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Study · Animal study (in vivo) · mouse · 2014

11 results

Role of AMPK and PPARγ1 in exercise-induced lipoprotein lipase in skeletal muscle.

Sasaki T, Nakata R, Inoue H, Shimizu M, Inoue J, Sato R

American journal of physiology. Endocrinology and metabolism18 Mar 2014Cited by 31 (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: Publisher copyright. Results still quote short attributed sentences.

Results from this study11

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

  1. 01AnimalAnimal study (in vivo)Mechanism

    In mice, AICAR increased gastrocnemius PPARγ1 mRNA.

    In plain wordsIn mice, AICAR increased PPARγ1 gene expression in muscle.

    Outcome
    IncreasePPARγ1 mRNA
    Study

    mousen: not reported in source

    gastrocnemius muscle
    Outcome group
    Receptor activity and mechanism · Musculoskeletal
    Studied dose
    Dose not stated · intraperitonealAs given in this study (mouse).

    Source sentences

    Summary
    When mice were intraperitoneally administered an AMP-activated protein kinase (AMPK) activator 5-aminoimidazole-4-carboxamide ribonucleoside (AICAR), the mRNA levels of the aforementioned three genes increased in gastrocnemius muscle.
    1 context sentence
    Summary · context
    Here we show that the mRNA levels of one of peroxisome proliferator-activated receptor (PPAR) family members, PPARγ1, and genes related to energy metabolism, including PPARγ coactivator-1 protein-1α (PGC-1α) and lipoprotein lipase (LPL), increased in the gastrocnemius muscle of habitual exercise-trained mice.
  2. 02AnimalAnimal study (in vivo)Mechanism

    In mice, AICAR increased gastrocnemius PGC-1α mRNA.

    In plain wordsIn mice, AICAR increased PGC-1α gene expression in muscle.

    Outcome
    IncreasePGC-1α mRNA
    Study

    mousen: not reported in source

    gastrocnemius muscle
    Outcome group
    Receptor activity and mechanism · Musculoskeletal
    Studied dose
    Dose not stated · intraperitonealAs given in this study (mouse).

    Source sentences

    Summary
    When mice were intraperitoneally administered an AMP-activated protein kinase (AMPK) activator 5-aminoimidazole-4-carboxamide ribonucleoside (AICAR), the mRNA levels of the aforementioned three genes increased in gastrocnemius muscle.
    1 context sentence
    Summary · context
    Here we show that the mRNA levels of one of peroxisome proliferator-activated receptor (PPAR) family members, PPARγ1, and genes related to energy metabolism, including PPARγ coactivator-1 protein-1α (PGC-1α) and lipoprotein lipase (LPL), increased in the gastrocnemius muscle of habitual exercise-trained mice.
  3. 03AnimalAnimal study (in vivo)Mechanism

    In mice, AICAR increased gastrocnemius LPL mRNA.

    In plain wordsIn mice, AICAR increased lipoprotein lipase gene expression in muscle.

    Outcome
    IncreaseLPL mRNA
    Study

    mousen: not reported in source

    gastrocnemius muscle
    Outcome group
    Receptor activity and mechanism · Musculoskeletal
    Studied dose
    Dose not stated · intraperitonealAs given in this study (mouse).

    Source sentences

    Summary
    When mice were intraperitoneally administered an AMP-activated protein kinase (AMPK) activator 5-aminoimidazole-4-carboxamide ribonucleoside (AICAR), the mRNA levels of the aforementioned three genes increased in gastrocnemius muscle.
    1 context sentence
    Summary · context
    Here we show that the mRNA levels of one of peroxisome proliferator-activated receptor (PPAR) family members, PPARγ1, and genes related to energy metabolism, including PPARγ coactivator-1 protein-1α (PGC-1α) and lipoprotein lipase (LPL), increased in the gastrocnemius muscle of habitual exercise-trained mice.
  4. 04LabIn vitro (cells)Mechanism

    In C2C12 myotubes, AICAR increased PPARγ1 mRNA.

    In plain wordsIn cells, AICAR increased PPARγ1 gene expression.

    Outcome
    IncreasePPARγ1 mRNA
    Study

    n: not reported in source

    C2C12 differentiated myotubes
    Outcome group
    Receptor activity and mechanism · Musculoskeletal
    Studied dose
    Dose not stated

    Source sentences

    Summary
    AICAR treatment to C2C12 differentiated myotubes also increased PPARγ1 mRNA levels, but not PPARα and -δ mRNA levels, concomitant with increased PGC-1α mRNA levels.
  5. 05LabIn vitro (cells)Mechanism

    In C2C12 myotubes, AICAR did not increase PPARα mRNA.

    In plain wordsIn cells, AICAR did not increase PPARα gene expression.

