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Study · Randomized controlled trial · n = 42 · 2010

5 results

Pre- versus postmenopausal age, estradiol, and peptide-secretagogue type determine pulsatile growth hormone secretion in healthy women: studies using submaximal agonist drive and an estrogen clamp.

Hudson SB, Schroeder DR, Bailey JN, Mielke KL, Erickson D, Miles JM, Bowers CY, Veldhuis JD

The Journal of clinical endocrinology and metabolism26 Oct 2009Cited by 11 (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 study5

1 result from studies that gave the peptide. 1 result from people.

  1. 01HumanRandomized controlled trialEfficacy outcome

    In healthy pre- and postmenopausal women, a half-maximal GHRP‑2 bolus stimulated more pulsatile GH secretion than a GHRH bolus of the same dose.

    In plain wordsIn healthy women, GHRP‑2 raised pulsatile growth hormone release more than GHRH at the same dose.

    Peptide
    GHRP-2
    Outcome
    IncreaseSubmaximally stimulated pulsatile GH secretion, GHRP-2 vs GHRH
    Study

    n = 42

    Comparator
    GHRH
    Outcome group
    Growth hormone and IGF-1 · Endocrine and hormones
    Studied dose
    0.33 mug/kg · iv bolusAs given in this study (human).

    Source sentences

    Summary
    Submaximally stimulated pulsatile GH secretion was positively determined by PRE vs. POST age (P < 0.001), E(2) repletion vs. depletion (P = 0.001) and GHRP-2 vs. GHRH stimulation (P < 0.001), after adjustment for AVF and basal secretion.
    2 context sentences
    Summary · context
    Community-dwelling healthy premenopausal (PRE, age 24 +/- 0.8 yr, n = 20) and postmenopausal (POST, age 63 +/- 1.8 yr, n = 22) women participated in the study.
    Summary · context
    Gonadal-axis down-regulation with leuprolide was followed by randomized addback of placebo or transdermal E(2) and separate-day iv bolus injections of a half-maximally stimulatory dose of GHRP-2 or GHRH (each 0.33 mug/kg).

Studies that did not test the peptide alone4

In this study, GHRP-2 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 GHRP-2.

  1. 02HumanNot a test of GHRP-2 aloneRandomized controlled trialEfficacy outcome

    In healthy women given GHRP‑2 or GHRH, pulsatile GH secretion was higher in premenopausal than in postmenopausal women, after adjustment for AVF and basal secretion.

    In plain wordsIn healthy women given GHRP‑2 or GHRH, younger premenopausal women released more pulsatile growth hormone than postmenopausal women.

    Peptide
    GHRP-2
    Outcome
    Not applicablePulsatile GH secretion, premenopausal vs postmenopausal age
    Study

    n = 42

    Outcome group
    Growth hormone and IGF-1 · Endocrine and hormones

    Source sentences

    Summary
    Submaximally stimulated pulsatile GH secretion was positively determined by PRE vs. POST age (P < 0.001), E(2) repletion vs. depletion (P = 0.001) and GHRP-2 vs. GHRH stimulation (P < 0.001), after adjustment for AVF and basal secretion.
    2 context sentences
    Summary · context
    Community-dwelling healthy premenopausal (PRE, age 24 +/- 0.8 yr, n = 20) and postmenopausal (POST, age 63 +/- 1.8 yr, n = 22) women participated in the study.
    Summary · context
    Gonadal-axis down-regulation with leuprolide was followed by randomized addback of placebo or transdermal E(2) and separate-day iv bolus injections of a half-maximally stimulatory dose of GHRP-2 or GHRH (each 0.33 mug/kg).

    In this study, GHRP-2 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 GHRP-2.

  2. 03HumanNot a test of GHRP-2 aloneRandomized controlled trialEfficacy outcome

    In healthy women given GHRP‑2 or GHRH, E2 repletion increased pulsatile GH secretion versus depletion.

    In plain wordsIn healthy women given GHRP‑2 or GHRH, restoring estradiol raised pulsatile growth hormone release compared with estradiol depletion.

