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- are hypotriglyceridemic;<br />

- exhibit antithrombotic and fibr<strong>in</strong>olytic activities;<br />

- exhibit anti<strong>in</strong>flammatory action;<br />

- reduce ischemia/reperfusion-<strong>in</strong>duced cellular damage. This effect is apparently due to the<br />

<strong>in</strong>corporation <strong>of</strong> eicosapentaenoic acid <strong>in</strong> membrane phospholipids.<br />

L<strong>in</strong>oleic acid (n-6) (LA) and alfa-l<strong>in</strong>olenic acid (n-3) (LNA) are two <strong>of</strong> the ma<strong>in</strong><br />

representative compounds, known as dietary essential fatty acids (EFA) because they prevent<br />

deficiency symptoms and cannot be synthesized by humans (1).<br />

Reduction <strong>of</strong> blood lipids and <strong>in</strong>hibition <strong>of</strong> LDL oxidation are the ma<strong>in</strong> therapeutic<br />

approaches to the treatment <strong>of</strong> atherosclerosis. Antioxidant agents, alone or <strong>in</strong> comb<strong>in</strong>ation<br />

with hypolipidaemic drugs are considered useful for this treatment. Food supplements<br />

conta<strong>in</strong><strong>in</strong>g such substances can serve as additional therapeutical agents (1).<br />

CLINICAL EXPERIMENT<br />

The aim <strong>of</strong> this work was to contribute to current knowledge <strong>of</strong> the <strong>in</strong>fluence <strong>of</strong> an<br />

antioxidant supplement type on metabolic and antioxidant status <strong>in</strong> a group <strong>of</strong> hyperlipidemic<br />

patients. Influence <strong>of</strong> complex food supplement conta<strong>in</strong><strong>in</strong>g tocopherol as antioxidant<br />

component and polyunsaturatd fatty acids as hypolipidaemic component on antioxidant status<br />

and parameters <strong>of</strong> lipid metabolism <strong>in</strong> 30 patients with hyperlipidaemia was studied. Food<br />

supplement (180 mg <strong>of</strong> eicosapentaneic acid EPA, 120 mg <strong>of</strong> docosahexaneic acid DHA, 1.12<br />

mg <strong>of</strong> vitam<strong>in</strong> E <strong>in</strong> 1 tbl.) was taken for 3 months, two tbl. daily; blood samples <strong>of</strong> each<br />

subject were taken <strong>in</strong> regular <strong>in</strong>tervals.<br />

METHODS<br />

Determ<strong>in</strong>ation <strong>of</strong> antioxidant activity<br />

Total antioxidant status was determ<strong>in</strong>ed us<strong>in</strong>g ABTS method (Randox Laboratories, USA).<br />

Serum AGE (Advanced Glycation End Products) were analysed fluorimetrically at<br />

350 nm/440 nm. Total amount <strong>of</strong> serum oxidation products „AOPP“ (Advanced Oxidation<br />

Prote<strong>in</strong> Products) was analysed spectrophotometrically accord<strong>in</strong>g to Witko-Sarsat et al. 1998<br />

(2), <strong>in</strong> Kalousová et al. 2001 modification (3).<br />

Biochemical parameters<br />

A set <strong>of</strong> biochemical parameters characteriz<strong>in</strong>g lipid metabolism was measured<br />

at Department <strong>of</strong> Cl<strong>in</strong>ical Biochemistry <strong>in</strong> the Kyjov Regional Hospital. Levels <strong>of</strong> total<br />

cholesterol, triacylglycerols, HDL and LDL – cholesterol, apolipoprote<strong>in</strong>e A and B, urea,<br />

creat<strong>in</strong><strong>in</strong>e, uric acid, alan<strong>in</strong>am<strong>in</strong>otransferase, aspartatam<strong>in</strong>otransferase, album<strong>in</strong> and glycated<br />

haemoglob<strong>in</strong> were determ<strong>in</strong>ed us<strong>in</strong>g automatically system HITACHI 717.<br />

HPLC analysis<br />

As parameters <strong>of</strong> antioxidant status levels <strong>of</strong> serum carotenoids, α-tocopherol and ret<strong>in</strong>ol<br />

were measured us<strong>in</strong>g HPLC method. Separation <strong>of</strong> carotenoids, ret<strong>in</strong>ol and α-tocopherol was<br />

carried out us<strong>in</strong>g the Biospher column C18 (4,6 mm × 150 mm, particulation size 7 μm),<br />

methanol as the mobile phase and flow rate 1.1 ml.m<strong>in</strong> -1 . Content <strong>of</strong> trans-all-ret<strong>in</strong>ol was<br />

detected at 325 nm, α-tocopherol at 289 nm and carotenoids at 450 nm.<br />

Sborník soutěže Studentské tvůrčí č<strong>in</strong>nosti Student 2006 a doktorské soutěže O cenu děkana 2005 a 2006<br />

Sekce DSP 2006, strana 211

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