Evidence map›Paper›PMID 42625289›Full record

ArticleJournal of cellular and molecular medicine2026

Corylin Confers Vasoprotection via JDP2-Nrf2 Antioxidant Axis against Chronic Kidney Disease-Induced Smooth Muscle Cell Remodelling.

Shang-En Huang, Chih-Le Lin, Kazunari K Yokoyama, Kai-Fang Hu, Bin-Nan Wu, Zen-Kong Dai, Meng-Xuan Lin, Yu-Hsin Tseng, Jong-Hau Hsu, Jwu-Lai Yeh

Abstract read
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Article in Journal of cellular and molecular medicine, 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

10 authors.

Shang-En HuangDepartment of Seafood Science, National Kaohsiung University of Science and Technology, Kaohsiung, Taiwan.ORCID 0000-0003-2324-9178
Chih-Le LinSchool of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan.
Kazunari K YokoyamaCell Therapy and Research Center, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan.ORCID 0000-0001-8508-7587
Kai-Fang HuDepartment of Dentistry, Division of Periodontics, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan.ORCID 0000-0001-8080-0339
Bin-Nan WuDepartment of Pharmacology, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan.ORCID 0000-0001-6593-5120
Zen-Kong DaiDepartment of Pediatrics, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan.
Meng-Xuan LinDepartment of Pharmacology, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan.
Yu-Hsin TsengDepartment of Pediatrics, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan.ORCID 0000-0002-2558-2209
Jong-Hau HsuDepartment of Pediatrics, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan.ORCID 0000-0002-2690-7247
Jwu-Lai YehDepartment of Pharmacology, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan.ORCID 0000-0001-7101-5865

Funding

Kaohsiung Medical University KMU-DK(N)115004 (JL Yeh)Kaohsiung Medical University KMU-TB114009-2 (JL Yeh)Kaohsiung Medical University Chung-Ho Memorial Hospital KMUH 114-4R48 (JH Hsu)National Science and Technology Council MOST 111-2314-B-037-075-MY3 (JH Hsu)National Science and Technology Council NSTC 112-2320-B-037-019-MY3 (JL Yeh)National Science and Technology Council NSTC 115-2320-B-992-001 (SE Huang)
6 · The paper itself

Abstract

Vascular calcification is a pathological process involving vascular smooth muscle cells (VSMCs) phenotypic switching into osteoblast-like cells within a calcium phosphate-deposited environment. This transformation is a critical risk factor for cardiovascular morbidity and mortality in patients with hyperphosphatemia due to chronic kidney disease. Corylin, a major compound derived from the Chinese medicine herb Psoralea corylifolia, is beneficial for the cardiovascular system. However, its role in modulating VSMC phenotypic switching and calcification remains to be elucidated. A vascular calcification rat model induced by vitamin D3 plus nicotine (VDN) was established to evaluate the therapeutic effects of corylin. The protective effects of corylin were evaluated in high phosphate-induced vessels and VSMCs using cytotoxicity assay, Alizarin red S staining, alkaline phosphatase staining, immunofluorescence, Western blot analysis, and qPCR. The interaction between Jun dimerisation protein 2 (JDP2) and Nrf2 was analysed using a ChIP-qPCR assay. Corylin treatment ameliorated arteriosclerotic lesions and oxidative stress in rats treated with VDN. We also observed that the cytoprotective effects of corylin prevented VSMC apoptosis and deposition of calcium phosphates. Additionally, corylin decreased calcium overload by inhibiting calcineurin and maintaining mitochondrial homeostasis. We identified a robust co-induction of JDP2 and Nrf2 in corylin-treated VSMCs, which contributed to reducing phenotypic switching and abrogating oxidative stress. Furthermore, Nrf2 knockdown by an inhibitor abolished JDP2 activation and the protective effects of corylin. Our study reveals that corylin exerts anti-arteriosclerotic and vasculoprotective effects targeting JDP2-Nrf2 activation, making it a potential treatment for vascular calcification.

Indexed as

AntioxidantsFlavonoidsMyocytes, Smooth MuscleNF-E2-Related Factor 2Renal Insufficiency, ChronicAnimalsApoptosisDisease Models, AnimalMaleMuscle, Smooth, VascularOxidative StressRatsRats, Sprague-DawleySignal TransductionVascular CalcificationAntioxidantscorylinFlavonoidsNF-E2-Related Factor 2corylinJDP2oxidative stressvascular calcificationVSMC phenotypic switching

Identifiers

PMID42625289
PMCPMC13494144

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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.