Literature DB >> 18177632

Swim stress exaggerates the hyperactive mesocortical dopamine system in a rodent model of autism.

Akane Nakasato1, Yasushi Nakatani, Yoshinari Seki, Naohisa Tsujino, Masahiro Umino, Hideho Arita.   

Abstract

Several clinical reports have suggested that there is a hyperactivation of the dopaminergic system in people with autism. Using rats exposed prenatally to valproic acid (VPA) as an animal model of autism, we measured dopamine (DA) levels in samples collected from the frontal cortex (FC) using in vivo microdialysis and HPLC. The basal DA level in FC was significantly higher in VPA-exposed rats relative to controls. Since the mesocortical DA system is known to be sensitive to physical and psychological stressors, we measured DA levels in FC before, during, and after a 60-min forced swim test (FST). There were further gradual increases in FC DA levels during the FST in the VPA-exposed rats, but not in the control rats. Behavioral analysis during the last 10 min of the FST revealed a significant decrease in active, escape-oriented behavior and an increase in immobility, which is thought to reflect the development of depressive behavior that disengages the animal from active forms of coping with stressful stimuli. These results suggest that this rodent model of autism exhibits a hyperactive mesocortical DA system, which is exaggerated by swim stress. This abnormality may be responsible for depressive and withdrawal behavior observed in autism.

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Year:  2007        PMID: 18177632     DOI: 10.1016/j.brainres.2007.11.043

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  17 in total

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Review 2.  Modeling dopamine dysfunction in autism spectrum disorder: From invertebrates to vertebrates.

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3.  Anhedonia and Hyperhedonia in Autism and Related Neurodevelopmental Disorders.

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4.  Augmentation effect of combination therapy of aripiprazole and antidepressants on forced swimming test in mice.

Authors:  Michel Bourin; Franck Chenu; Corina Prica; Martine Hascoët
Journal:  Psychopharmacology (Berl)       Date:  2009-06-11       Impact factor: 4.530

5.  Enteric short-chain fatty acids: microbial messengers of metabolism, mitochondria, and mind: implications in autism spectrum disorders.

Authors:  Derrick F MacFabe
Journal:  Microb Ecol Health Dis       Date:  2015-05-29

6.  GUT in FOCUS Symposium NOBEL FORUM, Karolinska Institutet, February 2nd 2015.

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7.  Genetic Variants of Angiotensin-Converting Enzyme Are Linked to Autism: A Case-Control Study.

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8.  Lipopolysaccharide Exposure Induces Maternal Hypozincemia, and Prenatal Zinc Treatment Prevents Autistic-Like Behaviors and Disturbances in the Striatal Dopaminergic and mTOR Systems of Offspring.

Authors:  Thiago Berti Kirsten; Gabriela P Chaves-Kirsten; Suene Bernardes; Cristoforo Scavone; Jorge E Sarkis; Maria Martha Bernardi; Luciano F Felicio
Journal:  PLoS One       Date:  2015-07-28       Impact factor: 3.240

9.  Enteric bacterial metabolites propionic and butyric acid modulate gene expression, including CREB-dependent catecholaminergic neurotransmission, in PC12 cells--possible relevance to autism spectrum disorders.

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Journal:  PLoS One       Date:  2014-08-29       Impact factor: 3.240

Review 10.  DNA methylome perturbations: an epigenetic basis for the emergingly heritable neurodevelopmental abnormalities associated with maternal smoking and maternal nicotine exposure†.

Authors:  Jordan M Buck; Li Yu; Valerie S Knopik; Jerry A Stitzel
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