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

15 results

MOTS-c primes adrenal cortex metabolism without directly driving steroidogenesis.

Blatkiewicz M, Kaminski K, Sobalska-Kwapis M, Szyszka M, Olechnowicz A, Jopek K, Rucinski M

Folia histochemica et cytobiologica11 Mar 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 study15

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

  1. 01AnimalAnimal study (in vivo)Mechanism

    In rats, 24 hours of MOTS‑c did not change expression of classical steroidogenic genes in adrenal tissue.

    In plain wordsIn rats, MOTS‑c did not change the activity of classic hormone-making genes in the adrenal gland compared with saline.

    Peptide
    MOTS-c
    Outcome
    No significant changeClassical steroidogenic gene expression
    Study

    ratn = 16

    Adult male Wistar rats
    Comparator
    Saline
    Outcome group
    Gene expression · Endocrine and hormones
    Studied dose
    0.1 μmol/24 h · subcutaneous · 24 hoursAs given in this study (rat).

    Source sentences

    Summary
    MOTS-c treatment did not alter classical steroidogenic genes or circulating corticosterone and aldosterone levels.
    2 context sentences
    Summary · context
    Adult male Wistar rats (n = 16) received continuous MOTS-c (0.1 μmol/24 h) or saline via subcutaneous micro-osmotic pumps for 24 hours.
    Summary · context
    Adrenal tissues were analyzed using qRT-PCR, immunohistochemistry, ELISA, and RNA-sequencing.
  2. 02AnimalAnimal study (in vivo)Efficacy outcome

    In rats, MOTS‑c did not change circulating corticosterone compared with saline.

    In plain wordsIn rats, MOTS‑c did not change blood corticosterone compared with saline.

    Peptide
    MOTS-c
    Outcome
    No significant changeCirculating corticosterone
    Study

    ratn = 16

    Adult male Wistar rats
    Comparator
    Saline
    Outcome group
    Stress hormones · Endocrine and hormones
    Studied dose
    0.1 μmol/24 h · subcutaneous · 24 hoursAs given in this study (rat).

    Source sentences

    Summary
    MOTS-c treatment did not alter classical steroidogenic genes or circulating corticosterone and aldosterone levels.
    2 context sentences
    Summary · context
    Adult male Wistar rats (n = 16) received continuous MOTS-c (0.1 μmol/24 h) or saline via subcutaneous micro-osmotic pumps for 24 hours.
    Summary · context
    Adrenal tissues were analyzed using qRT-PCR, immunohistochemistry, ELISA, and RNA-sequencing.
  3. 03AnimalAnimal study (in vivo)Efficacy outcome

    In rats, MOTS‑c did not change circulating aldosterone compared with saline.

    In plain wordsIn rats, MOTS‑c did not change blood aldosterone compared with saline.

    Peptide
    MOTS-c
    Outcome
    No significant changeCirculating aldosterone
    Study

    ratn = 16

    Adult male Wistar rats
    Comparator
    Saline
    Outcome group
    Stress hormones · Endocrine and hormones
    Studied dose
    0.1 μmol/24 h · subcutaneous · 24 hoursAs given in this study (rat).

    Source sentences

    Summary
    MOTS-c treatment did not alter classical steroidogenic genes or circulating corticosterone and aldosterone levels.
    2 context sentences
    Summary · context
    Adult male Wistar rats (n = 16) received continuous MOTS-c (0.1 μmol/24 h) or saline via subcutaneous micro-osmotic pumps for 24 hours.
    Summary · context
    Adrenal tissues were analyzed using qRT-PCR, immunohistochemistry, ELISA, and RNA-sequencing.
  4. 04AnimalAnimal study (in vivo)Mechanism

    In rat adrenal tissue, RNA sequencing identified differentially expressed genes after MOTS‑c treatment compared with saline.

    In plain wordsIn rats, MOTS‑c changed the activity of some adrenal genes compared with saline.

    Peptide
    MOTS-c
    Outcome
    MixedNumber of differentially expressed adrenal genes
    Study

    ratn = 16

    Adult male Wistar rats
    Comparator
    Saline
    Outcome group
    Gene expression · Endocrine and hormones
    Studied dose
    0.1 μmol/24 h · subcutaneous · 24 hoursAs given in this study (rat).

