Volume 23, Issue 4 (Scientific Journal of Hamadan University of Medical Sciences-Winter 2017)                   Avicenna J Clin Med 2017, 23(4): 345-351 | Back to browse issues page


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1- University of Mazandaran , a.hajizadeh@umz.ac.ir
2- University of Mazandaran
3- Amol University of Special Modern Technologies
Abstract:   (6195 Views)

Introduction: Recent studies have indicated that titanium dioxide nanoparticles (TiO2 NPs) are toxic for human. Silymarin is a well-known hepatoprotective drug. In this study, the nanoprecipitation technique was used for nanocrystals to improve the solubility of silymarin. The aim of this study was to analyze the protective role of silymarin and its nanocrystal on liver damage due to TiO2 NPs in rat.

Methods: In this experimental study, rats were divided to five groups in separate cages: Control, vehicle, toxic group (150 mg/kg TiO2 NPs for three weeks orally) as well as silymarin and silymarin NPs groups (100 mg/kg for three weeks orally after TiO2 NPs administration). Then, the serum level of aspartate transaminase (AST), alanine transaminase (ALT) and alkaline phosphatase (ALP) as well as the liver histological changes were investigated.

Results: Oral administration of Tio2 NPs resulted in significantly elevated levels of ALT, AST and ALP of serum and significantly increased the core diameter of hepatocytes (P < 0.05). Silymarin and its nanocrystal reduced the elevated liver enzyme levels and also decreased the core diameter of hepatocytes in toxic rats (P < 0.001).

Conclusion: : The results from the present study indicated that silymarin and its nanocrystal probably due to antioxidant effects cause hepatoprotective against TiO2 NPs-induced liver injury.  


 
 

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Type of Study: Original | Subject: Other Clinical Specialties

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