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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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Posters<br />

91.<br />

ANTIOXIDANT RESPONSE TO TREATMENT WITH NATUraL COMPOUNDS<br />

AND AN NO DONOR IN EXPERIMENTAL HYPERTENSION<br />

Ima Dovinová 1 , Zuzana Pakanová 2 , StanislavaVranková 1 , Oľga Pecháňová 1 ,<br />

Soňa Čačányiová 1 , František Kristek 1 and Helena Paulíková 2<br />

1<br />

Institute of Normal and Pathological Physiology, SAS, Bratislava;<br />

2<br />

Department of Biochemistry and Microbiology, Faculty of Chemical and Food<br />

Technology STU, Bratislava<br />

SOD enzymes play an important role in cardiovascular tissue by protecting NO against<br />

oxidative inactivation by superoxide. Both NO and superoxide are free radicals with<br />

unpaired electrons and can react with one another. Studies with pharmacologically inhibited<br />

SOD1 and SOD3 showed that NO cannot be released from endothelium without<br />

oxidative degradation, that is, SOD enzymes play an important role in vasodilatation and<br />

in protection of NO in blood vessel walls.<br />

In this study, we observed the effect of flavonoids (Alibernet red wine extract), melatonin,<br />

and an NO-donor, PETN, on antioxidant response of blood vessels and the heart in<br />

animal hypertension models, SHR and SHR-cp.<br />

The experiments show that in young hypertensive rats the Alibernet extract increased<br />

the activity of SOD and NOS in the left ventricle of SHR and the total antioxidant status<br />

in plasma.<br />

In adult hypertensive rats, the NO donor, PETN, increased SOD and GPx activities and<br />

decreased left ventricle damage.<br />

The results indicate that the most remarkable effects of the Alibernet red wine extract<br />

in young hypertensive rats, and of the PETN NO donor in adult hypertensive rats are<br />

related to protective effects of SOD enzymes in the heart.<br />

Ackowledgement: The work was supported by VEGA Grant No 2/0066/08.<br />

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

215

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