Evidence map›Paper›PMID 39940062›Full record

ArticleJournal of pineal research2025

Diurnal Variation in Melatonin-Mediated Cardiac Protection via Per2 Expression in Heart.

Ronghao Luo, Zebin Yang, Wanshi Liang, Yifei Chen, Yinhong Jie, Yang Zhang, Le Li

Abstract read
In one paragraph

Article in Journal of pineal research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
–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 synthesis or guideline pooled it.

  1. Pooled it
  2. Light therapy in medicine: where do we stand?Annals of translational medicine · 2026
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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

7 authors.

Ronghao LuoDepartment of Anesthesiology, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Zebin YangDepartment of Anesthesiology, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Wanshi LiangDepartment of Anesthesiology, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Yifei Chen
Yinhong Jie
Yang ZhangDivision of Orthopaedic Surgery, Department of Orthopaedics, Southern Medical University, Nanfang Hospital, Guangzhou, China.
Le LiDepartment of Anesthesiology, Zhujiang Hospital, Southern Medical University, Guangzhou, China.ORCID https://orcid.org/0000-0002-4999-2288

Funding

This research was supported by grants from the National Natural Science Foundation of China (No.82171357), the Natural Science Foundation of Guangdong Province (No.2022A1515011021), Science and Technology Program of Guangzhou (No. 202201011348) and the President Foundation of Zhujiang Hospital, Southern Medical University(yzjj2022rc06).
6 · The paper itself

Abstract

Myocardial ischemia/reperfusion (MIR) injury, a primary cause of mortality in acute myocardial infarction, exhibits diurnal variation associated with disruptions in diurnal rhythm. Melatonin (MLT), a potent antioxidant known for its cardioprotective properties, also demonstrates diurnal rhythmicity. This study aimed to investigate the time-dependent cardioprotective effects of MLT in MIR and to clarify the role of the circadian gene Per2 in mediating these effects. Using in vivo (mice) and in vitro (H9c2 cardiomyocytes) models of MIR, we administered MLT at two distinct diurnal time points: ZT1 and ZT13. We evaluated infarct size, cardiac function, apoptosis, and the expression levels of Per2 and other circadian genes. Pretreatment with MLT at ZT13 significantly reduced infarct size and enhanced cardiac function compared to ZT1 administration. This time-dependent cardioprotective effect correlated with the diurnal expression pattern of Per2, which was notably augmented by dark phase administration of MLT without phase alteration. Crucially, Per2 knockdown in both models abrogated the cardioprotective effects of MLT. Our findings underscore that MLT confers superior cardioprotection against MIR injury when administered at dark phase, aligning with the circadian variation of Per2 expression. These effects reveal the therapeutic potential of targeting the MLT-Per2 axis in chronotherapy to mitigate MIR injury.

Indexed as

Cardiotonic AgentsCircadian RhythmGene Expression RegulationMelatoninMyocardial Reperfusion InjuryMyocardiumMyocytes, CardiacPeriod Circadian ProteinsAnimalsCell LineMaleMiceMice, Inbred C57BLRatsCardiotonic AgentsMelatoninPer2 protein, mousePeriod Circadian Proteinsdiurnal variationmelatoninmyocardial ischemia/reperfusionPer2

Identifiers

PMID39940062
PMCPMC11822080

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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.