Aggressive encounters alter the activation of serotonergic neurons and the expression of 5-HT1A mRNA in the hamster dorsal raphe nucleus.
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Neurobiological mechanisms supporting experience-dependent resistance to social stressSerotonergic activation during courtship and aggression in the brown anole, Anolis sagreiActivation of 5-HT2a receptors in the basolateral amygdala promotes defeat-induced anxiety and the acquisition of conditioned defeat in Syrian hamsters.A double dissociation in the effects of 5-HT2A and 5-HT2C receptors on the acquisition and expression of conditioned defeat in Syrian hamsters.Stress-related serotonergic systems: implications for symptomatology of anxiety and affective disorders.Overlapping neurobiology of learned helplessness and conditioned defeat: implications for PTSD and mood disorders.5-hydroxytryptamine 2C receptors in the basolateral amygdala are involved in the expression of anxiety after uncontrollable traumatic stress.Behavioral characterization of escalated aggression induced by GABA(B) receptor activation in the dorsal raphe nucleus.Social status differences regulate the serotonergic system of a cichlid fish, Astatotilapia burtoni.Social opportunity rapidly regulates expression of CRF and CRF receptors in the brain during social ascent of a teleost fish, Astatotilapia burtoni.Repeated social defeat increases reactive emotional coping behavior and alters functional responses in serotonergic neurons in the rat dorsal raphe nucleus.A low-cost automated apparatus for investigating the effects of social defeat in Syrian hamsters.Regulation of dorsal raphe nucleus function by serotonin autoreceptors: a behavioral perspectiveDefeat-induced activation of the ventral medial prefrontal cortex is necessary for resistance to conditioned defeatGene expression in aminergic and peptidergic cells during aggression and defeat: relevance to violence, depression and drug abuseDay-night differences in neural activation in histaminergic and serotonergic areas with putative projections to the cerebrospinal fluid in a diurnal brain.Adverse experience during early life and adulthood interact to elevate tph2 mRNA expression in serotonergic neurons within the dorsal raphe nucleusAdverse early life experience and social stress during adulthood interact to increase serotonin transporter mRNA expression.Serotonin and arginine-vasopressin mediate sex differences in the regulation of dominance and aggression by the social brainStress-protective neural circuits: not all roads lead through the prefrontal cortex.Depression and substance use comorbidity: What we have learned from animal studies.Dominance status alters restraint-induced neural activity in brain regions controlling stress vulnerability.Behavioral control over shock blocks behavioral and neurochemical effects of later social defeat.Complex regional influence of photoperiod on the nycthemeral functioning of the dorsal and median raphé serotoninergic system in the Syrian hamster.Sex Differences in the Regulation of Offensive Aggression and Dominance by Arginine-Vasopressin.Fighting experience alters brain androgen receptor expression dependent on testosterone status.
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P2860
Aggressive encounters alter the activation of serotonergic neurons and the expression of 5-HT1A mRNA in the hamster dorsal raphe nucleus.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 09 April 2009
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Aggressive encounters alter th ...... hamster dorsal raphe nucleus.
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Aggressive encounters alter th ...... hamster dorsal raphe nucleus.
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type
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Aggressive encounters alter th ...... hamster dorsal raphe nucleus.
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Aggressive encounters alter th ...... hamster dorsal raphe nucleus.
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Aggressive encounters alter th ...... hamster dorsal raphe nucleus.
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Aggressive encounters alter th ...... hamster dorsal raphe nucleus.
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P2093
P2860
P1433
P1476
Aggressive encounters alter th ...... hamster dorsal raphe nucleus.
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P2093
C R Nicholas
K L Huhman
M A Cooper
M S Grober
P2860
P304
P356
10.1016/J.NEUROSCIENCE.2009.03.084
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P577
2009-04-09T00:00:00Z