Protective role of Edaravone against valproic acid induced changes in skin
Date
2017Author
Ozturk, Leyla Koc
Tunali, Sevim
Ipekci, Hazal
YARAT, AYŞEN
Yanardag, Refiye
Tunali-Akbay, Tugba
Alev, Burcin
OKTAY, NİHAL ŞEHKAR
ALTURFAN, EBRU IŞIK
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Valproic acid (VPA) is an antiepileptic drug known to have some adverse effects on gastrointestinal, neurologic, hematologic and reproductive systems. In this study, we investigated the effect of edaravone (3-methyl-1-pheny1-2pyrazofine-5-one), a potent free radical scavenger, on skin oxidative and inflammatory changes caused by VPA. Female rats were randomly divided into four groups: control, edaravone (30 mg/kg/day, i.p.), VPA (0.5 g/kg/day, i.p.), and VPA+edaravone (in same dose, i.p.). On the 8th day of experiment, all the animals were fasted overnight and then sacrificed under anesthesia. Malondialdehyde, glutathione, total sialic acid and total protein levels, superoxide dismutase, glutathioneS-transferase, catalase, glutathione peroxidase, Ne/KtATPase, myeloperoxidase and tissue factor activities were determined in homogenized skin samples. VPA administration significantly altered the skin oxidant and antioxidant balance which may cause skin cell damage. Edaravone, as an antioxidant, demonstrated its radical scavenger effect, especially on malondialdehyde level and glutathione-S-transferase activity. Edaravone, by preventing inflammatory and oxidative reactions, partly protected the skin against the changes observed after the VPA administration.
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