Evidence map›Paper›PMID 31907336›Full record

ArticleAging2020

Spermidine alleviates cardiac aging by improving mitochondrial biogenesis and function.

Junying Wang, Shaoqi Li, Ju Wang, Feixiang Wu, Yuhan Chen, Hao Zhang, Yubo Guo, Yan Lin, Lingxu Li, Xue Yu and 2 more

Open access · greenAbstract read
In one paragraph

Article in Aging, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed
5.2field-weighted citation impact, top 3% 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

72 citing papers in PubMed, 103 citations in OpenAlex.

  1. Article
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  11. Review
  12. Metabolic Regulation of Cardiovascular Aging.Current cardiology reports · 2025
    Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Spermidine enhances the heat tolerance ofApplied and environmental microbiology · 2025
    Article
  18. Article
  19. Review
  20. Article

12 more citing papers are in PubMed but not listed here.

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

12 authors at 4 institutions in 1 country.

Junying WangDepartment of Pathophysiology, Harbin Medical University, Harbin, China.
Shaoqi LiDepartment of Pathophysiology, Harbin Medical University, Harbin, China.
Ju WangDepartment of Pathophysiology, Harbin Medical University, Harbin, China.
Feixiang WuDepartment of Pathophysiology, Harbin Medical University, Harbin, China.
Yuhan ChenDepartment of Pathophysiology, Harbin Medical University, Harbin, China.
Hao ZhangDepartment of Pathophysiology, Harbin Medical University, Harbin, China.
Yubo GuoThe Second Affiliated Hospital of Harbin Medical University, Harbin, China.
Yan LinDepartment of Pathophysiology, Qiqihar Medical University, Qiqihar, Heilongjiang, China.
Lingxu LiDepartment of Pathophysiology, Harbin Medical University, Harbin, China.
Xue YuDepartment of Pathophysiology, Harbin Medical University, Harbin, China.
Ting LiuDepartment of Pathophysiology, Harbin Medical University, Harbin, China.
Yajun ZhaoDepartment of Pathophysiology, Harbin Medical University, Harbin, China.
Harbin Medical University · CNAffiliated Hospital of Hebei University · CNBeijing Health Vocational College · CNQiqihar Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Polyamines have been shown to delay cellular and organismal aging and to provide cardiovascular protection in humans. Because age-related cardiovascular dysfunction is often accompanied by impaired mitochondrial biogenesis and function, we explored the ability of spermidine (SPD), a major mammalian polyamine, to attenuate cardiac aging through activation of mitochondrial biogenesis. Cardiac polyamine levels were reduced in aged (24-month-old) rats. Six-week SPD supplementation restored cardiac polyamine content, preserved myocardial ultrastructure, and inhibited mitochondrial dysfunction. Immunoblotting showed that ornithine decarboxylase (ODC) and SPD/spermine N1-acetyltransferase (SSAT) were downregulated and upregulated, respectively, in the myocardium of older rats. These changes were paralleled by age-dependent downregulation of components of the sirtuin-1/peroxisome proliferator-activated receptor gamma coactivator alpha (SIRT1/PGC-1α) signaling pathway, an important regulator of mitochondrial biogenesis. SPD administration increased SIRT1, PGC-1α, nuclear respiratory factors 1 and 2 (NRF1, NRF2), and mitochondrial transcription factor A (TFAM) expression; decreased ROS production; and improved OXPHOS performance in senescent (H

Indexed as

Cellular SenescenceOrganelle BiogenesisAnimalsBiomarkersHydrogen PeroxideMitochondriaMyocytes, CardiacPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaPolyaminesProtein TransportRatsReactive Oxygen SpeciesSignal TransductionSirtuin 1SpermidineBiomarkersHydrogen PeroxidePeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaPolyaminesReactive Oxygen SpeciesSirtuin 1Spermidinemitochondrial biogenesisPGC-1αpolyamine metabolismSIRT1spermidine

Identifiers

PMID31907336
PMCPMC6977682
OpenAlexW2999558194

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.