Evidence map›Paper›PMID 26662641›Full record

ArticleJournal of neurochemistry2016

Administration of low dose estrogen attenuates gliosis and protects neurons in acute spinal cord injury in rats.

Supriti Samantaray, Arabinda Das, Denise C Matzelle, Shan P Yu, Ling Wei, Abhay Varma, Swapan K Ray, Naren L Banik

Open access · greenAbstract read
In one paragraph

Article in Journal of neurochemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
3.3field-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

33 citing papers in PubMed, 47 citations in OpenAlex.

  1. Review
  2. Article
  3. Hormonal interventions in skin wounds - a mini review.Molecular medicine (Cambridge, Mass.) · 2024
    Review
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  15. The Pathophysiology of Osteoporosis after Spinal Cord Injury.International journal of molecular sciences · 2021
    Review
  16. Article
  17. Hematogenous Macrophages: A New Therapeutic Target for Spinal Cord Injury.Frontiers in cell and developmental biology · 2021
    Review
  18. 17Mediators of inflammation · 2021
    Article
  19. Review
  20. Article
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

8 authors at 3 institutions in 1 country.

Supriti SamantarayDepartment of Neurology and Neurosurgery, Medical University of South Carolina, Charleston, South Carolina, USA.
Arabinda DasDepartment of Neurology and Neurosurgery, Medical University of South Carolina, Charleston, South Carolina, USA.
Denise C MatzelleDepartment of Neurology and Neurosurgery, Medical University of South Carolina, Charleston, South Carolina, USA.
Shan P YuDepartment of Anesthesia, Emory University School of Medicine, Atlanta, GA, USA.
Ling WeiDepartment of Anesthesia, Emory University School of Medicine, Atlanta, GA, USA.
Abhay VarmaDepartment of Neurology and Neurosurgery, Medical University of South Carolina, Charleston, South Carolina, USA.
Swapan K RayDepartment of Pathology, Microbiology, and Immunology, University of South Carolina School of Medicine, Columbia, South Carolina, USA.
Naren L BanikDepartment of Neurology and Neurosurgery, Medical University of South Carolina, Charleston, South Carolina, USA.
Medical University of South Carolina · USEmory University · USUniversity of South Carolina · US

Funding

ROLE OF PROTEINASE IN SPINAL CORD INJURYR01NS031622 · NINDS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI BANIK, NAREN L · 1994 to 2011
$3.4M
ESTROGEN EFFICACY IN SPINAL CORD INJURYR01NS045967 · NINDS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI BANIK, NAREN L · 2003 to 2006
$996k
Hormonal Intervention Protects Axon-myelin to Promote Functional Recovery in SCII01BX001262 · VA · RALPH H JOHNSON VA MEDICAL CENTER · PI BANIK, NAREN L · 2013 to 2025
–
Regulation of inflammatory T Cells and Neuroprotection by Calpain Inhibitor in MSI01BX002349 · VA · RALPH H JOHNSON VA MEDICAL CENTER · PI BANIK, NAREN L · 2014 to 2017
–
BLRD VA I01 BX001262BLRD VA I01 BX002349NINDS NIH HHS R01 NS031622NINDS NIH HHS R01 NS045967NINDS NIH HHS R01-NS31622NINDS NIH HHS R01 NS45967
6 · The paper itself

Abstract

Spinal cord injury (SCI) is a debilitating condition with neurological deficits and loss of motor function that, depending on the severity, may lead to paralysis. The only treatment currently available is methylprednisolone, which is widely used and renders limited efficacy in SCI. Therefore, other therapeutic agents must be developed. The neuroprotective efficacy of estrogen in SCI was studied with a pre-clinical and pro-translational perspective. Acute SCI was induced in rats that were treated with low doses of estrogen (1, 5, 10, or 100 μg/kg) and compared with vehicle-treated injured rats or laminectomy control (sham) rats at 48 h post-SCI. Changes in gliosis and other pro-inflammatory responses, expression and activity of proteolytic enzymes (e.g., calpain, caspase-3), apoptosis of neurons in SCI, and cell death were monitored via Western blotting and immunohistochemistry. Negligible pro-inflammatory responses or proteolytic events and very low levels of neuronal death were found in sham rats. In contrast, vehicle-treated SCI rats showed profound pro-inflammatory responses with reactive gliosis, elevated expression and activity of calpain and caspase-3, elevated Bax:Bcl-2 ratio, and high levels of neuronal death in lesion and caudal regions of the injured spinal cord. Estrogen treatment at each dose reduced pro-inflammatory and proteolytic activities and protected neurons in the caudal penumbra in acute SCI. Estrogen treatment at 10 μg was found to be as effective as 100 μg in ameliorating the above parameters in injured animals. Results from this investigation indicated that estrogen at a low dose could be a promising therapeutic agent for treating acute SCI. Experimental studies with low dose estrogen therapy in acute spinal cord injury (SCI) demonstrated the potential for multi-active beneficial outcomes. Estrogen has been found to ameliorate several degenerative pathways following SCI. Thus, such early protective effects may even lead to functional recovery in long term injury. Studies are underway in chronic SCI in a follow up manuscript.

Indexed as

AnimalsCell DeathDisease Models, AnimalEstrogensGliosisMaleNeuronsNeuroprotective AgentsRats, Sprague-DawleyRecovery of FunctionSpinal CordSpinal Cord InjuriesEstrogensNeuroprotective Agentsacute spinal cord injurycalpainestrogenestrogen receptorsgliosisneuroprotection

Identifiers

PMID26662641
PMCPMC5374720
OpenAlexW2289470861

What OpenQuestion holds

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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.