THE POSSIBLE PROTECTIVE ROLE OF N-ACETYLCYSTEINE AGAINST TRAMADOL- INDUCED NEPHROTOXICITY IN THE ADULT ALBINO RATS (LIGHT AND ELECTRON MICROSCOPIC STUDY)

Abd El-Aziz Mohammed Abo-Youssef, Ahmed Mostafa Kamal, Wahed Yousre Mohammed Abd El-Aziz
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Abstract

Background: Tramadol is nephrotoxic in over doses N-acetylcysteine is effective against inflammatory processes and oxidative stress. Objective: Study of tramadol-induced nephrotoxicity on the rats and assess the possible protection of N-acetylcysteine. Material and Methods: Forty adult albino rats were obtained from the breading animal house of Faculty of Pharmacy, Al-Azhar University. The rats were housed in the animal house at Faculty of Pharmacy, Al-Azhar University under the suitable and standard conditions of temperature and feeding from January, 2021 till February, 2021. The rats were divided into four groups Group I (control group): the rats of this group was given 30 ml /kg saline daily for thirty days orally; group II (treated with tramadol): the rats of this group were given l5.5 mg /kg tramadol orally daily for thirty days; Group III (Toxic dose tramadol): The rats of this group were given 30 mg /kg tramadol orally daily for thirty days; Group IV (treated with toxic dose of tramadol and N-acetyl cysteine): The rats of this group were given 30 mg /kg tramadol and N-acetylcysteine 100 mg/kg orally daily for thirty days. The rats at the last day of the experiment were killed and their kidneys were collected for histological evaluation using hematoxylin and eosin and Masson trichrome, and examined under light and transmission electron microscope. Also, Blood samples were taken for measurement of urea and creatinine. The data obtained from biochemical results for all groups were expressed as means and subjected to statistical analysis. Results: Treatment of rats with toxic dose of tramadol (group III) showed marked damage in the renal tissues, The damage in the renal tissues was improved in rats that were given N-acetylcysteine together with tramadol (group IV). However, tramadol that was given in a therapeutic dose (Group II) did not cause any damage in the kidney. Conclusion: N-acetylcysteine partially improves the tramadol –induced nephrotoxicity.
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正乙酰半胱氨酸对成年白化大鼠因曲马多引起的肾毒性可能具有保护作用(光镜和电子显微镜研究)
背景:过量服用曲马多会对肾脏产生毒性,而 N-乙酰半胱氨酸能有效对抗炎症过程和氧化应激。研究目的研究曲马多诱导的大鼠肾毒性,并评估 N-乙酰半胱氨酸可能的保护作用。材料与方法40 只成年白化大鼠来自爱资哈尔大学药学院的饲养动物房。从 2021 年 1 月到 2021 年 2 月,这些大鼠被饲养在爱资哈尔大学药学院的动物房中,温度和喂养条件均符合标准。大鼠被分为四组 I组(对照组):该组大鼠每天口服30毫升/千克生理盐水,持续30天;II组(曲马多治疗组):该组大鼠每天口服l5.5毫克/千克曲马多,持续30天;III组(毒性剂量曲马多组):该组大鼠每天口服l5.5毫克/千克曲马多,持续30天;III组(毒性剂量曲马多组):该组大鼠每天口服l5.5毫克/千克曲马多,持续30天:该组大鼠每天口服30毫克/千克曲马多,持续30天;第四组(有毒剂量曲马多和N-乙酰半胱氨酸治疗):该组大鼠每天口服30毫克/千克曲马多,持续30天:该组大鼠每天口服 30 毫克/千克曲马多和 100 毫克/千克 N-乙酰半胱氨酸,为期 30 天。实验最后一天杀死大鼠,收集其肾脏,使用苏木精、伊红和马森三色染色法进行组织学评估,并在光镜和透射电子显微镜下进行检查。此外,还采集血液样本测量尿素和肌酐。所有组的生化结果数据均以均值表示,并进行统计分析。结果给大鼠服用有毒剂量的曲马多(第三组)后,肾脏组织明显受损。然而,以治疗剂量给药的曲马多(II 组)不会对肾脏造成任何损害。结论N-乙酰半胱氨酸可部分改善曲马多引起的肾毒性。
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