Evidence map›Paper›PMID 35119333›Full record

ArticleAmerican journal of physiology. Heart and circulatory physiology2022

SGLT2 inhibition potentiates the cardiovascular, renal, and metabolic effects of sGC stimulation in hypertensive rats with prolonged exposure to high-fat diet.

Virginia Reverte, Francisca Rodriguez, Lidia Oltra, Juan M Moreno, María T Llinás, Courtney M Shea, Chad D Schwartzkopf, Emmanuel S Buys, Jaime L Masferrer, F Javier Salazar

Open access · hybridAbstract read
In one paragraph

Article in American journal of physiology. Heart and circulatory physiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.5field-weighted citation impact, top 16% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Soluble guanylate cyclase stimulators and activators as potential antihypertensive drugs.Hypertension research : official journal of the Japanese Society of Hypertension · 2025
    Review
  5. Article
  6. Guidelines on models of diabetic heart disease.American journal of physiology. Heart and circulatory physiology · 2022
    Review
  7. 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

10 authors at 2 institutions in 2 countries.

Virginia ReverteDepartment of Physiology, School of Medicine, CEIR Mare Nostrum University of Murcia, Murcia, Spain.
Francisca RodriguezDepartment of Physiology, School of Medicine, CEIR Mare Nostrum University of Murcia, Murcia, Spain.ORCID 0000-0002-8500-921X
Lidia OltraBiomedical Research Institute, Murcia, Spain.
Juan M MorenoDepartment of Physiology, School of Medicine, CEIR Mare Nostrum University of Murcia, Murcia, Spain.
María T LlinásDepartment of Physiology, School of Medicine, CEIR Mare Nostrum University of Murcia, Murcia, Spain.ORCID 0000-0002-9857-9940
Courtney M SheaCyclerion Therapeutics, Cambridge, Massachusetts.
Chad D SchwartzkopfCyclerion Therapeutics, Cambridge, Massachusetts.
Emmanuel S BuysCyclerion Therapeutics, Cambridge, Massachusetts.
Jaime L MasferrerCyclerion Therapeutics, Cambridge, Massachusetts.
F Javier SalazarDepartment of Physiology, School of Medicine, CEIR Mare Nostrum University of Murcia, Murcia, Spain.ORCID 0000-0003-4185-6692
Universidad de Murcia · ESCyclerion (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prolonged high-fat diet (HFD) accelerates the cardiovascular, renal, and metabolic dysfunction in hypertensive rats with altered renal development (ARDev). Soluble guanylate cyclase (sGC) stimulation or sodium-glucose cotransporter 2 (SGLT2) inhibition may improve cardiovascular, renal, and metabolic function in settings of hypertension and obesity. This study examined whether 6 wk treatment with an SGLT2 inhibitor (empagliflozin, 7 mg/kg/day) enhances the cardiovascular, renal, and metabolic effects of a sGC stimulator (praliciguat, 10 mg/kg/day) in hypertensive rats with ARDev and prolonged exposure to HFD. Arterial pressure (AP), renal vascular resistance (RVR), fat abdominal volume (FAV), insulin resistance, leptin and triglycerides levels, and intrarenal infiltration of inflammatory cells were higher, but cardiac output and creatinine clearance were lower in hypertensive rats (

Indexed as

HypertensionInsulin ResistanceAnimalsBenzhydryl CompoundsCreatinineDiet, High-FatGlucoseLeptinRatsSodium-Glucose Transporter 2Soluble Guanylyl CyclaseTriglyceridesBenzhydryl CompoundsCreatinineGlucoseLeptinSodium-Glucose Transporter 2Soluble Guanylyl CyclaseTriglycerideshigh-fat diethypertensioninsulin resistancesGC stimulationSGLT2 inhibition

Identifiers

PMID35119333
PMCPMC8917931
OpenAlexW4210792865

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.