Hyperbaric Oxygen Therapy Alleviates Social Behavior Dysfunction and Neuroinflammation in a Mouse Model for Autism Spectrum Disorders

被引:10
|
作者
Fischer, Inbar [1 ]
Shohat, Sophie [2 ]
Levy, Gilad [1 ]
Bar, Ela [3 ,4 ]
Trangle, Sari Schokoroy [3 ]
Efrati, Shai [1 ,5 ]
Barak, Boaz [1 ,3 ]
机构
[1] Tel Aviv Univ, Sagol Sch Neurosci, IL-69978 Tel Aviv, Israel
[2] Tel Aviv Univ, Dept Biomed Engn, IL-69978 Tel Aviv, Israel
[3] Tel Aviv Univ, Sch Psychol Sci, IL-69978 Tel Aviv, Israel
[4] Tel Aviv Univ, Fac Life Sci, Sch Neurobiol Biochem & Biophys, IL-69978 Tel Aviv, Israel
[5] Shamir Med Ctr Assaf Harofeh, Sagol Ctr Hyperbar Med & Res, IL-70330 Beer Yaagov, Israel
关键词
autism spectrum disorder; Phelan McDermid syndrome; hyperbaric oxygen therapy; neuroinflammation; social behavior; hypoperfusion; Shank3; neurodevelopmental disorders; microglia; Igf-1; Hif1a; GROWTH-FACTOR-I; CEREBROSPINAL-FLUID; BRAIN; SHANK3; IMPROVE; PREVALENCE; ACTIVATION; MUTATIONS; MICROGLIA; CIRCUITS;
D O I
10.3390/ijms231911077
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Autism spectrum disorder (ASD) is a multifactorial neurodevelopmental disorder (NDD) characterized by impaired social communication and repetitive behavior, among other symptoms. ASD is highly heritable, with SHANK3 being one of the high-risk genes for ASD. In recent years, knowledge has been growing regarding the neuroplasticity effect induced by hyperbaric oxygen therapy (HBOT) and its potential use for ASD. Here, we characterized the effect of HBOT on a mouse model for ASD with the human genetic condition of InsG3680 mutation in the Shank3 gene. As compared to placebo, HBOT improved social behavior and reduced neuroinflammation in the cortex of the InsG3680((+/+)) mice. Specifically, HBOT induced upregulation of Insulin-like growth factor 1 (Igf1) expression levels and reduced the number of Iba1-positive cells in the mouse model for ASD compared to placebo control. Together, our research suggests that HBOT has the potential to improve the clinical outcome of ASD by ameliorating some of the core pathophysiological processes responsible for the development of the disorder.
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页数:14
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