Key result
5-fluorouracil treatment in guinea pigs impaired the myocardial antioxidant defense system, lowering superoxide dismutase and glutathione peroxidase activities and increasing malondialdehyde levels.
Why the study?
Does 5-fluorouracil impair myocardial antioxidant defense capacity in guinea pigs?
Does 5-fluorouracil impair myocardial antioxidant defense capacity in guinea pigs?
5-fluorouracil induces myocardial oxidative stress in guinea pigs, providing a potential mechanism for its clinical cardiotoxicity.
5-FU induces myocardial oxidative stress in guinea pigs; hypothesis-generating for cardiotoxicity mechanisms but should not change practice.
Antioxidant defense capacity was investigated in myocardial tissue from guinea pigs treated with 5-fluorouracil (5-FU) at a dose of 400 mg/kg/d daily for 5 d administered intraperitonally. Treatment with 5-FU lowered the activities of cardiac superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px) accompanied by higher catalase (CAT) activity. Further, antioxidant potential (AOP) values were lower but oxidation resistance (OR) and malondialdehyde (MDA) levels were higher in the 5-FU-treated tissue. With regard to myocardial iron (Fe) and copper (Cu) levels, no significant differences were found between the groups. Results suggest that 5-FU treatment causes impairment in the myocardial antioxidant defense system and leads to cardiac peroxidation. It has been postulated that these changes might be responsible for the 5-FU cardiotoxicity seen in some patients, and antioxidant therapy might provide a therapeutic advantage.
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İlker Durak (2000) studied this question. 5-fluorouracil vs. Control group was evaluated on Antioxidant defense capacity. 5-fluorouracil treatment in guinea pigs impaired the myocardial antioxidant defense system, lowering superoxide dismutase and glutathione peroxidase activities and increasing malondialdehyde levels.
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