A Systematic Review of the Valproic-Acid-Induced Rodent Model of Autism
Autism spectrum disorder (ASD) is a neurodevelopmental disorder characterised by repetitive behaviours, cognitive rigidity/inflexibility, and social-affective impairment. Unfortunately, few pharmacological treatments exist to alleviate these socio-behavioural impairments. Prenatal administration of...
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Published in | Developmental neuroscience Vol. 42; no. 1; p. 12 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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Switzerland
2020
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Abstract | Autism spectrum disorder (ASD) is a neurodevelopmental disorder characterised by repetitive behaviours, cognitive rigidity/inflexibility, and social-affective impairment. Unfortunately, few pharmacological treatments exist to alleviate these socio-behavioural impairments. Prenatal administration of valproic acid (VPA) has become an accepted animal model of ASD and has been extensively used to explore new pharmacotherapies in rodents. We conducted a systematic review of the behavioural impairments induced by the VPA model in rodents, with specific reference to 3 core socio-behavioural alterations associated with ASD: repetitive behaviours, cognitive rigidity/inflexibility, and social-affective impairment. We systematically reviewed studies attempting to alleviate these core behavioural alterations using pharmacological means. We include 132 studies exploring the prenatal effects of VPA in rodents. Gestational exposure to VPA in rodents has significant effects on rodent-equivalent measures of the 3 core behavioural traits characteristic of ASD in humans, inducing social impairments, repetitive behaviour, and cognitive rigidity/inflexibility after birth. This model's validity has seen it used to test potential drug treatments for ASD and is likely to continue doing so. We conclude the rodent VPA model may be suitable to examine future therapeutic interventions for ASD, providing an overview of the progress made so far. |
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AbstractList | Autism spectrum disorder (ASD) is a neurodevelopmental disorder characterised by repetitive behaviours, cognitive rigidity/inflexibility, and social-affective impairment. Unfortunately, few pharmacological treatments exist to alleviate these socio-behavioural impairments. Prenatal administration of valproic acid (VPA) has become an accepted animal model of ASD and has been extensively used to explore new pharmacotherapies in rodents. We conducted a systematic review of the behavioural impairments induced by the VPA model in rodents, with specific reference to 3 core socio-behavioural alterations associated with ASD: repetitive behaviours, cognitive rigidity/inflexibility, and social-affective impairment. We systematically reviewed studies attempting to alleviate these core behavioural alterations using pharmacological means. We include 132 studies exploring the prenatal effects of VPA in rodents. Gestational exposure to VPA in rodents has significant effects on rodent-equivalent measures of the 3 core behavioural traits characteristic of ASD in humans, inducing social impairments, repetitive behaviour, and cognitive rigidity/inflexibility after birth. This model's validity has seen it used to test potential drug treatments for ASD and is likely to continue doing so. We conclude the rodent VPA model may be suitable to examine future therapeutic interventions for ASD, providing an overview of the progress made so far. |
Author | Mamo, John Albrecht, Matthew Takechi, Ryu Vaccarezza, Mauro Chaliha, Devahuti Al-Salami, Hani Lam, Virginie |
Author_xml | – sequence: 1 givenname: Devahuti surname: Chaliha fullname: Chaliha, Devahuti organization: School of Public Health, Curtin Health Innovation Research Institute, Perth, Washington, Australia – sequence: 2 givenname: Matthew surname: Albrecht fullname: Albrecht, Matthew organization: School of Public Health, Curtin Health Innovation Research Institute, Perth, Washington, Australia – sequence: 3 givenname: Mauro surname: Vaccarezza fullname: Vaccarezza, Mauro organization: School of Pharmacy and Biomedical Science, Curtin Health Innovation Research Institute, Perth, Washington, Australia – sequence: 4 givenname: Ryu surname: Takechi fullname: Takechi, Ryu organization: School of Public Health, Curtin Health Innovation Research Institute, Perth, Washington, Australia – sequence: 5 givenname: Virginie surname: Lam fullname: Lam, Virginie organization: School of Public Health, Curtin Health Innovation Research Institute, Perth, Washington, Australia – sequence: 6 givenname: Hani surname: Al-Salami fullname: Al-Salami, Hani organization: School of Pharmacy and Biomedical Science, Curtin Health Innovation Research Institute, Perth, Washington, Australia – sequence: 7 givenname: John surname: Mamo fullname: Mamo, John email: j.mamo@curtin.edu.au organization: School of Public Health, Curtin Health Innovation Research Institute, Perth, Washington, Australia, j.mamo@curtin.edu.au |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/32810856$$D View this record in MEDLINE/PubMed |
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