AI Article Synopsis

  • Autism spectrum disorder (ASD) is a complex neurodevelopmental disorder marked by difficulties in social communication and repetitive behaviors, with no current drug to cure its core symptoms.
  • Research indicates that issues with mitochondrial fatty acid oxidation (FAO) might play a role in ASD, highlighting a potential area for developing new therapeutic approaches.
  • PPAR receptors, when activated, can enhance FAO and may offer a pathway for treatment, with compounds like resveratrol showing promise for improving metabolic and inflammatory processes related to ASD.

Article Abstract

Autism spectrum disorder (ASD) is a neurodevelopmental disorder characterized by defective social communication and interaction and restricted, repetitive behavior with a complex, multifactorial etiology. Despite an increasing worldwide prevalence of ASD, there is currently no pharmacological cure to treat core symptoms of ASD. Clinical evidence and molecular data support the role of impaired mitochondrial fatty acid oxidation (FAO) in ASD. The recognition of defects in energy metabolism in ASD may be important for better understanding ASD and developing therapeutic intervention. The nuclear peroxisome proliferator-activated receptors (PPAR) α, δ, and γ are ligand-activated receptors with distinct physiological functions in regulating lipid and glucose metabolism, as well as inflammatory response. PPAR activation allows a coordinated up-regulation of numerous FAO enzymes, resulting in significant PPAR-driven increases in mitochondrial FAO flux. Resveratrol (RSV) is a polyphenolic compound which exhibits metabolic, antioxidant, and anti-inflammatory properties, pointing to possible applications in ASD therapeutics. In this study, we review the evidence for the existing links between ASD and impaired mitochondrial FAO and review the potential implications for regulation of mitochondrial FAO in ASD by PPAR activators, including RSV.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6515064PMC
http://dx.doi.org/10.3390/ijms20081878DOI Listing

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