Evidence mapPaperPMID 38980593Full record

ReviewMolecular and cellular biochemistry2025

Insight into the cardioprotective effects of melatonin: shining a spotlight on intercellular Sirt signaling communication.

Alireza Yaghoobi, Malihe Rezaee, Neda Hedayati, Atoosa Keshavarzmotamed, Mohammad Amin Khalilzad, Reitel Russel, Zatollah Asemi, Hasan Rajabi Moghadam, Alireza Mafi

Abstract readReview
PubMed Publisher
In one paragraph

Review in Molecular and cellular biochemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Melatonin and angiogenesis potential in stem cells.Stem cell research & therapy · 2025
    Review
  5. Review
  6. 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

9 authors.

Alireza Yaghoobi *School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Malihe Rezaee *School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Neda Hedayati *School of Medicine, Iran University of Medical Science, Tehran, Iran.
Atoosa KeshavarzmotamedStudent Research Committee, Guilan University of Medical Sciences, Rasht, Iran.
Mohammad Amin KhalilzadSchool of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Reitel RusselDepartment of Cell Systems and Anatomy, UT Health. Long School of Medicine, San Antonio, TX, USA. reiter@uthscsa.edu.
Zatollah AsemiResearch Center for Biochemistry and Nutrition in Metabolic Diseases, Institute for Basic Sciences, Kashan University of Medical Sciences, Kashan, Iran. asemi_r@yahoo.com.ORCID http://orcid.org/0000-0001-5265-4792
Hasan Rajabi MoghadamDepartment of Cardiology, Faculty of Medicine, Kashan University of Medical Sciences, Kashan, Iran.
Alireza MafiDepartment of Clinical Biochemistry, School of Pharmacy and Pharmaceutical Sciences, Isfahan University of Medical Sciences, Isfahan, Iran. armafi.m@gmail.com.ORCID http://orcid.org/0000-0002-9485-0326

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cardiovascular diseases (CVDs) are the leading causes of death and illness worldwide. While there have been advancements in the treatment of CVDs using medication and medical procedures, these conventional methods have limited effectiveness in halting the progression of heart diseases to complete heart failure. However, in recent years, the hormone melatonin has shown promise as a protective agent for the heart. Melatonin, which is secreted by the pineal gland and regulates our sleep-wake cycle, plays a role in various biological processes including oxidative stress, mitochondrial function, and cell death. The Sirtuin (Sirt) family of proteins has gained attention for their involvement in many cellular functions related to heart health. It has been well established that melatonin activates the Sirt signaling pathways, leading to several beneficial effects on the heart. These include preserving mitochondrial function, reducing oxidative stress, decreasing inflammation, preventing cell death, and regulating autophagy in cardiac cells. Therefore, melatonin could play crucial roles in ameliorating various cardiovascular pathologies, such as sepsis, drug toxicity-induced myocardial injury, myocardial ischemia-reperfusion injury, hypertension, heart failure, and diabetic cardiomyopathy. These effects may be partly attributed to the modulation of different Sirt family members by melatonin. This review summarizes the existing body of literature highlighting the cardioprotective effects of melatonin, specifically the ones including modulation of Sirt signaling pathways. Also, we discuss the potential use of melatonin-Sirt interactions as a forthcoming therapeutic target for managing and preventing CVDs.

Indexed as

Cardiotonic AgentsCardiovascular DiseasesMelatoninSignal TransductionSirtuinsAnimalsHumansOxidative StressCardiotonic AgentsMelatoninSirtuinsApoptosisCardiovascular diseaseInflammationMelatoninMelatonin receptorMyocardial ischemia/reperfusionOxidative stressSirtuinTranslational medicine

Identifiers

PMID38980593

What Socratic holds

Textmetadata
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 Socratic graph.