Evidence map›Paper›PMID 40897766›Full record

ArticleScientific reports2025

Klotho protein alleviates heart ischemia/reperfusion injury and oxidative stress through regulation of the NOS/MMP pathway.

Agnieszka Olejnik, Anna Krzywonos-Zawadzka, Izabela Sambor, Andrzej Mysiak, Iwona Bil-Lula

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

5 authors.

Agnieszka OlejnikDivision of Clinical Chemistry and Laboratory Haematology, Department of Medical Laboratory Diagnostics, Faculty of Pharmacy, Wroclaw Medical University, Borowska 211A St., 50-556, Wrocław, Poland. agnieszka.olejnik@umw.edu.pl.ORCID http://orcid.org/0000-0001-5130-7609
Anna Krzywonos-ZawadzkaDivision of Clinical Chemistry and Laboratory Haematology, Department of Medical Laboratory Diagnostics, Faculty of Pharmacy, Wroclaw Medical University, Borowska 211A St., 50-556, Wrocław, Poland.ORCID http://orcid.org/0000-0003-3534-7306
Izabela SamborDepartment of Biochemistry and Molecular Biology, Wroclaw University of Environmental and Life Sciences, Wrocław, Poland.
Andrzej MysiakInstitute of Heart Diseases, Wroclaw Medical University, Wrocław, Poland.ORCID http://orcid.org/0000-0002-4728-2565
Iwona Bil-LulaDivision of Clinical Chemistry and Laboratory Haematology, Department of Medical Laboratory Diagnostics, Faculty of Pharmacy, Wroclaw Medical University, Borowska 211A St., 50-556, Wrocław, Poland.ORCID http://orcid.org/0000-0002-2769-0166

Funding

National Science Centre Poland 2019/33/N/NZ3/01649
6 · The paper itself

Abstract

Heart ischemia/reperfusion injury (IRI) significantly contributes to cardiac damage through oxidative and nitrosative stress, where the dysregulation of nitric oxide synthases (NOS) and the subsequent activation of matrix metalloproteinases (MMPs) are observed. Klotho is a multifunctional protein crucial in ageing, metabolism, and ion homeostasis. It has been confirmed that Klotho serves as a critical protective factor across multiple biological systems, with its roles in neuroprotection, cardiovascular health, and renal function being particularly noteworthy. This study aimed to investigate the protective role of Klotho protein against oxidative and nitrosative stress in heart IRI through regulation of the NOS/MMP pathway. The study utilised in vitro human cardiomyocyte culture and ex vivo isolated rat hearts subjected to IRI. Recombinant Klotho protein was administered to evaluate its effects on heart mechanical function, gene and protein expression of NOS isoforms, oxidative and nitrosative stress markers, MMP activity, and lipid metabolism. Administration of Klotho significantly improved heart mechanical and contractile function following ischemia/reperfusion. Klotho normalised the expression and synthesis of endothelial NOS and inducible NOS, resulting in reduced production of reactive nitrogen species and attenuated nitrosative stress. It also limited oxidative damage, reflected by decreased protein oxidation, and restored fatty acid metabolism. Additionally, Klotho regulated MMP-2 and MMP-9 synthesis and activity, thereby protecting heart contractile proteins from degradation. The Klotho protein exhibits significant cardioprotection in IRI by mitigating oxidative and nitrosative stress through the modulation of the NOS/MMP signalling pathway. These findings highlight the therapeutic potential of Klotho in managing ischemic heart conditions and myocardial injury.

Indexed as

GlucuronidaseMatrix MetalloproteinasesMyocardial Reperfusion InjuryNitric Oxide SynthaseOxidative StressAnimalsHumansKlotho ProteinsMaleMyocytes, CardiacNitrosative StressRatsSignal TransductionGlucuronidaseKlotho ProteinsKL protein, humanMatrix MetalloproteinasesNitric Oxide Synthase

Identifiers

PMID40897766
PMCPMC12405471

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Registered trials

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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.