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Study · Ex vivo tissue · rat · 2004

8 results

Mechanism of ipamorelin-evoked insulin release from the pancreas of normal and diabetic rats.

Adeghate E, Ponery AS

Neuro endocrinology letters1 Dec 2004

PMID15665799 (opens in a new tab)PepBankPUB-15665799

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 study8

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

  1. 01LabEx vivo tissueEfficacy outcome

    In pancreatic tissue from normal rats, ipamorelin increased insulin secretion.

    In plain wordsIn lab tests on rat pancreatic tissue, ipamorelin increased insulin release.

    Peptide
    Ipamorelin
    Outcome
    IncreaseInsulin secretion, normal rats
    Study

    ratn: not reported in source

    pancreatic tissue fragments of normal rats
    Outcome group
    Glycemic control · Endocrine and hormones
    Studied dose
    10(-12) - 10(-6) MAs given in this study (rat).

    Source sentences

    Summary
    Ipamorelin evoked significant (p<0.04) increases in insulin secretion from the pancreas of normal and diabetic rats.
    1 context sentence
    Summary · context
    Four weeks after the induction of diabetes, pancreatic tissue fragments of normal and diabetic rats were removed and incubated with different concentrations (10(-12) - 10(-6) M) of IPA.
  2. 02LabEx vivo tissueEfficacy outcome

    In pancreatic tissue from streptozotocin-diabetic rats, ipamorelin increased insulin secretion.

    In plain wordsIn lab tests on pancreatic tissue from diabetic rats, ipamorelin increased insulin release.

    Peptide
    Ipamorelin
    Outcome
    IncreaseInsulin secretion, diabetic rats
    Study

    ratn: not reported in source

    pancreatic tissue fragments of streptozotocin-diabetic rats
    Outcome group
    Glycemic control · Endocrine and hormones
    Studied dose
    10(-12) - 10(-6) MAs given in this study (rat).

    Source sentences

    Summary
    Ipamorelin evoked significant (p<0.04) increases in insulin secretion from the pancreas of normal and diabetic rats.
    1 context sentence
    Summary · context
    Four weeks after the induction of diabetes, pancreatic tissue fragments of normal and diabetic rats were removed and incubated with different concentrations (10(-12) - 10(-6) M) of IPA.

Studies that did not test the peptide alone6

In this study, Ipamorelin 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 Ipamorelin.

  1. 03LabNot a test of Ipamorelin aloneEx vivo tissueMechanism

    In rat pancreatic tissue, diltiazem significantly inhibited ipamorelin-evoked insulin secretion.

    In plain wordsIn lab tests on rat pancreatic tissue, diltiazem reduced the insulin release triggered by ipamorelin.

    Peptide
    Ipamorelin
    Outcome
    DecreaseDiltiazem effect on ipamorelin-evoked insulin secretion
    Study

    ratn: not reported in source

    pancreatic tissue fragments of normal and diabetic rats
    Outcome group
    Glycemic control · Endocrine and hormones

    Source sentences

    Summary
    Either diltiazem or yohimbine or propranolol or a combination of atropine, propranolol and yohimbine inhibited IPA-evoked insulin secretion significantly (p<0.03) from the pancreas of normal and diabetic rats.
    1 context sentence
    Summary · context
    Four weeks after the induction of diabetes, pancreatic tissue fragments of normal and diabetic rats were removed and incubated with different concentrations (10(-12) - 10(-6) M) of IPA.

    In this study, Ipamorelin 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 Ipamorelin.

  2. 04LabNot a test of Ipamorelin aloneEx vivo tissueMechanism

    In rat pancreatic tissue, yohimbine significantly inhibited ipamorelin-evoked insulin secretion.

    In plain wordsIn lab tests on rat pancreatic tissue, yohimbine reduced the insulin release triggered by ipamorelin.

    Peptide
    Ipamorelin
    Outcome
    DecreaseYohimbine effect on ipamorelin-evoked insulin secretion
    Study

    ratn: not reported in source

    pancreatic tissue fragments of normal and diabetic rats
    Outcome group
    Glycemic control · Endocrine and hormones

    Source sentences

    Summary
    Either diltiazem or yohimbine or propranolol or a combination of atropine, propranolol and yohimbine inhibited IPA-evoked insulin secretion significantly (p<0.03) from the pancreas of normal and diabetic rats.
    1 context sentence
    Summary · context
    Four weeks after the induction of diabetes, pancreatic tissue fragments of normal and diabetic rats were removed and incubated with different concentrations (10(-12) - 10(-6) M) of IPA.

