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XXII. BIOCHEMICKÝ ZJAZD - Jesseniova lekárska fakulta

XXII. BIOCHEMICKÝ ZJAZD - Jesseniova lekárska fakulta

XXII. BIOCHEMICKÝ ZJAZD - Jesseniova lekárska fakulta

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Lectures<br />

THE ROLE OF ANGIOTENSIN II AND OXYTOCIN IN REGULATION OF<br />

ADIPOCYTE CELL SIZE<br />

Katarína Kršková, Daniela Ježová, Lucia Gajdošechová,<br />

Miroslava Eckertová and Štefan Zorad<br />

Institute of Experimental Endocrinology, Slovak Academy of Sciences, Bratislava<br />

It is well recognized that adipocytes produce a number of proteins collectively named<br />

adipokines and thus adipose tissue plays a central role in development of cardiovascular<br />

and metabolic disorders. It has been shown that hypertrofic adipocytes produce more<br />

proinflammatory and insulin sensitivity decreasing adipokines (Zorad et al. 2006). This<br />

study presents treatment with angiotensin II receptor type I blocker (ARB) or with oxytocin<br />

in order to manipulate adipose tissue morphology with stimulated production of<br />

insulin sensitizing adipokines.<br />

Chronic ARB treatment reduced adipose tissue mass, adipocyte size, leptin and TNFα<br />

gene expression and leads to an elevation of serum adiponectin concetration, adiponectin<br />

and PPARγ gene expression in adipose tissue without a change in food intake. Oxytocin<br />

treatment did not affect the adipose tissue mass and food intake in rats. Despite that, the<br />

adipocyte diameter was significantly decreased and it was accompanied by a significant<br />

elevation of gene expression of aP2, PPARγ, GLUT4, leptin, ACE and CD31.<br />

Our results demonstrate positive effects of renin-angiotensin system inhibition on fat<br />

tissue remodeling and insulin sensitivity. Our oxytocin data suggests a new approach to<br />

modulate adipose tissue morphology in order to stimulate expression of insulin sensitivity<br />

markers. We assume that oxytocin increases both adipogenesis and angiogenesis<br />

in adipose tissue.<br />

This work was supported by grant VEGA 2/0162/08.<br />

112 <strong>XXII</strong>. Biochemistry Congress, Martin

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