Evidence map›Paper›PMID 35657963›Full record

ArticlePloS one2022

Mechanistic insights gained from cell and molecular analysis of the neuroprotective potential of bioactive natural compounds in an immortalized hippocampal cell line.

Harris A Weisz, Deborah R Boone, William S Coggins, Gabrielle A Edwards, Hannah E Willey, Steven G Widen, Dionicio Siegel, Andrew T Nelson, Donald S Prough, Helen L Hellmich

Abstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. Review
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

10 authors.

Harris A WeiszDepartment of Anesthesiology, The University of Texas Medical Branch at Galveston, Galveston, Texas, United States of America.
Deborah R BooneDepartment of Anesthesiology, The University of Texas Medical Branch at Galveston, Galveston, Texas, United States of America.
William S CogginsDepartment of Neurosurgery, The University of Arkansas for Medical Sciences, Little Rock, Arkansas, United States of America.
Gabrielle A EdwardsDepartment of Anesthesiology, The University of Texas Medical Branch at Galveston, Galveston, Texas, United States of America.
Hannah E WilleyTulane University School of Medicine, New Orleans, Louisiana, United States of America.
Steven G WidenDepartment of Biochemistry & Molecular Biology, The University of Texas Medical Branch at Galveston, Galveston, Texas, United States of America.
Dionicio SiegelSkaggs School of Pharmacy and Pharmaceutical Sciences, The University of California San Diego, San Diego, California, United States of America.
Andrew T NelsonDepartment of Pathology, The University of Texas Southwestern Medical Center, Dallas, Texas, United States of America.
Donald S ProughDepartment of Anesthesiology, The University of Texas Medical Branch at Galveston, Galveston, Texas, United States of America.
Helen L HellmichDepartment of Anesthesiology, The University of Texas Medical Branch at Galveston, Galveston, Texas, United States of America.ORCID 0000-0002-7500-4490

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Evaluating novel compounds for neuroprotective effects in animal models of traumatic brain injury (TBI) is a protracted, labor-intensive and costly effort. However, the present lack of effective treatment options for TBI, despite decades of research, shows the critical need for alternative methods for screening new drug candidates with neuroprotective properties. Because natural products have been a leading source of new therapeutic agents for human diseases, we used an in vitro model of stretch injury to rapidly assess pro-survival effects of three bioactive compounds, two isolated from natural products (clovanemagnolol [CM], vinaxanthone [VX]) and the third, a dietary compound (pterostilbene [PT]) found in blueberries. The stretch injury experiments were not used to validate drug efficacy in a comprehensive manner but used primarily, as proof-of-principle, to demonstrate that the neuroprotective potential of each bioactive agent can be quickly assessed in an immortalized hippocampal cell line in lieu of comprehensive testing in animal models of TBI. To gain mechanistic insights into potential molecular mechanisms of neuroprotective effects, we performed a pathway-specific PCR array analysis of the effects of CM on the rat hippocampus and microRNA sequencing analysis of the effects of VX and PT on cultured hippocampal progenitor neurons. We show that the neuroprotective properties of these natural compounds are associated with altered expression of several genes or microRNAs that have functional roles in neurodegeneration or cell survival. Our approach could help in quickly assessing multiple natural products for neuroprotective properties and expedite the process of new drug discovery for TBI therapeutics.

Indexed as

Biological ProductsBrain Injuries, TraumaticNeuroprotective AgentsAnimalsCell LineDisease Models, AnimalHippocampusRatsBiological ProductsNeuroprotective Agents

Identifiers

PMID35657963
PMCPMC9165808

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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.