    Outcome
    No significant changePPARα mRNA
    Study

    n: not reported in source

    C2C12 differentiated myotubes
    Outcome group
    Receptor activity and mechanism · Musculoskeletal
    Studied dose
    Dose not stated

    Source sentences

    Summary
    AICAR treatment to C2C12 differentiated myotubes also increased PPARγ1 mRNA levels, but not PPARα and -δ mRNA levels, concomitant with increased PGC-1α mRNA levels.
  6. 06LabIn vitro (cells)Mechanism

    In C2C12 myotubes, AICAR did not increase PPARδ mRNA.

    In plain wordsIn cells, AICAR did not increase PPARδ gene expression.

    Outcome
    No significant changePPARδ mRNA
    Study

    n: not reported in source

    C2C12 differentiated myotubes
    Outcome group
    Receptor activity and mechanism · Musculoskeletal
    Studied dose
    Dose not stated

    Source sentences

    Summary
    AICAR treatment to C2C12 differentiated myotubes also increased PPARγ1 mRNA levels, but not PPARα and -δ mRNA levels, concomitant with increased PGC-1α mRNA levels.
  7. 07LabIn vitro (cells)Mechanism

    In C2C12 myotubes, AICAR increased PGC-1α mRNA.

    In plain wordsIn cells, AICAR increased PGC-1α gene expression.

    Outcome
    IncreasePGC-1α mRNA
    Study

    n: not reported in source

    C2C12 differentiated myotubes
    Outcome group
    Receptor activity and mechanism · Musculoskeletal
    Studied dose
    Dose not stated

    Source sentences

    Summary
    AICAR treatment to C2C12 differentiated myotubes also increased PPARγ1 mRNA levels, but not PPARα and -δ mRNA levels, concomitant with increased PGC-1α mRNA levels.
  8. 08LabIn vitro (cells)Mechanism

    In C2C12 cells, AICAR increased PPARγ1 mRNA half-life nearly threefold through AMPK activation.

    In plain wordsIn cells, AICAR increased PPARγ1 mRNA half-life nearly threefold.

    Outcome
    IncreasePPARγ1 mRNA half-life
    Study

    n: not reported in source

    C2C12 myotubes
    Outcome group
    Receptor activity and mechanism · Musculoskeletal
    Studied dose
    Dose not stated

    Measurements

    PPARγ1 mRNA half-life
    4 h
    before AICAR-associated increase
    PPARγ1 mRNA half-life
    12 h
    after AICAR-associated increase

    Source sentences

    Summary
    AICAR treatment increased the half-life of PPARγ1 mRNA nearly threefold (4-12 h) by activating AMPK.
  9. 09LabIn vitro (cells)Mechanism

    In C2C12 myotubes, AICAR increased LPL gene expression.

    In plain wordsIn cells, AICAR increased lipoprotein lipase gene expression.

    Outcome
    IncreaseLPL gene expression
    Study

    n: not reported in source

    C2C12 myotubes
    Outcome group
    Receptor activity and mechanism · Musculoskeletal
    Studied dose
    Dose not stated

    Source sentences

    Summary
    In contrast, when PPARγ1 expression was suppressed in C2C12 myotubes, LPL mRNA levels were significantly reduced, and the effect of AICAR on increased LPL gene expression was almost completely blocked.

Studies that did not test the peptide alone2

In this study, AICAR (acadesine) 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 AICAR (acadesine).

  1. 10LabNot a test of AICAR (acadesine) aloneIn vitro (cells)Mechanism

    In C2C12 myotubes, compound C blocked the effects of AICAR on gene expression.

    In plain wordsIn cells, compound C blocked AICAR's effects on gene expression.

    Outcome
    DecreaseBlockade of AICAR effects by compound C
    Study

    n: not reported in source

    C2C12 differentiated myotubes
    Outcome group
    Receptor activity and mechanism · Musculoskeletal

    Source sentences

    Summary
    An AMPK inhibitor, compound C, blocked these AICAR effects.
    1 context sentence
    Summary · context
    AICAR treatment to C2C12 differentiated myotubes also increased PPARγ1 mRNA levels, but not PPARα and -δ mRNA levels, concomitant with increased PGC-1α mRNA levels.

    In this study, AICAR (acadesine) 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 AICAR (acadesine).

  2. 11LabNot a test of AICAR (acadesine) aloneIn vitro (cells)Mechanism

    In C2C12 myotubes, PPARγ1 suppression reduced LPL mRNA and almost completely blocked the AICAR-induced increase in LPL expression.

    In plain wordsIn cells, suppressing PPARγ1 reduced LPL expression and almost completely blocked its increase with AICAR.

    Outcome
    DecreaseLPL mRNA after PPARγ1 suppression
    Study

    n: not reported in source

    PPARγ1-suppressed C2C12 myotubes
    Outcome group
    Receptor activity and mechanism · Musculoskeletal

    Source sentences

    Summary
    In contrast, when PPARγ1 expression was suppressed in C2C12 myotubes, LPL mRNA levels were significantly reduced, and the effect of AICAR on increased LPL gene expression was almost completely blocked.

    In this study, AICAR (acadesine) 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 AICAR (acadesine).

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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