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Study · Animal study (in vivo) · mouse · 2026

24 results

Nicotinamide Mononucleotide Improves High-Fat Diet-Induced Myocardial Damage of Aging Mice through the Sirt3/PINK1/Parkin Signaling Pathway.

Wen X, Chen YN, Han YC, Wang JP, Dong WH, Wang ZP, Wang T, Xiong ZE

The Journal of nutrition26 Feb 2026

Summary

The text of this summary is not shown here, because the article license does not allow reuse. Read it at the source (opens in a new tab)

Text rights: Publisher copyright. Results still quote short attributed sentences.

Results from this study24

22 results from studies that gave the peptide. No result from this study comes from people.

  1. 01AnimalAnimal study (in vivo)Efficacy outcome

    In aging mice, NMN reduced heart index compared with the HFD group.

    In plain wordsIn aging mice, NMN reduced heart index compared with the high-fat-diet group.

    Outcome
    DecreaseHeart index
    Study

    mousen: not reported in source

    aging male C57BL/6J mice receiving high-fat diet
    Comparator
    HFD group
    Outcome group
    Heart function · Cardiovascular
    Studied dose
    400 mg/kg · drinking water · 7 moAs given in this study (mouse).

    Source sentences

    Summary
    Compared with the HFD group, NMN treatment significantly reduced the heart index, ameliorated myocardial fibrosis
    1 context sentence
    Summary · context
    Male C57BL/6J mice (14-month-old) were assigned to 3 groups: normal diet, HFD, and HFD + NMN. NMN was added to their drinking water at a dose of 400 mg/kg for 7 mo.
  2. 02AnimalAnimal study (in vivo)Efficacy outcome

    In aging mice, NMN ameliorated myocardial fibrosis compared with the HFD group.

    In plain wordsIn aging mice, NMN reduced heart scarring compared with the high-fat-diet group.

    Outcome
    DecreaseMyocardial fibrosis
    Study

    mousen: not reported in source

    aging male C57BL/6J mice receiving high-fat diet
    Comparator
    HFD group
    Outcome group
    Heart function · Cardiovascular
    Studied dose
    400 mg/kg · drinking water · 7 moAs given in this study (mouse).

    Source sentences

    Summary
    Compared with the HFD group, NMN treatment significantly reduced the heart index, ameliorated myocardial fibrosis
    1 context sentence
    Summary · context
    Male C57BL/6J mice (14-month-old) were assigned to 3 groups: normal diet, HFD, and HFD + NMN. NMN was added to their drinking water at a dose of 400 mg/kg for 7 mo.
  3. 03AnimalAnimal study (in vivo)Mechanism

    In aging mice, NMN decreased cardiac Serpine1 expression compared with the HFD group.

    In plain wordsIn aging mice, NMN reduced heart Serpine1 expression compared with the high-fat-diet group.

    Outcome
    DecreaseSerpine1 expression
    Study

    mousen: not reported in source

    aging male C57BL/6J mice receiving high-fat diet
    Comparator
    HFD group
    Outcome group
    Aging markers · Cardiovascular
    Studied dose
    400 mg/kg · drinking water · 7 moAs given in this study (mouse).

    Source sentences

    Summary
    and decreased the expression concentrations of senescence-associated secretory phenotype markers (Serpine1, MMP3, CXCL-1, CXCL-10, and P16; P < 0.05)
    1 context sentence
    Summary · context
    Male C57BL/6J mice (14-month-old) were assigned to 3 groups: normal diet, HFD, and HFD + NMN. NMN was added to their drinking water at a dose of 400 mg/kg for 7 mo.
  4. 04AnimalAnimal study (in vivo)Mechanism

    In aging mice, NMN decreased cardiac MMP3 expression compared with the HFD group.

    In plain wordsIn aging mice, NMN reduced heart MMP3 expression compared with the high-fat-diet group.