    Measurements

    Differentially expressed genes
    39 genes
    MOTS-c vs saline

    Source sentences

    Summary
    RNA-seq identified 39 differentially expressed genes, notably upregulation of purinergic receptor P2ry4 (4.3-fold, P < 0.05) - a novel MOTS-C target enhancing calcium signaling.
    2 context sentences
    Summary · context
    Adult male Wistar rats (n = 16) received continuous MOTS-c (0.1 μmol/24 h) or saline via subcutaneous micro-osmotic pumps for 24 hours.
    Summary · context
    Adrenal tissues were analyzed using qRT-PCR, immunohistochemistry, ELISA, and RNA-sequencing.
  5. 05AnimalAnimal study (in vivo)Mechanism

    In rat adrenal tissue, MOTS‑c upregulated the purinergic receptor gene P2ry4.

    In plain wordsIn rats, MOTS‑c raised the activity of the P2ry4 gene in the adrenal gland.

    Peptide
    MOTS-c
    Outcome
    IncreaseP2ry4 expression
    Study

    ratn = 16

    Adult male Wistar rats
    Comparator
    Saline
    Outcome group
    Gene expression · Endocrine and hormones
    Studied dose
    0.1 μmol/24 h · subcutaneous · 24 hoursAs given in this study (rat).

    Measurements

    P2ry4 fold change
    4.3 fold
    MOTS-c vs saline

    Source sentences

    Summary
    RNA-seq identified 39 differentially expressed genes, notably upregulation of purinergic receptor P2ry4 (4.3-fold, P < 0.05) - a novel MOTS-C target enhancing calcium signaling.
    2 context sentences
    Summary · context
    Adult male Wistar rats (n = 16) received continuous MOTS-c (0.1 μmol/24 h) or saline via subcutaneous micro-osmotic pumps for 24 hours.
    Summary · context
    Adrenal tissues were analyzed using qRT-PCR, immunohistochemistry, ELISA, and RNA-sequencing.
  6. 06AnimalAnimal study (in vivo)Mechanism

    In rat adrenal tissue, MOTS‑c upregulated Apoc4.

    In plain wordsIn rats, MOTS‑c raised the activity of the Apoc4 gene in the adrenal gland.

    Peptide
    MOTS-c
    Outcome
    IncreaseApoc4 expression
    Study

    ratn = 16

    Adult male Wistar rats
    Comparator
    Saline
    Outcome group
    Gene expression · Endocrine and hormones
    Studied dose
    0.1 μmol/24 h · subcutaneous · 24 hoursAs given in this study (rat).

    Source sentences

    Summary
    Additional changes included upregulation of Apoc4 and downregulation of stress markers Bag3 and Smurf2, mitochondrial carrier Slc25a30, and peroxisomal factor Pex11a.
    2 context sentences
    Summary · context
    Adult male Wistar rats (n = 16) received continuous MOTS-c (0.1 μmol/24 h) or saline via subcutaneous micro-osmotic pumps for 24 hours.
    Summary · context
    Adrenal tissues were analyzed using qRT-PCR, immunohistochemistry, ELISA, and RNA-sequencing.
  7. 07AnimalAnimal study (in vivo)Mechanism

    In rat adrenal tissue, MOTS‑c downregulated the stress marker Bag3.

    In plain wordsIn rats, MOTS‑c lowered the activity of the Bag3 stress gene in the adrenal gland.

    Peptide
    MOTS-c
    Outcome
    DecreaseBag3 expression
    Study

    ratn = 16

    Adult male Wistar rats
    Comparator
    Saline
    Outcome group
    Gene expression · Endocrine and hormones
    Studied dose
    0.1 μmol/24 h · subcutaneous · 24 hoursAs given in this study (rat).

    Source sentences

    Summary
    Additional changes included upregulation of Apoc4 and downregulation of stress markers Bag3 and Smurf2, mitochondrial carrier Slc25a30, and peroxisomal factor Pex11a.
    2 context sentences
    Summary · context
    Adult male Wistar rats (n = 16) received continuous MOTS-c (0.1 μmol/24 h) or saline via subcutaneous micro-osmotic pumps for 24 hours.
    Summary · context
    Adrenal tissues were analyzed using qRT-PCR, immunohistochemistry, ELISA, and RNA-sequencing.
  8. 08AnimalAnimal study (in vivo)Mechanism

    In rat adrenal tissue, MOTS‑c downregulated the stress marker Smurf2.

    In plain wordsIn rats, MOTS‑c lowered the activity of the Smurf2 stress gene in the adrenal gland.

    Peptide
    MOTS-c
    Outcome
    DecreaseSmurf2 expression
    Study

    ratn = 16

    Adult male Wistar rats
    Comparator
    Saline
    Outcome group
    Gene expression · Endocrine and hormones
    Studied dose
    0.1 μmol/24 h · subcutaneous · 24 hoursAs given in this study (rat).

