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Study · Animal study (in vivo) · mouse · 2018

10 results

Impact of Perfluorooctane Sulfonate on Reproductive Ability of Female Mice through Suppression of Estrogen Receptor α-Activated Kisspeptin Neurons.

Wang X, Bai Y, Tang C, Cao X, Chang F, Chen L

Toxicological sciences : an official journal of the Society of Toxicology1 Oct 2018Cited by 47 (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 study10

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

  1. 01AnimalAnimal study (in vivo)Efficacy outcome

    In female mice exposed to PFOS, the GPR54 agonist kisspeptin‑10 corrected the prolongation of diestrus.

    In plain wordsIn mice exposed to a pollutant, kisspeptin‑10 corrected the longer resting phase of the cycle.

    Outcome
    DecreaseDiestrus prolongation in PFOS mice
    Study

    mousen: not reported in source

    Female mice exposed to PFOS
    Outcome group
    Sex hormones and fertility · Reproductive and sexual health
    Studied dose
    Dose not stated

    Source sentences

    Summary
    The administration of GPR54 agonist kisspeptin-10 in PFOS-mice could correct the prolongation of diestrus and reduction of corpora luteum, and recover the LH-surge and the levels of LH and GnRH.
  2. 02AnimalAnimal study (in vivo)Efficacy outcome

    In female mice exposed to PFOS, kisspeptin‑10 corrected the reduction of corpora luteum.

    In plain wordsIn mice exposed to a pollutant, kisspeptin‑10 restored the lower number of corpora luteum.

    Outcome
    IncreaseCorpora luteum number in PFOS mice
    Study

    mousen: not reported in source

    Female mice exposed to PFOS
    Outcome group
    Sex hormones and fertility · Reproductive and sexual health
    Studied dose
    Dose not stated

    Source sentences

    Summary
    The administration of GPR54 agonist kisspeptin-10 in PFOS-mice could correct the prolongation of diestrus and reduction of corpora luteum, and recover the LH-surge and the levels of LH and GnRH.
  3. 03AnimalAnimal study (in vivo)Efficacy outcome

    In female mice exposed to PFOS, kisspeptin‑10 recovered the LH surge.

    In plain wordsIn mice exposed to a pollutant, kisspeptin‑10 restored the LH surge.

    Outcome
    IncreaseLH surge in PFOS mice
    Study

    mousen: not reported in source

    Female mice exposed to PFOS
    Outcome group
    Sex hormones and fertility · Reproductive and sexual health
    Studied dose
    Dose not stated

    Source sentences

    Summary
    The administration of GPR54 agonist kisspeptin-10 in PFOS-mice could correct the prolongation of diestrus and reduction of corpora luteum, and recover the LH-surge and the levels of LH and GnRH.
  4. 04AnimalAnimal study (in vivo)Efficacy outcome

    In female mice exposed to PFOS, kisspeptin‑10 recovered the level of LH.

    In plain wordsIn mice exposed to a pollutant, kisspeptin‑10 restored LH levels.

    Outcome
    IncreaseLH level in PFOS mice
    Study

    mousen: not reported in source

    Female mice exposed to PFOS
    Outcome group
    Sex hormones and fertility · Reproductive and sexual health
    Studied dose
    Dose not stated

    Source sentences

    Summary
    The administration of GPR54 agonist kisspeptin-10 in PFOS-mice could correct the prolongation of diestrus and reduction of corpora luteum, and recover the LH-surge and the levels of LH and GnRH.
  5. 05AnimalAnimal study (in vivo)Efficacy outcome

    In female mice exposed to PFOS, kisspeptin‑10 recovered the level of GnRH.

    In plain wordsIn mice exposed to a pollutant, kisspeptin‑10 restored GnRH levels.

    Outcome
    IncreaseGnRH level in PFOS mice
    Study

    mousen: not reported in source

    Female mice exposed to PFOS
    Outcome group
    Sex hormones and fertility · Reproductive and sexual health
    Studied dose
    Dose not stated

    Source sentences

    Summary
    The administration of GPR54 agonist kisspeptin-10 in PFOS-mice could correct the prolongation of diestrus and reduction of corpora luteum, and recover the LH-surge and the levels of LH and GnRH.

Natural levels measured4

These results measure the body's own peptide. Nobody was given the peptide. They are not evidence about taking it. They are left out of key results, evidence counts and charts.

  1. 06AnimalEndogenous levelAnimal study (in vivo)Mechanism

    In female mice, PFOS suppressed the increase in the number of AVPV-kisspeptin neurons and in AVPV-kisspeptin expression seen in proestrus or after high-dose estradiol.

