Skip to content

Study · Animal study (in vivo) · mouse · 2025

12 results

Kisspeptin-54 Restores Blood-Brain Barrier Integrity via GATA-4 in Ischemic Stroke.

Shan W, Lan H, Wu Y, Xu Q, You M, Ma R

Chemical biology & drug design1 Jun 2025Cited by 2 (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 study12

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

  1. 01AnimalAnimal study (in vivo)Efficacy outcome

    In mice with middle cerebral artery occlusion, prophylactic Kisspeptin‑54 reduced cerebral infarct volume by 42%.

    In plain wordsIn mice with stroke, Kisspeptin‑54 given beforehand reduced the size of the brain damage by 42%.

    Outcome
    DecreaseCerebral infarct volume
    Study

    mousen: not reported in source

    middle cerebral artery occlusion (MCAO)
    Outcome group
    Neuroprotection · Nervous system and cognition
    Studied dose
    Dose not stated

    Measurements

    Infarct volume reduction
    42%
    prophylactic Kisspeptin-54

    Source sentences

    Summary
    Prophylactic Kisspeptin-54 reduced cerebral infarct volume by 42%
    1 context sentence
    Summary · context
    In vivo, mice underwent middle cerebral artery occlusion (MCAO), and cerebral infarct volume, neurological function, and blood-brain barrier (BBB) permeability were evaluated.
  2. 02AnimalAnimal study (in vivo)Efficacy outcome

    In mice with middle cerebral artery occlusion, prophylactic Kisspeptin‑54 enhanced neurological performance by 49%.

    In plain wordsIn mice with stroke, Kisspeptin‑54 given beforehand improved nerve function scores by 49%.

    Outcome
    IncreaseNeurological performance
    Study

    mousen: not reported in source

    middle cerebral artery occlusion (MCAO)
    Outcome group
    Neuroprotection · Nervous system and cognition
    Studied dose
    Dose not stated

    Measurements

    Neurological performance improvement
    49%
    prophylactic Kisspeptin-54

    Source sentences

    Summary
    Prophylactic Kisspeptin-54 reduced cerebral infarct volume by 42%, enhanced neurological performance by 49%
    1 context sentence
    Summary · context
    In vivo, mice underwent middle cerebral artery occlusion (MCAO), and cerebral infarct volume, neurological function, and blood-brain barrier (BBB) permeability were evaluated.
  3. 03AnimalAnimal study (in vivo)Efficacy outcome

    In mice with middle cerebral artery occlusion, prophylactic Kisspeptin‑54 decreased blood-brain barrier leakage by 26%.

    In plain wordsIn mice with stroke, Kisspeptin‑54 given beforehand reduced leakage across the blood-brain barrier by 26%.

    Outcome
    DecreaseBlood-brain barrier leakage
    Study

    mousen: not reported in source

    middle cerebral artery occlusion (MCAO)
    Outcome group
    Neuroprotection · Nervous system and cognition
    Studied dose
    Dose not stated

    Measurements

    BBB leakage reduction
    26%
    prophylactic Kisspeptin-54

    Source sentences

    Summary
    Prophylactic Kisspeptin-54 reduced cerebral infarct volume by 42%, enhanced neurological performance by 49%, and decreased BBB leakage by 26%
    1 context sentence
    Summary · context
    In vivo, mice underwent middle cerebral artery occlusion (MCAO), and cerebral infarct volume, neurological function, and blood-brain barrier (BBB) permeability were evaluated.
  4. 04AnimalAnimal study (in vivo)Efficacy outcome

    In mice with middle cerebral artery occlusion, prophylactic Kisspeptin‑54 produced near-complete occludin recovery.

    In plain wordsIn mice with stroke, Kisspeptin‑54 given beforehand nearly restored occludin, a barrier protein.

    Outcome
    IncreaseOccludin recovery
    Study

    mousen: not reported in source

    middle cerebral artery occlusion (MCAO)
    Outcome group
    Neuroprotection · Nervous system and cognition
    Studied dose
    Dose not stated

    Source sentences

    Summary
    with near-complete occludin recovery.
    1 context sentence
    Summary · context
    In vivo, mice underwent middle cerebral artery occlusion (MCAO), and cerebral infarct volume, neurological function, and blood-brain barrier (BBB) permeability were evaluated.
  5. 05LabIn vitro (cells)Efficacy outcome

    In HBMVECs exposed to oxygen-glucose deprivation/reperfusion, Kisspeptin‑54 reduced paracellular flux by 48%.

