Evidence map›Paper›PMID 35366264›Full record

ArticlePathophysiology : the official journal of the International Society for Pathophysiology2021

The Angiotensin-Converting Enzyme Inhibitor Lisinopril Mitigates Memory and Motor Deficits in a

Jimiece Thomas, Haddon Smith, C Aaron Smith, Lori Coward, Gregory Gorman, Maria De Luca, Patricia Jumbo-Lucioni

Open access · goldAbstract read
In one paragraph

Article in Pathophysiology : the official journal of the International Society for Pathophysiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.2field-weighted citation impact, top 26% 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

16 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. [Drug repositioning prediction based on dynamic feature learning on heterogeneous graphs].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2026
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  10. Modeling Path Importance for Effective Alzheimer's Disease Drug Repurposing.Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing · 2024
    Article
  11. Metabolic Disorder Therapeutics and their Effects on Memory.CNS & neurological disorders drug targets · 2024
    Review
  12. Review
  13. Article
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  16. 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

7 authors at 3 institutions in 1 country.

Jimiece ThomasMcWhorter School of Pharmacy, Samford University, Birmingham, AL 35229, USA.
Haddon SmithMcWhorter School of Pharmacy, Samford University, Birmingham, AL 35229, USA.
C Aaron SmithMcWhorter School of Pharmacy, Samford University, Birmingham, AL 35229, USA.
Lori CowardPharmaceutical Sciences Research Institute, McWhorter School of Pharmacy, Samford University, Birmingham, AL 35229, USA.
Gregory GormanPharmaceutical Sciences Research Institute, McWhorter School of Pharmacy, Samford University, Birmingham, AL 35229, USA.
Maria De LucaDepartment of Nutrition Sciences, School of Health Professions, University of Alabama, Birmingham, AL 35233, USA.ORCID 0000-0001-6345-7508
Patricia Jumbo-LucioniPharmaceutical, Social, and Administrative Sciences, McWhorter School of Pharmacy, Samford University, Birmingham, AL 35229, USA.
Samford University · USUniversity of Alabama · USUniversity of Alabama at Birmingham · US

Funding

Syndecan-4 as a molecular link between adipose tissue and agingR21AG063197 · NIA · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI DE LUCA, MARIA, NAGAREDDY, PRABHAKARA REDDY · 2020 to 2021
$408k
McWhorter School of Pharmacy-Samford University Dean's Innovation GrantNIH HHS R21AG063197Samford University Faculty Development Grant
6 · The paper itself

Abstract

The use of angiotensin-converting enzyme inhibitors (ACEis) has been reported to reduce symptoms of cognitive decline in patients with Alzheimer’s disease (AD). Yet, the protective role of ACEis against AD symptoms is still controversial. Here, we aimed at determining whether oral treatment with the ACEi lisinopril has beneficial effects on cognitive and physical functions in a Drosophila melanogaster model of AD that overexpresses the human amyloid precursor protein and the human β-site APP-cleaving enzyme in neurons. We found a significant impairment in learning and memory as well as in climbing ability in young AD flies compared to control flies. After evaluation of the kynurenine pathway of tryptophan metabolism, we also found that AD flies displayed a >30-fold increase in the levels of the neurotoxic 3-hydroxykynurenine (3-HK) in their heads. Furthermore, compared to control flies, AD flies had significantly higher levels of the reactive oxygen species (ROS) hydrogen peroxide in their muscle-enriched thoraces. Lisinopril significantly improved deficits in learning and memory and climbing ability in AD flies. The positive impact of lisinopril on physical function might be, in part, explained by a significant reduction in ROS levels in the thoraces of the lisinopril-fed AD flies. However, lisinopril did not affect the levels of 3-HK. In conclusion, our findings provide novel and relevant insights into the therapeutic potential of ACEis in a preclinical AD model.

Indexed as

agingAlzheimer’s diseaseangiotensin-converting enzyme inhibitorsDrosophilakynurenine pathway of tryptophan metabolism

Identifiers

PMID35366264
PMCPMC8830455
OpenAlexW3177017858

What OpenQuestion holds

Textmetadata
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.