Interactive effects of cadmium and titanium dioxide nanoparticles on hepatic tissue in rats: Ameliorative role of coenzyme 10 via modulation of the NF-κB and TNFα pathway

被引:1
作者
Abd-Elhakim, Yasmina M. [1 ]
Hashem, Mohamed M. M. [2 ]
Abo-EL-Sooud, Khaled [2 ]
Mousa, Mohamed R. [3 ]
Soliman, Ahmed M. [2 ]
Mouneir, Samar M. [2 ]
Ismail, Sameh H. [4 ]
Hassan, Bayan A. [5 ]
El-Nour, Hayat H. M. [6 ]
机构
[1] Zagazig Univ, Fac Vet Med, Dept Forens Med & Toxicol, Zagazig 44519, Egypt
[2] Cairo Univ, Fac Vet Med, Dept Pharmacol, Giza 12211, Egypt
[3] Cairo Univ, Fac Vet Med, Dept Pathol, Giza 12211, Egypt
[4] Cairo Univ, Fac Nanotechnol Postgrad Studies, Sheikh Zayed Campus, 6th October City 12588, Giza, Egypt
[5] Future Univ, Fac Pharm, Pharmacol Dept, Cairo 11835, Egypt
[6] Anim Reprod Res Inst, Biol Reprod Dept, Giza 3514805, Egypt
关键词
Titanium dioxide nanoparticles; Cadmium; Coenzyme; 10; Liver; Oxidative stress; Inflammation; INDUCED OXIDATIVE STRESS; LIPID-PEROXIDATION; TIO2; NANOPARTICLES; IN-VIVO; VITAMIN-E; LIVER; TOXICITY; EXPOSURE; BIOACCUMULATION; INFLAMMATION;
D O I
10.1016/j.fct.2023.114191
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
This study investigated the effect of oral dosing of titanium dioxide nanoparticles (TNPs) and cadmium (Cd2+) on rat liver and the potential protective role of coenzyme Q10 (CQ10) against TNPs and Cd2+-induced hepatic injury. Seventy male Sprague Dawley rats were divided into seven groups and orally given distilled water, corn oil, CQ10 (10 mg/kg b.wt), TNPs (50 mg/kg b.wt), Cd2+ (5 mg/kg b.wt), TNPs + Cd2+, or TNPs + Cd2++CQ10 by gastric gavage for 60 successive days. The results showed that individual or mutual exposure to TNPs and Cd2+ significantly increased the serum levels of various hepatic enzymes and lipids, depleted the hepatic content of antioxidant enzymes, and increased malondialdehyde. Moreover, the hepatic titanium and Cd2+ content were increased considerably in TNPs and/or Cd2+-exposed rats. Furthermore, marked histopathological perturbations with increased immunoexpression of tumor necrosis factor-alpha and nuclear factor kappa B were evident in TNPs and/or Cd2+-exposed rats. However, CQ10 significantly counteracted the damaging effect of combined exposure of TNPs and Cd2+ on the liver. The study concluded that TNPs and Cd2+ exposure harm hepatic function and its architecture, particularly at their mutual exposure, but CQ10 could be a candidate protective agent against TNPs and Cd2+ hepatotoxic impacts.
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页数:13
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