Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.754074
Title: Psychopathologies characterised by social deficits : neurobiological mechanisms and treatment implications
Author: Pantouli, Fani
ISNI:       0000 0004 7427 1372
Awarding Body: St George's, University of London
Current Institution: St George's, University of London
Date of Award: 2017
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Abstract:
Autism spectrum disorder (ASD) is characterised by impairment in the social domain and is often comorbid with depression and social anxiety. Several neuronal systems have been implicated in the neuropathology of ASD, yet the underlining neurobiology remains unclear, with no effective treatment being identified. Therefore, we utilised a well-validated mouse neurobiological candidate systems and we detected dysregulation of opioid, oxytocin, vasopressin, glutamate and dopamine in this model. Current ASD pharmacotherapy is only symptomatic and does not target core symptomatology. Intranasal oxytocin is a promising target for the treatment of ASD with known acute effects on related ASD-like symptomatology, but little currently is known about the effect of chronic exposure to the drug. Therefore, we performed a battery of behavioural experiments to assess the efficacy and neurobiological consequences of chronic oxytocin administration in the Fmr1 KO and wild-type mice. We observed restoration of sociability but not stereotypy upon acute and chronic oxytocin treatment in the mutants and prevention of comorbid anxiety following chronic oxytocin administration. Opposingly, detrimental effects in sociability, stereotypy and emotionality following chronic oxytocin treatment were detected in wild-type mice. Differential regulation of several transcripts was detected in Fmr1 KO and wild-type mice. Lastly, we investigated the effect of chronic exposure to social-defeat stress (CSS), a common psychopathology characterised by impairment in sociability and depression on central nicotinic acetylcholine receptor (nAchR) subtype and D2 dopamine receptor density. While CSS did not affect 07* and CI4P2* nAChR binding, it downregulated D2. These findings offer better understanding of the neurobiology underpinning psychopathologies characterised by social deficit and highlight chronic OXT as an effective pharmacotherapy for their treatment. Nonetheless, our findings reveal potential safety concerns of its chronic use in healthy subjects with intact oxytocinergic system.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.754074  DOI: Not available
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