The development of agonistic behavior in male golden hamsters : from behavior to brain

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The development of agonistic behavior in male golden hamsters : from behavior to brain

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dc.contributor.advisor Delville, Yvon
dc.creator Taravosh-Lahn, Kereshmeh
dc.date.accessioned 2012-09-06T21:11:23Z
dc.date.available 2012-09-06T21:11:23Z
dc.date.created 2008-08
dc.date.issued 2012-09-06
dc.identifier.uri http://hdl.handle.net/2152/17799
dc.description.abstract In male golden hamsters, puberty is marked by dramatic changes in agonistic behavior. Attack frequency gradually decreases as agonistic behavior evolves from play fighting to adult aggression. Attack types change as targets of attack mature from play fighting to adult attacks. In adult hamsters, serotonin plays an inhibitory role in aggression. Thus, the decline in attack frequency during puberty could be associated with an up-regulation of the activity of the serotonergic system. In adults, acute Fluoxetine treatment inhibited aggressive behavior at all doses. In juveniles, only the highest dose reduced attack frequency. Interestingly, juveniles treated with the lowest dose showed an increase in aggressive behavior. Attack type was also affected as treatment with Fluoxetine accelerated the maturation of attack targets. This same effect had been observed in previous studies in response to chronic social stress and dexamethasone treatment. Consequently, the role of cortisol on the development of the serotonergic system was also investigated. Furthermore, the density of serotonin innervation in the anterior hypothalamus and medial amygdala was found to be higher in adults than juveniles and consistent with the inhibition of attacks by the high dose of Fluoxetine. However, the differential effects of Fluoxetine at the lower doses were investigated through analysis of different serotonin receptor subtypes. In adult hamsters, aggression can be facilitated by activation of 5-HT₃ receptors and inhibited by 5-HT[subscript 1A] receptors. During puberty, the density of immunoreactive 5-HT1A receptors increased in the anterior hypothalamus and medial amydala while 5-HT₃ receptor immunoreactivity did not change. Thus, it is possible that in these areas the ratio of 5-HT₃ to 5-HT[subscript 1A] receptors decreases during puberty. This change is consistent with the decline in the frequency of offensive responses during puberty. The functionality of 5-HT[subscript 1A] and 5-HT₃ receptors on offensive aggression in juveniles was tested via peripheral injections of a 5-HT[subscript 1A] receptor agonist and a 5-HT₃ receptors antagonist. At the high dose, both drug treatments inhibited attack frequency and attack repetition. Together, these data examine the role of the serotonergic system on the development of agonistic behavior.
dc.format.medium electronic
dc.language.iso eng
dc.rights Copyright © is held by the author. Presentation of this material on the Libraries' web site by University Libraries, The University of Texas at Austin was made possible under a limited license grant from the author who has retained all copyrights in the works.
dc.subject.lcsh Agonistic behavior in animals
dc.subject.lcsh Fluoxetine
dc.subject.lcsh Hamsters
dc.subject.lcsh Brain chemistry
dc.title The development of agonistic behavior in male golden hamsters : from behavior to brain
dc.description.department Neuroscience
dc.type.genre Thesis
dc.type.material text
thesis.degree.department Neuroscience
thesis.degree.discipline Neuroscience
thesis.degree.grantor The University of Texas at Austin
thesis.degree.level Doctoral
thesis.degree.name Doctor of Philosophy

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