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Acta Physiologica Congress

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Acta Physiologica 2007; Volume 191, Supplement 658
Joint Meeting of The Slovak Physiological Society, The Physiological Society and The Federation of European Physiological Societies
9/11/2007-9/14/2007
Bratislava, Slovakia


ALCOHOL INTAKE ALTERS ENDOCRINE ACTIVITY OF RAT ADIPOSE TISSUE
Abstract number: PTH11-93

Pravdova1 E., Macho1 L., Fickova1 M.

1Institute of Experimental Endocrinology, Slovak Academy of Sciences, Bratislava, Slovak Republic; [email protected]

Aims: 

We have studied the effect of short and long-term alcohol intake on serum levels and gene expression in rat adipose tissue of three adipokines – leptin, adiponectin and resistin.

Methods: 

Alcohol (A10, A28) and control (C) Wistar rats were fed standard laboratory diet ad libitum. Rats had ad libitum access to 6% ethanol solution in tap water as the only drinking fluid. Pair-fed (PF) animals had the same caloric intake in the form of pelleted diet as A rats had consumed during the preceding 24 h. Gene expression of adipokines in epididymal adipose tissue was determined by the rtPCR method and serum levels of adipokines by ELISA method.

Results: 

Alcohol intake (A10, A28) significantly increased serum concentrations of all three adipokines compared to C. Alcohol consumption (A10, A28) resulted in the decrease of leptin and adiponectin mRNA levels in adipose tissue. Resistin gene expression in adipose tissue was not affected neither by short or long-time alcohol intake. Only increased adiponectin gene expression positively correlated with elevated adiponectin serum levels.

Conclusion: 

We demonstrated that both short and long-term alcohol intake altered serum levels of leptin, adiponectin and resistin and also modified adipokines gene expression in epididymal adipose tissue. Increased adipokines serum concentrations could be involved in changed metabolic processes manifested by smaller adipocyte size, increased glycemia, attenuation of insulin effect on glucose transport in isolated adipocytes, decreased liver glycogen content, and modified serum and liver lipid profile.

This study was supported by the grant VEGA 2/7044/27.

To cite this abstract, please use the following information:
Acta Physiologica 2007; Volume 191, Supplement 658 :PTH11-93

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