Evidence map›Paper›PMID 35659370›Full record

ReviewAdvances in pharmacology (San Diego, Calif.)2022

The CYP/20-HETE/GPR75 axis in hypertension.

Ghezal Froogh, Victor Garcia, Michal Laniado Schwartzman

Open access · greenAbstract readReview
In one paragraph

Review in Advances in pharmacology (San Diego, Calif.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
43.8field-weighted citation impact, top 1% 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

22 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Arachidonic acid in aging: New roles for old players.Journal of advanced research · 2025
    Review
  14. Article
  15. 20-HETE and Hypertension.Hypertension (Dallas, Tex. : 1979) · 2024
    Article
  16. Article
  17. Article
  18. International journal of general medicine · 2024
    Article
  19. Review
  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

3 authors at 1 institution in 1 country.

Ghezal FrooghDepartment of Pharmacology, New York Medical College School of Medicine, Valhalla, NY, United States.
Victor GarciaDepartment of Pharmacology, New York Medical College School of Medicine, Valhalla, NY, United States.
Michal Laniado SchwartzmanDepartment of Pharmacology, New York Medical College School of Medicine, Valhalla, NY, United States. Electronic address: michal_schwartzman@nymc.edu.
New York Medical College · US

Funding

Molecular Mechanisms of 20-HETE-mediated Vascular Dysfunction and HypertensionR01HL139793 · NHLBI · NEW YORK MEDICAL COLLEGE · PI SCHWARTZMAN, MICHAL LANIADO · 2018 to 2021
$2.7M
NHLBI NIH HHS R01 HL139793
6 · The paper itself

Abstract

20-Hydroxyeicosatetraenoic acid (20-HETE) is a bioactive lipid generated from the ω-hydroxylation of arachidonic acid (AA) by enzymes of the cytochrome P450 (CYP) family, primarily the CYP4A and CYP4F subfamilies. 20-HETE is most notably identified as a modulator of vascular tone, regulator of renal function, and a contributor to the onset and development of hypertension and cardiovascular disease. 20-HETE-mediated signaling promotes hypertension by sensitizing the vasculature to constrictor stimuli, inducing endothelial dysfunction, and potentiating vascular inflammation. These bioactions are driven by the activation of the G-protein coupled receptor 75 (GPR75), a 20-HETE receptor (20HR). Given the capacity of 20-HETE signaling to drive pro-hypertensive mechanisms, the CYP/20-HETE/GPR75 axis has the potential to be a significant therapeutic target for the treatment of hypertension and cardiovascular diseases associated with increases in blood pressure. In this chapter, we review 20-HETE-mediated cellular mechanisms that promote hypertension, highlight important data in humans such as genetic variants in the CYP genes that potentiate 20-HETE production and describe recent findings in humans with 20HR/GPR75 mutations. Special emphasis is given to the 20HR and respective receptor blockers that have the potential to pave a path to translational and clinical studies for the treatment of 20-HETE-driven hypertension, and obesity/metabolic syndrome.

Indexed as

Cardiovascular DiseasesHypertensionBlood PressureCytochrome P-450 CYP4ACytochrome P-450 Enzyme SystemHumansHydroxyeicosatetraenoic AcidsReceptors, G-Protein-Coupled20-hydroxy-5,8,11,14-eicosatetraenoic acidCytochrome P-450 CYP4ACytochrome P-450 Enzyme SystemGPR75 protein, humanHydroxyeicosatetraenoic AcidsReceptors, G-Protein-Coupled20-HETECardiovascular diseaseCytochrome P450GPR75Hypertension

Identifiers

PMID35659370
PMCPMC10123763
OpenAlexW4225345689

What Socratic 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 Socratic graph.