Evidence map›Paper›PMID 32616652›Full record

ArticleThe Journal of biological chemistry2020

Garcinoic acid prevents β-amyloid (Aβ) deposition in the mouse brain.

Rita Marinelli, Pierangelo Torquato, Desirée Bartolini, Cristina Mas-Bargues, Guido Bellezza, Antimo Gioiello, Consuelo Borras, Antonella De Luca, Francesca Fallarino, Bartolomeo Sebastiani and 8 more

Abstract read
In one paragraph

Article in The Journal of biological chemistry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
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

14 citing papers in PubMed.

  1. Article
  2. Article
  3. Acetylcholinesterase inhibiting withanolides from Curvularia pseudobrachyspora, an endophytic fungus of Withania somnifera (L.) Dunal.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2026
    Article
  4. Review
  5. Review
  6. Modulation ofMicroorganisms · 2024
    Article
  7. Article
  8. Article
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  11. Article
  12. Article
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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

18 authors.

Rita MarinelliDepartment of Pharmaceutical Sciences, University of Perugia, Perugia, Italy.ORCID 0000-0001-6746-449X
Pierangelo TorquatoDepartment of Pharmaceutical Sciences, University of Perugia, Perugia, Italy.
Desirée BartoliniDepartment of Pharmaceutical Sciences, University of Perugia, Perugia, Italy.ORCID 0000-0003-3849-757X
Cristina Mas-BarguesFreshage Research Group, Dept. of Physiology, Faculty of Medicine, University of Valencia, CIBERFES, INCLIVA, Valencia, Spain.
Guido BellezzaDepartment of Experimental Medicine, Section of Anatomic Pathology and Histology, Medical School, University of Perugia, Perugia, Italy.
Antimo GioielloDepartment of Pharmaceutical Sciences, University of Perugia, Perugia, Italy.
Consuelo BorrasFreshage Research Group, Dept. of Physiology, Faculty of Medicine, University of Valencia, CIBERFES, INCLIVA, Valencia, Spain.ORCID 0000-0003-4606-1792
Antonella De LucaDepartment of Experimental Medicine, University of Perugia, Perugia, Italy.
Francesca FallarinoDepartment of Experimental Medicine, University of Perugia, Perugia, Italy.
Bartolomeo SebastianiDepartment of Pharmaceutical Sciences, University of Perugia, Perugia, Italy.
Sridhar ManiDepartments of Medicine, Genetics and Molecular Pharmacology, Albert Einstein College of Medicine, Bronx, New York USA.ORCID 0000-0003-4132-6157
Angelo SidoniDepartment of Experimental Medicine, Section of Anatomic Pathology and Histology, Medical School, University of Perugia, Perugia, Italy.
Jose ViñaFreshage Research Group, Dept. of Physiology, Faculty of Medicine, University of Valencia, CIBERFES, INCLIVA, Valencia, Spain.
Manuela LeriDepartment of Experimental and Clinical Biomedical Sciences, University of Florence, Italy.
Monica BucciantiniDepartment of Experimental and Clinical Biomedical Sciences, University of Florence, Italy.
Pamela NardielloDepartment of Experimental and Clinical Biomedical Sciences, University of Florence, Italy.
Fiorella CasamentiDepartment of Experimental and Clinical Biomedical Sciences, University of Florence, Italy.
Francesco GalliDepartment of Pharmaceutical Sciences, University of Perugia, Perugia, Italy francesco.galli@unipg.it.ORCID 0000-0003-3626-051X

Funding

Developmental PBDE exposure, gut microbiome, and diabetesR01ES030197 · NIEHS · UNIVERSITY OF WASHINGTON · PI Julia Yue Cui, Haiwei Gu · 2019 to 2026
$5.0M
Microbial Metabolite Mimics, PXR and Colitis-Induced Colorectal CancerR01CA222469 · NCI · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI MANI, SRIDHAR · 2018 to 2022
$2.3M
Chemical Modulation of Orphan Nuclear Receptor FunctionR01CA127231 · NCI · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI MANI, SRIDHAR · 2009 to 2014
$1.6M
Development of Novel Drugs to Alleviate CPT-11 ToxicityR01CA161879 · NCI · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI MANI, SRIDHAR, REDINBO, MATTHEW R · 2012 to 2016
$1.6M
NCI NIH HHS R01 CA127231NCI NIH HHS R01 CA161879NCI NIH HHS R01 CA222469NIEHS NIH HHS R01 ES030197
6 · The paper itself

Abstract

Garcinoic acid (GA or δ-T3-13'COOH), is a natural vitamin E metabolite that has preliminarily been identified as a modulator of nuclear receptors involved in β-amyloid (Aβ) metabolism and progression of Alzheimer's disease (AD). In this study, we investigated GA's effects on Aβ oligomer formation and deposition. Specifically, we compared them with those of other vitamin E analogs and the soy isoflavone genistein, a natural agonist of peroxisome proliferator-activated receptor γ (PPARγ) that has therapeutic potential for managing AD. GA significantly reduced Aβ aggregation and accumulation in mouse cortical astrocytes. Similarly to genistein, GA up-regulated PPARγ expression and apolipoprotein E (ApoE) efflux in these cells with an efficacy that was comparable with that of its metabolic precursor δ-tocotrienol and higher than those of α-tocopherol metabolites. Unlike for genistein and the other vitamin E compounds, the GA-induced restoration of ApoE efflux was not affected by pharmacological inhibition of PPARγ activity, and specific activation of pregnane X receptor (PXR) was observed together with ApoE and multidrug resistance protein 1 (MDR1) membrane transporter up-regulation in both the mouse astrocytes and brain tissue. These effects of GA were associated with reduced Aβ deposition in the brain of TgCRND8 mice, a transgenic AD model. In conclusion, GA holds potential for preventing Aβ oligomerization and deposition in the brain. The mechanistic aspects of GA's properties appear to be distinct from those of other vitamin E metabolites and of genistein.

Indexed as

Amyloid beta-PeptidesAnimalsBenzopyransBrainMaleMiceProtein AggregatesProtein Aggregation, PathologicalVitamin EAmyloid beta-PeptidesBenzopyransgarcinoic acidProtein AggregatesVitamin E)Alzheimer diseaseAlzheimer's diseaseamyloid-beta (AB)apolipoprotein E (ApoEgarcinoic acidgenisteinneurodegenerative diseaseperoxisome proliferator-activated receptor gamma (PPARγ)peroxisome proliferator-activated receptor (PPAR)pregnane X receptor (PXR)protein aggregationtocopheroltocotrienolvitamin E

Identifiers

PMID32616652
PMCPMC7450134

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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.