Evidence map›Paper›PMID 35327604›Full record

ReviewBiomolecules2022

Emerging Roles for G Protein-Coupled Estrogen Receptor 1 in Cardio-Renal Health: Implications for Aging.

Ravneet Singh, Victoria L Nasci, Ginger Guthrie, Lale A Ertuglu, Maryam K Butt, Annet Kirabo, Eman Y Gohar

Abstract readReview
In one paragraph

Review in Biomolecules, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
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

12 citing papers in PubMed.

  1. Circulating GPER-1, 8-Iso-Prostaglandin FJournal of clinical medicine · 2026
    Article
  2. GPER1 activation regulates renal purinergic P2YAmerican journal of physiology. Regulatory, integrative and comparative physiology · 2026
    Article
  3. Review
  4. Article
  5. Review
  6. Research progress and prospect of MAPK signaling pathway in knee osteoarthritis.European journal of orthopaedic surgery & traumatology : orthopedie traumatologie · 2025
    Review
  7. Observational
  8. Article
  9. Review
  10. Review
  11. Review
  12. 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.

Ravneet SinghDivision of Nephrology and Hypertension, Vanderbilt University Medical Center, Medical Research Building IV, Nashville, TN 37232, USA.
Victoria L NasciDivision of Nephrology and Hypertension, Vanderbilt University Medical Center, Medical Research Building IV, Nashville, TN 37232, USA.ORCID 0000-0002-1891-8974
Ginger GuthrieDivision of Nephrology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL 35233, USA.
Lale A ErtugluDivision of Clinical Pharmacology, Vanderbilt University Medical Center, Nashville, TN 37232, USA.ORCID 0000-0002-6318-4199
Maryam K ButtDivision of Nephrology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL 35233, USA.
Annet KiraboDivision of Clinical Pharmacology, Vanderbilt University Medical Center, Nashville, TN 37232, USA.ORCID 0000-0001-8580-9359
Eman Y GoharDivision of Nephrology and Hypertension, Vanderbilt University Medical Center, Medical Research Building IV, Nashville, TN 37232, USA.

Funding

Sex Differences in Renal Sodium HandlingR00DK119413 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI GOHAR, EMAN · 2021 to 2023
$740k
NIDDK NIH HHS R00 DK119413
6 · The paper itself

Abstract

Cardiovascular (CV) and renal diseases are increasingly prevalent in the United States and globally. CV-related mortality is the leading cause of death in the United States, while renal-related mortality is the 8th. Despite advanced therapeutics, both diseases persist, warranting continued exploration of disease mechanisms to develop novel therapeutics and advance clinical outcomes for cardio-renal health. CV and renal diseases increase with age, and there are sex differences evident in both the prevalence and progression of CV and renal disease. These age and sex differences seen in cardio-renal health implicate sex hormones as potentially important regulators to be studied. One such regulator is G protein-coupled estrogen receptor 1 (GPER1). GPER1 has been implicated in estrogen signaling and is expressed in a variety of tissues including the heart, vasculature, and kidney. GPER1 has been shown to be protective against CV and renal diseases in different experimental animal models. GPER1 actions involve multiple signaling pathways: interaction with aldosterone and endothelin-1 signaling, stimulation of the release of nitric oxide, and reduction in oxidative stress, inflammation, and immune infiltration. This review will discuss the current literature regarding GPER1 and cardio-renal health, particularly in the context of aging. Improving our understanding of GPER1-evoked mechanisms may reveal novel therapeutics aimed at improving cardio-renal health and clinical outcomes in the elderly.

Indexed as

Estrogen Receptor alphaReceptors, G-Protein-CoupledAgingAnimalsEstrogensFemaleGTP-Binding ProteinsKidneyMaleEstrogen Receptor alphaEstrogensGTP-Binding ProteinsReceptors, G-Protein-Coupledendothelin-1GPR30heartkidneynitric oxidepostmenopausal womenRAASROS

Identifiers

PMID35327604
PMCPMC8946600

What Socratic 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 Socratic graph.