    Outcome
    DecreaseMMP3 expression
    Study

    mousen: not reported in source

    aging male C57BL/6J mice receiving high-fat diet
    Comparator
    HFD group
    Outcome group
    Aging markers · Cardiovascular
    Studied dose
    400 mg/kg · drinking water · 7 moAs given in this study (mouse).

    Source sentences

    Summary
    and decreased the expression concentrations of senescence-associated secretory phenotype markers (Serpine1, MMP3, CXCL-1, CXCL-10, and P16; P < 0.05)
    1 context sentence
    Summary · context
    Male C57BL/6J mice (14-month-old) were assigned to 3 groups: normal diet, HFD, and HFD + NMN. NMN was added to their drinking water at a dose of 400 mg/kg for 7 mo.
  5. 05AnimalAnimal study (in vivo)Mechanism

    In aging mice, NMN decreased cardiac CXCL-1 expression compared with the HFD group.

    In plain wordsIn aging mice, NMN reduced heart CXCL-1 expression compared with the high-fat-diet group.

    Outcome
    DecreaseCXCL-1 expression
    Study

    mousen: not reported in source

    aging male C57BL/6J mice receiving high-fat diet
    Comparator
    HFD group
    Outcome group
    Aging markers · Cardiovascular
    Studied dose
    400 mg/kg · drinking water · 7 moAs given in this study (mouse).

    Source sentences

    Summary
    and decreased the expression concentrations of senescence-associated secretory phenotype markers (Serpine1, MMP3, CXCL-1, CXCL-10, and P16; P < 0.05)
    1 context sentence
    Summary · context
    Male C57BL/6J mice (14-month-old) were assigned to 3 groups: normal diet, HFD, and HFD + NMN. NMN was added to their drinking water at a dose of 400 mg/kg for 7 mo.
  6. 06AnimalAnimal study (in vivo)Mechanism

    In aging mice, NMN decreased cardiac CXCL-10 expression compared with the HFD group.

    In plain wordsIn aging mice, NMN reduced heart CXCL-10 expression compared with the high-fat-diet group.

    Outcome
    DecreaseCXCL-10 expression
    Study

    mousen: not reported in source

    aging male C57BL/6J mice receiving high-fat diet
    Comparator
    HFD group
    Outcome group
    Aging markers · Cardiovascular
    Studied dose
    400 mg/kg · drinking water · 7 moAs given in this study (mouse).

    Source sentences

    Summary
    and decreased the expression concentrations of senescence-associated secretory phenotype markers (Serpine1, MMP3, CXCL-1, CXCL-10, and P16; P < 0.05)
    1 context sentence
    Summary · context
    Male C57BL/6J mice (14-month-old) were assigned to 3 groups: normal diet, HFD, and HFD + NMN. NMN was added to their drinking water at a dose of 400 mg/kg for 7 mo.
  7. 07AnimalAnimal study (in vivo)Mechanism

    In aging mice, NMN decreased cardiac P16 expression compared with the HFD group.

    In plain wordsIn aging mice, NMN reduced heart P16 expression compared with the high-fat-diet group.

    Outcome
    DecreaseP16 expression
    Study

    mousen: not reported in source

    aging male C57BL/6J mice receiving high-fat diet
    Comparator
    HFD group
    Outcome group
    Aging markers · Cardiovascular
    Studied dose
    400 mg/kg · drinking water · 7 moAs given in this study (mouse).

    Source sentences

    Summary
    and decreased the expression concentrations of senescence-associated secretory phenotype markers (Serpine1, MMP3, CXCL-1, CXCL-10, and P16; P < 0.05)
    1 context sentence
    Summary · context
    Male C57BL/6J mice (14-month-old) were assigned to 3 groups: normal diet, HFD, and HFD + NMN. NMN was added to their drinking water at a dose of 400 mg/kg for 7 mo.
  8. 08AnimalAnimal study (in vivo)Mechanism

    In aging mice, NMN decreased cardiac P21 expression compared with the HFD group.

