Evidence map›Paper›PMID 23349763›Full record

ArticlePloS one2013

The multifaceted effects of agmatine on functional recovery after spinal cord injury through Modulations of BMP-2/4/7 expressions in neurons and glial cells.

Yu Mi Park, Won Taek Lee, Kiran Kumar Bokara, Su Kyoung Seo, Seung Hwa Park, Jae Hwan Kim, Midori A Yenari, Kyung Ah Park, Jong Eun Lee

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.3field-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

18 citing papers in PubMed, 39 citations in OpenAlex.

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  9. Bone morphogenic protein signaling in spinal cord injury.Neuroimmunology and neuroinflammation · 2021
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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

9 authors at 3 institutions in 2 countries.

Yu Mi ParkDepartment of Anatomy, Yonsei University College of Medicine, Seoul, Republic of Korea.
Won Taek Lee
Kiran Kumar Bokara
Su Kyoung Seo
Seung Hwa Park
Jae Hwan Kim
Midori A Yenari
Kyung Ah Park
Jong Eun Lee
Yonsei University · KRKonkuk University · KRSan Francisco VA Medical Center · US

Funding

Inflammatory Mechanisms in Cerebral IschemiaR01NS040516 · NINDS · STANFORD UNIVERSITY · PI YENARI, MIDORI A · 2001 to 2014
$4.6M
NINDS NIH HHS NS40516NINDS NIH HHS R01 NS040516
6 · The paper itself

Abstract

Presently, few treatments for spinal cord injury (SCI) are available and none have facilitated neural regeneration and/or significant functional improvement. Agmatine (Agm), a guanidinium compound formed from decarboxylation of L-arginine by arginine decarboxylase, is a neurotransmitter/neuromodulator and been reported to exert neuroprotective effects in central nervous system injury models including SCI. The purpose of this study was to demonstrate the multifaceted effects of Agm on functional recovery and remyelinating events following SCI. Compression SCI in mice was produced by placing a 15 g/mm(2) weight for 1 min at thoracic vertebra (Th) 9 segment. Mice that received an intraperitoneal (i.p.) injection of Agm (100 mg/kg/day) within 1 hour after SCI until 35 days showed improvement in locomotor recovery and bladder function. Emphasis was made on the analysis of remyelination events, neuronal cell preservation and ablation of glial scar area following SCI. Agm treatment significantly inhibited the demyelination events, neuronal loss and glial scar around the lesion site. In light of recent findings that expressions of bone morphogenetic proteins (BMPs) are modulated in the neuronal and glial cell population after SCI, we hypothesized whether Agm could modulate BMP- 2/4/7 expressions in neurons, astrocytes, oligodendrocytes and play key role in promoting the neuronal and glial cell survival in the injured spinal cord. The results from computer assisted stereological toolbox analysis (CAST) demonstrate that Agm treatment dramatically increased BMP- 2/7 expressions in neurons and oligodendrocytes. On the other hand, BMP- 4 expressions were significantly decreased in astrocytes and oligodendrocytes around the lesion site. Together, our results reveal that Agm treatment improved neurological and histological outcomes, induced oligodendrogenesis, protected neurons, and decreased glial scar formation through modulating the BMP- 2/4/7 expressions following SCI.

Indexed as

AgmatineAnimalsBlotting, WesternBone Morphogenetic Protein 2Bone Morphogenetic Protein 4Bone Morphogenetic Protein 7Bone Morphogenetic ProteinsGlial Fibrillary Acidic ProteinImmunohistochemistryInjections, IntraperitonealMaleMiceMice, Inbred ICRMicroscopy, ConfocalMicroscopy, Electron, TransmissionMotor ActivityAgmatineBmp2 protein, mouseBone Morphogenetic Protein 2Bone Morphogenetic Protein 4Bone Morphogenetic Protein 7Bone Morphogenetic ProteinsGlial Fibrillary Acidic Protein

Identifiers

PMID23349763
PMCPMC3549976
OpenAlexW2004161433

What OpenQuestion holds

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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.