Evidence map›Paper›PMID 20731659›Full record

ArticleBrain pathology (Zurich, Switzerland)2011

Methylene blue reduces aβ levels and rescues early cognitive deficit by increasing proteasome activity.

David X Medina, Antonella Caccamo, Salvatore Oddo

Abstract read
In one paragraph

Article in Brain pathology (Zurich, Switzerland), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 91 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
91citing papers in PubMed, 1 pooled it
9.6field-weighted citation impact, top 1% 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

91 citing papers in PubMed, 1 synthesis or guideline pooled it, 193 citations in OpenAlex.

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  14. The effects of acute Methylene Blue administration on cerebral blood flow and metabolism in humans and rats.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2023
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  19. Mechanisms associated with the dysregulation of mitochondrial function due to lead exposure and possible implications on the development of Alzheimer's disease.Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine · 2022
    Review
  20. Review

31 more citing papers are in PubMed but not listed here.

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

3 authors at 1 institution in 1 country.

David X MedinaDepartment of Physiology and The Barshop Institute for Longevity and Aging Studies, University of Texas Health Science Center at San Antonio, San Antonio, TX 78229-3900, USA.
Antonella Caccamo
Salvatore Oddo
The University of Texas Health Science Center at San Antonio · US

Funding

Molecular Mechanisms of Memory Loss in a Transgenic Model of Alzheimer DiseaseR00AG029729 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI ODDO, SALVATORE · 2008 to 2010
$745k
Molecular Mechanisms of Memory Loss in a Transgenic Model of Alzheimer DiseaseK99AG029729 · NIA · UNIVERSITY OF CALIFORNIA-IRVINE · PI ODDO, SALVATORE · 2007 to 2008
$119k
NIA NIH HHS K99 AG029729NIA NIH HHS R00 AG029729
6 · The paper itself

Abstract

Promising results have emerged from a phase II clinical trial testing methylene blue (MB) as a potential therapeutic for Alzheimer disease (AD), where improvements in cognitive functions of AD patients after 6 months of MB administration have been reported. Despite these reports, no preclinical testing of MB in mammals has been published, and thus its mechanism of action in relation to AD pathology remains unknown. In order to elucidate the effects of MB on AD pathology and to determine its mechanism of action, we used a mouse model (3xTg-AD) that develops age-dependent accumulation of Aβ and tau and cognitive decline. Here, we report that chronic dietary MB treatment reduces Aβ levels and improves learning and memory deficits in the 3xTg-AD mice. The mechanisms underlying the effects of MB on Aβ pathology appears to be mediated by an increase in Aβ clearance as we show that MB increases the chymotrypsin- and trypsin-like activities of the proteasome in the brain. To our knowledge, this is the first report showing that MB increases proteasome function and ameliorates AD-like pathology in vivo. Overall, the data presented here support the use of MB for the treatment of AD and offer a possible mechanism of action.

Indexed as

Alzheimer DiseaseAmyloid beta-PeptidesAnimalsBlotting, WesternCognition DisordersDisease Models, AnimalEnzyme InhibitorsEnzyme-Linked Immunosorbent AssayImmunohistochemistryMaleMethylene BlueMiceMice, TransgenicProteasome Endopeptidase Complextau ProteinsAmyloid beta-PeptidesEnzyme InhibitorsMethylene BlueProteasome Endopeptidase Complextau Proteins

Identifiers

PMID20731659
PMCPMC2992595
OpenAlexW1946583083

What OpenQuestion holds

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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.