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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 />

ATOrvaSTATIN CHANGES MEMBraNE LIPID FLUIDITY IN<br />

MITOCHONDRIA ISOLATED frOM varIOUS TISSUES OF raTS<br />

Iveta Waczulíková 1 , Oľga Uličná 2 , Oľga Vančová 2 , Jarmila Kucharská 2 ,<br />

Veronika Ilovská 1 and Libuša Šikurová 1<br />

1<br />

Faculty of Mathematics, Physics and Informatics, 2 Pharmacobiochemical Lab.,<br />

3 rd Med. Clinic, Faculty of Medicine, Comenius University, Bratislava, Slovakia<br />

Atorvastatin is a potent cholesterol-lowering agent with well-described benefits and<br />

adverse effects manifested in clinical practice. Hypercholesterolemia leads to alterations<br />

in lipid composition and fluidity of blood cell plasma membranes and atorvastatin was<br />

reported to reverse these alterations. Little is known how the hypercholesterolemic<br />

condition and its therapy may influence mitochondrial membrane properties. We have<br />

examined the effect of two selected doses of atorvastatin on membrane lipid fluidity<br />

and function of mitochondria isolated from liver, heart and skeletal muscles of control<br />

and hypercholesterolemic rats. Wistar rats were on a high cholesterol diet for 8 weeks.<br />

Atorvastatin was administered per os either at a low or high dose (10/80 mg/kg/day, resp.)<br />

for 4 weeks. Fluidity was assessed spectrofluorometrically and functional parameters of<br />

mitochondria with a Clark oxygen electrode.<br />

Hypercholesterolemic condition affected the investigated properties of mitochondria in<br />

a tissue-dependent manner. This is likely the reason of an ambiguous action of atorvastatin<br />

on membrane fluidity. Atorvastatin seems to eliminate certain types of membrane<br />

damage induced by hypercholesterolemia, if it is controlled by an appropriate dosage.<br />

However, on average, it tended to fluidize the membranes and compromise capacity of<br />

mitochondrial respiratory chain as well as the rate of ATP formation in mitochondria in<br />

both, healthy and hypercholesterolemic rats.<br />

Acknowledgement: Supported by the grants: VEGA 1/0328/10 and 1/0293/08.<br />

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

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