Journal of
Toxicology and Environmental Health Sciences

  • Abbreviation: J. Toxicol. Environ. Health Sci.
  • Language: English
  • ISSN: 2006-9820
  • DOI: 10.5897/JTEHS
  • Start Year: 2009
  • Published Articles: 194

Full Length Research Paper

Combined arsenic and di-(2-ethylhexyl) phthalate exposure elicits responses in brain ATPases different from hepatic and renal activities in rats

Olusegun K. Afolabi
  • Olusegun K. Afolabi
  • Department of Biochemistry, Faculty of Basic Medical Sciences, Ladoke Akintola University of Technology, Ogbomoso, Nigeria.
  • Google Scholar
Regina N. Ugbaja
  • Regina N. Ugbaja
  • Department of Biochemistry, College of Biosciences, Federal University of Agriculture, Abeokuta, Nigeria.
  • Google Scholar
Oladipo Ademuyiwa
  • Oladipo Ademuyiwa
  • Department of Biochemistry, College of Biosciences, Federal University of Agriculture, Abeokuta, Nigeria.
  • Google Scholar


  •  Received: 16 January 2016
  •  Accepted: 16 March 2016
  •  Published: 31 July 2016

Abstract

Arsenic and di-(2-ethylhexyl) phthalate (DEHP) are environmentally ubiquitous and epidemiologically important toxic agents that millions of people are currently exposed to, worldwide. Although the adverse impact due to exposure to either arsenic or DEHP are documented, the toxicological effects of co-exposure to these agents are largely unknown. In this study, exposure to these chemicals was investigated for their effects on ATPase activities in the brain, liver and kidney of rats. Male Wistar rats were exposed daily to 100 mg L-1 arsenic via drinking water and to 100 mg DEHP kg-1 body weight in corn oil either individually or concurrently for 30 days. Toxicity was assessed by evaluating changes in body and organ weights, as well as, Na+/K+-, Ca2+-, Mg2+- and total ATPase activities in the brain, liver and kidney. Exposure to either arsenic or DEHP resulted in drastic reduction in activities of the enzymes in the compartments investigated, except in the brain where Na+/K+- and Mg2+- ATPases had their activities significantly increased. Also, DEHP displayed no effect on the total ATPase and Ca2+ ATPase in the kidney and brain, respectively. Interestingly, co-exposure to these toxicants significantly stimulated the activities of all these enzymes in the brain. In this compartment, combined treatment resulted in an additive interaction between the toxicants and a potentiation effect of arsenic on DEHP with regards to the Na+/K+- ATPase activity and Ca2+- ATPase activity, respectively. Our findings demonstrate tissue specific response to combined arsenic and DEHP exposure in rats with the effect on the brain significantly different from other compartments.

Key words: Arsenic, di-(2-ethylhexyl) phthalate, Na+/K+-ATPase, Ca2+-ATPase, co-exposure.