Age-related hypertrophy of adipose tissue has been associated with a significant decrease
in the number of angiotensin II receptors. The aim of this study was to investigate
the characteristics of angiotensin II receptors in hypertrophic adipose tissue in
animal obesity model using rats postnatally treated with monosodium glutamate. Angiotensin
II is known to induce hypertrophy in several tissues of the cardiovascular system
and might do the same in fat tissue. The expression and binding properties of angiotensin
II AT1 receptors in epididymal fat tissue of adult rats were studied using membrane-binding,
RT-PCR, and immunoblotting. The amount of AT1 receptor mRNA did not differ significantly between obese and control rats. Despite
that glutamate-treated rats displayed approximately 4-times more AT1 receptor immunoreactive protein content in fat tissue cell membranes than the controls
did. In contrast, binding experiments showed a significant (40.3 ± 6.2 %) decrease
of 125I-Sar1-Ile8-angiotensin II-binding to fat tissue cell membranes in obese rats compared to controls.
In conclusion, the present study provides evidence for the low binding properties
associated with an accumulation of AT1 receptor protein in cell membranes of the fat tissue of rats with glutamate-induced
obesity. Discrepancies among angiotensin II-binding, AT1 receptor protein, and AT1 receptor mRNA levels indicate a possible defect in the receptor protein, which remains
to be identified. The results obtained support a role of angiotensin II and AT1 receptors in the pathogenesis of obesity.
Key words:
AT1 Receptor - Fat Tissue - MSG Rat
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Štefan Zórad
Institute of Experimental Endocrinology
Slovak Academy of Sciences
Vlarska 3
833 06 Bratislava
Slovak Republic
Telefon: + 421 (2) 54 77-28 00
Fax: + 421 (2) 54 77-42 47
eMail: ueenstef@savba.sk