    In plain wordsIn aging mice, NMN reduced heart P21 expression compared with the high-fat-diet group.

    Outcome
    DecreaseP21 expression
    Study

    mousen: not reported in source

    aging male C57BL/6J mice receiving high-fat diet
    Comparator
    HFD group
    Outcome group
    Aging markers · Cardiovascular
    Studied dose
    400 mg/kg · drinking water · 7 moAs given in this study (mouse).

    Source sentences

    Summary
    senescence markers (P21 and β-galactosidase (β-gal); P < 0.01)
    1 context sentence
    Summary · context
    Male C57BL/6J mice (14-month-old) were assigned to 3 groups: normal diet, HFD, and HFD + NMN. NMN was added to their drinking water at a dose of 400 mg/kg for 7 mo.
  9. 09AnimalAnimal study (in vivo)Mechanism

    In aging mice, NMN decreased cardiac β-galactosidase expression compared with the HFD group.

    In plain wordsIn aging mice, NMN reduced heart β-galactosidase expression compared with the high-fat-diet group.

    Outcome
    Decreaseβ-galactosidase expression
    Study

    mousen: not reported in source

    aging male C57BL/6J mice receiving high-fat diet
    Comparator
    HFD group
    Outcome group
    Aging markers · Cardiovascular
    Studied dose
    400 mg/kg · drinking water · 7 moAs given in this study (mouse).

    Source sentences

    Summary
    senescence markers (P21 and β-galactosidase (β-gal); P < 0.01)
    1 context sentence
    Summary · context
    Male C57BL/6J mice (14-month-old) were assigned to 3 groups: normal diet, HFD, and HFD + NMN. NMN was added to their drinking water at a dose of 400 mg/kg for 7 mo.
  10. 10AnimalAnimal study (in vivo)Mechanism

    In aging mice, NMN decreased cardiac IL-1β expression compared with the HFD group.

    In plain wordsIn aging mice, NMN reduced heart IL-1β expression compared with the high-fat-diet group.

    Outcome
    DecreaseIL-1β expression
    Study

    mousen: not reported in source

    aging male C57BL/6J mice receiving high-fat diet
    Comparator
    HFD group
    Outcome group
    Inflammation markers · Cardiovascular
    Studied dose
    400 mg/kg · drinking water · 7 moAs given in this study (mouse).

    Source sentences

    Summary
    proinflammatory cytokines [interleukin (IL)-1β and tumor necrosis factor α; P < 0.05]
    1 context sentence
    Summary · context
    Male C57BL/6J mice (14-month-old) were assigned to 3 groups: normal diet, HFD, and HFD + NMN. NMN was added to their drinking water at a dose of 400 mg/kg for 7 mo.
  11. 11AnimalAnimal study (in vivo)Mechanism

    In aging mice, NMN decreased cardiac tumor necrosis factor α expression compared with the HFD group.

    In plain wordsIn aging mice, NMN reduced heart tumor necrosis factor α compared with the high-fat-diet group.

    Outcome
    DecreaseTNF-α expression
    Study

    mousen: not reported in source

    aging male C57BL/6J mice receiving high-fat diet
    Comparator
    HFD group
    Outcome group
    Inflammation markers · Cardiovascular
    Studied dose
    400 mg/kg · drinking water · 7 moAs given in this study (mouse).

    Source sentences

    Summary
    proinflammatory cytokines [interleukin (IL)-1β and tumor necrosis factor α; P < 0.05]
    1 context sentence
    Summary · context
    Male C57BL/6J mice (14-month-old) were assigned to 3 groups: normal diet, HFD, and HFD + NMN. NMN was added to their drinking water at a dose of 400 mg/kg for 7 mo.
  12. 12AnimalAnimal study (in vivo)Mechanism

    In aging mice, NMN decreased the cardiac Bax/Bcl-2 ratio compared with the HFD group.

