Skip to content

Study · Randomized controlled trial · n = 24 · 2018

7 results

Exenatide Increases IL-1RA Concentration and Induces Nrf-2‒Keap-1‒Regulated Antioxidant Enzymes: Relevance to β-Cell Function.

Dandona P, Ghanim H, Abuaysheh S, Green K, Dhindsa S, Makdissi A, Batra M, Kuhadiya ND, Chaudhuri A

The Journal of clinical endocrinology and metabolism1 Mar 2018Cited by 15 (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

7 results from studies that gave the peptide. 7 results from people.

  1. 01HumanRandomized controlled trialMechanism

    In patients with obesity and T2DM, exenatide increased plasma IL-1RA concentration.

    In plain wordsIn patients with obesity and diabetes, exenatide increased an anti-inflammatory protein in blood.

    Outcome
    IncreaseIL-1RA concentration
    Study

    n = 24

    Outcome group
    Inflammation markers · Immune and inflammation
    Studied dose
    10 μg twice a day · 12 weeksAs given in this study (human).

    Measurements

    IL-1RA increase
    61%
    exenatide
    IL-1RA concentration
    318 pg/mL
    before exenatide
    IL-1RA concentration
    456 pg/mL
    after exenatide

    Source sentences

    Summary
    Exenatide increased IL-1RA concentration by 61% (from 318 ± 53 to 456 ± 88 pg/mL; P < 0.05).
    1 context sentence
    Summary · context
    Twenty-four patients with obesity and type 2 diabetes receiving combined oral and insulin therapy were randomly assigned to receive either exenatide 10 μg or placebo twice a day for 12 weeks.
  2. 02HumanRandomized controlled trialMechanism

    In patients with obesity and T2DM, exenatide suppressed mononuclear-cell Keap-1 protein.

    In plain wordsIn patients with obesity and diabetes, exenatide reduced Keap-1 protein in blood immune cells.

    Outcome
    DecreaseKeap-1 protein
    Study

    n = 24

    Outcome group
    Inflammation markers · Immune and inflammation
    Studied dose
    10 μg twice a day · 12 weeksAs given in this study (human).

    Source sentences

    Summary
    Exenatide treatment also suppressed Keap-1 protein (P < 0.05) and increased messenger RNA expression of NQO-1, glutathione S-transferase PI, heme oxygenase-1, and p21 and increased NAD(P)H dehydrogenase [quinone] 1 protein (P < 0.05) in mononuclear cells.
    1 context sentence
    Summary · context
    Twenty-four patients with obesity and type 2 diabetes receiving combined oral and insulin therapy were randomly assigned to receive either exenatide 10 μg or placebo twice a day for 12 weeks.
  3. 03HumanRandomized controlled trialMechanism

    In patients with obesity and T2DM, exenatide increased mononuclear-cell NQO-1 mRNA expression.

    In plain wordsIn patients with obesity and diabetes, exenatide increased NQO-1 gene activity in blood immune cells.

    Outcome
    IncreaseNQO-1 mRNA
    Study

    n = 24

    Outcome group
    Inflammation markers · Immune and inflammation
    Studied dose
    10 μg twice a day · 12 weeksAs given in this study (human).

    Source sentences

    Summary
    Exenatide treatment also suppressed Keap-1 protein (P < 0.05) and increased messenger RNA expression of NQO-1, glutathione S-transferase PI, heme oxygenase-1, and p21 and increased NAD(P)H dehydrogenase [quinone] 1 protein (P < 0.05) in mononuclear cells.
    1 context sentence
    Summary · context
    Twenty-four patients with obesity and type 2 diabetes receiving combined oral and insulin therapy were randomly assigned to receive either exenatide 10 μg or placebo twice a day for 12 weeks.
  4. 04HumanRandomized controlled trialMechanism

    In patients with obesity and T2DM, exenatide increased mononuclear-cell glutathione S-transferase PI mRNA expression.

    In plain wordsIn patients with obesity and diabetes, exenatide increased glutathione S-transferase PI gene activity in blood immune cells.

    Outcome
    IncreaseGlutathione S-transferase PI mRNA
    Study

    n = 24

    Outcome group
    Inflammation markers · Immune and inflammation
    Studied dose
    10 μg twice a day · 12 weeksAs given in this study (human).

