Evidence map›Paper›PMID 32077471›Full record

ArticleJournal of neuropathology and experimental neurology2020

l-Serine Reduces Spinal Cord Pathology in a Vervet Model of Preclinical ALS/MND.

David A Davis, Paul Alan Cox, Sandra Anne Banack, Patricia D Lecusay, Susanna P Garamszegi, Matthew J Hagan, James T Powell, James S Metcalf, Roberta M Palmour, Amy Beierschmitt and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of neuropathology and experimental neurology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
3.8field-weighted citation impact, top 5% 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

31 citing papers in PubMed, 1 synthesis or guideline pooled it, 59 citations in OpenAlex.

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  4. Life Course Exposure to Cyanobacteria and Amyotrophic Lateral Sclerosis Survival.International journal of environmental research and public health · 2025
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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

12 authors at 3 institutions in 3 countries.

David A DavisDepartment of Neurology, Miller School of Medicine, University of Miami, Miami, Florida.
Paul Alan CoxDepartment of Neurology, Miller School of Medicine, University of Miami, Miami, Florida.
Sandra Anne BanackDepartment of Neurology, Miller School of Medicine, University of Miami, Miami, Florida.
Patricia D Lecusay
Susanna P Garamszegi
Matthew J HaganDepartment of Neurology, Miller School of Medicine, University of Miami, Miami, Florida.
James T PowellBrain Chemistry Labs, Jackson Hole, Wyoming.
James S MetcalfBrain Chemistry Labs, Jackson Hole, Wyoming.
Roberta M PalmourBehavioural Science Foundation, St. Kitts and Nevis, West Indies.
Amy BeierschmittBehavioural Science Foundation, St. Kitts and Nevis, West Indies.
Walter G BradleyDepartment of Neurology, Miller School of Medicine, University of Miami, Miami, Florida.
Deborah C MashDepartment of Neurology, Miller School of Medicine, University of Miami, Miami, Florida.
University of Miami · USMcGill University · CARoss University School of Veterinary Medicine · KN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The early neuropathological features of amyotrophic lateral sclerosis/motor neuron disease (ALS/MND) are protein aggregates in motor neurons and microglial activation. Similar pathology characterizes Guamanian ALS/Parkinsonism dementia complex, which may be triggered by the cyanotoxin β-N-methylamino-l-alanine (BMAA). We report here the occurrence of ALS/MND-type pathological changes in vervets (Chlorocebus sabaeus; n = 8) fed oral doses of a dry powder of BMAA HCl salt (210 mg/kg/day) for 140 days. Spinal cords and brains from toxin-exposed vervets were compared to controls fed rice flour (210 mg/kg/day) and to vervets coadministered equal amounts of BMAA and l-serine (210 mg/kg/day). Immunohistochemistry and quantitative image analysis were used to examine markers of ALS/MND and glial activation. UHPLC-MS/MS was used to confirm BMAA exposures in dosed vervets. Motor neuron degeneration was demonstrated in BMAA-dosed vervets by TDP-43+ proteinopathy in anterior horn cells, by reactive astrogliosis, by activated microglia, and by damage to myelinated axons in the lateral corticospinal tracts. Vervets dosed with BMAA + l-serine displayed reduced neuropathological changes. This study demonstrates that chronic dietary exposure to BMAA causes ALS/MND-type pathological changes in the vervet and coadministration of l-serine reduces the amount of reactive gliosis and the number of protein inclusions in motor neurons.

Indexed as

Amino Acids, DiaminoAmyotrophic Lateral SclerosisAnimalsChlorocebus aethiopsCyanobacteria ToxinsDisease Models, AnimalMaleMicrogliaMotor Neuron DiseaseMotor NeuronsPyramidal TractsSerineSpinal CordAmino Acids, Diaminobeta-N-methylamino-L-alanineCyanobacteria ToxinsSerineALS/MNDBMAACyanobacteriaGuam ALS/PDCMotor neuronsNeurofibrillary tanglesTDP-43

Identifiers

PMID32077471
PMCPMC7092359
OpenAlexW3007929261

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.