due to increased postreceptor signaling within adipocytes.
- No significant changes were observed in lymphocyte beta-AR number or alpha 2-AR-mediated effects.