ScienceDirect® Home Skip Main Navigation Links
You have guest access to ScienceDirect. Find out more.
 
Home
Browse
My Settings
Alerts
Help
 Quick Search
 Search tips (Opens new window)
    Clear all fields    
Food and Chemical Toxicology
Volume 45, Issue 4, April 2007, Pages 543-550
 
Font Size: Decrease Font Size  Increase Font Size
 Abstract - selected
Article
Purchase PDF (187 K)

 
 
 
Related Articles in ScienceDirect
View More Related Articles
 
View Record in Scopus
 
doi:10.1016/j.fct.2006.07.024    How to Cite or Link Using DOI (Opens New Window)
Copyright © 2006 Published by Elsevier Ltd.

Ginkgo biloba extract protects against mercury(II)-induced oxidative tissue damage in rats

Göksel Şenera, Corresponding Author Contact Information, E-mail The Corresponding Author, E-mail The Corresponding Author, Özer Sehirlia, Ayfer Tozanb, Ayliz Velioğlu-Övunçc, Nursal Gedikd and Gülden Z. Omurtagb

aMarmara University, School of Pharmacy, Department of Pharmacology, Istanbul, Turkey

bMarmara University, School of Pharmacy, Department of Pharmaceutical Toxicology, Istanbul, Turkey

cMarmara University, Vocational School of Health Related Professions, Istanbul, Turkey

dKasımpasa Military Hospital, Division of Biochemistry, Istanbul, Turkey


Received 8 October 2005; 
accepted 25 July 2006. 
Available online 30 August 2006.

Purchase the full-text article



References and further reading may be available for this article. To view references and further reading you must purchase this article.

Abstract

Mercury(II) is a highly toxic metal which induces oxidative stress in the body. In this study we aimed to investigate the possible protective effect of Ginkgo biloba (EGb), an antioxidant agent, against experimental mercury toxicity in rat model. Following a single dose of 5 mg/kg mercuric chloride (HgCl2; Hg group) either saline or EGb (150 mg/kg) was administered for 5 days. After decapitation of the rats trunk blood was obtained and the tissue samples from the brain, lung, liver, and kidney were taken for the determination of malondialdehyde (MDA) and glutathione (GSH) levels, myeloperoxidase (MPO) activity and collagen contents. Formation of reactive oxygen species in the tissue samples was monitored by chemiluminescence (CL) technique. BUN, creatinin, ALT, and AST levels and tumor necrosis factor-greek small letter alpha (TNF-greek small letter alpha) and lactate dehydrogenase (LDH) activity were assayed in serum samples. The results revealed that HgCl2 induced oxidative damage caused significant decrease in GSH level, significant increase in MDA level, MPO activity and collagen content of the tissues. Treatment of rats with EGb significantly increased the GSH level and decreased the MDA level, MPO activity, and collagen contents. Similarly, serum ALT, AST and BUN levels, as well as LDH and TNF-greek small letter alpha, were elevated in the Hg group as compared to control group. On the other hand, EGb treatment reversed all these biochemical indices. Our results implicate that mercury-induced oxidative damage in brain, lung, liver, and kidney tissues protected by G. biloba extract, with its antioxidant effects.

Keywords: Mercury chloride; Ginkgo biloba; Lipid peroxidation; TNF-greek small letter alpha

Article Outline

1. Introduction
2. Materials and methods
2.1. Animals
2.2. Experimental design
2.3. Assays
2.4. Chemiluminescence (CL) assay
2.5. Malondialdehyde and glutathione assays
2.6. Myeloperoxidase activity
2.7. Tissue Collagen measurement
2.8. Statistics
3. Results
4. Discussion
Acknowledgements
References






 
Home
Browse
My Settings
Alerts
Help
Elsevier.com (Opens new window)
About ScienceDirect  |  Contact Us  |  Terms & Conditions  |  Privacy Policy
Copyright © 2008 Elsevier B.V. All rights reserved. ScienceDirect® is a registered trademark of Elsevier B.V.