    Source sentences

    Summary
    Additional changes included upregulation of Apoc4 and downregulation of stress markers Bag3 and Smurf2, mitochondrial carrier Slc25a30, and peroxisomal factor Pex11a.
    2 context sentences
    Summary · context
    Adult male Wistar rats (n = 16) received continuous MOTS-c (0.1 μmol/24 h) or saline via subcutaneous micro-osmotic pumps for 24 hours.
    Summary · context
    Adrenal tissues were analyzed using qRT-PCR, immunohistochemistry, ELISA, and RNA-sequencing.
  9. 09AnimalAnimal study (in vivo)Mechanism

    In rat adrenal tissue, MOTS‑c downregulated the mitochondrial carrier gene Slc25a30.

    In plain wordsIn rats, MOTS‑c lowered the activity of the Slc25a30 gene in the adrenal gland.

    Peptide
    MOTS-c
    Outcome
    DecreaseSlc25a30 expression
    Study

    ratn = 16

    Adult male Wistar rats
    Comparator
    Saline
    Outcome group
    Gene expression · Endocrine and hormones
    Studied dose
    0.1 μmol/24 h · subcutaneous · 24 hoursAs given in this study (rat).

    Source sentences

    Summary
    Additional changes included upregulation of Apoc4 and downregulation of stress markers Bag3 and Smurf2, mitochondrial carrier Slc25a30, and peroxisomal factor Pex11a.
    2 context sentences
    Summary · context
    Adult male Wistar rats (n = 16) received continuous MOTS-c (0.1 μmol/24 h) or saline via subcutaneous micro-osmotic pumps for 24 hours.
    Summary · context
    Adrenal tissues were analyzed using qRT-PCR, immunohistochemistry, ELISA, and RNA-sequencing.
  10. 10AnimalAnimal study (in vivo)Mechanism

    In rat adrenal tissue, MOTS‑c downregulated the peroxisomal factor Pex11a.

    In plain wordsIn rats, MOTS‑c lowered the activity of the Pex11a gene in the adrenal gland.

    Peptide
    MOTS-c
    Outcome
    DecreasePex11a expression
    Study

    ratn = 16

    Adult male Wistar rats
    Comparator
    Saline
    Outcome group
    Gene expression · Endocrine and hormones
    Studied dose
    0.1 μmol/24 h · subcutaneous · 24 hoursAs given in this study (rat).

    Source sentences

    Summary
    Additional changes included upregulation of Apoc4 and downregulation of stress markers Bag3 and Smurf2, mitochondrial carrier Slc25a30, and peroxisomal factor Pex11a.
    2 context sentences
    Summary · context
    Adult male Wistar rats (n = 16) received continuous MOTS-c (0.1 μmol/24 h) or saline via subcutaneous micro-osmotic pumps for 24 hours.
    Summary · context
    Adrenal tissues were analyzed using qRT-PCR, immunohistochemistry, ELISA, and RNA-sequencing.
  11. 11AnimalAnimal study (in vivo)Mechanism

    In rat adrenal tissue, gene set enrichment analysis showed that MOTS‑c inhibited the cAMP response pathway.

    In plain wordsIn rats, gene analysis showed MOTS‑c lowered the cAMP response pathway in the adrenal gland.

    Peptide
    MOTS-c
    Outcome
    DecreasecAMP response pathway
    Study

    ratn = 16

    Adult male Wistar rats
    Comparator
    Saline
    Outcome group
    Receptor activity and mechanism · Endocrine and hormones
    Studied dose
    0.1 μmol/24 h · subcutaneous · 24 hoursAs given in this study (rat).

    Source sentences

    Summary
    Gene Set Enrichment Analysis revealed inhibition of cAMP response, mitophagy, and histone deacetylation pathways, alongside activation of cell proliferation, indicating metabolic reprogramming without steroidogenic activation.
    2 context sentences
    Summary · context
    Adult male Wistar rats (n = 16) received continuous MOTS-c (0.1 μmol/24 h) or saline via subcutaneous micro-osmotic pumps for 24 hours.
    Summary · context
    Adrenal tissues were analyzed using qRT-PCR, immunohistochemistry, ELISA, and RNA-sequencing.
  12. 12AnimalAnimal study (in vivo)Mechanism

    In rat adrenal tissue, gene set enrichment analysis showed that MOTS‑c inhibited the mitophagy pathway.

    In plain wordsIn rats, gene analysis showed MOTS‑c lowered the mitophagy pathway in the adrenal gland.

    Peptide
    MOTS-c
    Outcome
    DecreaseMitophagy pathway
    Study

    ratn = 16

    Adult male Wistar rats
    Comparator
    Saline
    Outcome group
    Mitochondrial function · Endocrine and hormones
    Studied dose
    0.1 μmol/24 h · subcutaneous · 24 hoursAs given in this study (rat).