    Peptide
    GHRP-2
    Outcome
    IncreasePulsatile GH secretion, E2 repletion vs depletion
    Study

    n = 42

    Outcome group
    Growth hormone and IGF-1 · Endocrine and hormones

    Source sentences

    Summary
    Submaximally stimulated pulsatile GH secretion was positively determined by PRE vs. POST age (P < 0.001), E(2) repletion vs. depletion (P = 0.001) and GHRP-2 vs. GHRH stimulation (P < 0.001), after adjustment for AVF and basal secretion.
    2 context sentences
    Summary · context
    Community-dwelling healthy premenopausal (PRE, age 24 +/- 0.8 yr, n = 20) and postmenopausal (POST, age 63 +/- 1.8 yr, n = 22) women participated in the study.
    Summary · context
    Gonadal-axis down-regulation with leuprolide was followed by randomized addback of placebo or transdermal E(2) and separate-day iv bolus injections of a half-maximally stimulatory dose of GHRP-2 or GHRH (each 0.33 mug/kg).

    In this study, GHRP-2 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 GHRP-2.

  3. 04HumanNot a test of GHRP-2 aloneRandomized controlled trialEfficacy outcome

    In healthy pre- and postmenopausal women, E2 versus placebo elevated fasting mean GH concentrations.

    In plain wordsIn healthy women, estradiol raised fasting growth hormone levels compared with placebo.

    Peptide
    GHRP-2
    Outcome
    IncreaseFasting mean GH concentration with E2
    Study

    n = 42

    Comparator
    Placebo
    Outcome group
    Growth hormone and IGF-1 · Endocrine and hormones

    Source sentences

    Summary
    E(2) vs. placebo elevated fasting mean GH concentrations in both PRE and POST women (P = 0.006) but increased basal (nonpulsatile) GH secretion in PRE only (P = 0.002).
    2 context sentences
    Summary · context
    Community-dwelling healthy premenopausal (PRE, age 24 +/- 0.8 yr, n = 20) and postmenopausal (POST, age 63 +/- 1.8 yr, n = 22) women participated in the study.
    Summary · context
    Gonadal-axis down-regulation with leuprolide was followed by randomized addback of placebo or transdermal E(2) and separate-day iv bolus injections of a half-maximally stimulatory dose of GHRP-2 or GHRH (each 0.33 mug/kg).

    In this study, GHRP-2 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 GHRP-2.

  4. 05HumanNot a test of GHRP-2 aloneRandomized controlled trialEfficacy outcome

    In healthy premenopausal women only, E2 versus placebo increased basal (nonpulsatile) GH secretion.

    In plain wordsIn healthy premenopausal women only, estradiol raised basal growth hormone release compared with placebo.

    Peptide
    GHRP-2
    Outcome
    IncreaseBasal (nonpulsatile) GH secretion with E2
    Study

    n = 42

    Comparator
    Placebo
    Outcome group
    Growth hormone and IGF-1 · Endocrine and hormones

    Source sentences

    Summary
    E(2) vs. placebo elevated fasting mean GH concentrations in both PRE and POST women (P = 0.006) but increased basal (nonpulsatile) GH secretion in PRE only (P = 0.002).
    2 context sentences
    Summary · context
    Community-dwelling healthy premenopausal (PRE, age 24 +/- 0.8 yr, n = 20) and postmenopausal (POST, age 63 +/- 1.8 yr, n = 22) women participated in the study.
    Summary · context
    Gonadal-axis down-regulation with leuprolide was followed by randomized addback of placebo or transdermal E(2) and separate-day iv bolus injections of a half-maximally stimulatory dose of GHRP-2 or GHRH (each 0.33 mug/kg).

    In this study, GHRP-2 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 GHRP-2.

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, 16:37 UTC

    Study data updated · source update from Europe PMC

  2. Version 2

    13 Oct 2026, 21:44 UTC

    Study results updated

  3. Version 1

    13 Oct 2026, 16:31 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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