    In plain wordsIn aging mice, NMN reduced the heart Bax/Bcl-2 ratio compared with the high-fat-diet group.

    Outcome
    DecreaseBax/Bcl-2 ratio
    Study

    mousen: not reported in source

    aging male C57BL/6J mice receiving high-fat diet
    Comparator
    HFD group
    Outcome group
    Heart function · Cardiovascular
    Studied dose
    400 mg/kg · drinking water · 7 moAs given in this study (mouse).

    Source sentences

    Summary
    and apoptotic indicators (Bax/Bcl-2 ratio and cleaved caspase-3; P < 0.01).
    1 context sentence
    Summary · context
    Male C57BL/6J mice (14-month-old) were assigned to 3 groups: normal diet, HFD, and HFD + NMN. NMN was added to their drinking water at a dose of 400 mg/kg for 7 mo.
  13. 13AnimalAnimal study (in vivo)Mechanism

    In aging mice, NMN decreased cardiac cleaved caspase-3 compared with the HFD group.

    In plain wordsIn aging mice, NMN reduced heart cleaved caspase-3 compared with the high-fat-diet group.

    Outcome
    DecreaseCleaved caspase-3
    Study

    mousen: not reported in source

    aging male C57BL/6J mice receiving high-fat diet
    Comparator
    HFD group
    Outcome group
    Heart function · Cardiovascular
    Studied dose
    400 mg/kg · drinking water · 7 moAs given in this study (mouse).

    Source sentences

    Summary
    and apoptotic indicators (Bax/Bcl-2 ratio and cleaved caspase-3; P < 0.01).
    1 context sentence
    Summary · context
    Male C57BL/6J mice (14-month-old) were assigned to 3 groups: normal diet, HFD, and HFD + NMN. NMN was added to their drinking water at a dose of 400 mg/kg for 7 mo.
  14. 14AnimalAnimal study (in vivo)Mechanism

    In aging mice, NMN increased cardiac IL-10 concentration compared with the HFD group.

    In plain wordsIn aging mice, NMN increased heart IL-10 compared with the high-fat-diet group.

    Outcome
    IncreaseIL-10 concentration
    Study

    mousen: not reported in source

    aging male C57BL/6J mice receiving high-fat diet
    Comparator
    HFD group
    Outcome group
    Inflammation markers · Cardiovascular
    Studied dose
    400 mg/kg · drinking water · 7 moAs given in this study (mouse).

    Source sentences

    Summary
    Conversely, NMN treatment upregulated the concentrations of anti-inflammatory factor IL-10 (P < 0.01) in cardiac tissue.
    1 context sentence
    Summary · context
    Male C57BL/6J mice (14-month-old) were assigned to 3 groups: normal diet, HFD, and HFD + NMN. NMN was added to their drinking water at a dose of 400 mg/kg for 7 mo.
  15. 15AnimalAnimal study (in vivo)Mechanism

    In aging mice, NMN increased cardiac Sirt3 protein concentration compared with the HFD group.

    In plain wordsIn aging mice, NMN increased heart Sirt3 protein compared with the high-fat-diet group.

    Outcome
    IncreaseSirt3 concentration
    Study

    mousen: not reported in source

    aging male C57BL/6J mice receiving high-fat diet
    Comparator
    HFD group
    Outcome group
    Mitochondrial function · Cardiovascular
    Studied dose
    400 mg/kg · drinking water · 7 moAs given in this study (mouse).

    Source sentences

    Summary
    Furthermore, NMN treatment increased protein concentrations of Sirt3, PINK1, and Parkin (P < 0.01), and enhanced autophagy-lysosomal markers, including LC3-II/LC3-I ratio and transcription factor EB (TFEB) (P < 0.05), and decreased p62 concentrations (P < 0.01) in cardiac tissue.
    1 context sentence
    Summary · context
    Male C57BL/6J mice (14-month-old) were assigned to 3 groups: normal diet, HFD, and HFD + NMN. NMN was added to their drinking water at a dose of 400 mg/kg for 7 mo.
  16. 16AnimalAnimal study (in vivo)Mechanism

    In aging mice, NMN increased cardiac PINK1 protein concentration compared with the HFD group.

