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Study · Animal study (in vivo) · mouse · 2025

9 results

Nicotinamide mononucleotide protects against diabetic nephropathy via IL-6/Rab5-mediated crosstalk between proximal tubular epithelial cells and podocytes.

Zha DQ, Gao P, Wu XY

World journal of diabetes1 Oct 2025Cited by 2 (Europe PMC)

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: CC BY-NC. Results still quote short attributed sentences.

Results from this study9

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

  1. 01AnimalAnimal study (in vivo)Efficacy outcome

    In diabetic mice, NMN reduced podocyte injury.

    In plain wordsIn diabetic mice, NMN reduced podocyte injury.

    Outcome
    DecreasePodocyte injury
    Study

    mousen: not reported in source

    streptozotocin-induced diabetic nephropathy
    Outcome group
    Kidney function · Kidney and urinary
    Studied dose
    Dose not stated · 8 weeksAs given in this study (mouse).

    Source sentences

    Summary
    NMN treatment of diabetic mice markedly reduced podocyte injury, glomerular hypertrophy, foot-process effacement, and urinary albumin excretion.
    1 context sentence
    Summary · context
    In vivo, DN was induced in mice using streptozotocin, and mice then received NMN, insulin, or both treatments over an 8-week period.
  2. 02AnimalAnimal study (in vivo)Efficacy outcome

    In diabetic mice, NMN reduced glomerular hypertrophy.

    In plain wordsIn diabetic mice, NMN reduced enlargement of kidney glomeruli.

    Outcome
    DecreaseGlomerular hypertrophy
    Study

    mousen: not reported in source

    streptozotocin-induced diabetic nephropathy
    Outcome group
    Kidney function · Kidney and urinary
    Studied dose
    Dose not stated · 8 weeksAs given in this study (mouse).

    Source sentences

    Summary
    NMN treatment of diabetic mice markedly reduced podocyte injury, glomerular hypertrophy, foot-process effacement, and urinary albumin excretion.
    1 context sentence
    Summary · context
    In vivo, DN was induced in mice using streptozotocin, and mice then received NMN, insulin, or both treatments over an 8-week period.
  3. 03AnimalAnimal study (in vivo)Efficacy outcome

    In diabetic mice, NMN reduced foot-process effacement.

    In plain wordsIn diabetic mice, NMN reduced damage to podocyte foot processes.

    Outcome
    DecreaseFoot-process effacement
    Study

    mousen: not reported in source

    streptozotocin-induced diabetic nephropathy
    Outcome group
    Kidney function · Kidney and urinary
    Studied dose
    Dose not stated · 8 weeksAs given in this study (mouse).

    Source sentences

    Summary
    NMN treatment of diabetic mice markedly reduced podocyte injury, glomerular hypertrophy, foot-process effacement, and urinary albumin excretion.
    1 context sentence
    Summary · context
    In vivo, DN was induced in mice using streptozotocin, and mice then received NMN, insulin, or both treatments over an 8-week period.
  4. 04AnimalAnimal study (in vivo)Efficacy outcome

    In diabetic mice, NMN reduced urinary albumin excretion.

    In plain wordsIn diabetic mice, NMN reduced albumin loss in urine.

    Outcome
    DecreaseUrinary albumin excretion
    Study

    mousen: not reported in source

    streptozotocin-induced diabetic nephropathy
    Outcome group
    Kidney function · Kidney and urinary
    Studied dose
    Dose not stated · 8 weeksAs given in this study (mouse).

    Source sentences

    Summary
    NMN treatment of diabetic mice markedly reduced podocyte injury, glomerular hypertrophy, foot-process effacement, and urinary albumin excretion.
    1 context sentence
    Summary · context
    In vivo, DN was induced in mice using streptozotocin, and mice then received NMN, insulin, or both treatments over an 8-week period.
  5. 05LabIn vitro (cells)Mechanism

    In PTECs, NMN suppressed epithelial-mesenchymal transition.

