Evidence map›Paper›PMID 41746444›Full record

ArticleMolecular biology reports2026

Cardiac drug potential: exploring individual and combined cardiac drugs to promote differentiation of adipose-derived stem cells into cardiomyocytes.

Hessah Alshammari, Jawahir Abuhaimed, Seham Alshehri, Abdulaziz Siyal, Sameerah Shaheen, Sara Abou Al-Saud

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Article in Molecular biology reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Hessah AlshammariDepartment of Anatomy and Stem Cell Unit, College of medicine, King Saud University, Riyadh, Saudi Arabia. healshammari@ksu.edu.sa.ORCID http://orcid.org/0000-0001-9366-7776
Jawahir AbuhaimedCollege of Medicine, Alfaisal University, Riyadh, Saudi Arabia.
Seham AlshehriDepartment of Anatomy and Stem Cell Unit, College of medicine, King Saud University, Riyadh, Saudi Arabia.
Abdulaziz SiyalDepartment of Anatomy and Stem Cell Unit, College of medicine, King Saud University, Riyadh, Saudi Arabia.
Sameerah ShaheenDepartment of Anatomy and Stem Cell Unit, College of medicine, King Saud University, Riyadh, Saudi Arabia.
Sara Abou Al-SaudCardiac Sciences Department, College of medicine, King Saud University, Riyadh, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundStem cell–based cardiac regenerative medicine holds significant promise for regenerating damaged cardiomyocyte by cardiomyocyte differentiation. Among stem cell types, adipose-derived stem cells (ADSCs) are the most extensively studied due to their ease of isolation and expansion, yet current differentiation protocols remain inefficient and poorly reproducible. Given the well-established roles of certain cardiac drugs—such as Salbutamol, Ivabradine, and Entresto—their potential influence on the regulation of cardiomyocyte differentiation may provide a valuable foundation for advancing differentiation protocols. This study investigates the potential of clinically approved cardiac drugs to enhance ADSC differentiation into cardiomyocytes. 

methodsADSCs were isolated from adipose tissue after liposuction surgery from healthy female patients (n = 6, age 23–40 year) using enzymatic methods. ADSCs at early passages (2–3) were treated with Salbutamol, Ivabradine, or Entresto for 21 days. Subsequently, RT-PCR was performed for pluripotency markers (OCT4, NANOG, and SOX2) and cardiac-specific genes (GATA4, NKX2.5, cTNNI, α-MHC).

resultTreatment of ADSCs with each cardiac drug independently led to downregulation of pluripotency-markers compared to controls which indicate a loss of stemness. This was accompanied by increased expression of some early cardiomyocyte markers and slight increase in late cardiomyocyte markers expression, indicating commitment toward cardiac lineage commitment. In light of these results, a combination of these drugs have improved the differentiation of ADSCs into cardiomyocytes and significantly increase gene expression of early cardiomyocyte markers and late cardiomyocyte markers.

conclusionClinically approved cardiac drugs promote ADSC differentiation toward the cardiomyocyte lineage, offering a novel and safe approach for cardiac regenerative medicine.

Indexed as

Adipose TissueCardiovascular AgentsCell DifferentiationMyocytes, CardiacStem CellsAdultAlbuterolCells, CulturedFemaleHumansIvabradineRegenerative MedicineAlbuterolCardiovascular AgentsIvabradineAdipose-derived stem cellsCardiac regenerationCardiomyocyte differentiationEntrestoIvabradineSalbutamolStem cells therapy

Identifiers

PMID41746444
PMCPMC12945984

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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.