    In this study, Ipamorelin 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 Ipamorelin.

  3. 05LabNot a test of Ipamorelin aloneEx vivo tissueMechanism

    In rat pancreatic tissue, propranolol significantly inhibited ipamorelin-evoked insulin secretion.

    In plain wordsIn lab tests on rat pancreatic tissue, propranolol reduced the insulin release triggered by ipamorelin.

    Peptide
    Ipamorelin
    Outcome
    DecreasePropranolol effect on ipamorelin-evoked insulin secretion
    Study

    ratn: not reported in source

    pancreatic tissue fragments of normal and diabetic rats
    Outcome group
    Glycemic control · Endocrine and hormones

    Source sentences

    Summary
    Either diltiazem or yohimbine or propranolol or a combination of atropine, propranolol and yohimbine inhibited IPA-evoked insulin secretion significantly (p<0.03) from the pancreas of normal and diabetic rats.
    1 context sentence
    Summary · context
    Four weeks after the induction of diabetes, pancreatic tissue fragments of normal and diabetic rats were removed and incubated with different concentrations (10(-12) - 10(-6) M) of IPA.

    In this study, Ipamorelin 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 Ipamorelin.

  4. 06LabNot a test of Ipamorelin aloneEx vivo tissueMechanism

    In rat pancreatic tissue, the combination of atropine, propranolol and yohimbine significantly inhibited ipamorelin-evoked insulin secretion.

    In plain wordsIn lab tests on rat pancreatic tissue, a combination of three blockers reduced the insulin release triggered by ipamorelin.

    Peptide
    Ipamorelin
    Outcome
    DecreaseAtropine, propranolol and yohimbine combination effect on ipamorelin-evoked insulin secretion
    Study

    ratn: not reported in source

    pancreatic tissue fragments of normal and diabetic rats
    Outcome group
    Glycemic control · Endocrine and hormones

    Source sentences

    Summary
    Either diltiazem or yohimbine or propranolol or a combination of atropine, propranolol and yohimbine inhibited IPA-evoked insulin secretion significantly (p<0.03) from the pancreas of normal and diabetic rats.
    1 context sentence
    Summary · context
    Four weeks after the induction of diabetes, pancreatic tissue fragments of normal and diabetic rats were removed and incubated with different concentrations (10(-12) - 10(-6) M) of IPA.

    In this study, Ipamorelin 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 Ipamorelin.

  5. 07LabNot a test of Ipamorelin aloneEx vivo tissueMechanism

    In pancreatic tissue from diabetic rats, atropine significantly reduced ipamorelin-induced insulin secretion.

    In plain wordsIn lab tests on pancreatic tissue from diabetic rats, atropine reduced the insulin release triggered by ipamorelin.

    Peptide
    Ipamorelin
    Outcome
    DecreaseAtropine effect on ipamorelin-induced insulin secretion, diabetic rats
    Study

    ratn: not reported in source

    pancreatic tissue fragments of streptozotocin-diabetic rats
    Outcome group
    Glycemic control · Endocrine and hormones

    Source sentences

    Summary
    Atropine caused a significant (p<0.007) reduction in the IPA-induced insulin secretion in diabetic but not in normal rats.
    1 context sentence
    Summary · context
    Four weeks after the induction of diabetes, pancreatic tissue fragments of normal and diabetic rats were removed and incubated with different concentrations (10(-12) - 10(-6) M) of IPA.

    In this study, Ipamorelin 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 Ipamorelin.

  6. 08LabNot a test of Ipamorelin aloneEx vivo tissueMechanism

    In pancreatic tissue from normal rats, atropine did not significantly reduce ipamorelin-induced insulin secretion.

    In plain wordsIn lab tests on pancreatic tissue from normal rats, atropine did not reduce the insulin release triggered by ipamorelin.

    Peptide
    Ipamorelin
    Outcome
    No significant changeAtropine effect on ipamorelin-induced insulin secretion, normal rats
    Study

    ratn: not reported in source

    pancreatic tissue fragments of normal rats
    Outcome group
    Glycemic control · Endocrine and hormones

    Source sentences

    Summary
    Atropine caused a significant (p<0.007) reduction in the IPA-induced insulin secretion in diabetic but not in normal rats.
    1 context sentence
    Summary · context
    Four weeks after the induction of diabetes, pancreatic tissue fragments of normal and diabetic rats were removed and incubated with different concentrations (10(-12) - 10(-6) M) of IPA.

    In this study, Ipamorelin 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 Ipamorelin.

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, 03:13 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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