Searching for just a few words should be enough to get started. If you need to make more complex queries, use the tips below to guide you.
Article type: Research Article
Authors: Amiri, Asghar* | Mirhoseiny, Zahra
Affiliations: Department of Chemistry, Payame Noor University, Tehran, Iran
Correspondence: [*] Corresponding author: Asghar Amiri, Department of Chemistry, Payame Noor University, P.O. BOX 19395-3697, Tehran, Iran. Tel.: +98 9133401546; E-mail: a.amiri@pnu.ac.ir.
Abstract: The aim of this research was to test the chelation potency of deferasirox (DFS or ICL670)) and deferiprone (L1) in mobilization of arsenic in arsenic-exposed rats. Male Wistar rats were exposed to 60 mg/kg body weight sodium arsenite in drinking water for six weeks, followed by treatment with DFS (80 mg/kg body weight, oral, once daily), L1(100 mg/kg body weight, oral, once daily) alone or in combination, for six consecutive days. After chelation therapy, these rats were anesthetized by ether vapor, were immobilized by cervical dislocation and then their heart, liver, kidneys, intestine and blood were sampled for clinical hematological variables and determination of arsenic and iron concentration by Inductively Coupled Plasma/Optical Emission Spectrometry (ICP-OES). Comparison of single and combined therapy showed that the combined chelation therapy (DFS+L1) is more effective in depleting arsenic concentration from soft tissues. No effects of arsenic or any of the two treatments (L1 or DFS) on WBC, RBC and Hb were observed. Interestingly, platelet counts showed a decrease in arsenic exposure. The obtained Results of combined treatment should be confirmed by a different experimental model before extrapolation to other systems.
Keywords: Chelation therapy, deferasirox, deferiprone, arsenic toxicity, rats
DOI: 10.3233/MGC-160215
Journal: Main Group Chemistry, vol. 16, no. 1, pp. 1-5, 2017
IOS Press, Inc.
6751 Tepper Drive
Clifton, VA 20124
USA
Tel: +1 703 830 6300
Fax: +1 703 830 2300
sales@iospress.com
For editorial issues, like the status of your submitted paper or proposals, write to editorial@iospress.nl
IOS Press
Nieuwe Hemweg 6B
1013 BG Amsterdam
The Netherlands
Tel: +31 20 688 3355
Fax: +31 20 687 0091
info@iospress.nl
For editorial issues, permissions, book requests, submissions and proceedings, contact the Amsterdam office info@iospress.nl
Inspirees International (China Office)
Ciyunsi Beili 207(CapitaLand), Bld 1, 7-901
100025, Beijing
China
Free service line: 400 661 8717
Fax: +86 10 8446 7947
china@iospress.cn
For editorial issues, like the status of your submitted paper or proposals, write to editorial@iospress.nl
如果您在出版方面需要帮助或有任何建, 件至: editorial@iospress.nl