Evidence map›Paper›PMID 38041171›Full record

ArticleBiological research2023

Melatonin alleviates pyroptosis by regulating the SIRT3/FOXO3α/ROS axis and interacting with apoptosis in Atherosclerosis progression.

Lin Cong, Xiankun Liu, Yiming Bai, Qin Qin, Lili Zhao, Ying Shi, Yunpeng Bai, Zhigang Guo

Open access · goldAbstract read
In one paragraph

Article in Biological research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

26 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Review
  16. Article
  17. Macrophage pyroptosis in atherosclerosis: therapeutic potential.Acta biochimica et biophysica Sinica · 2025
    Review
  18. Article
  19. Roles of SIRT3 in aging and aging-related diseases.International journal of biological sciences · 2025
    Review
  20. 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

8 authors at 3 institutions in 1 country.

Lin CongAcademy of Medical Engineering and Translational Medicine, Tianjin University, Tianjin, China.
Xiankun LiuTianjin Institute of Cardiovascular Diseases, Chest Hospital, Tianjin University, Tianjin, China.
Yiming BaiTianjin Institute of Cardiovascular Diseases, Chest Hospital, Tianjin University, Tianjin, China.
Qin QinTianjin Institute of Cardiovascular Diseases, Chest Hospital, Tianjin University, Tianjin, China.
Lili ZhaoTianjin Institute of Cardiovascular Diseases, Chest Hospital, Tianjin University, Tianjin, China.
Ying ShiTianjin Institute of Cardiovascular Diseases, Chest Hospital, Tianjin University, Tianjin, China.
Yunpeng BaiDepartment of Cardiac Surgery, Chest Hospital, Tianjin University, Tianjin, China. oliverwhite@126.com.
Zhigang GuoAcademy of Medical Engineering and Translational Medicine, Tianjin University, Tianjin, China. zhigangguo2022@126.com.
Tianjin University · CNTianjin Chest Hospital · CNTianjin Municipal Education Commission · CN

Funding

Natural Fund Project of Tianjin Science and Technology Bureau 20JCZDJC00810Scientific Research Project of Integrated Traditional Chinese and Western Medicine of Tianjin Health Commission 2021204Tianjin Key Medical Discipline (Specialty) Construction Project TJYXZDXK-042A
6 · The paper itself

Abstract

backgroundAtherosclerosis (AS), a significant contributor to cardiovascular disease (CVD), is steadily rising with the aging of the global population. Pyroptosis and apoptosis, both caspase-mediated cell death mechanisms, play an essential role in the occurrence and progression of AS. The human pineal gland primarily produces melatonin (MT), an indoleamine hormone with powerful anti-oxidative, anti-pyroptotic, and anti-apoptotic properties. This study examined MT's anti-oxidative stress and anti-pyroptotic effects on human THP-1 macrophages treated with nicotine.

methodsIn vitro, THP-1 macrophages were induced by 1 µM nicotine to form a pyroptosis model and performed 30 mM MT for treatment. In vivo, ApoE

resultsMT downregulated pyroptosis, whose changes were paralleled by a reduction in reactive oxygen species (ROS) production, reversal of sirtuin3 (SIRT3), and Forkhead box O3 (FOXO3α) upregulation. MT also inhibited apoptosis, mainly caused by the interaction of caspase-1 and caspase-3 proteins. Vivo studies confirmed that nicotine could accelerate plaque formation. Moreover, mice treated with MT showed a reduction in AS lesion area.

conclusionsMT alleviates pyroptosis by regulating the SIRT3/FOXO3α/ROS axis and interacting with apoptosis. Importantly, our understanding of the inhibitory pathways for macrophage pyroptosis will allow us to identify other novel therapeutic targets that will help treat, prevent, and reduce AS-associated mortality.

Indexed as

AtherosclerosisMelatoninSirtuin 3AnimalsApoptosisCaspasesHumansMiceNicotinePyroptosisReactive Oxygen SpeciesCaspasesMelatoninNicotineReactive Oxygen SpeciesSIRT3 protein, humanSirtuin 3ApoptosisAtherosclerosis (AS)Melatonin (MT)PyroptosisSIRT3/FOXO3α/ROS axis

Identifiers

PMID38041171
PMCPMC10693060
OpenAlexW4389258137

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.