Hashim Mariam, Anjum Sumaira, Mujahid Huma, Alotaibi Khalid S, Albattal Shatha B, Ghamry Heba I, Soliman Mohamed Mohamed
Department of Biotechnology, Kinnaird College for Women University, Jail Road, Lahore 54000, Pakistan.
Institute of Biochemistry and Biotechnology, University of Veterinary and Animal Sciences, Lahore 54000, Pakistan.
Toxicol Res (Camb). 2025 Mar 17;14(2):tfaf037. doi: 10.1093/toxres/tfaf037. eCollection 2025 Apr.
Thymoquinone (THQ), a strong antioxidant and anti-inflammatory bioactive compound has been reported in numerous studies to prevent the hepatorenal toxicity caused by various xenobiotics. Similarly, the zinc oxide nanoparticles (ZnONPs) have been used to protect against the hepatorenal damages caused by oxidative stress due to their potent antioxidant properties. The aim of this study was to synthesize and investigate the possible protective effects of THQ, ZnONPs and THQ-loaded ZnONPs against CCl induced hepatorenal toxicity in albino rats. ZnONPs and THQ-loaded ZnONPs were synthesized and characterized by various techniques. For the in-vivo study, thirty albino rats were randomly divided into five groups of six rats each. The control group received normal saline and 2 group (injury group) received CCl only. The 3 group (T1-group) received CCl + ZnONPs, the 4 group (T2-group) received CCl + THQ, and the 5 group (T3-group) received CCl + THQ-loaded ZnONPs. Renal and hepatic biomarkers (total bilirubin, AST, ALT, ALP, blood urea nitrogen and creatinine), lipid profiles, antioxidant levels and histopathological studies were investigated. The synthesized NPs showed a spherical shape with an average size of 16-30 nm and exhibited hexagonal structures. Results showed that THQ-loaded ZnONPs resulted in a decrease in liver and kidney biomarkers as well as a reduction in TC, TG, and LDL levels compared to groups received ZnONPs and THQ alone. CAT, SOD, GR and DPPH-radical scavenging ability were maintained at normal levels in group T3, which received THQ-loaded ZnONPs compared to T1 and T2 groups. Hepatic histopathological analysis revealed a reduction in hydropic degeneration and hepatocyte congestion in the central veins, alongside a decrease in tubular cell swelling and normalization of renal histology in the THQ-loaded ZnONPs groups. In conclusion, results of this investigation demonstrate that THQ-loaded ZnONPs can act as an efficient protectant and antioxidant against oxidative stress and hepatorenal toxicity caused by various xenobiotics.
百里醌(THQ)是一种强大的抗氧化和抗炎生物活性化合物,众多研究报告称其可预防各种异源生物引起的肝肾毒性。同样,氧化锌纳米颗粒(ZnONPs)因其强大的抗氧化特性,已被用于保护机体免受氧化应激引起的肝肾损伤。本研究的目的是合成并研究THQ、ZnONPs和负载THQ的ZnONPs对白化大鼠四氯化碳诱导的肝肾毒性的可能保护作用。通过各种技术合成并表征了ZnONPs和负载THQ的ZnONPs。在体内研究中,将30只白化大鼠随机分为五组,每组六只。对照组接受生理盐水,第2组(损伤组)仅接受四氯化碳。第3组(T1组)接受四氯化碳+ZnONPs,第4组(T2组)接受四氯化碳+THQ,第5组(T3组)接受四氯化碳+负载THQ的ZnONPs。研究了肾和肝生物标志物(总胆红素、谷草转氨酶、谷丙转氨酶、碱性磷酸酶、血尿素氮和肌酐)、血脂谱、抗氧化水平和组织病理学。合成的纳米颗粒呈球形,平均尺寸为16 - 30纳米,并呈现六边形结构。结果表明,与单独接受ZnONPs和THQ的组相比,负载THQ的ZnONPs使肝脏和肾脏生物标志物降低,同时总胆固醇、甘油三酯和低密度脂蛋白水平也降低。与T1组和T2组相比,接受负载THQ的ZnONPs的T3组中过氧化氢酶、超氧化物歧化酶、谷胱甘肽还原酶和二苯基苦味酰基自由基清除能力维持在正常水平。肝脏组织病理学分析显示,负载THQ的ZnONPs组中央静脉的水样变性和肝细胞充血减少,同时肾小管细胞肿胀减少,肾脏组织学恢复正常。总之,本研究结果表明,负载THQ的ZnONPs可作为一种有效的保护剂和抗氧化剂,对抗各种异源生物引起的氧化应激和肝肾毒性。