TY - JOUR
T1 - Subacute oral exposure to benzo[α]pyrene (B[α]P) increases aggressiveness and affects consummatory aspects of sexual behaviour in male mice
AU - Bouayed, Jaouad
AU - Desor, Frédéric
AU - Soulimani, Rachid
PY - 2009/9/30
Y1 - 2009/9/30
N2 - Benzo[α]pyrene (B[α]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[α]P increases aggressiveness and affects copulatory behaviour in male mice. Indeed, after 3 weeks of exposure to B[α]P at 0.02 and 0.2 mg/kg, we have observed that B[α]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[α]P 0.02 mg/kg-treated mice were found. On the other hand, we have found that subacute exposure (4 weeks) to B[α]P, does not affect the appetitive aspects and sexual motivation in copulatory behaviour because the latency to the first mount between control and B[α]P-treated male mice was not significantly different. We have nevertheless, surprisingly found that B[α]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[α]P improves the consummatory aspects of sexual behaviour, we cannot conclude that this neurotoxic pollutant has advantage of sexual function because B[α]P has been shown to alter the monoaminergic neurotransmitter system and causes endocrine dysregulation via toxic effect.
AB - Benzo[α]pyrene (B[α]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[α]P increases aggressiveness and affects copulatory behaviour in male mice. Indeed, after 3 weeks of exposure to B[α]P at 0.02 and 0.2 mg/kg, we have observed that B[α]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[α]P 0.02 mg/kg-treated mice were found. On the other hand, we have found that subacute exposure (4 weeks) to B[α]P, does not affect the appetitive aspects and sexual motivation in copulatory behaviour because the latency to the first mount between control and B[α]P-treated male mice was not significantly different. We have nevertheless, surprisingly found that B[α]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[α]P improves the consummatory aspects of sexual behaviour, we cannot conclude that this neurotoxic pollutant has advantage of sexual function because B[α]P has been shown to alter the monoaminergic neurotransmitter system and causes endocrine dysregulation via toxic effect.
KW - Aggressive behaviour
KW - Aggressiveness
KW - Benzo[α]pyrene (B[α]P)
KW - Male mice
KW - Neurotoxic
KW - Sexual behaviour
UR - http://www.scopus.com/inward/record.url?scp=67649743511&partnerID=8YFLogxK
U2 - 10.1016/j.jhazmat.2009.03.131
DO - 10.1016/j.jhazmat.2009.03.131
M3 - Article
C2 - 19414216
AN - SCOPUS:67649743511
SN - 0304-3894
VL - 169
SP - 581
EP - 585
JO - Journal of Hazardous Materials
JF - Journal of Hazardous Materials
IS - 1-3
ER -