    In plain wordsIn aging mice, NMN increased heart PINK1 protein compared with the high-fat-diet group.

    Outcome
    IncreasePINK1 concentration
    Study

    mousen: not reported in source

    aging male C57BL/6J mice receiving high-fat diet
    Comparator
    HFD group
    Outcome group
    Mitochondrial function · Cardiovascular
    Studied dose
    400 mg/kg · drinking water · 7 moAs given in this study (mouse).

    Source sentences

    Summary
    Furthermore, NMN treatment increased protein concentrations of Sirt3, PINK1, and Parkin (P < 0.01), and enhanced autophagy-lysosomal markers, including LC3-II/LC3-I ratio and transcription factor EB (TFEB) (P < 0.05), and decreased p62 concentrations (P < 0.01) in cardiac tissue.
    1 context sentence
    Summary · context
    Male C57BL/6J mice (14-month-old) were assigned to 3 groups: normal diet, HFD, and HFD + NMN. NMN was added to their drinking water at a dose of 400 mg/kg for 7 mo.
  17. 17AnimalAnimal study (in vivo)Mechanism

    In aging mice, NMN increased cardiac Parkin protein concentration compared with the HFD group.

    In plain wordsIn aging mice, NMN increased heart Parkin protein compared with the high-fat-diet group.

    Outcome
    IncreaseParkin concentration
    Study

    mousen: not reported in source

    aging male C57BL/6J mice receiving high-fat diet
    Comparator
    HFD group
    Outcome group
    Mitochondrial function · Cardiovascular
    Studied dose
    400 mg/kg · drinking water · 7 moAs given in this study (mouse).

    Source sentences

    Summary
    Furthermore, NMN treatment increased protein concentrations of Sirt3, PINK1, and Parkin (P < 0.01), and enhanced autophagy-lysosomal markers, including LC3-II/LC3-I ratio and transcription factor EB (TFEB) (P < 0.05), and decreased p62 concentrations (P < 0.01) in cardiac tissue.
    1 context sentence
    Summary · context
    Male C57BL/6J mice (14-month-old) were assigned to 3 groups: normal diet, HFD, and HFD + NMN. NMN was added to their drinking water at a dose of 400 mg/kg for 7 mo.
  18. 18AnimalAnimal study (in vivo)Mechanism

    In aging mice, NMN increased the cardiac LC3-II/LC3-I ratio compared with the HFD group.

    In plain wordsIn aging mice, NMN increased the heart LC3-II/LC3-I ratio compared with the high-fat-diet group.

    Outcome
    IncreaseLC3-II/LC3-I ratio
    Study

    mousen: not reported in source

    aging male C57BL/6J mice receiving high-fat diet
    Comparator
    HFD group
    Outcome group
    Mitochondrial function · Cardiovascular
    Studied dose
    400 mg/kg · drinking water · 7 moAs given in this study (mouse).

    Source sentences

    Summary
    Furthermore, NMN treatment increased protein concentrations of Sirt3, PINK1, and Parkin (P < 0.01), and enhanced autophagy-lysosomal markers, including LC3-II/LC3-I ratio and transcription factor EB (TFEB) (P < 0.05), and decreased p62 concentrations (P < 0.01) in cardiac tissue.
    1 context sentence
    Summary · context
    Male C57BL/6J mice (14-month-old) were assigned to 3 groups: normal diet, HFD, and HFD + NMN. NMN was added to their drinking water at a dose of 400 mg/kg for 7 mo.
  19. 19AnimalAnimal study (in vivo)Mechanism

    In aging mice, NMN increased cardiac TFEB concentration compared with the HFD group.

    In plain wordsIn aging mice, NMN increased heart TFEB compared with the high-fat-diet group.

