The protective effect of naringenin on ciprofloxacin-induced cardiovascular toxicity in rats

Z. Ulutas, Sigbetullah Kurutkan, O. Ozhan, A. Yıldız, Ahmet Ulu, Leyla Buyukkorkmaz, N. Vardı, B. Ateş, H. Parlakpınar
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Abstract

Aim: Ciprofloxacin (CIPRO) is an antibiotic in the quinolone group. It can exert cardiotoxic effects on the cardiovascular system through potential arrhythmic and oxidative stress. Naringenin (NRG) is a flavonoid compound found in various plant sources. It may protect the heart by lowering oxidative stress and inflammation. In this study, protective effects of NRG against CIPRO-induced cardiotoxicity was explored. Material and Methods: Thirty-two adult male Sprague-Dawley rats were divided into four groups by simple randomization: Control, CIPRO (50 mg/kg CIPRO intraperitoneally (i.p.) twice a day for 7 days), NRG (25 mg/kg NRG oral gavage (p.o.), 28 days), and NRG+CIPRO (25 mg/kg NRG p.o. for 28 days, 50 mg/kg CIPRO i.p. twice a day from the 22nd day). Data on heart rate, blood pressure (BP), and electrocardiography (ECG) were recorded. The samples (heart and descending aorta) were prepared for histopathology and biochemical analysis. Malondialdehyde (MDA) and total glutathione (tGSH) levels, as well as superoxide dismutase (SOD) activity were evaluated in the heart tissue. Results: The CIPRO group showed histopathological abnormalities such as infiltration and interstitial oedema. In the NRG+CIPRO group, infiltration was significantly reduced. In the NRG group, SOD activity greatly increased, while in the NRG+CIPRO group, tGSH level significantly increased. The control, CIPRO, and NRG+CIPRO groups showed significantly higher systolic and mean BP measurements than the NRG group. In comparison to the CIPRO and control groups, the QT interval was longer in the NRG group. Conclusion: NRG can reduce CIPRO-induced cardiac damage in rats by increasing antioxidant enzymes and decreasing oxidative stress. With our histopathological evaluation, we have shown that CIPRO-induced cardiotoxicity may be ameliorated by pretreatment with NRG. NRG may also be effective in BP regulation. It should be kept in mind it is important to use NRG with caution and at appropriate doses, as it may prolong the QT interval.
柚皮素对环丙沙星致大鼠心血管毒性的保护作用
目的:环丙沙星(CIPRO)是喹诺酮类药物中的一种抗生素。它可以通过潜在的心律失常和氧化应激对心血管系统施加心脏毒性作用。柚皮素(Naringenin, NRG)是一种黄酮类化合物,存在于多种植物中。它可以通过降低氧化应激和炎症来保护心脏。本研究探讨了NRG对cipro诱导的心脏毒性的保护作用。材料与方法:将32只成年雄性Sprague-Dawley大鼠简单随机分为4组:对照组、CIPRO (50 mg/kg CIPRO腹腔灌胃(1次)2次,连用7 d)、NRG (25 mg/kg NRG灌胃(1次),连用28 d)、NRG+CIPRO (25 mg/kg NRG灌胃,连用28 d, 50 mg/kg CIPRO 1次,连用22 d)。记录心率、血压(BP)和心电图(ECG)数据。取标本(心脏和降主动脉)进行组织病理学和生化分析。评估心脏组织中丙二醛(MDA)和总谷胱甘肽(tGSH)水平以及超氧化物歧化酶(SOD)活性。结果:CIPRO组出现浸润、间质水肿等组织病理异常。NRG+CIPRO组细胞浸润明显减少。NRG组SOD活性显著升高,NRG+CIPRO组tGSH水平显著升高。对照组、CIPRO组和NRG+CIPRO组的收缩压和平均血压测量值明显高于NRG组。与CIPRO组和对照组相比,NRG组QT间期更长。结论:NRG可通过提高抗氧化酶水平、降低氧化应激来减轻cipro所致大鼠心脏损伤。通过我们的组织病理学评估,我们已经表明,经NRG预处理后,cipro诱导的心脏毒性可能会得到改善。NRG在BP监管中也可能有效。应记住,谨慎使用NRG和适当剂量是很重要的,因为它可能延长QT间期。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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