Evidence map›Paper›PMID 24582784›Full record

ArticleJournal of stroke and cerebrovascular diseases : the official journal of National Stroke Association

Alpha 1-antitrypsin therapy mitigated ischemic stroke damage in rats.

Huong L Moldthan, Aaron C Hirko, Jeffrey S Thinschmidt, Maria B Grant, Zhimin Li, Joanna Peris, Yuanqing Lu, Ahmed S Elshikha, Michael A King, Jeffrey A Hughes and 1 more

Open access · greenAbstract readComparative Study
In one paragraph

Article in Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

23 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
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  8. Ceruletide and Alpha-1 Antitrypsin as a Novel Combination Therapy for Ischemic Stroke.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2022
    Article
  9. Review
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  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Transcriptomic Analysis ofFrontiers in psychiatry · 2019
    Article
  17. Alpha 1 Antitrypsin Gene Therapy Extends the Lifespan of Lupus-Prone Mice.Molecular therapy. Methods & clinical development · 2018
    Article
  18. Article
  19. Alpha-1 Antitrypsin Therapy for Autoimmune Disorders.Chronic obstructive pulmonary diseases (Miami, Fla.) · 2018
    Article
  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

11 authors at 4 institutions in 2 countries.

Huong L MoldthanDepartment of Pharmaceutics, University of Florida College of Pharmacy, Gainesville, Florida.
Aaron C HirkoDepartment of Pharmacology and Therapeutics, University of Florida College of Medicine, Gainesville, Florida.
Jeffrey S ThinschmidtDepartment of Pharmacology and Therapeutics, University of Florida College of Medicine, Gainesville, Florida.
Maria B GrantDepartment of Pharmacology and Therapeutics, University of Florida College of Medicine, Gainesville, Florida.
Zhimin LiDepartment of Pharmacodynamics, University of Florida College of Pharmacy, Gainesville, Florida.
Joanna PerisDepartment of Pharmacodynamics, University of Florida College of Pharmacy, Gainesville, Florida.
Yuanqing LuDepartment of Pharmaceutics, University of Florida College of Pharmacy, Gainesville, Florida.
Ahmed S ElshikhaDepartment of Pharmaceutics, University of Florida College of Pharmacy, Gainesville, Florida; Department of Pharmaceutics, Faculty of Pharmacy, Zagazig University, Zagazig, Sharkia, Egypt.
Michael A KingDepartment of Pharmacology and Therapeutics, University of Florida College of Medicine, Gainesville, Florida; Department of Veterans Affairs Medical Center, Gainesville, Florida.
Jeffrey A HughesMonsanto Co., Chemistry, St Louis, Missouri.
Sihong SongDepartment of Pharmaceutics, University of Florida College of Pharmacy, Gainesville, Florida. Electronic address: shsong@ufl.edu.
Florida College · USUniversity of Florida · USMonsanto (United States) · USZagazig University · EG

Funding

System Gene Delivery for Alzheimer's Disease- SupplementP01AG010485 · NIA · UNIVERSITY OF NORTH TEXAS HLTH SCI CTR · PI ZOLOTUKHIN, SERGEI · 1991 to 2009
$11.3M
Strategies for Sustained Effect of AAV-mediated Correction of Pompe DiseaseP01DK058327 · NIDDK · UNIVERSITY OF FLORIDA · PI CAMPBELL-THOMPSON, MARTHA · 2000 to 2009
$11.0M
NIA NIH HHS P01 AG010485NIA NIH HHS P01-AG10485NIDDK NIH HHS DK58327NIDDK NIH HHS P01 DK058327
6 · The paper itself

Abstract

Our objective is to develop a new therapy for the treatment of stroke. Currently, the only effective therapy for acute ischemic stroke is the thrombolytic agent recombinant tissue plasminogen activator. α1-Antitrypsin (AAT), a serine proteinase inhibitor with potent anti-inflammatory, anti-apoptotic, antimicrobial, and cytoprotective activities, could be beneficial in stroke. The goal of this study is to test whether AAT can improve ischemic stroke outcome in an established rat model. Middle cerebral artery occlusion was induced in male rats via intracranial (i.c.) microinjection of endothelin-1. Five to 10 minutes after stroke induction, rats received either i.c. or intravenous delivery of human AAT. Cylinder and vibrissae tests were used to evaluate sensorimotor function before and 72 hours after middle cerebral artery occlusion. Infarct volumes were examined via either 2,3,5-triphenyltetrazolium chloride assay or magnetic resonance imaging 72 hours after middle cerebral artery occlusion. Despite equivalent initial strokes, at 72 hours, the infarct volumes of the human AAT treatment groups (local and systemic injection) were statistically significantly reduced by 83% and 63% (P < .0001 and P < .05, respectively) compared with control rats. Human AAT significantly limited sensory motor system deficits. Human AAT could be a potential novel therapeutic drug for the protection against neurodegeneration after ischemic stroke, but more studies are needed to investigate the protective mechanisms and efficacy in other animal models.

Indexed as

alpha 1-AntitrypsinAnimalsBrainCytoprotectionDisease Models, AnimalEndothelin-1HumansInfarction, Middle Cerebral ArteryInjections, IntravenousMagnetic Resonance ImagingMaleMicroinjectionsMotor ActivityNeuroprotective AgentsRats, Sprague-DawleySensory Thresholdsalpha 1-AntitrypsinEndothelin-1Neuroprotective AgentsSERPINA1 protein, humanalpha 1-antitrypsinanti-inflammationendothelin-1–induced MCAOinflammationIschemic strokeneuroprotection

Identifiers

PMID24582784
PMCPMC4035453
OpenAlexW2029527746

What OpenQuestion holds

Textmetadata
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.