Orabi Sahar Hassan, Allam Tamer S, Shawky Sherif Mohamed, Tahoun Enas Abd El-Aziz, Khalifa Hanem K, Almeer Rafa, Abdel-Daim Mohamed M, El-Borai Nermeen Borai, Mousa Ahmed Abdelmoniem
Department of Biochemistry and Chemistry of Nutrition, Faculty of Veterinary Medicine, University of Sadat City, Sadat City, Menofia 32897, Egypt.
Department of Clinical Pathology, Faculty of Veterinary Medicine, University of Sadat City, Sadat City, Menofia 32897, Egypt.
Biology (Basel). 2020 Oct 23;9(11):352. doi: 10.3390/biology9110352.
The present study aimed to investigate the protective effect of argan oil (AO) against nephrotoxic effects following overdose and long-term administration of betamethasone (BM). The phytochemical compositions of AO were assessed using GC/MS. Forty eight male Wister albino rats were divided into six groups and treated for 3 successive weeks. The control group was orally administrated distilled water daily, the BM group received BM (1 mg/kg, IM, day after day), AO/0.5 and AO/1 groups received AO (0.5 mL/kg, 1 mL/kg, orally, daily, respectively), BM + AO/0.5 group and BM + AO/1 group. The results revealed that BM induced hematological changes, including reduction of red blood cells with leukocytosis, neutrophilia, monocytosis, lymphocytopenia, and thrombocytopenia. Moreover, BM caused a significant increase of serum urea and creatinine levels, and renal malondialdehyde and nitric oxide contents with significant decrease of reduced glutathione content. BM also caused vascular, degenerative, and inflammatory histopathological alterations in kidney, along with an increase in the Bax/Bcl-2 ratio, activation of caspase-3, and decrease of proliferating cell nuclear antigen expression. Conversely, the concomitant administration of AO (0.5, 1 mL/kg) with BM ameliorated the aforementioned hematological, biochemical, pathological, and histochemical BM adverse effects. In conclusion, AO has protective effects against BM-induced renal damage, possibly via its antioxidant, anti-apoptotic, and proliferative properties.
本研究旨在探讨过量和长期给予倍他米松(BM)后,阿甘油(AO)对肾毒性作用的保护效果。使用气相色谱/质谱联用仪(GC/MS)评估AO的植物化学成分。将48只雄性Wister白化大鼠分为6组,并连续治疗3周。对照组每日口服蒸馏水,BM组接受BM(1mg/kg,肌肉注射,每日),AO/0.5组和AO/1组分别每日口服AO(0.5mL/kg,1mL/kg),BM + AO/0.5组和BM + AO/1组。结果显示,BM引起血液学变化,包括红细胞减少伴白细胞增多、中性粒细胞增多、单核细胞增多、淋巴细胞减少和血小板减少。此外,BM导致血清尿素和肌酐水平显著升高,肾丙二醛和一氧化氮含量显著增加,还原型谷胱甘肽含量显著降低。BM还引起肾脏血管、退行性和炎症性组织病理学改变,同时Bax/Bcl-2比值增加、半胱天冬酶-3激活以及增殖细胞核抗原表达降低。相反,AO(0.5、1mL/kg)与BM联合给药改善了上述血液学、生化、病理和组织化学方面的BM不良反应。总之,AO对BM诱导的肾损伤具有保护作用,可能是通过其抗氧化、抗凋亡和增殖特性实现的。