Evidence map›Paper›PMID 38617797›Full record

ArticleInternational journal of nanomedicine2024

Carbon Dots Derived from

Liyang Dong, Yafang Zhao, Juan Luo, Xiaopeng Li, Shuxian Wang, Menghan Li, Peng Zou, Hui Kong, Qingguo Wang, Yan Zhao and 1 more

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Exploring the Cardioprotective Potential ofCardiovascular & hematological disorders drug targets · 2026
    Article
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  4. Article
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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

11 authors at 1 institution in 1 country.

Liyang Dong *School of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, People's Republic of China.
Yafang Zhao *School of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, People's Republic of China.
Juan LuoSchool of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, People's Republic of China.
Xiaopeng LiSchool of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, People's Republic of China.
Shuxian WangSchool of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, People's Republic of China.
Menghan LiSchool of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, People's Republic of China.
Peng ZouSchool of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, People's Republic of China.
Hui KongSchool of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, People's Republic of China.ORCID 0000-0002-1382-7985
Qingguo WangSchool of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, People's Republic of China.
Yan ZhaoSchool of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, People's Republic of China.
Huihua QuSchool of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, People's Republic of China.
Beijing University of Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Acute myocardial infarction (AMI) is a common cardiovascular disease in clinic. Currently, there is no specific treatment for AMI. Carbon dots (CDs) have been reported to show excellent biological activities, which hold promise for the development of novel nanomedicines for the treatment of cardiovascular diseases. Methods: In this study, we firstly prepared CDs from the natural herb Results: The results showed that pretreatment with CRC-CDs significantly reduced serum levels of cardiac enzymes (CK-MB, LDH, AST) and lipids (TC, TG, LDL) and reduced st-segment elevation and myocardial infarct size on the ECG in AMI rats. Importantly, cardiac ejection fraction (EF) and shortening fraction (FS) were markedly elevated, as was ATPase activity. In addition, CRC-CDs could significantly increase the levels of superoxide dismutase (SOD), reduced glutathione (GSH), catalase (CAT), and reduce the levels of malondialdehyde (MDA) and reactive oxygen species (ROS) in myocardial tissue, thereby exerting cardioprotective effect by enhancing the antioxidant capacity of myocardial tissue. Moreover, the TUNEL staining image showed that positive apoptotic cells were markedly declined after CRC-CDs treatment, which indicate that CRC-CDs could inhibit cardiomyocyte apoptosis. Importantly, The protective effect of CRC-CDs on H Conclusion: Taken together, CRC-CDs has the potential for clinical application as an anti-myocardial ischemia drug candidate, which not only provides evidence for further broadening the biological application of cardiovascular diseases, but also offers potential hope for the application of nanomedicine to treat intractable diseases.

Indexed as

Myocardial InfarctionMyocardial IschemiaAnimalsCarbonHydrogen PeroxideMyocardiumRatsCarbonHydrogen Peroxideacute myocardial infarctioncarbon dotsCurcumae Radix Carbonisataoxidative stress

Identifiers

PMID38617797
PMCPMC11012788
OpenAlexW4394575861

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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 OpenQuestion graph.