![]() |
|
|
Vol. 31, Issue 3, 306-311, March 2003
Department of Anatomy and Cell Biology, Queen's University,
Kingston, Ontario, Canada (P.G.F.); Department of Pharmacology, Wayne
State University School of Medicine, Detroit, Michigan (L.L.);
Department of Environmental and Occupational Health, University of
Montreal, Montreal, Quebec, Canada (R.T.); Hormones/Growth/Development
Research Group, Ottawa Health Research Institute, Ottawa, Ontario,
Canada (N.T.); California National Primate Research Center, University
of California, Davis, California (C.V.); and Department of Pathology,
London Health Sciences Centre, London, Ontario, Canada (M.M.)
We have investigated the potential of the male reproductive tract
to accumulate trichloroethylene (TCE) and its metabolites, including
chloral, trichloroethanol (TCOH), trichloroacetic acid (TCA), and
dichloroacetic acid (DCA). Human seminal fluid and urine samples from
eight mechanics diagnosed with clinical infertility and exposed to TCE
occupationally were analyzed. In in vivo experimental studies, TCE and
its metabolites were determined in epididymis and testis of mice
exposed to TCE (1000 ppm) by inhalation for 1 to 4 weeks. In other
studies, incubations of monkey epididymal microsomes were performed in
the presence of TCE and NADPH. Our results showed that seminal fluid
from all eight subjects contained TCE, chloral, and TCOH. DCA was
present in samples from two subjects, and only one contained TCA. TCA
and/or TCOH were also identified in urine samples from only two
subjects. TCE, chloral, and TCOH were detected in murine epididymis
after inhalation exposure with TCE for 1 to 4 weeks. Levels of TCE and
chloral were similar throughout the entire exposure period. TCOH levels
were similar at 1 and 2 weeks but increased significantly after 4 weeks
of TCE exposure. Chloral was identified in microsomal incubations with
TCE in monkey epididymis. CYP2E1, a P450 that metabolizes TCE, was
localized in human and monkey epididymal epithelium and testicular
Leydig cells. These results indicated that TCE is metabolized in the reproductive tract of the mouse and monkey. Furthermore, TCE and its
metabolites accumulated in seminal fluid, and suggested associations between production of TCE metabolites, reproductive toxicity, and
impaired fertility.
This article has been cited by other articles:
![]() |
P.-G. Forkert, R. M. Baldwin, B. Millen, L. H. Lash, D. A. Putt, M. A. Shultz, and K. S. Collins PULMONARY BIOACTIVATION OF TRICHLOROETHYLENE TO CHLORAL HYDRATE: RELATIVE CONTRIBUTIONS OF CYP2E1, CYP2F, AND CYP2B1 Drug Metab. Dispos., October 1, 2005; 33(10): 1429 - 1437. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Xu, N. Tanphaichitr, P.-G. Forkert, A. Anupriwan, W. Weerachatyanukul, R. Vincent, A. Leader, and M. G. Wade Exposure to Trichloroethylene and its Metabolites Causes Impairment of Sperm Fertilizing Ability in Mice Toxicol. Sci., December 1, 2004; 82(2): 590 - 597. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. B. DuTeaux, T. Berger, R. A. Hess, B. L. Sartini, and M. G. Miller Male Reproductive Toxicity of Trichloroethylene: Sperm Protein Oxidation and Decreased Fertilizing Ability Biol Reprod, May 1, 2004; 70(5): 1518 - 1526. [Abstract] [Full Text] [PDF] |
||||