Roy K, De A U, Sengupta C
Division of Medicinal and Pharmaceutical Chemistry, Department of Pharmaceutical Technology, Jadavpur University, Calcutta 700032.
Indian J Exp Biol. 2000 Jun;38(6):580-6.
In different sets of experiment lipid peroxidation induction capacity of two drugs, viz., ceftizoxime sodium, a third generation cephalosporin antibiotic, and acyclovir, an antiviral agent, was studied using goat whole blood as the lipid source. Ceftizoxime sodium caused significant extent of lipid peroxidation. Lipid peroxidation being a toxicity mediating process, such observation may be related to the toxic potential of the drug. Insignificant induction of lipid peroxidation was found in case of acyclovir and this is in good agreement with the safety record of the drug. Glutathione and ascorbic acid could significantly reduce ceftizoxime sodium induced lipid peroxidation, suggesting that free radical scavenging action of antioxidants may be exploited by possible antioxidant co-therapy to reduce iatrogenicity of the drug in persons with impaired endogenous antioxidant defence. Glutathione and ascorbic acid appear to be promising candidates for further investigation in this regard.
在不同的实验中,以山羊全血作为脂质来源,研究了两种药物(即第三代头孢菌素抗生素头孢唑肟钠和抗病毒药物阿昔洛韦)诱导脂质过氧化的能力。头孢唑肟钠引起了显著程度的脂质过氧化。脂质过氧化是一个介导毒性的过程,这样的观察结果可能与该药物的潜在毒性有关。在阿昔洛韦的情况下,发现脂质过氧化诱导不显著,这与该药物的安全记录相符。谷胱甘肽和抗坏血酸可以显著降低头孢唑肟钠诱导的脂质过氧化,这表明抗氧化剂的自由基清除作用可能通过可能的抗氧化剂联合疗法来利用,以降低内源性抗氧化防御受损者中该药物的医源性。谷胱甘肽和抗坏血酸似乎是在这方面进一步研究的有希望的候选者。