    Source sentences

    Summary
    Exenatide treatment also suppressed Keap-1 protein (P < 0.05) and increased messenger RNA expression of NQO-1, glutathione S-transferase PI, heme oxygenase-1, and p21 and increased NAD(P)H dehydrogenase [quinone] 1 protein (P < 0.05) in mononuclear cells.
    1 context sentence
    Summary · context
    Twenty-four patients with obesity and type 2 diabetes receiving combined oral and insulin therapy were randomly assigned to receive either exenatide 10 μg or placebo twice a day for 12 weeks.
  5. 05HumanRandomized controlled trialMechanism

    In patients with obesity and T2DM, exenatide increased mononuclear-cell heme oxygenase-1 mRNA expression.

    In plain wordsIn patients with obesity and diabetes, exenatide increased heme oxygenase-1 gene activity in blood immune cells.

    Outcome
    IncreaseHeme oxygenase-1 mRNA
    Study

    n = 24

    Outcome group
    Inflammation markers · Immune and inflammation
    Studied dose
    10 μg twice a day · 12 weeksAs given in this study (human).

    Source sentences

    Summary
    Exenatide treatment also suppressed Keap-1 protein (P < 0.05) and increased messenger RNA expression of NQO-1, glutathione S-transferase PI, heme oxygenase-1, and p21 and increased NAD(P)H dehydrogenase [quinone] 1 protein (P < 0.05) in mononuclear cells.
    1 context sentence
    Summary · context
    Twenty-four patients with obesity and type 2 diabetes receiving combined oral and insulin therapy were randomly assigned to receive either exenatide 10 μg or placebo twice a day for 12 weeks.
  6. 06HumanRandomized controlled trialMechanism

    In patients with obesity and T2DM, exenatide increased mononuclear-cell p21 mRNA expression.

    In plain wordsIn patients with obesity and diabetes, exenatide increased p21 gene activity in blood immune cells.

    Outcome
    Increasep21 mRNA
    Study

    n = 24

    Outcome group
    Inflammation markers · Immune and inflammation
    Studied dose
    10 μg twice a day · 12 weeksAs given in this study (human).

    Source sentences

    Summary
    Exenatide treatment also suppressed Keap-1 protein (P < 0.05) and increased messenger RNA expression of NQO-1, glutathione S-transferase PI, heme oxygenase-1, and p21 and increased NAD(P)H dehydrogenase [quinone] 1 protein (P < 0.05) in mononuclear cells.
    1 context sentence
    Summary · context
    Twenty-four patients with obesity and type 2 diabetes receiving combined oral and insulin therapy were randomly assigned to receive either exenatide 10 μg or placebo twice a day for 12 weeks.
  7. 07HumanRandomized controlled trialMechanism

    In patients with obesity and T2DM, exenatide increased mononuclear-cell NAD(P)H dehydrogenase [quinone] 1 protein.

    In plain wordsIn patients with obesity and diabetes, exenatide increased an antioxidant enzyme protein in blood immune cells.

    Outcome
    IncreaseNAD(P)H dehydrogenase [quinone] 1 protein
    Study

    n = 24

    Outcome group
    Inflammation markers · Immune and inflammation
    Studied dose
    10 μg twice a day · 12 weeksAs given in this study (human).

    Source sentences

    Summary
    Exenatide treatment also suppressed Keap-1 protein (P < 0.05) and increased messenger RNA expression of NQO-1, glutathione S-transferase PI, heme oxygenase-1, and p21 and increased NAD(P)H dehydrogenase [quinone] 1 protein (P < 0.05) in mononuclear cells.
    1 context sentence
    Summary · context
    Twenty-four patients with obesity and type 2 diabetes receiving combined oral and insulin therapy were randomly assigned to receive either exenatide 10 μg or placebo twice a day for 12 weeks.

AI wrote and checked these results. AI can make mistakes, so check important results against the source.

Registered trials1

Trials this study reports on, or that list this study as a reference. Registry data from ClinicalTrials.gov.

1 trial · 1 completed · 1 with posted results · source ClinicalTrials.gov (opens in a new tab)

CompletedPhase 2Results postedNCT01154933

Exeantide in Type 2 Diabetes on Insulin

University at Buffalon = 24Apr 2008 to Nov 2011

Type 2 Diabetes

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.