    Source sentences

    Summary
    Gene Set Enrichment Analysis revealed inhibition of cAMP response, mitophagy, and histone deacetylation pathways, alongside activation of cell proliferation, indicating metabolic reprogramming without steroidogenic activation.
    2 context sentences
    Summary · context
    Adult male Wistar rats (n = 16) received continuous MOTS-c (0.1 μmol/24 h) or saline via subcutaneous micro-osmotic pumps for 24 hours.
    Summary · context
    Adrenal tissues were analyzed using qRT-PCR, immunohistochemistry, ELISA, and RNA-sequencing.
  13. 13AnimalAnimal study (in vivo)Mechanism

    In rat adrenal tissue, gene set enrichment analysis showed that MOTS‑c inhibited the histone deacetylation pathway.

    In plain wordsIn rats, gene analysis showed MOTS‑c lowered the histone deacetylation pathway in the adrenal gland.

    Peptide
    MOTS-c
    Outcome
    DecreaseHistone deacetylation pathway
    Study

    ratn = 16

    Adult male Wistar rats
    Comparator
    Saline
    Outcome group
    Receptor activity and mechanism · Endocrine and hormones
    Studied dose
    0.1 μmol/24 h · subcutaneous · 24 hoursAs given in this study (rat).

    Source sentences

    Summary
    Gene Set Enrichment Analysis revealed inhibition of cAMP response, mitophagy, and histone deacetylation pathways, alongside activation of cell proliferation, indicating metabolic reprogramming without steroidogenic activation.
    2 context sentences
    Summary · context
    Adult male Wistar rats (n = 16) received continuous MOTS-c (0.1 μmol/24 h) or saline via subcutaneous micro-osmotic pumps for 24 hours.
    Summary · context
    Adrenal tissues were analyzed using qRT-PCR, immunohistochemistry, ELISA, and RNA-sequencing.
  14. 14AnimalAnimal study (in vivo)Mechanism

    In rat adrenal tissue, gene set enrichment analysis showed that MOTS‑c activated the cell proliferation pathway.

    In plain wordsIn rats, gene analysis showed MOTS‑c raised the cell growth pathway in the adrenal gland.

    Peptide
    MOTS-c
    Outcome
    IncreaseCell proliferation pathway
    Study

    ratn = 16

    Adult male Wistar rats
    Comparator
    Saline
    Outcome group
    Receptor activity and mechanism · Endocrine and hormones
    Studied dose
    0.1 μmol/24 h · subcutaneous · 24 hoursAs given in this study (rat).

    Source sentences

    Summary
    Gene Set Enrichment Analysis revealed inhibition of cAMP response, mitophagy, and histone deacetylation pathways, alongside activation of cell proliferation, indicating metabolic reprogramming without steroidogenic activation.
    2 context sentences
    Summary · context
    Adult male Wistar rats (n = 16) received continuous MOTS-c (0.1 μmol/24 h) or saline via subcutaneous micro-osmotic pumps for 24 hours.
    Summary · context
    Adrenal tissues were analyzed using qRT-PCR, immunohistochemistry, ELISA, and RNA-sequencing.

Natural levels measured1

These results measure the body's own peptide. Nobody was given the peptide. They are not evidence about taking it. They are left out of key results, evidence counts and charts.

  1. 15AnimalEndogenous levelAnimal study (in vivo)Other

    In rat adrenal cortex, the body's own MOTS‑c was expressed at higher levels in the zona fasciculata and reticularis than in the zona glomerulosa.

    In plain wordsIn rats, the body's own MOTS‑c was higher in two inner layers of the adrenal cortex than in the outer layer.

    Peptide
    MOTS-c
    Outcome
    Not applicableMOTS-c expression across adrenal cortex zones
    Study

    ratn: not reported in source

    Adult male Wistar rats
    Outcome group
    Mitochondrial function · Endocrine and hormones

    Source sentences

    Summary
    MOTS-c showed significantly higher expression in ZF/ZR vs. ZG.
    2 context sentences
    Summary · context
    Adult male Wistar rats (n = 16) received continuous MOTS-c (0.1 μmol/24 h) or saline via subcutaneous micro-osmotic pumps for 24 hours.
    Summary · context
    Adrenal tissues were analyzed using qRT-PCR, immunohistochemistry, ELISA, and RNA-sequencing.

    This result measures the body's own MOTS-c. Nobody was given the peptide. It is not evidence about taking it.

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

    9 Oct 2026, 18:17 UTC

    Study results updated

  2. Version 1

    9 Oct 2026, 02:47 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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