Skip to content

Study · Animal study (in vivo) · rat · 2012

7 results

Amelioration of neurodegenerative changes in cellular and rat models of diabetes-related Alzheimer's disease by exendin-4.

Chen S, Liu AR, An FM, Yao WB, Gao XD

Age (Dordrecht, Netherlands)8 Sept 2011Cited by 106 (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 study7

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

  1. 01AnimalAnimal study (in vivo)Efficacy outcome

    In ICV-STZ-treated rats, twice-daily exendin‑4 improved Morris water maze learning and memory performance versus saline.

    In plain wordsIn rats given ICV-STZ, exendin‑4 improved maze learning and memory performance compared with saline.

    Outcome
    IncreaseLearning and memory performance
    Study

    ratn: not reported in source

    ICV-STZ diabetes-related Alzheimer-like changes
    Comparator
    Saline
    Outcome group
    Cognition and memory · Nervous system and cognition
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Fourteen days following ICV-STZ injection, rats treated with twice-daily Ex-4 had better learning and memory performance in the Morris water maze test compared with rats treated with saline.
  2. 02AnimalAnimal study (in vivo)Efficacy outcome

    In ICV-STZ-treated rats, exendin‑4 protected hippocampal neurons against degeneration.

    In plain wordsIn rats given ICV-STZ, exendin‑4 protected hippocampal nerve cells against degeneration.

    Outcome
    DecreaseHippocampal neuron degeneration
    Study

    ratn: not reported in source

    ICV-STZ diabetes-related Alzheimer-like changes
    Outcome group
    Neuroprotection · Nervous system and cognition
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Additionally, histopathological evaluation confirmed the protective effects of Ex-4 treatment on hippocampal neurons against degeneration.
    1 context sentence
    Summary · context
    In rat models, bilateral ICV-STZ administration was used to produce impaired insulin signaling in the brain.
  3. 03AnimalAnimal study (in vivo)Mechanism

    In ICV-STZ-treated rats, exendin‑4 reversed tau hyperphosphorylation.

    In plain wordsIn rats given ICV-STZ, exendin‑4 reversed excessive tau phosphorylation.

    Outcome
    DecreaseTau hyperphosphorylation
    Study

    ratn: not reported in source

    ICV-STZ diabetes-related Alzheimer-like changes
    Outcome group
    Neuroprotection · Nervous system and cognition
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Furthermore, we demonstrated that Ex-4 reversed ICV-STZ-induced tau hyperphosphorylation through downregulation of GSK-3β activity, a key kinase in both DM and AD.
    1 context sentence
    Summary · context
    In rat models, bilateral ICV-STZ administration was used to produce impaired insulin signaling in the brain.
  4. 04AnimalAnimal study (in vivo)Mechanism

    In ICV-STZ-treated rats, exendin‑4 downregulated GSK-3β activity as part of reversing tau hyperphosphorylation.

    In plain wordsIn rats given ICV-STZ, exendin‑4 reduced GSK-3β activity as part of reversing excessive tau phosphorylation.

    Outcome
    DecreaseGSK-3β activity
    Study

    ratn: not reported in source

    ICV-STZ diabetes-related Alzheimer-like changes
    Outcome group
    Receptor activity and mechanism · Nervous system and cognition
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Furthermore, we demonstrated that Ex-4 reversed ICV-STZ-induced tau hyperphosphorylation through downregulation of GSK-3β activity, a key kinase in both DM and AD.
    1 context sentence
    Summary · context
    In rat models, bilateral ICV-STZ administration was used to produce impaired insulin signaling in the brain.

Studies that did not test the peptide alone3

In this study, Exenatide (exendin-4) 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 Exenatide (exendin-4).

  1. 05LabNot a test of Exenatide (exendin-4) aloneIn vitro (cells)Efficacy outcome

    In high-glucose PC12 cells, GLP-1/exendin‑4 protected against reduced viability.

    In plain wordsIn cells exposed to high glucose, GLP-1/exendin‑4 protected against loss of cell viability.

    Outcome
    IncreaseCell viability
    Study

    n: not reported in source

    High-glucose PC12 cells
    Outcome group
    Neuroprotection · Nervous system and cognition

    Source sentences

    Summary
    Our study demonstrated that GLP-1/Ex-4 could exert a protective effect against reduced viability of PC12 cells caused by high glucose and that this protective effect was mediated via the PI3-kinase pathway.

    In this study, Exenatide (exendin-4) 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 Exenatide (exendin-4).

  2. 06LabNot a test of Exenatide (exendin-4) aloneIn vitro (cells)Mechanism

    In high-glucose PC12 cells, PI3-kinase signaling mediated the protective effect of GLP-1/exendin‑4.

    In plain wordsIn cells exposed to high glucose, PI3-kinase signaling mediated protection from GLP-1/exendin‑4.

    Outcome
    Not applicablePI3-kinase mediation
    Study

    n: not reported in source

    High-glucose PC12 cells
    Outcome group
    Receptor activity and mechanism · Nervous system and cognition

    Source sentences

    Summary
    Our study demonstrated that GLP-1/Ex-4 could exert a protective effect against reduced viability of PC12 cells caused by high glucose and that this protective effect was mediated via the PI3-kinase pathway.

    In this study, Exenatide (exendin-4) 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 Exenatide (exendin-4).

  3. 07LabNot a test of Exenatide (exendin-4) aloneIn vitro (cells)Efficacy outcome

    In PC12 cells, GLP-1/exendin‑4 reduced oxidative stress-induced injury.

    In plain wordsIn cells, GLP-1/exendin‑4 reduced injury from oxidative stress.

    Outcome
    DecreaseOxidative injury
    Study

    n: not reported in source

    Oxidative stress in PC12 cells
    Outcome group
    Neuroprotection · Nervous system and cognition

    Source sentences

    Summary
    In addition, GLP-1/Ex-4 ameliorated oxidative stress-induced injury in PC12 cells.

    In this study, Exenatide (exendin-4) 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 Exenatide (exendin-4).

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

    22 Oct 2026, 02:26 UTC

    Study results updated

  2. Version 1

    21 Oct 2026, 18:59 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

PepBank is a research reference. Talk to a doctor before you use any peptide.