Diphenyl Diselenide Protects Against Hematological and Immunological Alterations Induced by Mercury in Mice

被引:24
作者
Brandao, Ricardo [1 ]
Borges, Lysandro Pinto [1 ]
de Oliveira, Renata [1 ]
Rocha, Joao B. T. [1 ]
Nogueira, Cristina W. [1 ]
机构
[1] Univ Fed Santa Maria, Dept Quim, Ctr Ciencias Nat & Exatas, BR-97105900 Santa Maria, RS, Brazil
关键词
Mercury; Selenium; Diphenyl diselenide; Hematological; Immunological;
D O I
10.1002/jbt.20242
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mercury is a heavy metal that can cause a variety of toxic effects on the organism, such as hematological and immunological alterations. In the present investigation, deleterious effects of mercury-intoxication in mice and a possible protective effect of diphenyl diselenide (PhSe)2 were studied. Male adult Swiss albino mice received daily a pretreatment with (PhSe)(2) (15.6 mg/kg, orally) for 1 week. After this week, mice received daily mercuric chloride (1 mg/kg, subcutaneously) for 2 weeks. A number of hematological (erythrocytes, leukocytes, platelets, hemoglobin, hematocrit, reticulocytes, and leukocytes differential) and immunological (immunoglobulin G and M plasma concentration) parameters were evaluated. Another biomarker of tissue damage, lactate dehydrogenase (LDH), was also determined. The results demonstrated that mercury exposure caused a reduction in the erythrocyte, hematocrit, hemoglobin, leukocyte, and platelet counts and an increase in the reticulocyte percentages. (PhSe)2 was effective in protecting against the reduction in hematocrit, hemoglobin, and leukocyte levels. (PhSe)2 ameliorated reticulocyte percentages increased by mercury. However, (PhSe)2 was partially effective in preventing against the decrease in erythrocyte and platelet counts. Immunoglobulin G and M concentrations and LDH activity were increased by mercury exposure, and (PhSe)2 was effective in protecting against these effects. In conclusion, (PhSe)2 was effective in protecting against hematological and immunological alterations induced by mercury in mice. (C) 2008 Wiley Periodicals, Inc. J Biochem Mol Toxicol 22:311-319, 2008; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10:1002/jbt.20242
引用
收藏
页码:311 / 319
页数:9
相关论文
共 59 条
[1]  
[Anonymous], 1991, DOC THRESH LIM VAL B
[2]   Diphenyl diselenide reduces temporarily hyperglycemia: Possible relationship with oxidative stress [J].
Barbosa, N. B. V. ;
Rocha, J. B. T. ;
Wondracek, D. C. ;
Perottoni, J. ;
Zeni, G. ;
Nogueira, C. W. .
CHEMICO-BIOLOGICAL INTERACTIONS, 2006, 163 (03) :230-238
[3]  
BENCKO V, 1990, Journal of Hygiene Epidemiology Microbiology and Immunology (Prague), V34, P9
[4]  
BIGAZZI PE, 2000, TXB AUTOIMMUNE DIS, P753
[5]   Benzo(a)pyrene-induced anemia and splenomegaly in NZB/WF1 mice [J].
Booker, CD ;
White, KL .
FOOD AND CHEMICAL TOXICOLOGY, 2005, 43 (09) :1423-1431
[6]   Acute liver damage induced by 2-nitropropane in rats: Effect of diphenyl diselenide on antioxidant defenses [J].
Borges, LP ;
Nogueira, CW ;
Panatieri, RB ;
Rocha, JBT ;
Zeni, G .
CHEMICO-BIOLOGICAL INTERACTIONS, 2006, 160 (02) :99-107
[7]   Protective effect of diphenyl diselenide on acute liver damage induced by 2-nitropropane in rats [J].
Borges, LP ;
Borges, VC ;
Moro, AV ;
Nogueira, CW ;
Rocha, JBT ;
Zeni, G .
TOXICOLOGY, 2005, 210 (01) :1-8
[8]  
CHATTERJEE GC, 1975, INT J VITAM NUTR RES, V45, P284
[9]  
Clarkson T. W., 1988, BIOL MONITORING TOXI, P199
[10]   The toxicology of mercury [J].
Clarkson, TW .
CRITICAL REVIEWS IN CLINICAL LABORATORY SCIENCES, 1997, 34 (04) :369-403