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dc.contributor.authorSmith, Karen L.
dc.contributor.authorFord, Gemma K.
dc.contributor.authorFinn, David P.
dc.date.accessioned2013-01-15T10:39:17Z
dc.date.available2013-01-15T10:39:17Z
dc.date.issued2012
dc.identifier.citationSmith KL, Ford GK, Jessop DS, Finn DP (2012) 'Behavioural, neurochemical and neuroendocrine effects of the endogenous beta-carboline harmane in fear-conditioned rats'. Journal Of Psychopharmacology, .en_US
dc.identifier.urihttp://hdl.handle.net/10379/3135
dc.description.abstractThe putative endogenous imidazoline binding site ligand harmane enhances neuronal activation in response to psychological stress and alters behaviour in animal models of anxiety and antidepressant efficacy. However, the neurobiological mechanisms underlying harmane's psychotropic effects are poorly understood. We investigated the effects of intraperitoneal injection of harmane (2.5 and 10 mg/kg) on fear-conditioned behaviour, hypothalamo-pituitary-adrenal axis activity, and monoaminergic activity within specific fear-associated areas of the rat brain. Harmane had no significant effect on the duration of contextually induced freezing or 22 kHz ultrasonic vocalisations and did not alter the contextually induced suppression of motor activity, including rearing. Harmane reduced the duration of rearing and tended to increase freezing in non-fear-conditioned controls, suggesting potential sedative effects. Harmane increased plasma ACTH and corticosterone concentrations, and serotonin (in hypothalamus, amygdaloid cortex, prefrontal cortex and hippocampus) and noradrenaline (prefrontal cortex) content, irrespective of fear-conditioning. Furthermore, harmane reduced dopamine and serotonin turnover in the PFC and hypothalamus, and serotonin turnover in the amygdaloid cortex in both fear-conditioned and non-fear-conditioned rats. In contrast, harmane increased dopamine and noradrenaline content and reduced dopamine turnover in the amygdala of fear-conditioned rats only, suggesting differential effects on catecholaminergic transmission in the presence and absence of fear. The precise mechanism(s) mediating these effects of harmane remain to be determined but may involve its inhibitory action on monoamine oxidases. These findings support a role for harmane as a neuromodulator, altering behaviour, brain neurochemistry and neuroendocrine function.en_US
dc.formatapplication/pdfen_US
dc.language.isoenen_US
dc.relation.ispartofJournal Of Psychopharmacologyen
dc.subjectImidazoline binding sitesen_US
dc.subjectBeta-carbolineen_US
dc.subjectHarmaneen_US
dc.subjectFear conditioningen_US
dc.subjectMonoamineen_US
dc.subjectHPA axisen_US
dc.subjectBrainen_US
dc.subjectRaten_US
dc.subjectPharmacology and Therapeuticsen_US
dc.titleBehavioural, neurochemical and neuroendocrine effects of the endogenous beta-carboline harmane in fear-conditioned ratsen_US
dc.typeArticleen_US
dc.date.updated2013-01-09T15:09:42Z
dc.local.publishedsourcehttp://jop.sagepub.com/content/early/2012/09/23/0269881112460108.fullen_US
dc.description.peer-reviewedpeer-reviewed
dc.contributor.funder|~|
dc.internal.rssid2780089
dc.local.contactDavid Finn, Dept. Of Pharmacology &, Therapeutics, Nui, Galway. 5280 Email: david.finn@nuigalway.ie
dc.local.copyrightcheckedYes
dc.local.versionACCEPTED
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