Treatment in Early Life Prevents Autism Symptoms From Developing in Mice

Autism Help Concept

Timing is key when treating developmental disorders.

Identifying the window of development could reveal ideal time to intervene in autism.

Timing is key when treating developmental disorders. Blocking an overactive signaling pathway during the first five weeks of life prevents autism symptoms from ever developing in mice, according to new research published in JNeurosci.

The brain develops capabilities, like language, during specific spans of time called critical periods. The symptoms of disorders like autism arise during a set critical period; administering a targeted intervention only during the critical period could prevent the disorder from ever taking shape without the burden of a life-long treatment.

Early Life Treatment Prevents Autism Symptoms From Developing in Mice

Treatment with rapamycin for 4 weeks prevents the onset of social deficits in three-chamber social approach (left) and social novelty (right) testing. Credit: Gibson et al., JNeurosci 2021

Gibson et al. compared intervention timing in a genetic mouse model of Tuberous Sclerosis Complex (TSC), a neurodevelopmental disorder with high rates of autism spectrum disorder. The research team administered the drug rapamycin to inhibit mTOR signaling, a pathway that is overactive in people and animals with TSC. After four weeks of treatment starting at one week of life, mutant mice displayed normal social behaviors and normal activity in cerebellar Purkinje neurons, even after four weeks without treatment. These results raise the possibility that treatment covering critical periods of development could prevent autism symptoms from ever manifesting. As TSC is often diagnosed in utero in humans, defining these critical periods may provide an opportunity to prevent development of autism behaviors.

Reference: “A Critical Period for Development of Cerebellar-Mediated Autism-Relevant Social Behavior” by Jennifer M. Gibson, Cleone P. Howland, Chongyu Ren, Cyrena Howland, Alexandra Vernino and Peter T. Tsai, 21 February 2022, JNeurosci.
DOI: 10.1523/JNEUROSCI.1230-21.2021

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