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Study · Not a test of the peptide alone · 2017

3 results

Geniposide protects pancreatic β cells from high glucose-mediated injury by activation of AMP-activated protein kinase.

Liu C, Hao Y, Yin F, Zhang Y, Liu J

Cell biology international4 Apr 2017Cited by 14 (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 study3

No result from this study comes from a test of the peptide.

Studies that did not test the peptide alone3

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. 01LabNot a test of AICAR (acadesine) aloneIn vitro (cells)Mechanism

    In high-glucose-treated INS-1 cells, AICAR potentiated geniposide-induced HO-1 protein elevation.

    In plain wordsIn cells, AICAR enhanced the rise in HO-1 protein with geniposide compared with geniposide alone.

    Outcome
    IncreaseHO-1 protein
    Study

    ratn: not reported in source

    INS-1 pancreatic beta cells
    Comparator
    geniposide alone
    Outcome group
    Receptor activity and mechanism · Metabolic and weight

    Source sentences

    Summary
    but AICAR, an AMPK activator, potentiated the role of geniposide on the protein levels of HO-1, Bcl-2, and Bax.
    2 context sentences
    Summary · context
    Data suggested that geniposide obviously prevented the cell damage induced by high (25 mM) glucose in INS-1 cells, which increased the protein levels of cell apoptosis-associated enzymes, including heme oxygenase-1 (HO-1), and Bcl-2, but apparently attenuated the protein level of Bax, an apoptotic protein.
    Summary · context
    In the present study, we investigated the role of 5'-AMP-activated protein kinase (AMPK) in high glucose induced cell injury and explored the associated molecular mechanisms in rat INS-1 pancreatic β cells.

    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. 02LabNot a test of AICAR (acadesine) aloneIn vitro (cells)Mechanism

    In high-glucose-treated INS-1 cells, AICAR potentiated geniposide-induced Bcl-2 protein elevation.

    In plain wordsIn cells, AICAR enhanced the rise in Bcl-2 protein with geniposide compared with geniposide alone.

    Outcome
    IncreaseBcl-2 protein
    Study

    ratn: not reported in source

    INS-1 pancreatic beta cells
    Comparator
    geniposide alone
    Outcome group
    Receptor activity and mechanism · Metabolic and weight

    Source sentences

    Summary
    but AICAR, an AMPK activator, potentiated the role of geniposide on the protein levels of HO-1, Bcl-2, and Bax.
    2 context sentences
    Summary · context
    Data suggested that geniposide obviously prevented the cell damage induced by high (25 mM) glucose in INS-1 cells, which increased the protein levels of cell apoptosis-associated enzymes, including heme oxygenase-1 (HO-1), and Bcl-2, but apparently attenuated the protein level of Bax, an apoptotic protein.
    Summary · context
    In the present study, we investigated the role of 5'-AMP-activated protein kinase (AMPK) in high glucose induced cell injury and explored the associated molecular mechanisms in rat INS-1 pancreatic β cells.

    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).

  3. 03LabNot a test of AICAR (acadesine) aloneIn vitro (cells)Mechanism

    In high-glucose-treated INS-1 cells, AICAR potentiated geniposide-induced Bax protein reduction.

    In plain wordsIn cells, AICAR enhanced the reduction in Bax protein with geniposide compared with geniposide alone.

    Outcome
    DecreaseBax protein
    Study

    ratn: not reported in source

    INS-1 pancreatic beta cells
    Comparator
    geniposide alone
    Outcome group
    Receptor activity and mechanism · Metabolic and weight

    Source sentences

    Summary
    but AICAR, an AMPK activator, potentiated the role of geniposide on the protein levels of HO-1, Bcl-2, and Bax.
    2 context sentences
    Summary · context
    Data suggested that geniposide obviously prevented the cell damage induced by high (25 mM) glucose in INS-1 cells, which increased the protein levels of cell apoptosis-associated enzymes, including heme oxygenase-1 (HO-1), and Bcl-2, but apparently attenuated the protein level of Bax, an apoptotic protein.
    Summary · context
    In the present study, we investigated the role of 5'-AMP-activated protein kinase (AMPK) in high glucose induced cell injury and explored the associated molecular mechanisms in rat INS-1 pancreatic β cells.

    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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