    In plain wordsIn cells, Kisspeptin‑54 reduced leakage between brain blood vessel cells by 48%.

    Outcome
    DecreaseParacellular flux
    Study

    humann: not reported in source

    human brain microvascular endothelial cells (HBMVECs) exposed to oxygen-glucose deprivation/reperfusion
    Outcome group
    Neuroprotection · Nervous system and cognition
    Studied dose
    Dose not stated

    Measurements

    Paracellular flux reduction
    48%
    HBMVECs

    Source sentences

    Summary
    In vitro: Kisspeptin-54 treatment reduced paracellular flux by 48% and increased transendothelial resistance by 60%.
    1 context sentence
    Summary · context
    In vitro, human brain microvascular endothelial cells (HBMVECs) were exposed to oxygen-glucose deprivation/reperfusion (OGD/R) to assess the effects of Kisspeptin-54 on paracellular flux and transendothelial electrical resistance (TEER).
  6. 06LabIn vitro (cells)Efficacy outcome

    In HBMVECs exposed to oxygen-glucose deprivation/reperfusion, Kisspeptin‑54 increased transendothelial resistance by 60%.

    In plain wordsIn cells, Kisspeptin‑54 strengthened a brain blood vessel cell barrier, with 60% higher resistance.

    Outcome
    IncreaseTransendothelial electrical resistance
    Study

    humann: not reported in source

    human brain microvascular endothelial cells (HBMVECs) exposed to oxygen-glucose deprivation/reperfusion
    Outcome group
    Neuroprotection · Nervous system and cognition
    Studied dose
    Dose not stated

    Measurements

    Transendothelial resistance increase
    60%
    HBMVECs

    Source sentences

    Summary
    In vitro: Kisspeptin-54 treatment reduced paracellular flux by 48% and increased transendothelial resistance by 60%.
    1 context sentence
    Summary · context
    In vitro, human brain microvascular endothelial cells (HBMVECs) were exposed to oxygen-glucose deprivation/reperfusion (OGD/R) to assess the effects of Kisspeptin-54 on paracellular flux and transendothelial electrical resistance (TEER).

Natural levels measured3

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. 07AnimalEndogenous levelAnimal study (in vivo)Mechanism

    In mice with middle cerebral artery occlusion, cortical ischemia downregulated KISS1 mRNA.

    In plain wordsIn mice with stroke, the gene for the body's own kisspeptin was less active in the brain cortex.

    Outcome
    DecreaseKISS1 mRNA after cortical ischemia
    Study

    mousen: not reported in source

    middle cerebral artery occlusion (MCAO)
    Outcome group
    Neuroprotection · Nervous system and cognition

    Measurements

    KISS1 mRNA reduction
    59%
    cortical ischemia

    Source sentences

    Summary
    cortical ischemia downregulated KISS-1 metastasis-suppressor (KISS1, 59% mRNA; 55% protein)
    1 context sentence
    Summary · context
    In vivo, mice underwent middle cerebral artery occlusion (MCAO), and cerebral infarct volume, neurological function, and blood-brain barrier (BBB) permeability were evaluated.

    This result measures the body's own Kisspeptin-54 (metastin). Nobody was given the peptide. It is not evidence about taking it.

  2. 08AnimalEndogenous levelAnimal study (in vivo)Mechanism

    In mice with middle cerebral artery occlusion, cortical ischemia downregulated KISS1 protein.

    In plain wordsIn mice with stroke, the body's own kisspeptin protein was lower in the brain cortex.

    Outcome
    DecreaseKISS1 protein after cortical ischemia
    Study

    mousen: not reported in source

    middle cerebral artery occlusion (MCAO)
    Outcome group
    Neuroprotection · Nervous system and cognition

    Measurements

    KISS1 protein reduction
    55%
    cortical ischemia

    Source sentences

    Summary
    cortical ischemia downregulated KISS-1 metastasis-suppressor (KISS1, 59% mRNA; 55% protein)
    1 context sentence
    Summary · context
    In vivo, mice underwent middle cerebral artery occlusion (MCAO), and cerebral infarct volume, neurological function, and blood-brain barrier (BBB) permeability were evaluated.

    This result measures the body's own Kisspeptin-54 (metastin). Nobody was given the peptide. It is not evidence about taking it.

  3. 09AnimalEndogenous levelAnimal study (in vivo)Mechanism

    In mice with middle cerebral artery occlusion, circulating Kisspeptin‑54 declined by 32%.

