Subacute oral exposure to benzo[α]pyrene (B[α]P) increases aggressiveness and affects consummatory aspects of sexual behaviour in male mice

被引:16
作者
Bouayed, Jaouad [1 ]
Desor, Frederic [1 ]
Soulimani, Rachid [1 ]
机构
[1] Univ Paul Verlaine Metz INPL INRA, UR AFPA, F-57040 Metz, France
关键词
Benzo[alpha]pyrene (B[alpha]P); Male mice; Aggressiveness; Aggressive behaviour; Sexual behaviour; Neurotoxic; POLYCYCLIC AROMATIC-HYDROCARBONS; MESSENGER-RNA EXPRESSION; ANXIETY-RELATED BEHAVIOR; OXIDATIVE STRESS; MALONDIALDEHYDE LEVELS; ESTROGENIC ACTIVITY; ANTIOXIDANT ENZYME; MAJOR DEPRESSION; BRAIN-REGIONS; MOUSE-BRAIN;
D O I
10.1016/j.jhazmat.2009.03.131
中图分类号
X [环境科学、安全科学];
学科分类号
083001 [环境科学];
摘要
Benzo[alpha]pyrene (B[alpha]P) is a neurotoxic pollutant which is also able to affect some behaviour and cognitive function. Here we report that a subacute oral exposure to B[alpha]P increases aggressiveness and affects copulatory behaviour in male mice. Indeed, after 3 weeks of exposure to B[alpha]P at 0.02 and 0.2 mg/kg, we have observed that B[alpha]P 0.02 mg/kg-treated male mice are more aggressive than control mice in resident-intruder test because a significant decrease in the latency time of the first attack and a significant increase in the number of attacks in B[alpha]P 0.02 mg/kg-treated mice were found. On the other hand, we have found that subacute exposure (4 weeks) to B[alpha]P, does not affect the appetitive aspects and sexual motivation in copulatory behaviour because the latency to the first mount between control and B[alpha]P-treated male mice was not significantly different. We have nevertheless, surprisingly found that B[alpha]P (0.02-0.2)mg/kg-treated mice have performed significantly more sexual behavioural acts including mounting, intromission latency and intromission frequency than control mice. Although these last results suggest that B[alpha]P improves the consummatory aspects of sexual behaviour, we cannot conclude that this neurotoxic pollutant has advantage of sexual function because B[alpha]P has been shown to alter the monoaminergic neurotransmitter system and causes endocrine dysregulation via toxic effect. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:581 / 585
页数:5
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