Evidence map›Paper›PMID 33016313›Full record

ReviewClinical science (London, England : 1979)2020

Brain angiotensin converting enzyme-2 in central cardiovascular regulation.

Mazher Mohammed, Clara Berdasco, Eric Lazartigues

Open access · greenAbstract readReview
In one paragraph

Review in Clinical science (London, England : 1979), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.9field-weighted citation impact, top 12% 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

19 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
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  15. Review
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  17. Stress and the "extended" autonomic system.Autonomic neuroscience : basic & clinical · 2021
    Review
  18. Review
  19. Sensory Afferent Renal Nerve Activated GαiFrontiers in physiology · 2021
    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

3 authors at 2 institutions in 1 country.

Mazher MohammedDepartment of Pharmacology and Experimental Therapeutics, Louisiana State University Health Sciences Center, New Orleans, LA 70112, U.S.A.
Clara BerdascoDepartment of Pharmacology and Experimental Therapeutics, Louisiana State University Health Sciences Center, New Orleans, LA 70112, U.S.A.
Eric LazartiguesDepartment of Pharmacology and Experimental Therapeutics, Louisiana State University Health Sciences Center, New Orleans, LA 70112, U.S.A.
Southeast Louisiana Veterans Health Care System · USLouisiana State University Health Sciences Center New Orleans · US

Funding

Targeting ACE2 ubiquitination for hypertensionR01HL150592 · NHLBI · LSU HEALTH SCIENCES CENTER · PI LAZARTIGUES, ERIC D · 2020 to 2023
$2.4M
Targeting ADAM17 maturation in resistant hypertension.R01HL163588 · NHLBI · LSU HEALTH SCIENCES CENTER · PI LAZARTIGUES, ERIC D · 2022 to 2025
$2.2M
New strategies to restore ACE2 compensatory activity in neurogenic hypertensionI01BX004294 · VA · SOUTHEAST LOUISIANA VETERANS HEALTH CARE · PI LAZARTIGUES, ERIC D · 2018 to 2021
–
BLRD VA I01 BX004294NHLBI NIH HHS R01 HL150592NHLBI NIH HHS R01 HL163588
6 · The paper itself

Abstract

The brain renin-angiotensin system (RAS) plays an important role in the regulation of autonomic and neuroendocrine functions, and maintains cardiovascular homeostasis. Ang-II is the major effector molecule of RAS and exerts most of its physiological functions, including blood pressure (BP) regulation, via activation of AT1 receptors. Dysregulation of brain RAS in the central nervous system results in increased Ang-II synthesis that leads to sympathetic outflow and hypertension. Brain angiotensin (Ang) converting enzyme-2 (ACE2) was discovered two decades ago as an RAS component, exhibiting a counter-regulatory role and opposing the adverse cardiovascular effects produced by Ang-II. Studies using synthetic compounds that can sustain the elevation of ACE2 activity or genetically overexpressed ACE2 in specific brain regions found various beneficial effects on cardiovascular function. More recently, ACE2 has been shown to play critical roles in neuro-inflammation, gut dysbiosis and the regulation of stress and anxiety-like behaviors. In the present review, we aim to highlight the anatomical locations and functional implication of brain ACE2 related to its BP regulation via modulation of the sympathetic nervous system and discuss the recent developments and future directions in the ACE2-mediated central cardiovascular regulation.

Indexed as

Angiotensin-Converting Enzyme 2AnimalsBrainCardiovascular SystemHumansModels, BiologicalRenin-Angiotensin SystemStress, PhysiologicalAngiotensin-Converting Enzyme 2autonomic nervous systemcardiovascular physiologyHPA axisneuro–immune interactionsrenin-angiotensin system

Identifiers

PMID33016313
PMCPMC7640374
OpenAlexW3089441201

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.