Literature DB >> 20659492

Evaluation of cytotoxicity and oxidative DNA damaging effects of di(2-ethylhexyl)-phthalate (DEHP) and mono(2-ethylhexyl)-phthalate (MEHP) on MA-10 Leydig cells and protection by selenium.

Pinar Erkekoglu1, Walid Rachidi, Ozge Gursoy Yuzugullu, Belma Giray, Alain Favier, Mehmet Ozturk, Filiz Hincal.   

Abstract

Di(2-ethylhexyl)-phthalate (DEHP) is the most abundantly used phthalate derivative, inevitable environmental exposure of which is suspected to contribute to the increasing incidence of testicular dysgenesis syndrome in humans. Oxidative stress and mitochondrial dysfunction in germ cells are suggested to contribute to phthalate-induced disruption of spermatogenesis in rodents, and Leydig cells are one of the main targets of phthalates' testicular toxicity. Selenium is known to be involved in the modulation of intracellular redox equilibrium, and plays a critical role in testis, sperm, and reproduction. This study was aimed to investigate the oxidative stress potential of DEHP and its consequences in testicular cells, and examine the possible protective effects of selenium using the MA-10 mouse Leydig tumor cell line as a model. In the presence and absence of selenium compounds [30 nM sodium selenite (SS), and 10 μM selenomethionine (SM)], the effects of exposure to DEHP and its main metabolite mono(2-ethylhexyl)-phthalate (MEHP) on the cell viability, enzymatic and non-enzymatic antioxidant status, ROS production, p53 expression, and DNA damage by alkaline Comet assay were investigated. The overall results of this study demonstrated the cytotoxicity and genotoxicity potential of DEHP, where MEHP was found to be more potent than the parent compound. SS and SM produced almost the same level of protection against antioxidant status modifying effects, ROS and p53 inducing potentials, and DNA damaging effects of the two phthalate derivatives. It was thus shown that DEHP produced oxidative stress in MA-10 cells, and selenium supplementation appeared to be an effective redox regulator in the experimental conditions used in this study, emphasizing the critical importance of the appropriate selenium status. Copyright (c) 2010 Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20659492     DOI: 10.1016/j.taap.2010.07.016

Source DB:  PubMed          Journal:  Toxicol Appl Pharmacol        ISSN: 0041-008X            Impact factor:   4.219


  41 in total

1.  Low doses of selenium specifically stimulate the repair of oxidative DNA damage in LNCaP prostate cancer cells.

Authors:  Viviana de Rosa; Pinar Erkekoğlu; Anne Forestier; Alain Favier; Filiz Hincal; Alan M Diamond; Thierry Douki; Walid Rachidi
Journal:  Free Radic Res       Date:  2012-01-25

2.  Urinary metabolites of di(2-ethylhexyl) phthalate relation to sperm motility, reactive oxygen species generation, and apoptosis in polyvinyl chloride workers.

Authors:  Li-Ping Huang; Ching-Chang Lee; Jer-Pei Fan; Po-Hsiu Kuo; Tung-Sheng Shih; Ping-Chi Hsu
Journal:  Int Arch Occup Environ Health       Date:  2013-08-31       Impact factor: 3.015

Review 3.  Chemical compounds from anthropogenic environment and immune evasion mechanisms: potential interactions.

Authors:  Julia Kravchenko; Emanuela Corsini; Marc A Williams; William Decker; Masoud H Manjili; Takemi Otsuki; Neetu Singh; Faha Al-Mulla; Rabeah Al-Temaimi; Amedeo Amedei; Anna Maria Colacci; Monica Vaccari; Chiara Mondello; A Ivana Scovassi; Jayadev Raju; Roslida A Hamid; Lorenzo Memeo; Stefano Forte; Rabindra Roy; Jordan Woodrick; Hosni K Salem; Elizabeth P Ryan; Dustin G Brown; William H Bisson; Leroy Lowe; H Kim Lyerly
Journal:  Carcinogenesis       Date:  2015-05-22       Impact factor: 4.944

4.  Urinary phthalate metabolites in relation to biomarkers of inflammation and oxidative stress: NHANES 1999-2006.

Authors:  Kelly K Ferguson; Rita Loch-Caruso; John D Meeker
Journal:  Environ Res       Date:  2011-02-23       Impact factor: 6.498

5.  [Effect of Di-(2-ethylhcxyl) phthalate exposure on blood-testis barrier integrity in rats].

Authors:  Lian-Ju Shen; Xiang-Liang Tang; Chun-Lan Long; Xi-Ning Cao; Yi Wei; Yang-Cai Wang; Mang Sun; Yue Zhou; Yang Liu; Bo Liu; Fang-Yuan Huang; Guang-Hui Wei
Journal:  Nan Fang Yi Ke Da Xue Xue Bao       Date:  2017-09-20

6.  Mono-2-ethylhexyl phthalate disrupts neurulation and modifies the embryonic redox environment and gene expression.

Authors:  Karilyn E Sant; Dana C Dolinoy; Joseph L Jilek; Maureen A Sartor; Craig Harris
Journal:  Reprod Toxicol       Date:  2016-05-07       Impact factor: 3.143

Review 7.  SEXUAL DIMORPHISM IN SELENIUM METABOLISM AND SELENOPROTEINS.

Authors:  Lucia A Seale; Ashley N Ogawa-Wong; Marla J Berry
Journal:  Free Radic Biol Med       Date:  2018-03-21       Impact factor: 7.376

8.  Mono-(2-ethylhexyl) phthalate induces oxidative stress and inhibits growth of mouse ovarian antral follicles.

Authors:  Wei Wang; Zelieann R Craig; Mallikarjuna S Basavarajappa; Katlyn S Hafner; Jodi A Flaws
Journal:  Biol Reprod       Date:  2012-12-27       Impact factor: 4.285

9.  Determination of phthalates and their by-products in tissues of roach (Rutilus rutilus) from the Orge river (France).

Authors:  A S Valton; C Serre-Dargnat; M Blanchard; F Alliot; M Chevreuil; Marie Jeanne Teil
Journal:  Environ Sci Pollut Res Int       Date:  2014-06-26       Impact factor: 4.223

10.  Effects of mono-(2-ethylhexyl) phthalate (MEHP) on chicken germ cells cultured in vitro.

Authors:  Edith Guibert; Bérénice Prieur; Ronan Cariou; Frédérique Courant; Jean Philippe Antignac; Bertrand Pain; Jean Pierre Brillard; Pascal Froment
Journal:  Environ Sci Pollut Res Int       Date:  2013-01-25       Impact factor: 4.223

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