Evidence map›Paper›PMID 27138068›Full record

ArticleBrain research2016

Membrane lipid peroxidation in neurodegeneration: Role of thrombin and proteinase-activated receptor-1.

Bruce A Citron, Syed Ameenuddin, K Uchida, William Z Suo, Karen SantaCruz, Barry W Festoff

Open access · greenAbstract read
In one paragraph

Article in Brain research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

17 citing papers in PubMed, 27 citations in OpenAlex.

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  17. 4-Hydroxy-2-nonenal: a critical target in oxidative stress?American journal of physiology. Cell physiology · 2016
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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

6 authors at 3 institutions in 2 countries.

Bruce A CitronNeurobiology Research Laboratory, Department of Veterans Affairs Medical Center, Kansas City, Missouri 64128; Departments of Neurology, University of Kansas Medical Center, Kansas City, Kansas 66170.
Syed AmeenuddinNeurobiology Research Laboratory, Department of Veterans Affairs Medical Center, Kansas City, Missouri 64128.
K UchidaLaboratory of Food and Biodynamics, Graduate School of Bioagricultural Sciences, Nagoya University, Nagoya 464-8601, Japan.
William Z SuoNeurobiology Research Laboratory, Department of Veterans Affairs Medical Center, Kansas City, Missouri 64128; Departments of Neurology, University of Kansas Medical Center, Kansas City, Kansas 66170.
Karen SantaCruzNeurobiology Research Laboratory, Department of Veterans Affairs Medical Center, Kansas City, Missouri 64128; Departments of Pathology and Laboratory Medicine University of Kansas Medical Center, Kansas City, Kansas 66170.
Barry W FestoffNeurobiology Research Laboratory, Department of Veterans Affairs Medical Center, Kansas City, Missouri 64128; Departments of Neurology, University of Kansas Medical Center, Kansas City, Kansas 66170; Departments of Pharmacology, Toxicology and Therapeutics, University of Kansas Medical Center, Kansas City, Kansas 66170; Departments of Molecular and Integrative Physiology, University of Kansas Medical Center, Kansas City, Kansas 66170. Electronic address: bwfestoff@mac.com.
University of Kansas Medical Center · USNagoya University · JPVeterans Health Administration · US

Funding

Preventing TBI-Induced Chronic Functional Loss with a Neuroprotective AntioxidantI01RX001520 · VA · VA NEW JERSEY HEALTH CARE SYSTEM · PI CITRON, BRUCE A. · 2015 to 2020
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RRD VA I01 RX001520
6 · The paper itself

Abstract

Thrombin and membrane lipid peroxidation (MLP) have been implicated in various central nervous system (CNS) disorders from CNS trauma to stroke, Alzheimer's (AD) and Parkinson's (PD) diseases. Because thrombin also induces MLP in platelets and its involvement in neurodegenerative diseases we hypothesized that its deleterious effects might, in part, involve formation of MLP in neuronal cells. We previously showed that thrombin induced caspase-3 mediated apoptosis in motor neurons, via a proteinase-activated receptor (PAR1). We have now investigated thrombin's influence on the oxidative state of neurons leading to induction of MLP-protein adducts. Translational relevance of thrombin-induced MLP is supported by increased levels of 4-hydroxynonenal-protein adducts (HNEPA) in AD and PD brains. We now report for the first time that thrombin dose-dependently induces formation of HNEPA in NSC34 mouse motor neuron cells using anti-HNE and anti-acrolein monoclonal antibodies. The most prominent immunoreactive band, in SDS-PAGE, was at ∼54kDa. Membrane fractions displayed higher amounts of the protein-adduct than cytosolic fractions. Thrombin induced MLP was mediated, at least in part, through PAR1 since a PAR1 active peptide, PAR1AP, also elevated HNEPA levels. Of interest, glutamate and Fe2SO4 also increased the ∼54kDa HNEPA band in these cells but to a lesser extent. Taken together our results implicate the involvement of thrombin and MLP in neuronal cell loss observed in various CNS degenerative and traumatic pathologies.

Indexed as

Lipid PeroxidationAcroleinAldehydesAlzheimer DiseaseAnimalsCells, CulturedCytoplasmDose-Response Relationship, DrugHumansMembrane LipidsMiceMotor NeuronsParkinson DiseaseReceptor, PAR-1Thrombin4-hydroxy-2-nonenalAcroleinAldehydesMembrane LipidsReceptor, PAR-1ThrombinApoptosisMembrane lipid peroxidationNeurodegenerative diseasesReactive oxygenSpinal cord injury

Identifiers

PMID27138068
PMCPMC9035224
OpenAlexW2344182823

What OpenQuestion holds

Textmetadata
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.