    In plain wordsIn mice with stroke, the body's own Kisspeptin‑54 in the blood was lower.

    Outcome
    DecreaseCirculating Kisspeptin-54 after cortical ischemia
    Study

    mousen: not reported in source

    middle cerebral artery occlusion (MCAO)
    Outcome group
    Neuroprotection · Nervous system and cognition

    Measurements

    Circulating Kisspeptin-54 decline
    32%
    cortical ischemia

    Source sentences

    Summary
    with a 32% decline in circulating Kisspeptin-54.
    1 context sentence
    Summary · context
    In vivo, mice underwent middle cerebral artery occlusion (MCAO), and cerebral infarct volume, neurological function, and blood-brain barrier (BBB) permeability were evaluated.

    This result measures the body's own Kisspeptin-54 (metastin). Nobody was given the peptide. It is not evidence about taking it.

Studies that did not test the peptide alone3

In this study, Kisspeptin-54 (metastin) 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-54 (metastin).

  1. 10LabNot a test of Kisspeptin-54 (metastin) aloneIn vitro (cells)Mechanism

    In HBMVECs, GATA-4 silencing abolished Kisspeptin‑54-induced occludin restoration.

    In plain wordsIn cells, silencing the GATA-4 gene stopped Kisspeptin‑54 from restoring occludin.

    Outcome
    DecreaseKisspeptin-54-induced occludin restoration after GATA-4 silencing
    Study

    humann: not reported in source

    human brain microvascular endothelial cells (HBMVECs) with GATA-4 silencing
    Outcome group
    Receptor activity and mechanism · Nervous system and cognition

    Source sentences

    Summary
    GATA-4 silencing abolished Kisspeptin-54-induced occludin restoration, increasing permeability by 65% and diminishing barrier resistance by 28%.
    1 context sentence
    Summary · context
    Additionally, GATA-4 was silenced to investigate its role in mediating protection.

    In this study, Kisspeptin-54 (metastin) 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-54 (metastin).

  2. 11LabNot a test of Kisspeptin-54 (metastin) aloneIn vitro (cells)Mechanism

    In HBMVECs treated with Kisspeptin‑54, GATA-4 silencing increased permeability by 65%.

    In plain wordsIn cells, silencing the GATA-4 gene increased barrier leakiness by 65% in the presence of Kisspeptin‑54.

    Outcome
    IncreasePermeability after GATA-4 silencing with Kisspeptin-54
    Study

    humann: not reported in source

    human brain microvascular endothelial cells (HBMVECs) with GATA-4 silencing
    Outcome group
    Receptor activity and mechanism · Nervous system and cognition

    Measurements

    Permeability increase
    65%
    GATA-4 silencing

    Source sentences

    Summary
    GATA-4 silencing abolished Kisspeptin-54-induced occludin restoration, increasing permeability by 65% and diminishing barrier resistance by 28%.
    1 context sentence
    Summary · context
    Additionally, GATA-4 was silenced to investigate its role in mediating protection.

    In this study, Kisspeptin-54 (metastin) 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-54 (metastin).

  3. 12LabNot a test of Kisspeptin-54 (metastin) aloneIn vitro (cells)Mechanism

    In HBMVECs treated with Kisspeptin‑54, GATA-4 silencing diminished barrier resistance by 28%.

    In plain wordsIn cells, silencing the GATA-4 gene lowered barrier resistance by 28% in the presence of Kisspeptin‑54.

    Outcome
    DecreaseBarrier resistance after GATA-4 silencing with Kisspeptin-54
    Study

    humann: not reported in source

    human brain microvascular endothelial cells (HBMVECs) with GATA-4 silencing
    Outcome group
    Receptor activity and mechanism · Nervous system and cognition

    Measurements

    Barrier resistance reduction
    28%
    GATA-4 silencing

    Source sentences

    Summary
    GATA-4 silencing abolished Kisspeptin-54-induced occludin restoration, increasing permeability by 65% and diminishing barrier resistance by 28%.
    1 context sentence
    Summary · context
    Additionally, GATA-4 was silenced to investigate its role in mediating protection.

    In this study, Kisspeptin-54 (metastin) 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-54 (metastin).

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

    13 Oct 2026, 21:44 UTC

    Study results updated

  2. Version 1

    13 Oct 2026, 16:31 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

PepBank is a research reference. Talk to a doctor before you use any peptide.