Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2013 Dec 12:2013:397524.
doi: 10.1155/2013/397524. eCollection 2013.

Cytotoxic effects of benzene metabolites on human sperm function: an in vitro study

Affiliations

Cytotoxic effects of benzene metabolites on human sperm function: an in vitro study

Priyanka Mandani et al. ISRN Toxicol. .

Abstract

In recent years, individuals are rampantly exposed to vapours of benzene, through paint, plastic, petroleum industries, fuel exhaust, and tobacco smoke. Hence the present investigation was directed towards determining the effect of benzene metabolites, namely, phenol-hydroquinone and catechol, on the motility, viability, and nuclear integrity of the human spermatozoa. From the results obtained it was clear that exposure to phenol-hydroquinone caused a significant decline in both, sperm motility and viability. Exposure to a phenol-hydroquinone (Phase I) microenvironment may therefore inhibit metabolically active enzymes, thus impeding ATP production, and in turn lowers sperm motility and viability. In addition, the present study also revealed that both metabolites of benzene caused significant denaturation of sperm nuclear DNA. Hence, exposure to phenol-hydroquinone in vitro could have resulted in generation of free radicals and altered membrane function, which is reflected by a decline in the motility, viability, and loss of sperm nuclear DNA integrity. In Phase II, the exposure of human sperm in vitro to varied concentrations of catechol caused only insignificant changes in sperm motility and viability as compared to those observed on exposure to phenol-hydroquinone. Hence, exposure to catechol appeared to have less toxic effects than those of phenol-hydroquinone.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Comparison of motility between phenol-hydroquinone and catechol treated spermatozoa.
Figure 2
Figure 2
Comparison of viability between phenol-hydroquinone and catechol treated spermatozoa.

References

    1. Wallace L. Environmental exposure to benzene: an update. Environmental Health Perspectives. 1996;104(supplement 6):1129–1136. - PMC - PubMed
    1. Agency for Toxic Substances and Disease Registry ATSDR. US DHHS. PB/98/101157/AS. Agency for Toxic Substances and Disease Registry; 1997. Toxicological profile for benzene.
    1. Weisel CP. Benzene exposure: an overview of monitoring methods and their findings. Chemico-Biological Interactions. 2010;184(1-2):58–66. - PMC - PubMed
    1. Sabourin PJ, Chen BT, Lucier G. Effect of dose on the absorption and excretion of [14C] benzene administered orally or by inhalation in rats and mice. Toxicology and Applied Pharmacology. 1987;87(2):325–336. - PubMed
    1. McDonald TA, Holland NT, Skibola C, Duramad P, Smith MT. Hypothesis: phenol and hydroquinone derived mainly from diet and gastrointestinal flora activity are causal factors in leukemia. Leukemia. 2001;15(1):10–20. - PubMed

LinkOut - more resources