High-Fat Diet Exacerbates Autistic-Like Restricted Repetitive Behaviors and Social Abnormalities in CC2D1A Conditional Knockout Mice
- PMID: 36445635
- DOI: 10.1007/s12035-022-03146-1
High-Fat Diet Exacerbates Autistic-Like Restricted Repetitive Behaviors and Social Abnormalities in CC2D1A Conditional Knockout Mice
Abstract
Autism spectrum disorder (ASD) represents a heterogeneous group of neurodevelopmental disorders characterized by deficits in social communication, social interaction, and the presence of restricted repetitive behaviors. The cause of ASD involves complex interactions between genetic and environmental factors. Haploinsufficiency of the Coiled-coil and C2 domain containing 1A (Cc2d1a) gene is causally linked to ASD, and obesity has been associated with worse outcomes for ASD. High-fat diet (HFD) feeding leads to the development of obesity and metabolic dysfunction; however, the effect of HFD on pre-existing autistic-like phenotypes remains to be clarified. Here, we report that male Cc2d1a conditional knockout (cKO) mice fed with HFD, from weaning onwards and throughout the experimental period, show a marked aggravation in autistic-like phenotypes, manifested in increased restricted repetitive behaviors and impaired performance in the preference for social novelty, but not in sociability and cognitive impairments assessed using the object location memory, novel object recognition, and Morris water maze tests. HFD feeding also results in increased numbers of reactive microglia and astrocytes, and exacerbates reductions in dendritic complexity and spine density of hippocampal CA1 pyramidal neurons. Furthermore, we demonstrate that chronic treatment with minocycline, a semisynthetic tetracycline-derived antibiotic, rescues the observed behavioral and morphological deficits in Cc2d1a cKO mice fed with HFD. Collectively, these findings highlight an aggravating role of HFD in pre-existing autistic-like phenotypes and suggest that minocycline treatment can alleviate abnormal neuronal morphology and behavioral symptoms associated with ASD resulted from the interplay between genetic and environmental risk factors.
Keywords: Autism spectrum disorder; CC2D1A; High-fat diet; Minocycline; Repetitive behaviors; Social deficits.
© 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.
References
-
- Baron-Cohen S, Belmonte MK (2005) Autism: a window onto the development of the social and the analytic brain. Annu Rev Neurosci 28:109–126. https://doi.org/10.1146/annurev.neuro.27.070203.144137 - DOI
-
- Chen JA, Peñagarikano O, Belgard TG, Swarup V, Geschwind DH (2015) The emerging picture of autism spectrum disorder: genetics and pathology. Annu Rev Pathol 10:111–144. https://doi.org/10.1146/annurev-pathol-012414-040405 - DOI
-
- Heavner WE, Smith SEP (2020) Resolving the synaptic versus developmental dichotomy of autism risk genes. Trends Neurosci 43(4):227–241. https://doi.org/10.1016/j.tins.2020.01.009 - DOI
-
- Satterstrom FK, Kosmicki JA, Wang J, Breen MS, Rubeis SD, An JY et al (2020) Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of Autism. Cell 180(3):568–584. https://doi.org/10.1016/j.cell.2019.12.036 - DOI
-
- Miles JH (2011) Autism spectrum disorders-a genetics review. Genet Med 13(4):278–294. https://doi.org/10.1097/GIM.0b013e3181ff67ba - DOI
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous