Evidence map›Paper›PMID 28561773›Full record

ReviewInternational journal of molecular sciences2017

Can Co-Activation of Nrf2 and Neurotrophic Signaling Pathway Slow Alzheimer's Disease?

Kelsey E Murphy, Joshua J Park

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 8% 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

31 citing papers in PubMed, 1 synthesis or guideline pooled it, 53 citations in OpenAlex.

  1. Pooled it
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  7. Sargachromenol Isolated fromMarine drugs · 2022
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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

2 authors at 1 institution in 1 country.

Kelsey E MurphyDepartment of Neurosciences, College of Medicine and Life Sciences, University of Toledo, Toledo, OH 43614, USA. kelsey.murphy@rockets.utoledo.edu.
Joshua J ParkDepartment of Neurosciences, College of Medicine and Life Sciences, University of Toledo, Toledo, OH 43614, USA. joshua.park2@utoledo.edu.
University of Toledo · US

Funding

Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Mehboob A Hussain · 2013 to 2026
$24.3M
A BBB-permeable neurotrophic polysaccharide, midi-GAGRR21AG053590 · NIA · UNIVERSITY OF TOLEDO HEALTH SCI CAMPUS · PI PARK, JOSHUA JIN-HYOUK · 2016 to 2017
$417k
NIA NIH HHS R21 AG053590NIDDK NIH HHS P30 DK020572
6 · The paper itself

Abstract

Alzheimer's disease (AD) is a multifaceted disease that is hard to treat by single-modal treatment. AD starts with amyloid peptides, mitochondrial dysfunction, and oxidative stress and later is accompanied with chronic endoplasmic reticulum (ER) stress and autophagy dysfunction, resulting in more complicated pathogenesis. Currently, few treatments can modify the complicated pathogenic progress of AD. Compared to the treatment with exogenous antioxidants, the activation of global antioxidant defense system via Nrf2 looks more promising in attenuating oxidative stress in AD brains. Accompanying the activation of the Nrf2-mediated antioxidant defense system that reduce the AD-causative factor, oxidative stress, it is also necessary to activate the neurotrophic signaling pathway that replaces damaged organelles and molecules with new ones. Thus, the dual actions to activate both the Nrf2 antioxidant system and neurotrophic signaling pathway are expected to provide a better strategy to modify AD pathogenesis. Here, we review the current understanding of AD pathogenesis and neuronal defense systems and discuss a possible way to co-activate the Nrf2 antioxidant system and neurotrophic signaling pathway with the hope of helping to find a better strategy to slow AD.

Indexed as

Signal TransductionAlzheimer DiseaseAnimalsAntioxidantsBrainDisease ProgressionHumansNeuronsNF-E2-Related Factor 2Oxidative StressAntioxidantsNFE2L2 protein, humanNF-E2-Related Factor 2Alzheimer’s diseaseamyloid peptidemitochondrial damagenatural productsneurotrophic signaling pathwayNrf2oxidative stress

Identifiers

PMID28561773
PMCPMC5485992
OpenAlexW2619541264

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.