Antipurinergic therapy corrects the autism-like features in the Fragile X (Fmr1 knockout) mouse model

• Published in: Molecular autism Vol. 6; no. 1; p. 1
• Main Authors: Naviaux, Jane C, Wang, Lin, Li, Kefeng, Bright, A Taylor, Alaynick, William A, Williams, Kenneth R, Powell, Susan B, Naviaux, Robert K
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 13-01-2015; BioMed Central
• Subjects: Analysis; Autism; Care and treatment; Complications and side effects; Glutamate; Mass spectrometry; Physiological aspects; Autism spectrum disorders; Metabolomics; Mitochondria; Cell danger response (CDR); Environment; Genetics; Fragile X syndrome; Maternal immune activation (MIA); Metabolism; Antipurinergic therapy (APT); Purinergic signaling
• ISSN: 2040-2392; 2040-2392
• DOI: 10.1186/2040-2392-6-1

This study was designed to test a new approach to drug treatment of autism spectrum disorders (ASDs) in the Fragile X (Fmr1) knockout mouse model.
We used behavioral analysis, mass spectrometry, metabolomics, electron microscopy, and western analysis to test the hypothesis that the disturbances in social behavior, novelty preference, metabolism, and synapse structure are treatable with antipurinergic therapy (APT).
Weekly treatment with the purinergic antagonist suramin (20 mg/kg intraperitoneally), started at 9 weeks of age, restored normal social behavior, and improved metabolism, and brain synaptosomal structure. Abnormalities in synaptosomal glutamate, endocannabinoid, purinergic, and IP3 receptor expression, complement C1q, TDP43, and amyloid β precursor protein (APP) were corrected. Comprehensive metabolomic analysis identified 20 biochemical pathways associated with symptom improvements. Seventeen pathways were shared with human ASD, and 11 were shared with the maternal immune activation (MIA) model of ASD. These metabolic pathways were previously identified as functionally related mediators of the evolutionarily conserved cell danger response (CDR).
The data show that antipurinergic therapy improves the multisystem, ASD-like features of both the environmental MIA, and the genetic Fragile X models. These abnormalities appeared to be traceable to mitochondria and regulated by purinergic signaling.