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Study · Animal study (in vivo) · rat · 2004

6 results

Pituitary and gonadal effects of GnRH (gonadotropin releasing hormone) analogues in two peripubertal female rat models.

Roth C, Hegemann F, Hildebrandt J, Balzer I, Witt A, Wuttke W, Jarry H

Pediatric research6 Nov 2003Cited by 7 (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 study6

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

  1. 01AnimalAnimal study (in vivo)Mechanism

    In ovariectomized rats, triptorelin inhibited pituitary LHbeta mRNA compared with controls.

    In plain wordsIn rats, triptorelin reduced pituitary LHbeta gene expression compared with controls.

    Outcome
    DecreasePituitary LHbeta mRNA
    Study

    ratn: not reported in source

    Prepubertal ovariectomized female rats
    Comparator
    Controls
    Outcome group
    Receptor activity and mechanism · Endocrine and hormones
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Pituitary gonadotropin subunit LHbeta mRNA levels were inhibited in all groups except controls
    1 context sentence
    Summary · context
    To compare modes of action and effectiveness of GnRH analogues and assess treatment combinations of agonistic (triptorelin) and antagonistic (cetrorelix acetate) GnRH analogues with established treatment, we used prepubertal 31-d-old ovariectomized female rats.
  2. 02AnimalAnimal study (in vivo)Mechanism

    In ovariectomized rats, triptorelin stimulated pituitary GnRH receptor mRNA.

    In plain wordsIn rats, triptorelin increased pituitary GnRH receptor gene expression.

    Outcome
    IncreasePituitary GnRH receptor mRNA
    Study

    ratn: not reported in source

    Prepubertal ovariectomized female rats
    Outcome group
    Receptor activity and mechanism · Endocrine and hormones
    Studied dose
    Dose not stated

    Source sentences

    Summary
    but pituitary GnRH receptor mRNA was stimulated by agonist yet unaffected by combined analogues.
    1 context sentence
    Summary · context
    To compare modes of action and effectiveness of GnRH analogues and assess treatment combinations of agonistic (triptorelin) and antagonistic (cetrorelix acetate) GnRH analogues with established treatment, we used prepubertal 31-d-old ovariectomized female rats.
  3. 03LabEx vivo tissueMechanism

    In explanted rat ovaries, triptorelin did not significantly reduce GnRH receptor mRNA after incubation.

    In plain wordsIn lab tests on rat ovaries, triptorelin did not significantly reduce GnRH receptor gene expression.

    Outcome
    No significant changeOvarian GnRH receptor mRNA
    Study

    ratn: not reported in source

    Explanted rat ovaries
    Outcome group
    Receptor activity and mechanism · Endocrine and hormones
    Studied dose
    10-6 M · 4 hAs given in this study (rat).

    Source sentences

    Summary
    After 4 h, GnRH receptor mRNA levels were significantly reduced by antagonist but not agonist.
    1 context sentence
    Summary · context
    Explanted ovaries were incubated with either analogue, both 10-6 M.

Studies that did not test the peptide alone3

In this study, Triptorelin (Trelstar, Decapeptyl) 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 Triptorelin (Trelstar, Decapeptyl).

  1. 04AnimalNot a test of Triptorelin (Trelstar, Decapeptyl) aloneAnimal study (in vivo)Mechanism

    In ovariectomized rats, combined triptorelin and cetrorelix reduced serum LH versus controls.

    In plain wordsIn rats, combined triptorelin and cetrorelix reduced blood LH compared with controls.

    Outcome
    DecreaseSerum LH with combined analogues
    Study

    ratn: not reported in source

    Prepubertal ovariectomized female rats
    Comparator
    Controls
    Outcome group
    Receptor activity and mechanism · Endocrine and hormones

    Measurements

    LH
    0.52 ng/mL
    combined agonist/antagonist after 5 d
    LH
    4.9 ng/mL
    controls

    Source sentences

    Summary
    Combined agonist/antagonist was second most effective of the treatments (after 5 d treatment, LH 0.52 +/- 0.15 versus 4.9 +/- 1.1 ng/mL in controls; p < 0.01).
    1 context sentence
    Summary · context
    To compare modes of action and effectiveness of GnRH analogues and assess treatment combinations of agonistic (triptorelin) and antagonistic (cetrorelix acetate) GnRH analogues with established treatment, we used prepubertal 31-d-old ovariectomized female rats.

    In this study, Triptorelin (Trelstar, Decapeptyl) 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 Triptorelin (Trelstar, Decapeptyl).

  2. 05AnimalNot a test of Triptorelin (Trelstar, Decapeptyl) aloneAnimal study (in vivo)Mechanism

    In ovariectomized rats, combined triptorelin and cetrorelix inhibited pituitary LHbeta mRNA compared with controls.

    In plain wordsIn rats, combined triptorelin and cetrorelix reduced pituitary LHbeta gene expression compared with controls.

    Outcome
    DecreasePituitary LHbeta mRNA with combined analogues
    Study

    ratn: not reported in source

    Prepubertal ovariectomized female rats
    Comparator
    Controls
    Outcome group
    Receptor activity and mechanism · Endocrine and hormones

    Source sentences

    Summary
    Pituitary gonadotropin subunit LHbeta mRNA levels were inhibited in all groups except controls
    1 context sentence
    Summary · context
    To compare modes of action and effectiveness of GnRH analogues and assess treatment combinations of agonistic (triptorelin) and antagonistic (cetrorelix acetate) GnRH analogues with established treatment, we used prepubertal 31-d-old ovariectomized female rats.

    In this study, Triptorelin (Trelstar, Decapeptyl) 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 Triptorelin (Trelstar, Decapeptyl).

  3. 06AnimalNot a test of Triptorelin (Trelstar, Decapeptyl) aloneAnimal study (in vivo)Mechanism

    In ovariectomized rats, combined triptorelin and cetrorelix did not affect pituitary GnRH receptor mRNA.

    In plain wordsIn rats, combined triptorelin and cetrorelix did not affect pituitary GnRH receptor gene expression.

    Outcome
    No significant changePituitary GnRH receptor mRNA with combined analogues
    Study

    ratn: not reported in source

    Prepubertal ovariectomized female rats
    Outcome group
    Receptor activity and mechanism · Endocrine and hormones

    Source sentences

    Summary
    but pituitary GnRH receptor mRNA was stimulated by agonist yet unaffected by combined analogues.
    1 context sentence
    Summary · context
    To compare modes of action and effectiveness of GnRH analogues and assess treatment combinations of agonistic (triptorelin) and antagonistic (cetrorelix acetate) GnRH analogues with established treatment, we used prepubertal 31-d-old ovariectomized female rats.

    In this study, Triptorelin (Trelstar, Decapeptyl) 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 Triptorelin (Trelstar, Decapeptyl).

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 3Current

    27 Oct 2026, 16:35 UTC

    Study data updated · source update from Europe PMC

  2. Version 2

    22 Oct 2026, 02:26 UTC

    Study results updated

  3. Version 1

    21 Oct 2026, 18:59 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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