Eugenol Mitigates γ-rays-induced Acute Renal Destructive Impacts in Rats

A. Elkady, R. Ebrahim, W. A. El khouly
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Abstract

A CUTE renal injury is a common and hazardous distress of γ-rays’ exposure. The aim of the current study is to explore the role of eugenol on γ-rays-induced acute kidney lesions in rats. The rats were separated into four groups (n=6). The control group received saline for two weeks. The eugenol group received i.p. 20 mg/kg Eugenol for two weeks. The γ-rays group was pretreated with saline for a week, then whole-body exposed to 8 Gy γ-rays and saline treatment continued for another week. The rats in γ-rays+ eugenol group received Eugenol for a week pre-irradiation, then were exposed to γ-rays and eugenol treatment continued for another week. The blood and kidney samples were collected for histopathological and biochemical investigations. It was observed that exposure to γ-rays induced atrophy of glomeruli with increasing capsular space, expanded renal tubules and congested inter tubular blood vessels. Histological changes were accompanied by significant decreases in the level of antioxidants: reduced glutathione content (GSH), and superoxide dismutase (SOD), and catalase (CAT) activities with a significant increase of malondialdehyde (MDA; end-product of lipid peroxidation), indicating oxidative stress. Significant increases in the levels of inflammatory markers, tumor necrosis factor-alpha (TNF-α) and interleukin-1 Beta (IL-1β) levels were recorded also. Kidney damage was substantiated by significant increases in urea, creatinine, lactate dehydrogenase (LDH), γ-glutamyltransferase (γGT), and disturbance of electrolytes balance; elevated sodium (Na + ), and decreased potassium (K + ). Eugenol treatment has significantly improved histological damage oxidative stress and inflammatory-biomarkers, which was accompanied by significant amelioration of kidney functions. It could be concluded that eugenol may alleviate acute kidney injury resulting from γ -rays exposure through its antioxidant and anti-inflammatory properties.
丁香酚减轻γ射线引起的大鼠急性肾破坏作用
急性肾损伤是一种常见的、危险的γ射线暴露的痛苦。本研究旨在探讨丁香酚在γ射线致大鼠急性肾损伤中的作用。将大鼠分为4组(n=6)。对照组给予生理盐水治疗2周。丁香酚组给予丁香酚20 mg/kg ig,连续2周。γ射线组先用生理盐水预处理一周,然后全身暴露于8 Gy γ射线下,再继续生理盐水治疗一周。γ射线+丁香酚组大鼠先接受1周的丁香酚预照射,然后再进行γ射线照射,丁香酚继续治疗1周。采集血液和肾脏标本进行组织病理学和生化检查。观察到γ射线照射引起肾小球萎缩,囊腔增大,肾小管扩张,小管间血管充血。组织学变化伴随着抗氧化剂水平的显著降低:谷胱甘肽含量(GSH)、超氧化物歧化酶(SOD)和过氧化氢酶(CAT)活性降低,丙二醛(MDA)显著升高;脂质过氧化的最终产物),表明氧化应激。炎症标志物、肿瘤坏死因子-α (TNF-α)和白细胞介素-1β (IL-1β)水平也显著升高。肾损害表现为尿素、肌酐、乳酸脱氢酶(LDH)、γ-谷氨酰转移酶(γGT)显著升高,电解质平衡紊乱;钠(Na +)升高,钾(K +)降低。丁香酚治疗显著改善了组织损伤、氧化应激和炎症生物标志物,并伴有肾功能的显著改善。由此可见,丁香酚可能通过其抗氧化和抗炎作用减轻γ射线急性肾损伤。
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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