Evidence map›Paper›PMID 27167084›Full record

ArticleNeuroscience2016

MicroRNA 146a locally mediates distal axonal growth of dorsal root ganglia neurons under high glucose and sildenafil conditions.

Longfei Jia, Lei Wang, Michael Chopp, Yi Zhang, Alexandra Szalad, Zheng Gang Zhang

Open access · greenAbstract read
In one paragraph

Article in Neuroscience, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

29 citing papers in PubMed, 47 citations in OpenAlex.

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  12. Micro- and Nano-Devices for Studying Subcellular Biology.Small (Weinheim an der Bergstrasse, Germany) · 2021
    Review
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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 1 institution in 1 country.

Longfei JiaDepartment of Neurology, Henry Ford Hospital, 2799 W. Grand Boulevard, Detroit, MI 48202, United States.
Lei WangDepartment of Neurology, Henry Ford Hospital, 2799 W. Grand Boulevard, Detroit, MI 48202, United States.
Michael ChoppDepartment of Neurology, Henry Ford Hospital, 2799 W. Grand Boulevard, Detroit, MI 48202, United States; Department of Physics Oakland University, Rochester, MI 48309, United States.
Yi ZhangDepartment of Neurology, Henry Ford Hospital, 2799 W. Grand Boulevard, Detroit, MI 48202, United States.
Alexandra SzaladDepartment of Neurology, Henry Ford Hospital, 2799 W. Grand Boulevard, Detroit, MI 48202, United States.
Zheng Gang ZhangDepartment of Neurology, Henry Ford Hospital, 2799 W. Grand Boulevard, Detroit, MI 48202, United States. Electronic address: zhazh@neuro.hfh.edu.
Henry Ford Hospital · US

Funding

miR-17-92 exosome treatment of strokeR01NS088656 · NINDS · HENRY FORD HEALTH SYSTEM · PI CHOPP, MICHAEL · 2015 to 2019
$1.6M
MicroRNAs and neurogenesis after strokeR01NS075156 · NINDS · HENRY FORD HEALTH SYSTEM · PI ZHANG, ZHENG GANG · 2011 to 2015
$1.6M
Thymosin Beta4 Promotes the Recovery of Peripheral neuropathy in Type II DiabeticR01DK097519 · NIDDK · HENRY FORD HEALTH SYSTEM · PI WANG, LEI · 2013 to 2016
$1.3M
PDE5 is a Therapeutic Target for Peripheral Neuropathy in Diabetic MiceR01NS075084 · NINDS · HENRY FORD HEALTH SYSTEM · PI WANG, LEI · 2012 to 2015
$1.3M
NIDDK NIH HHS R01 DK097519NINDS NIH HHS R01 NS075084NINDS NIH HHS R01 NS075156NINDS NIH HHS R01 NS088656
6 · The paper itself

Abstract

Axonal loss contributes to induction of diabetic peripheral neuropathy. Sildenafil, a phosphodiesterase type 5 inhibitor, ameliorates neurological dysfunction in diabetic peripheral neuropathy. However, the direct effect of high glucose and sildenafil on axonal growth has not been extensively investigated. Using rat primary dorsal root ganglia (DRG) neurons cultured in a microfluidic chamber, we investigated the effect of axonal application of high glucose and sildenafil on distal axonal growth. We found that axonal, but not cell body, application of high glucose locally inhibited distal axonal growth. However, axonal application of sildenafil overcame high glucose-reduced axonal growth. Quantitative real-time RT-PCR (qRT-PCR) and Western blot analysis of distal axonal samples revealed that high glucose reduced axonal miR-146a levels and substantially increased miR-146a target genes, IRAK1 and TRAF6 in the axon. In contrast, sildenafil significantly reversed high glucose-reduced miR-146a levels and high glucose-increased IRAK1 and TRAF6. Gain- and loss-of function of miR-146a in DRG neurons revealed that miR-146a mediated the local effect of high glucose on the distal axonal growth. These in vitro data provide new insights into molecular mechanisms of diabetic peripheral neuropathy.

Indexed as

AnimalsArgonaute ProteinsAxonsCells, CulturedDEAD-box RNA HelicasesDiabetes Mellitus, ExperimentalDiabetic NeuropathiesGanglia, SpinalGlucoseInterleukin-1 Receptor-Associated KinasesMicroRNAsNeuronal OutgrowthNeuroprotective AgentsPhosphodiesterase 5 InhibitorsRats, WistarRibonuclease IIIAgo2 protein, ratArgonaute ProteinsDEAD-box RNA HelicasesDicer1 protein, ratGlucoseInterleukin-1 Receptor-Associated KinasesIRAK1 protein, ratMicroRNAsMIRN146 microRNA, ratNeuroprotective AgentsPhosphodiesterase 5 InhibitorsRibonuclease IIISildenafil CitrateTNF Receptor-Associated Factor 6axonal growthdiabetesmiR-146aperipheral neuropathysildenafil

Identifiers

PMID27167084
PMCPMC4905785
OpenAlexW2346613219

What OpenQuestion holds

Textmetadata
LicenceTDM
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.