کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
2013224 | 1067101 | 2012 | 8 صفحه PDF | دانلود رایگان |
In male rats, the dopamine agonist apomorphine (APO) generally facilitates copulatory behavior. However, disruptive effects of high APO doses have been reported. These have been interpreted in diverse ways, as products of a dopaminergic system that inhibits sexual behavior or as consequences of APO's stimulation of competing responses. To test the generality of these effects, we observed APO's impact on copulatory behavior in male hamsters. Several effects were observed, all attributable to a relatively high dose and involving the disruption of male behavior. More unexpectedly, APO treatment caused males to attack estrous stimulus females in the course of these tests. To clarify these effects, we observed the effects of APO on flank marking, a type of scent marking closely allied to aggression and dominance in hamsters. Treatment reliably decreased the latency of marking. It also increased the rate of marking when appropriate measures were taken to prevent this effect from being obscured by drug-induced cheek pouching. Together, these results confirm and extend APO's well-known ability to increase aggression. Further, they suggest that APO-induced aggression can intrude into other contexts so as to disrupt, or possibly facilitate, other forms of social behavior.
► Male hamsters received systemic injections of apomorphine, a dopamine agonist.
► These disrupted male sex behavior but facilitated flank-marking and fighting.
► All of these effects may be attributable to a drug-induced increase in aggression.
► But in other contexts, such an increase could facilitate sex behavior not disrupt it.
Journal: Pharmacology Biochemistry and Behavior - Volume 101, Issue 4, June 2012, Pages 520–527