Garca M Fatih, Kavak Servet, Gecit Ilhan, Meral Ismail, Demir Halit, Turan Mahfuz, Çeğin Bilal, Bektas Hava, Çankaya Hakan
Department of Otorhinolaryngology, University of Yuzuncu Yil, Van, Turkey
Department of Biophysics, University of Yuzuncu Yil, Van, Turkey.
Toxicol Ind Health. 2014 Jun;30(5):454-8. doi: 10.1177/0748233712457452. Epub 2012 Aug 29.
This study was designed to investigate whether extracorporeal shock wave lithotripsy (ESWL) exposure to parotid gland produces an oxidative stress in parotid glands of rats. Twelve male Wistar-albino rats, 6 months of age with an average body weight of 250-300 g, were divided randomly into two groups, each consisting of six rats. The animals in the first group did not receive any treatment and served as control. The left parotid glands of animals in group 2 (ESWL treated) received a thousand 18 kV shock waves after anesthetizing the rats with 50 mg/kg of ketamine. The animals in both groups were killed 72 hours after the ESWL treatment, and the parotid glands were harvested for the determination of lipid peroxidation product malondialdehyde (MDA), antioxidant glutathione (GSH) levels and the activities of antioxidant enzymes such as superoxide dismutase (SOD), GSH-Px and catalase (CAT). It was found that MDA level increased in parotid glands of rats after the ESWL treatment. The SOD, GSH-Px and CAT enzyme activities, and the level of antioxidant GSH decreased in parotid gland of rats after the ESWL treatment. It was concluded that short-term ESWL treatment caused an increase in the free radical production and a decrease in the antioxidant enzyme activity in parotid glands of ESWL-treated rats.
本研究旨在调查体外冲击波碎石术(ESWL)对腮腺的照射是否会在大鼠腮腺中产生氧化应激。12只6月龄、平均体重250 - 300克的雄性Wistar白化大鼠被随机分为两组,每组6只。第一组动物不接受任何治疗,作为对照组。用50毫克/千克氯胺酮麻醉大鼠后,对第二组(接受ESWL治疗)动物的左侧腮腺施加1000次18 kV冲击波。ESWL治疗72小时后,处死两组动物,摘取腮腺用于测定脂质过氧化产物丙二醛(MDA)、抗氧化剂谷胱甘肽(GSH)水平以及超氧化物歧化酶(SOD)、谷胱甘肽过氧化物酶(GSH-Px)和过氧化氢酶(CAT)等抗氧化酶的活性。结果发现,ESWL治疗后大鼠腮腺中的MDA水平升高。ESWL治疗后大鼠腮腺中的SOD、GSH-Px和CAT酶活性以及抗氧化剂GSH水平降低。得出的结论是,短期ESWL治疗导致接受ESWL治疗的大鼠腮腺中自由基产生增加,抗氧化酶活性降低。