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il\VOLVEMENT OF RETII\OIC ACID II{ - MSpace at the University of ...

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ADR group animals was fur<strong>the</strong>r confirmed by <strong>the</strong> echocardiogfaphy d<strong>at</strong>a which showed a<br />

significant decrease in <strong>the</strong> cardiac ouþut and left ventricular mass, indic<strong>at</strong>ing <strong>the</strong><br />

decompens<strong>at</strong>ion <strong>of</strong> cardiac function'<br />

The administr<strong>at</strong>ion <strong>of</strong> adriamycin also resulted in a decrease in animal body<br />

weight. The decrease in body weight <strong>of</strong> animals became significant during <strong>the</strong> second<br />

week <strong>of</strong> <strong>the</strong> tre<strong>at</strong>ment and continued throughout <strong>the</strong> third and fourth week after <strong>the</strong> first<br />

injection i.e. first and second week post-tre<strong>at</strong>ment. At three-week post-tre<strong>at</strong>ment, <strong>the</strong>re<br />

was an increase in total body weight, however, <strong>the</strong>se ADR group animals never achieved<br />

<strong>the</strong> weight comparable to <strong>the</strong> CONT group. The gain in body weight <strong>at</strong> 3-week posttre<strong>at</strong>ment<br />

can be <strong>at</strong>tributed to <strong>the</strong> development <strong>of</strong> ascites. The maximum decrease in body<br />

weight <strong>of</strong> adriamycin tre<strong>at</strong>ed animals was seen immedi<strong>at</strong>ely following <strong>the</strong> completion <strong>of</strong><br />

tre<strong>at</strong>ment with adriamycin. These d<strong>at</strong>a arc in agreement with o<strong>the</strong>r studies (Li et al. 2000;<br />

Siveski-Iliskovic et al. 1994; Siveski-Iliskovic et al' 1995).<br />

<strong>II</strong>I. The occurrence <strong>of</strong> oxid<strong>at</strong>ive stress and apoptosis<br />

Apoptosis and oxid<strong>at</strong>ive stress in cardiac myocytes exposed to adriamycin were<br />

assessed using an annexin and propidium iodide assay as well as CM-H2 DCFDA probe<br />

staining respectively. Tre<strong>at</strong>ment with adriamycin caused a significant increase in<br />

oxid<strong>at</strong>ive stress and this was accompanied by a significant increase in <strong>the</strong> number <strong>of</strong><br />

apoptotic cells. Tre<strong>at</strong>ment with antioxidant trolox in ADR+TROL group resulted in a<br />

significant decrease in <strong>the</strong> level <strong>of</strong> oxid<strong>at</strong>ive stress which correl<strong>at</strong>ed with a significant<br />

decrease in <strong>the</strong> occurïence <strong>of</strong> apoptosis due to adriamycin. This confirmed th<strong>at</strong><br />

antioxidant properties <strong>of</strong> trolox effectively prevented <strong>the</strong> occurrence <strong>of</strong> adriamycininduced<br />

apoptosis.<br />

t20

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