Evidence map›Paper›PMID 30995737›Full record

ReviewInternational journal of molecular sciences2019

Nuclear Peroxisome Proliferator-Activated Receptors (PPARs) as Therapeutic Targets of Resveratrol for Autism Spectrum Disorder.

Rita Barone, Renata Rizzo, Giovanni Tabbì, Michele Malaguarnera, Richard E Frye, Jean Bastin

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
4.4field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

25 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 4 institutions in 4 countries.

Rita BaroneChild Neurology and Psychiatry Unit, Department of Clinical and Experimental Medicine, University of Catania, 95123 Catania, Italy. rbarone@unict.it.ORCID 0000-0001-6302-2686
Renata RizzoChild Neurology and Psychiatry Unit, Department of Clinical and Experimental Medicine, University of Catania, 95123 Catania, Italy. rerizzo@unict.it.
Giovanni TabbìInstitute of Crystallography (IC), National Research Council (CNR), 95126 Catania, Italy. giovanni.tabbi@cnr.it.
Michele MalaguarneraLaboratory of Neurobiology, Centro Investigación Príncipe Felipe, 46012 Valencia, Spain. michele.malaguarnera@gmail.com.ORCID 0000-0002-7145-6377
Richard E FryeBarrow Neurologic Institute at Phoenix Children's Hospital, Phoenix, AZ 85016, USA. rfrye@phoenixchildrens.com.ORCID 0000-0003-4442-2937
Jean BastinCentre de Recherche des Cordeliers, 75006 Paris, France. jean.bastin@inserm.fr.
University of Catania · ITDélégation Paris 5 · FRNational Research Council · ITUniversity of Arizona · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

AnimalsAnti-Inflammatory AgentsAntioxidantsAutism Spectrum DisorderEnergy MetabolismFatty AcidsHumansMitochondriaMolecular Targeted TherapyOxidation-ReductionPeroxisome Proliferator-Activated ReceptorsResveratrolSignal TransductionAnti-Inflammatory AgentsAntioxidantsFatty AcidsPeroxisome Proliferator-Activated ReceptorsResveratrolautism spectrum disordersmitochondrial fatty acid β-oxidation metabolismPPARs agonistsresveratrol

Identifiers

PMID30995737
PMCPMC6515064
OpenAlexW2936437788

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.