    Outcome
    IncreaseTFEB concentration
    Study

    mousen: not reported in source

    aging male C57BL/6J mice receiving high-fat diet
    Comparator
    HFD group
    Outcome group
    Mitochondrial function · Cardiovascular
    Studied dose
    400 mg/kg · drinking water · 7 moAs given in this study (mouse).

    Source sentences

    Summary
    Furthermore, NMN treatment increased protein concentrations of Sirt3, PINK1, and Parkin (P < 0.01), and enhanced autophagy-lysosomal markers, including LC3-II/LC3-I ratio and transcription factor EB (TFEB) (P < 0.05), and decreased p62 concentrations (P < 0.01) in cardiac tissue.
    1 context sentence
    Summary · context
    Male C57BL/6J mice (14-month-old) were assigned to 3 groups: normal diet, HFD, and HFD + NMN. NMN was added to their drinking water at a dose of 400 mg/kg for 7 mo.
  20. 20AnimalAnimal study (in vivo)Mechanism

    In aging mice, NMN decreased cardiac p62 concentration compared with the HFD group.

    In plain wordsIn aging mice, NMN reduced heart p62 compared with the high-fat-diet group.

    Outcome
    Decreasep62 concentration
    Study

    mousen: not reported in source

    aging male C57BL/6J mice receiving high-fat diet
    Comparator
    HFD group
    Outcome group
    Mitochondrial function · Cardiovascular
    Studied dose
    400 mg/kg · drinking water · 7 moAs given in this study (mouse).

    Source sentences

    Summary
    Furthermore, NMN treatment increased protein concentrations of Sirt3, PINK1, and Parkin (P < 0.01), and enhanced autophagy-lysosomal markers, including LC3-II/LC3-I ratio and transcription factor EB (TFEB) (P < 0.05), and decreased p62 concentrations (P < 0.01) in cardiac tissue.
    1 context sentence
    Summary · context
    Male C57BL/6J mice (14-month-old) were assigned to 3 groups: normal diet, HFD, and HFD + NMN. NMN was added to their drinking water at a dose of 400 mg/kg for 7 mo.
  21. 21LabIn vitro (cells)Efficacy outcome

    In H9c2 cardiomyocytes, NMN attenuated palmitic-acid-induced cytotoxicity.

    In plain wordsIn heart cells, NMN reduced toxicity compared with palmitic acid exposure.

    Outcome
    DecreaseCytotoxicity
    Study

    n: not reported in source

    palmitic-acid-exposed H9c2 cardiomyocytes
    Comparator
    palmitic acid exposure
    Outcome group
    Heart function · Cardiovascular
    Studied dose
    Dose not stated

    Source sentences

    Summary
    In H9c2 cardiomyocytes, NMN treatment significantly attenuated PA-induced cytotoxicity (P < 0.01) and enhanced PA-induced impairment of autophagy flux.
    1 context sentence
    Summary · context
    In vitro, H9c2 cardiomyocytes were exposed to palmitic acid (PA) to establish a lipotoxicity model, and the effects of NMN on cell viability and autophagy flux were assessed by the Methyl Thiazol Tetrazolium (MTT) assay and mRFP-GFP-LC3 adenoviral transfection.
  22. 22LabIn vitro (cells)Mechanism

    In H9c2 cardiomyocytes, NMN reportedly enhanced palmitic-acid-induced impairment of autophagy flux, despite the abstract's opposing protective interpretation.

    In plain wordsIn heart cells, the result sentence reports greater autophagy impairment with NMN than with palmitic acid exposure.

