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  4. Postnatal exposure of 2,2′,3,3′,4,6′-hexachlorobiphenyl and 2,2′,3,4′,5′,6-hexachlorobiphenyl on sperm function and hormone levels in adult rats
 
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Postnatal exposure of 2,2′,3,3′,4,6′-hexachlorobiphenyl and 2,2′,3,4′,5′,6-hexachlorobiphenyl on sperm function and hormone levels in adult rats

Resource
Toxicology 187 (2-3): 117-126
Journal
Toxicology
Journal Issue
187
Pages
117-126
Date Issued
2003
Date
2003
Author(s)
Hsu, Ping-Chi
Li, Mei-Hui  
Yue Leon Guo  
DOI
10.1016/S0300-483X(03)00057-X
URI
http://ntur.lib.ntu.edu.tw//handle/246246/173636
Abstract
Polychlorinated biphenyls (PCBs) are known to affect reproductive system in animals and in accidentally or occupationally exposed humans. Information is lacking on effects of non-dioxin like chlorinated biphenyls (CB) congeners on male reproduction. The aim of this study is to determine whether treatment of postnatal non-dioxin like CB congeners affects sperm function and hormone levels in rats. Male Sprague-Dawley rats received either 2,2′,3,3′,4,6′-hexachlorobiphenyls (CB 132) or 2,2′,3,4′,5′,6-hexachlorobiphenyls (CB 149) by ip injection of 9.6 or 96 mg/kg at day 21. At 16 weeks, the animals were sacrificed; sperm quality and hormone levels were measured. Body weight, testis and cauda epididymis weights, sperm counts, ROS generation, acrosome reaction rate, serum thyroxine (T4), free T4 and testosterone (TT) concentrations were unaffected. However, treatment of CB 132 and CB 149 caused decreases in sperm motility, curvilinear velocity (VCL), average path velocity (VAP), straight-line velocity (VSL), amplitude of lateral head displacement (ALH) and beat cross frequency (BCF). Serum triiodothyronine (T3) level was significantly decreased in CB 132 9.6 mg/kg dose group compared with the controls. On the other hand, a significant decrease was found in free T3 concentration both in 96 mg/kg of CB 132 and CB 149 groups. In summary, this study showed that CB 132 and CB 149 affects serum levels of triiodothyronine as well as sperm motility, velocity and capability of penetrating oocytes. The mechanism of action and potential effects on human warrant further investigation. © 2003 Elsevier Science Ltd. All rights reserved.
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