PROTECTIVE EFFECT OF AQUEOUS EXTRACT OF MORINGA OLEIFERA LEAVES AGAINST POTASSIUM BROMATE-INDUCED RENAL TOXICITY IN RATS

A. Kamel, M. Fouad, Heba Mohamed
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Abstract

KBrO 3 is a vital component used in food, beer, pharmaceutical, and cosmetic productions; it produces moderate-to-dangerous toxic insults to a variety of organs. This study aimed to investigate if Moringa oleifera leaves aqueous extract (MOE) can protect rats from KBrO 3 -induced renal toxicity. Four experimental groups of male albino rats (Sprague Dawley) were used here (n=8): control, MOE (400 mg/kg body weight), KBrO 3 (100 mg/kg body weight), and KBrO 3 in combination with MOE groups. Daily for six weeks, each group received orally its unique treatment. After the experimental period kidneys and serum were collected for biochemical, molecular, and histological investigations. The KBrO 3 treatment was associated with a significant rise in serum levels of urea, creatinine, sodium, and potassium. KBrO 3 also caused a significant increase in the renal tissue levels of malondialdehyde and nitric oxide, while reducing the activities of antioxidant enzymes in the renal tissues. Moreover, KBrO 3 led to kidney inflammation and fibrosis by increasing the tumor necrosis factor-α, interleukin-6, and tumor growth factor-β1, which was followed by upregulation in the renal expression of miRNA 21 ( miR-21 ), miR-29 , and miR-192 . In comparison to the control group, histopathological evaluation of the KBrO 3 group revealed degenerative alterations and damage in the kidney tissues. Conversely, co-treatment with MOE revealed a noticeable alleviation of the harmful effects of KBrO 3 in almost all examined parameters. In conclusion, MOE could be utilized as an alternative therapy to alleviate the detrimental effects of KBrO 3 on kidneys due to its antioxidant, anti-inflammatory, and anti-fibrotic activities.
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辣木叶水提物对溴酸钾致大鼠肾毒性的保护作用
KBrO 3是食品、啤酒、制药和化妆品生产中使用的重要成分;它对多种器官产生中度到危险的毒性损害。本研究旨在探讨辣木叶水提物(MOE)对kbro3诱导的大鼠肾毒性的保护作用。选用雄性白化大鼠(Sprague Dawley) 4个实验组(n=8):对照组、MOE组(400 mg/kg体重)、kbro3组(100 mg/kg体重)、kbro3与MOE联合组。每天口服,连续6周。实验结束后,收集肾脏和血清进行生化、分子和组织学检查。kbro3治疗与血清尿素、肌酐、钠和钾水平显著升高相关。kbro3还引起肾组织丙二醛和一氧化氮水平的显著升高,同时降低肾组织中抗氧化酶的活性。此外,kbro3通过增加肿瘤坏死因子-α、白细胞介素-6和肿瘤生长因子-β1,导致肾脏炎症和纤维化,随后上调肾脏miRNA 21 (miR-21)、miR-29和miR-192的表达。与对照组相比,kbro3组的组织病理学评估显示肾脏组织出现退行性改变和损伤。相反,与MOE共同处理显示,在几乎所有检查参数中,kbro3的有害影响都明显减轻。综上所述,MOE具有抗氧化、抗炎和抗纤维化的作用,可以作为一种替代疗法来减轻KBrO - 3对肾脏的有害影响。
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