Evidence mapPaperPMID 37629047Full record

ReviewInternational journal of molecular sciences2023

New Therapeutics for Heart Failure: Focusing on cGMP Signaling.

Supachoke Mangmool, Ratchanee Duangrat, Warisara Parichatikanond, Hitoshi Kurose

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 10% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Systemic sclerosis, main culprits and involved signaling pathways.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2025
    Review
  4. Article
  5. Promoting proteostasis by cAMP/PKA and cGMP/PKG.Trends in molecular medicine · 2025
    Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. Review
  11. Adenosine AInternational journal of molecular sciences · 2024
    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

4 authors at 2 institutions in 2 countries.

Supachoke MangmoolDepartment of Pharmacology, Faculty of Science, Mahidol University, Bangkok 10400, Thailand.ORCID 0000-0003-3223-1551
Ratchanee DuangratDepartment of Pharmacology, Faculty of Science, Mahidol University, Bangkok 10400, Thailand.
Warisara ParichatikanondDepartment of Pharmacology, Faculty of Pharmacy, Mahidol University, Bangkok 10400, Thailand.ORCID 0000-0001-7851-2477
Hitoshi KurosePharmacology for Life Sciences, Graduate School of Pharmaceutical Sciences, Tokushima University, Tokushima 770-8505, Japan.
Mahidol University · THTokushima University · JP

Funding

Japan Society for the Promotion of Science 22K06646
6 · The paper itself

Abstract

Current drugs for treating heart failure (HF), for example, angiotensin II receptor blockers and β-blockers, possess specific target molecules involved in the regulation of the cardiac circulatory system. However, most clinically approved drugs are effective in the treatment of HF with reduced ejection fraction (HFrEF). Novel drug classes, including angiotensin receptor blocker/neprilysin inhibitor (ARNI), sodium-glucose co-transporter-2 (SGLT2) inhibitor, hyperpolarization-activated cyclic nucleotide-gated (HCN) channel blocker, soluble guanylyl cyclase (sGC) stimulator/activator, and cardiac myosin activator, have recently been introduced for HF intervention based on their proposed novel mechanisms. SGLT2 inhibitors have been shown to be effective not only for HFrEF but also for HF with preserved ejection fraction (HFpEF). In the myocardium, excess cyclic adenosine monophosphate (cAMP) stimulation has detrimental effects on HFrEF, whereas cyclic guanosine monophosphate (cGMP) signaling inhibits cAMP-mediated responses. Thus, molecules participating in cGMP signaling are promising targets of novel drugs for HF. In this review, we summarize molecular pathways of cGMP signaling and clinical trials of emerging drug classes targeting cGMP signaling in the treatment of HF.

Indexed as

Heart FailureSodium-Glucose Transporter 2 InhibitorsAngiotensin Receptor AntagonistsCalcium Channel BlockersCyclic AMPCyclic GMPHeartHumansMyocardiumStroke VolumeVasodilator AgentsAngiotensin Receptor AntagonistsCalcium Channel BlockersCyclic AMPCyclic GMPSodium-Glucose Transporter 2 InhibitorsVasodilator Agentscyclic guanosine monophosphate (cGMP) signalingdrugsheart failure (HF)natriuretic peptidessoluble guanylyl cyclase (sGC)

Identifiers

PMID37629047
PMCPMC10454066
OpenAlexW4385877311

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.