Evidence map›Paper›PMID 33368801›Full record

ArticleBrain pathology (Zurich, Switzerland)2021

Alleviation of extensive visual pathway dysfunction by a remyelinating drug in a chronic mouse model of multiple sclerosis.

Maria T Sekyi, Kelli Lauderdale, Kelley C Atkinson, Batis Golestany, Hawra Karim, Micah Feri, Joselyn S Soto, Cobi Diaz, Sung Hoon Kim, Marianne Cilluffo and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Brain pathology (Zurich, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 16% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
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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

13 authors at 3 institutions in 1 country.

Maria T SekyiDivision of Biomedical Sciences, Riverside School of Medicine, University of California, Riverside, CA, USA.
Kelli LauderdaleDivision of Biomedical Sciences, Riverside School of Medicine, University of California, Riverside, CA, USA.
Kelley C AtkinsonDivision of Biomedical Sciences, Riverside School of Medicine, University of California, Riverside, CA, USA.
Batis GolestanyDivision of Biomedical Sciences, Riverside School of Medicine, University of California, Riverside, CA, USA.
Hawra KarimDivision of Biomedical Sciences, Riverside School of Medicine, University of California, Riverside, CA, USA.
Micah FeriDivision of Biomedical Sciences, Riverside School of Medicine, University of California, Riverside, CA, USA.
Joselyn S SotoDivision of Biomedical Sciences, Riverside School of Medicine, University of California, Riverside, CA, USA.
Cobi DiazDivision of Biomedical Sciences, Riverside School of Medicine, University of California, Riverside, CA, USA.
Sung Hoon KimDepartment of Chemistry and Cancer Center, University of Illinois at Urbana-Champaign, Urbana, IL, USA.
Marianne CilluffoBRI Electron Microscopy Laboratory, Los Angeles School of Medicine, University of California, Los Angeles, CA, USA.
Steven NusinowitzStein Eye Institute, Los Angeles School of Medicine, University of California, Los Angeles, CA, USA.
John A KatzenellenbogenDepartment of Chemistry and Cancer Center, University of Illinois at Urbana-Champaign, Urbana, IL, USA.
Seema K Tiwari-WoodruffDivision of Biomedical Sciences, Riverside School of Medicine, University of California, Riverside, CA, USA.ORCID 0000-0001-7608-4763
University of California, Riverside · USUniversity of California, Los Angeles · USUniversity of Illinois Urbana-Champaign · US

Funding

Demyelination is coupled to neuronal hyperexcitability leading to seizuresR01NS111552 · NINDS · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI BINDER, DEVIN K, TIWARI-WOODRUFF, SEEMA K · 2020 to 2024
$1.9M
Novel Ligands and Mechanisms to Achieve Selective Nuclear Receptor ActivityR01DK015556 · NIDDK · UNIVERSITY OF ILLINOIS URBANA-CHAMPAIGN · PI KATZENELLENBOGEN, JOHN A. · 1986 to 2016
$1.6M
Stimulating oligodendrocyte progenitor cell differentiation and remyelinationR01NS081141 · NINDS · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI TIWARI-WOODRUFF, SEEMA K · 2014 to 2017
$1.3M
Breast Cancer Research Foundation BCRF-20-084National Multiple Sclerosis Society RG-1901-33349National Multiple Sclerosis Society RG 4853A3/2National Science Foundation DGE-1326120NIDDK NIH HHS R01 DK015556NINDS NIH HHS R01 DK015556NINDS NIH HHS R01 NS081141NINDS NIH HHS R01NS081141NINDS NIH HHS R01 NS111552NINDS NIH HHS R01NS111552
6 · The paper itself

Abstract

Visual deficits are among the most prevalent symptoms in patients with multiple sclerosis (MS). To understand deficits in the visual pathway during MS and potential treatment effects, we used experimental autoimmune encephalomyelitis (EAE), the most commonly used animal model of MS. The afferent visual pathway was assessed in vivo using optical coherence tomography (OCT), electroretinography (ERG), and visually evoked cortical potentials (VEPs). Inflammation, demyelination, and neurodegeneration were examined by immunohistochemistry ex vivo. In addition, an immunomodulatory, remyelinating agent, the estrogen receptor β ligand chloroindazole (IndCl), was tested for its therapeutic potential in the visual pathway. EAE produced functional deficits in visual system electrophysiology, including suppression of ERG and VEP waveform amplitudes and increased signal latencies. Therapeutic IndCl rescued overall visual system latency by VEP but had little impact on amplitude or ERG findings relative to vehicle. Faster VEP conduction in IndCl-treated mice was associated with enhanced myelin basic protein signal in all visual system structures examined. IndCl preserved retinal ganglion cells (RGCs) and oligodendrocyte density in the prechiasmatic white matter, but similar retinal nerve fiber layer thinning by OCT was noted in vehicle and IndCl-treated mice. Although IndCl differentially attenuated leukocyte and astrocyte staining signal throughout the structures analyzed, axolemmal varicosities were observed in all visual fiber tracts of mice with EAE irrespective of treatment, suggesting impaired axonal energy homeostasis. These data support incomplete functional recovery of VEP amplitude with IndCl, as fiber tracts displayed persistent axon pathology despite remyelination-induced decreases in latencies, evidenced by reduced optic nerve g-ratio in IndCl-treated mice. Although additional studies are required, these findings demonstrate the dynamics of visual pathway dysfunction and disability during EAE, along with the importance of early treatment to mitigate EAE-induced axon damage.

Indexed as

AnimalsAzo CompoundsEncephalomyelitis, Autoimmune, ExperimentalEvoked Potentials, VisualInflammationMiceMice, Inbred C57BLMultiple SclerosisNaphthalenesNerve DegenerationRemyelinationVisual PathwaysAzo Compoundschlorindazone DSNaphthalenesdemyelinationelectroretinogramestrogen receptor βexperimental autoimmune encephalomyelitisindazole chlorideinflammationmultiple sclerosismyelinneurodegenerationoptical coherence tomographyremyelinationvisual dysfunctionvisually evoked potentialsvisual pathway

Identifiers

PMID33368801
PMCPMC8018057
OpenAlexW3117955456

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Registered trials

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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.