    In plain wordsIn cells, NMN suppressed the transition of kidney tubular cells toward a mesenchymal state.

    Outcome
    DecreasePTEC EMT
    Study

    humann: not reported in source

    high-glucose PTECs
    Outcome group
    Receptor activity and mechanism · Kidney and urinary
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Mechanistically, NMN suppressed the EMT and IL-6 secretion by PTECs, inhibited Rab5 activation in podocytes, and prevented nephrin endocytosis, thereby preserving the cytoskeletal integrity and function of podocytes.
    1 context sentence
    Summary · context
    In vitro, human PTECs and murine podocytes were cultured under high-glucose conditions, and IL-6 neutralizing antibodies or NMN treatments were applied.
  6. 06LabIn vitro (cells)Mechanism

    In PTECs, NMN suppressed IL-6 secretion.

    In plain wordsIn cells, NMN reduced IL-6 release from kidney tubular cells.

    Outcome
    DecreasePTEC IL-6 secretion
    Study

    humann: not reported in source

    high-glucose PTECs
    Outcome group
    Inflammation markers · Kidney and urinary
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Mechanistically, NMN suppressed the EMT and IL-6 secretion by PTECs, inhibited Rab5 activation in podocytes, and prevented nephrin endocytosis, thereby preserving the cytoskeletal integrity and function of podocytes.
    1 context sentence
    Summary · context
    In vitro, human PTECs and murine podocytes were cultured under high-glucose conditions, and IL-6 neutralizing antibodies or NMN treatments were applied.
  7. 07LabIn vitro (cells)Mechanism

    In podocytes, NMN inhibited Rab5 activation.

    In plain wordsIn cells, NMN reduced Rab5 activation in podocytes.

    Outcome
    DecreaseRab5 activation
    Study

    mousen: not reported in source

    podocytes under high-glucose conditions
    Outcome group
    Receptor activity and mechanism · Kidney and urinary
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Mechanistically, NMN suppressed the EMT and IL-6 secretion by PTECs, inhibited Rab5 activation in podocytes, and prevented nephrin endocytosis, thereby preserving the cytoskeletal integrity and function of podocytes.
    1 context sentence
    Summary · context
    In vitro, human PTECs and murine podocytes were cultured under high-glucose conditions, and IL-6 neutralizing antibodies or NMN treatments were applied.
  8. 08LabIn vitro (cells)Mechanism

    In podocytes, NMN prevented nephrin endocytosis.

    In plain wordsIn cells, NMN prevented nephrin uptake into podocytes.

    Outcome
    DecreaseNephrin endocytosis
    Study

    mousen: not reported in source

    podocytes under high-glucose conditions
    Outcome group
    Receptor activity and mechanism · Kidney and urinary
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Mechanistically, NMN suppressed the EMT and IL-6 secretion by PTECs, inhibited Rab5 activation in podocytes, and prevented nephrin endocytosis, thereby preserving the cytoskeletal integrity and function of podocytes.
    1 context sentence
    Summary · context
    In vitro, human PTECs and murine podocytes were cultured under high-glucose conditions, and IL-6 neutralizing antibodies or NMN treatments were applied.
  9. 09LabIn vitro (cells)Efficacy outcome

    In podocytes, NMN preserved cytoskeletal integrity and function.

    In plain wordsIn cells, NMN preserved podocyte internal structure and function.

    Outcome
    Direction not reportedPodocyte cytoskeletal integrity and function
    Study

    mousen: not reported in source

    podocytes under high-glucose conditions
    Outcome group
    Kidney function · Kidney and urinary
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Mechanistically, NMN suppressed the EMT and IL-6 secretion by PTECs, inhibited Rab5 activation in podocytes, and prevented nephrin endocytosis, thereby preserving the cytoskeletal integrity and function of podocytes.
    1 context sentence
    Summary · context
    In vitro, human PTECs and murine podocytes were cultured under high-glucose conditions, and IL-6 neutralizing antibodies or NMN treatments were applied.

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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