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Study · Animal study (in vivo) · rat · 2001

6 results

Hormonal regulation of peripheral benzodiazepine receptor binding properties is mediated by subunit interaction.

Golani I, Weizman A, Leschiner S, Spanier I, Eckstein N, Limor R, Yanai J, Maaser K, Scherübl H, Weisinger G, Gavish M

Biochemistry1 Aug 2001Cited by 33 (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

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

  1. 01AnimalAnimal study (in vivo)Mechanism

    In female rats, triptorelin reduced ovarian PBR binding capacity by 40%.

    In plain wordsIn rats, triptorelin reduced ovarian receptor binding capacity by 40%.

    Outcome
    DecreaseOvarian PBR binding capacity
    Study

    ratn: not reported in source

    Adult female rats with pharmacological castration
    Outcome group
    Receptor activity and mechanism · Endocrine and hormones
    Studied dose
    Dose not stated

    Measurements

    PBR binding capacity reduction
    40%
    ovaries

    Source sentences

    Summary
    We found that PBR binding capacity dropped by 40 and 48% in ovaries and adrenals, respectively, following decapeptyl administration, as opposed to no change in the kidney.
    2 context sentences
    Summary · context
    To accomplish this, adult female rats were pharmacologically castrated using chronic administration of the gonadotropin-releasing hormone agonist decapeptyl (triptorelin-D-Trp(6)-LHRH).
    Summary · context
    Half of these rats received 17beta-estradiol as hormone replacement, while a control group received daily injections of vehicle only.
  2. 02AnimalAnimal study (in vivo)Mechanism

    In female rats, triptorelin reduced adrenal PBR binding capacity by 48%.

    In plain wordsIn rats, triptorelin reduced adrenal receptor binding capacity by 48%.

    Outcome
    DecreaseAdrenal PBR binding capacity
    Study

    ratn: not reported in source

    Adult female rats with pharmacological castration
    Outcome group
    Receptor activity and mechanism · Endocrine and hormones
    Studied dose
    Dose not stated

    Measurements

    PBR binding capacity reduction
    48%
    adrenals

    Source sentences

    Summary
    We found that PBR binding capacity dropped by 40 and 48% in ovaries and adrenals, respectively, following decapeptyl administration, as opposed to no change in the kidney.
    2 context sentences
    Summary · context
    To accomplish this, adult female rats were pharmacologically castrated using chronic administration of the gonadotropin-releasing hormone agonist decapeptyl (triptorelin-D-Trp(6)-LHRH).
    Summary · context
    Half of these rats received 17beta-estradiol as hormone replacement, while a control group received daily injections of vehicle only.
  3. 03AnimalAnimal study (in vivo)Mechanism

    In female rats, triptorelin did not change kidney PBR binding capacity.

    In plain wordsIn rats, triptorelin did not change kidney receptor binding capacity.

    Outcome
    No significant changeKidney PBR binding capacity
    Study

    ratn: not reported in source

    Adult female rats with pharmacological castration
    Outcome group
    Receptor activity and mechanism · Endocrine and hormones
    Studied dose
    Dose not stated

    Source sentences

    Summary
    We found that PBR binding capacity dropped by 40 and 48% in ovaries and adrenals, respectively, following decapeptyl administration, as opposed to no change in the kidney.
    2 context sentences
    Summary · context
    To accomplish this, adult female rats were pharmacologically castrated using chronic administration of the gonadotropin-releasing hormone agonist decapeptyl (triptorelin-D-Trp(6)-LHRH).
    Summary · context
    Half of these rats received 17beta-estradiol as hormone replacement, while a control group received daily injections of vehicle only.
  4. 04AnimalAnimal study (in vivo)Mechanism

    In female rats, the study found no evidence for transcriptional, posttranscriptional or translational mechanisms underlying triptorelin-induced PBR down-regulation.

    In plain wordsIn rats, the study found no evidence that transcription or translation explained triptorelin-related receptor reductions.

    Outcome
    Not applicableTranscriptional, posttranscriptional and translational regulation
    Study

    ratn: not reported in source

    Adult female rats with pharmacological castration
    Outcome group
    Receptor activity and mechanism · Endocrine and hormones
    Studied dose
    Dose not stated

    Source sentences

    Summary
    We did not find evidence for transcriptional, posttranscriptional, and translational mechanisms in this decapeptyl-induced down-regulation.
    2 context sentences
    Summary · context
    To accomplish this, adult female rats were pharmacologically castrated using chronic administration of the gonadotropin-releasing hormone agonist decapeptyl (triptorelin-D-Trp(6)-LHRH).
    Summary · context
    Half of these rats received 17beta-estradiol as hormone replacement, while a control group received daily injections of vehicle only.
  5. 05AnimalAnimal study (in vivo)Mechanism

    In female rats, triptorelin-associated PBR down-regulation coincided with changes in PBR subunit interactions.

    In plain wordsIn rats, triptorelin-related receptor reductions coincided with changes in interactions between receptor subunits.

    Outcome
    Direction not reportedPBR subunit interactions
    Study

    ratn: not reported in source

    Adult female rats with pharmacological castration
    Outcome group
    Receptor activity and mechanism · Endocrine and hormones
    Studied dose
    Dose not stated

    Source sentences

    Summary
    In contrast, immunoprecipitation of the PBR complex, using antibodies against the 18- and 32-kDa subunits of the complex, demonstrated that there were changes in PBR subunit interactions, consistent with the down-regulation of PBR binding capacity.
    2 context sentences
    Summary · context
    To accomplish this, adult female rats were pharmacologically castrated using chronic administration of the gonadotropin-releasing hormone agonist decapeptyl (triptorelin-D-Trp(6)-LHRH).
    Summary · context
    Half of these rats received 17beta-estradiol as hormone replacement, while a control group received daily injections of vehicle only.

Studies that did not test the peptide alone1

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

    In triptorelin-castrated female rats, estradiol replacement prevented the reduction in PBR density.

    In plain wordsIn rats given triptorelin, estradiol replacement prevented the reduction in receptor density.

    Outcome
    No significant changeEstradiol prevention of PBR down-regulation
    Study

    ratn: not reported in source

    Adult female rats with pharmacological castration
    Outcome group
    Receptor activity and mechanism · Endocrine and hormones

    Source sentences

    Summary
    This down-regulation of PBR densities was prevented by estradiol replacement.
    2 context sentences
    Summary · context
    To accomplish this, adult female rats were pharmacologically castrated using chronic administration of the gonadotropin-releasing hormone agonist decapeptyl (triptorelin-D-Trp(6)-LHRH).
    Summary · context
    Half of these rats received 17beta-estradiol as hormone replacement, while a control group received daily injections of vehicle only.

    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 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.

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