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Publication : Intermittent Hypobaric Hypoxia Ameliorates Autistic-Like Phenotypes in Mice.

First Author  Pan YD Year  2024
Journal  J Neurosci Volume  44
Issue  7 PubMed ID  38124211
Mgi Jnum  J:354122 Mgi Id  MGI:7719156
Doi  10.1523/JNEUROSCI.1665-23.2023 Citation  Pan YD, et al. (2024) Intermittent Hypobaric Hypoxia Ameliorates Autistic-Like Phenotypes in Mice. J Neurosci 44(7)
abstractText  Autism spectrum disorder (ASD) is a neurodevelopmental condition characterized by persistent deficits in social communication and stereotyped behaviors. Although major advances in basic research on autism have been achieved in the past decade, and behavioral interventions can mitigate the difficulties that individuals with autism experience, little is known about the many fundamental issues of the interventions, and no specific medication has demonstrated efficiency for the core symptoms of ASD. Intermittent hypobaric hypoxia (IHH) is characterized by repeated exposure to lowered atmospheric pressure and oxygen levels, which triggers multiple physiological adaptations in the body. Here, using two mouse models of ASD, male Shank3B (-/-) and Fmr1 (-/y) mice, we found that IHH training at an altitude of 5,000 m for 4 h per day, for 14 consecutive days, ameliorated autistic-like behaviors. Moreover, IHH training enhanced hypoxia inducible factor (HIF) 1alpha in the dorsal raphe nucleus (DRN) and activated the DRN serotonergic neurons. Infusion of cobalt chloride into the DRN, to mimic IHH in increasing HIF1alpha expression or genetically knockdown PHD2 to upregulate HIF1alpha expression in the DRN serotonergic neurons, alleviated autistic-like behaviors in Shank3B (-/-) mice. In contrast, downregulation of HIF1alpha in DRN serotonergic neurons induced compulsive behaviors. Furthermore, upregulating HIF1alpha in DRN serotonergic neurons increased the firing rates of these neurons, whereas downregulation of HIF1alpha in DRN serotonergic neurons decreased their firing rates. These findings suggest that IHH activated DRN serotonergic neurons via upregulation of HIF1alpha, and thus ameliorated autistic-like phenotypes, providing a novel therapeutic option for ASD.
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