Evidence map›Paper›PMID 35990729›Full record

ArticleFrontiers in behavioral neuroscience2022

Angiotensin-(1-7) improves cognitive function and reduces inflammation in mice following mild traumatic brain injury.

Ryan P Bruhns, Maha Ibrahim Sulaiman, Michael Gaub, Esther H Bae, Rachel B Davidson Knapp, Anna R Larson, Angela Smith, Deziree L Coleman, William D Staatz, Alexander J Sandweiss and 4 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Frontiers in behavioral neuroscience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06282965 (A Randomized, Double-blind, Placebo Controlled Study of the Safety and Efficacy of Angiotensin), which is not on this map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.5field-weighted citation impact, top 18% 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.

NCT06282965 phase1 / phase2recruitingnot on this mapstarted 2024, after this paper: background citation

A Randomized, Double-blind, Placebo Controlled Study of the Safety and Efficacy of Angiotensin (1-7) in Persons With Moderate to Severe Traumatic Brain Injury (TBI)

TypeinterventionalSponsorUniversity of ArizonaRan2024 to 2027Enrolled90ConditionsTraumatic Brain InjuryArmsAngiotensin (1-7), Sterile saline
3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Article
  3. Frontiers in neural circuits · 2025
    Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. The Renin Angiotensin System as a Therapeutic Target in Traumatic Brain Injury.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2023
    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

14 authors at 1 institution in 1 country.

Ryan P BruhnsDepartment of Pharmacology, College of Medicine and Health Sciences, University of Arizona, Tucson, AZ, United States.
Maha Ibrahim SulaimanDepartment of Pharmacology, College of Medicine and Health Sciences, University of Arizona, Tucson, AZ, United States.
Michael GaubDepartment of Pharmacology, College of Medicine and Health Sciences, University of Arizona, Tucson, AZ, United States.
Esther H BaeDepartment of Pharmacology, College of Medicine and Health Sciences, University of Arizona, Tucson, AZ, United States.
Rachel B Davidson KnappDepartment of Pharmacology, College of Medicine and Health Sciences, University of Arizona, Tucson, AZ, United States.
Anna R LarsonDepartment of Pharmacology, College of Medicine and Health Sciences, University of Arizona, Tucson, AZ, United States.
Angela SmithDepartment of Pharmacology, College of Medicine and Health Sciences, University of Arizona, Tucson, AZ, United States.
Deziree L ColemanDepartment of Pharmacology, College of Medicine and Health Sciences, University of Arizona, Tucson, AZ, United States.
William D StaatzDepartment of Pharmacology, College of Medicine and Health Sciences, University of Arizona, Tucson, AZ, United States.
Alexander J SandweissDepartment of Pharmacology, College of Medicine and Health Sciences, University of Arizona, Tucson, AZ, United States.
Bellal JosephDepartment of Surgery, College of Medicine and Health Sciences, University of Arizona, Tucson, AZ, United States.
Meredith HayDepartment of Physiology, College of Medicine and Health Sciences, University of Arizona, Tucson, AZ, United States.
Tally M Largent-MilnesDepartment of Pharmacology, College of Medicine and Health Sciences, University of Arizona, Tucson, AZ, United States.
Todd W VanderahDepartment of Pharmacology, College of Medicine and Health Sciences, University of Arizona, Tucson, AZ, United States.
University of Arizona · US

Funding

PNA5: A Novel Mas Receptor Agonist for Treatment of Cognitive Impairment in Patients at Risk for Vascular Dementia and Alzheimer's Disease Related Dementia: an FDA required Toxicology StudyU01AG082617 · NIA · UNIVERSITY OF ARIZONA · PI Meredith Hay, TODD W VANDERAH · 2023 to 2026
$8.0M
The Center of Excellence in Addiction Studies (CEAS)P30DA051355 · NIDA · UNIVERSITY OF ARIZONA · PI MILNES, TALLY MARIE · 2021 to 2025
$6.7M
Training in Cellular & Molecular BiologyT32GM136534 · NIGMS · UNIVERSITY OF WASHINGTON · PI Andrew Atwell Oberst, LARRY S ZWEIFEL · 2021 to 2026
$5.8M
Primary Afferent Transmission in the Trigeminal Dorsal HornF32DE022499 · NIDCR · OREGON HEALTH & SCIENCE UNIVERSITY · PI MILNES, TALLY MARIE · 2011 to 2014
$127k
NIA NIH HHS U01 AG082617NIDA NIH HHS P30 DA051355NIDCR NIH HHS F32 DE022499NIGMS NIH HHS T32 GM136534
6 · The paper itself

Abstract

Introduction: Traumatic brain injury (TBI) is a leading cause of disability in the US. Angiotensin 1-7 (Ang-1-7), an endogenous peptide, acts at the G protein coupled MAS1 receptors (MASR) to inhibit inflammatory mediators and decrease reactive oxygen species within the CNS. Few studies have identified whether Ang-(1-7) decreases cognitive impairment following closed TBI. This study examined the therapeutic effect of Ang-(1-7) on secondary injury observed in a murine model of mild TBI (mTBI) in a closed skull, single injury model. Materials and methods: Male mice ( Results: Administration of Ang-(1-7) daily for 5 days post-mTBI significantly increased cognitive function as compared to saline control-treated animals. Cortical and hippocampal structures showed less damage in the presence of Ang-(1-7), while Ang-(1-7) administration significantly changed the expression of pTau and GFAP in cortical and hippocampal regions as compared to control. Discussion: These are among the first studies to demonstrate that sustained administration of Ang-(1-7) following a closed-skull, single impact mTBI significantly improves neurologic outcomes, potentially offering a novel therapeutic modality for the prevention of long-term CNS impairment following such injuries.

Indexed as

angiotensin 1-7cognitive impairmentMas receptorpTautraumatic brain injury

Identifiers

PMID35990729
PMCPMC9386567
OpenAlexW4289838323

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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.