Evidence mapPaperPMID 41080652Full record

ReviewBiomaterials research2025

Nitric Oxide in Biomaterial-Based Therapies for Coronary Heart Disease: Mechanistic Insights, Current Advances, and Translational Prospects.

Jinpeng Sun, Zhiwen Wang, Yang Sun, Jiahui Zhang, Fangyuan Zhang, Junran Tong, Ran Gao, Xiaopeng Guo, Di Sun, Yumiao Wei

Abstract readReview
In one paragraph

Review in Biomaterials research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Hydrogen Radical-Mediated Nitric Oxide Reduction to Ammonia Over Synergistic PdAngewandte Chemie (International ed. in English) · 2026
    Article
  2. Isosakuranetin ameliorates hypertension in rats induced by L-NAME.Journal of pharmaceutical health care and sciences · 2025
    Article
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.

Jinpeng SunDepartment of Cardiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China.ORCID https://orcid.org/0009-0009-5350-6033
Zhiwen WangDepartment of Nephrology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China.
Yang SunDepartment of Medical Records Management and Statistics, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China.
Jiahui ZhangDepartment of Cardiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China.
Fangyuan ZhangSchool of Education, University of Nottingham, Nottingham, UK.
Junran TongDepartment of Cardiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China.
Ran GaoDepartment of Cardiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China.
Xiaopeng GuoDepartment of Radiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China.
Di SunDepartment of Plastic Surgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China.
Yumiao WeiDepartment of Cardiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China.ORCID https://orcid.org/0000-0001-8737-2699

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Coronary heart disease (CHD) remains a leading etiology of cardiovascular mortality globally. Endothelial dysfunction is now well-documented as the incipient pathological event in coronary atherosclerosis, with endogenous nitric oxide (NO) and nitric oxide synthase playing pivotal roles in regulating endothelial homeostasis via diverse signaling cascades. Over the past several decades, the pleiotropic functions of NO in cardiovascular physiology and pathophysiology have sparked substantial research interest in leveraging exogenous NO delivery strategies for atherosclerotic interventions. Beyond conventional NO-based pharmacotherapies, notable advancements have been achieved in the development of NO-releasing platforms and donor systems capable of spatiotemporally controlled and sustained NO delivery to target vascular tissues. This comprehensive review synthesizes current understanding of (a) the dual roles of endogenous NO in maintaining cardiovascular health and mediating pathological processes, (b) the enzymatic regulation of NO biosynthesis and its downstream signaling networks, and (c) the emerging translational potential of NO-based biomaterials in atherosclerotic management. Particular emphasis is placed on evaluating novel NO-donor systems and bioengineered constructs that exhibit therapeutic efficacy in preclinical models. Collectively, this analysis underscores the critical importance of NO-based biomaterials in advancing precision medicine approaches for CHDs, with implications for both diagnostic innovation and therapeutic optimization.

Identifiers

PMID41080652
PMCPMC12509227

What Socratic holds

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LicenceCC BY
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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.