Prophylactic role of α-lipoic acid and vitamin E against zinc oxide nanoparticles induced metabolic and immune disorders in rat's liver

被引:0
作者
Al-Rasheed, N. M. [1 ,2 ]
Al-Rasheed, N. M. [1 ,2 ]
Baky, N. A. Abdel [1 ]
Faddah, L. M. [1 ]
Fatani, A. J. [1 ]
Hasan, I. H. [1 ]
Mohamad, R. A. [3 ]
机构
[1] King Saud Univ, Fac Pharm, Dept Pharmacol, Riyadh, Saudi Arabia
[2] Princess Nora Bint Abdul Rahman Univ, Coll Pharm, Dept Pharmacol, Riyadh, Saudi Arabia
[3] King Saud Univ, Coll Med, Dept Anat, Riyadh 11461, Saudi Arabia
关键词
alpha-lipoic acid; Vitamin E; Zinc oxide nano-particles; Deoxyribonucleic acid; Tumor necrosis factor-alpha; C-REACTIVE PROTEIN; HEALTHY ADULT MICE; DNA-DAMAGE; ULTRAFINE PARTICLES; TITANIUM-DIOXIDE; OXIDATIVE DAMAGE; PULMONARY TOXICITY; LIPID-PEROXIDATION; SIGNALING PATHWAY; CARBON NANOTUBES;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
OBJECTIVES: Potential health hazard is associated with the wide use of nanoparticles. The prophylactic role of either alpha-lipoic acid (alpha-lip) or vitamin E (vit E) against the toxic effect of zinc oxide nano-particles (ZnO-NPs) induced metabolic disorder, inflammation and DNA damage in rat livers was studied. MATERIALS AND METHODS: ZnO-NPs were administered orally using two doses (600 mg and 1 g/kg body weight/day for 5 conscutive days). Some biomarkers of tissue damage, metabolic disorder, and DNA damage were investigated to explore the protective mechanisms of a-lip or vit E against ZnO-NPs induced hepatotoxicity. RESULTS: Co-administration of either alpha-lip (200 mg/kg body weight) or vit E (100 mg/kg body weight) daily for three weeks to ZnO-NPs intoxicated rats, significantly down-modulated the marked increase in serum ALT (marker of liver damage) and also serum glucose level (marker of metabolic disorder) as well as the pro-inflammatory biomarkers including nitric oxide (NO), tumor necrosis factor-alpha (TNF-alpha), interleukin-6 (IL-6), C-reactive protein (CRP), and immunoglobin G (IGg). Reduced glutathione level was decreased while caspase3 level was elevated in liver tissues of ZnO-NPs treated group compared with intoxicated one. Moreover histopathological examination of liver tissue supported the previous biochemical markers. Furthermore, ZnO-NPs induced hepatic oxidative DNA damage. CONCLUSIONS: Either alpha-lip or vit E proved to be hepatoprotective agents against ZnO-NPs toxicity because they ameliorated metabolic and immune disorders related to liver damage and modulated the previous measured parameters.
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收藏
页码:1813 / 1828
页数:16
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