    In plain wordsIn mice, a pollutant blocked the rise in the body's own kisspeptin cells and kisspeptin levels in one brain region.

    Outcome
    DecreaseAVPV-kisspeptin neuron number and expression
    Study

    mousen: not reported in source

    Proestrus mice and ovariectomized mice given high-dose estradiol benzoate
    Outcome group
    Receptor activity and mechanism · Reproductive and sexual health

    Source sentences

    Summary
    The number of AVPV-kisspeptin neurons and the AVPV-kisspeptin expression were increased in proestrus mice or OVX-mice treated with high-dose estradiol benzoate (0.05 mg/kg), which were suppressed by the administration of PFOS.

    This result measures the body's own Kisspeptin-10. Nobody was given the peptide. It is not evidence about taking it.

  2. 07LabEndogenous levelEx vivo tissueMechanism

    In mouse hypothalamic slices, 100 nM estradiol for 4 hours significantly increased AVPV-kisspeptin expression.

    In plain wordsIn lab tests on mouse brain slices, estradiol raised the body's own kisspeptin levels in one brain region.

    Outcome
    IncreaseAVPV-kisspeptin expression with estradiol
    Study

    mousen: not reported in source

    Hypothalamic slices incubated in estradiol
    Outcome group
    Receptor activity and mechanism · Reproductive and sexual health

    Source sentences

    Summary
    In hypothalamic slices incubated in 100 nM E2 for 4 h, the AVPV-kisspeptin expression was significantly enhanced

    This result measures the body's own Kisspeptin-10. Nobody was given the peptide. It is not evidence about taking it.

  3. 08LabEndogenous levelEx vivo tissueMechanism

    In mouse hypothalamic slices, the estradiol-induced rise in AVPV-kisspeptin expression was inhibited by PFOS in a dose-dependent manner or by the ERα antagonist MPP, but not by the ERβ antagonist PHTPP.

    In plain wordsIn lab tests on mouse brain slices, a pollutant blocked the estradiol rise in the body's own kisspeptin levels.

    Outcome
    DecreaseAVPV-kisspeptin expression with PFOS or ER antagonists
    Study

    mousen: not reported in source

    Hypothalamic slices incubated in estradiol
    Outcome group
    Receptor activity and mechanism · Reproductive and sexual health

    Source sentences

    Summary
    which was inhibited by PFOS in a dose-dependent manner or estrogen receptor α (ERα) antagonist MPP, but not ERβ antagonist PHTPP.

    This result measures the body's own Kisspeptin-10. Nobody was given the peptide. It is not evidence about taking it.

  4. 09LabEndogenous levelEx vivo tissueMechanism

    In mouse hypothalamic slices, the ERα agonist PPT, but not the ERβ agonist DPN, increased AVPV-kisspeptin expression, and this was sensitive to PFOS.

    In plain wordsIn lab tests on mouse brain slices, an estrogen receptor activator raised the body's own kisspeptin levels, and a pollutant blocked this.

    Outcome
    IncreaseAVPV-kisspeptin expression with ERα agonist PPT
    Study

    mousen: not reported in source

    Hypothalamic slices
    Outcome group
    Receptor activity and mechanism · Reproductive and sexual health

    Source sentences

    Summary
    The incubation of ERα agonist PPT rather than ERβ agonist DPN could increase the level of AVPV-kisspeptin expression, which was sensitive to the treatment with PFOS.

    This result measures the body's own Kisspeptin-10. Nobody was given the peptide. It is not evidence about taking it.

Studies that did not test the peptide alone1

In this study, Kisspeptin-10 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 Kisspeptin-10.

  1. 10AnimalNot a test of Kisspeptin-10 aloneAnimal study (in vivo)Mechanism

    In ovariectomized mice given high-dose estradiol, PFOS or the GPR54 antagonist P234 prevented the LH surge.

    In plain wordsIn mice, a pollutant or a kisspeptin receptor blocker prevented the LH surge.

    Outcome
    DecreaseLH surge with PFOS or GPR54 antagonist P234
    Study

    mousen: not reported in source

    Ovariectomized mice given high-dose estradiol
    Outcome group
    Sex hormones and fertility · Reproductive and sexual health

    Source sentences

    Summary
    The administration of PFOS or GPR54 antagonist P234 prevented the generation of LH-surge in OVX-mice treated with high-dose E2.

    In this study, Kisspeptin-10 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 Kisspeptin-10.

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

    10 Oct 2026, 09:43 UTC

    Study results updated

  2. Version 1

    9 Oct 2026, 03:04 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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