    Outcome
    IncreaseAutophagy flux impairment
    Study

    n: not reported in source

    palmitic-acid-exposed H9c2 cardiomyocytes
    Comparator
    palmitic acid exposure
    Outcome group
    Mitochondrial function · Cardiovascular
    Studied dose
    Dose not stated

    Source sentences

    Summary
    In H9c2 cardiomyocytes, NMN treatment significantly attenuated PA-induced cytotoxicity (P < 0.01) and enhanced PA-induced impairment of autophagy flux.
    1 context sentence
    Summary · context
    In vitro, H9c2 cardiomyocytes were exposed to palmitic acid (PA) to establish a lipotoxicity model, and the effects of NMN on cell viability and autophagy flux were assessed by the Methyl Thiazol Tetrazolium (MTT) assay and mRFP-GFP-LC3 adenoviral transfection.

Studies that did not test the peptide alone2

In this study, NMN (nicotinamide mononucleotide) was a lab tool or a carrier, part of a mix, or the subject of a lab method. These results are not evidence about taking NMN (nicotinamide mononucleotide).

  1. 23LabNot a test of NMN (nicotinamide mononucleotide) aloneIn vitro (cells)Mechanism

    In H9c2 cardiomyocytes, cotreatment with the Sirt3 inhibitor 3-TYP abolished NMN-associated cytoprotection.

    In plain wordsIn heart cells, adding 3-TYP abolished cell protection compared with NMN alone.

    Outcome
    DecreaseSirt3 dependence of cytoprotection
    Study

    n: not reported in source

    palmitic-acid-exposed H9c2 cardiomyocytes
    Comparator
    NMN without 3-TYP
    Outcome group
    Receptor activity and mechanism · Cardiovascular

    Source sentences

    Summary
    Notably, these protective effects were abolished by cotreatment with 3-TYP, a selective Sirt3 inhibitor.
    2 context sentences
    Summary · context
    In H9c2 cardiomyocytes, NMN treatment significantly attenuated PA-induced cytotoxicity (P < 0.01) and enhanced PA-induced impairment of autophagy flux.
    Summary · context
    In vitro, H9c2 cardiomyocytes were exposed to palmitic acid (PA) to establish a lipotoxicity model, and the effects of NMN on cell viability and autophagy flux were assessed by the Methyl Thiazol Tetrazolium (MTT) assay and mRFP-GFP-LC3 adenoviral transfection.

    In this study, NMN (nicotinamide mononucleotide) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking NMN (nicotinamide mononucleotide).

  2. 24LabNot a test of NMN (nicotinamide mononucleotide) aloneIn vitro (cells)Mechanism

    In H9c2 cardiomyocytes, 3-TYP abolished the autophagy-related effect described as protective for NMN.

    In plain wordsIn heart cells, adding 3-TYP abolished the reported autophagy-related protection compared with NMN alone.

    Outcome
    MixedSirt3 dependence of autophagy effect
    Study

    n: not reported in source

    palmitic-acid-exposed H9c2 cardiomyocytes
    Comparator
    NMN without 3-TYP
    Outcome group
    Receptor activity and mechanism · Cardiovascular

    Source sentences

    Summary
    Notably, these protective effects were abolished by cotreatment with 3-TYP, a selective Sirt3 inhibitor.
    2 context sentences
    Summary · context
    In H9c2 cardiomyocytes, NMN treatment significantly attenuated PA-induced cytotoxicity (P < 0.01) and enhanced PA-induced impairment of autophagy flux.
    Summary · context
    In vitro, H9c2 cardiomyocytes were exposed to palmitic acid (PA) to establish a lipotoxicity model, and the effects of NMN on cell viability and autophagy flux were assessed by the Methyl Thiazol Tetrazolium (MTT) assay and mRFP-GFP-LC3 adenoviral transfection.

    In this study, NMN (nicotinamide mononucleotide) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking NMN (nicotinamide mononucleotide).

AI wrote and checked these results. AI can make mistakes, so check important results against the source.

Version history

PepBank keeps every version of the data on this study. Status changes from Retraction Watch, Europe PMC and Crossref are listed with their source.

  1. Version 2Current

    21 Oct 2026, 15:58 UTC

    Study results updated

  2. Version 1

    21 Oct 2026, 12:50 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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