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

7 results

Neurotropic Effects of Cortexin on Models of Mental and Physical Developmental Delay.

Kurkin DV, Bakulin DA, Morkovin EI, Petrov VI, Strygin AV, Smirnov AV, Shmidt MV, Gorbunova JV, Kolosov YA, Ivanova OV, Krysanov IS, Dzhavakhyan MA and 7 more

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Zaborovsky AV, Saparova VB, Makarenko IE, Drai RI, Lugovik IA, Verlov NA, Burdakov VS

Biomedicines2 Apr 2025

Summary

Objective: To evaluate the efficacy of the neurotropic action of cortexin in models of mental and physical developmental delays in rat offspring. Methods: The neurotropic properties of bovine brain cortex polypeptides were studied using two models of mental and physical developmental delays in rats: toxic CNS damage (oral administration of ethanol during the last week of pregnancy) and neonatal trauma (ischemia-hypoxia). The drug was administered intramuscularly or rectally as suppositories for 20 days. Treatment efficacy was evaluated using the mNSS scale, open field, rotarod, and adhesive removal tests. A histological examination of the brain was subsequently performed. In a separate series of experiments in mice, the concentration of the test drug cortexin and the reference drug cerebrolysin was determined in blood and brain tissue samples using radioactive iodine (Na125I) labeling of these preparations. Results: Modeling developmental delay in rat offspring (due to the toxic effect of ethanol in late pregnancy or neonatal trauma) led to pronounced neurological deficits, manifested by decreased motor activity, and sensorimotor, and coordination disorders. Administration of cortexin in all forms reduced the severity of neurological deficits as measured by mNSS scores, improved motor activity in the Open Field test, enhanced performance in the Adhesive Removal and Rotarod tests, and decreased structural changes in brain tissues. Histological examination revealed reduced neuronal damage in multiple cortical regions, with a significant increase in normal, unchanged neurons compared to placebo groups. Comparison of the blood concentrations of labeled Na125I cortexin depending on the type of administration showed similar distribution profiles in brain tissues, primarily dependent on its blood concentration, which was influenced by the route of administration. Conclusions: The results indicate that brain polypeptides (cortexin), administered either intramuscularly or rectally, can reach the systemic circulation and cross the blood-brain barrier, as demonstrated by our distribution studies using radiolabeled preparations. These polypeptides exert comparable neurotropic effects in models of mental and physical developmental delays in offspring caused by neonatal trauma or the toxic effect of ethanol in late pregnancy in rats.
CC BYText from Europe PMC. Highlighted sentences are the source of results.

Results from this study7

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

  1. 01AnimalAnimal study (in vivo)Efficacy outcome

    In rat offspring with developmental delay, Cortexin reduced neurological deficits measured by mNSS.

    In plain wordsIn rats with developmental delay, Cortexin reduced neurological deficits.

    Outcome
    DecreasemNSS neurological deficit
    Study

    ratn: not reported in source

    Developmental delay after prenatal ethanol or neonatal ischemia-hypoxia
    Outcome group
    Neuroprotection · Nervous system and cognition
    Studied dose
    Dose not stated · intramuscular or rectal · 20 daysAs given in this study (rat).

    Source sentences

    Summary
    Administration of cortexin in all forms reduced the severity of neurological deficits as measured by mNSS scores, improved motor activity in the Open Field test, enhanced performance in the Adhesive Removal and Rotarod tests, and decreased structural changes in brain tissues.
    2 context sentences
    Summary · context
    The neurotropic properties of bovine brain cortex polypeptides were studied using two models of mental and physical developmental delays in rats: toxic CNS damage (oral administration of ethanol during the last week of pregnancy) and neonatal trauma (ischemia-hypoxia).
    Summary · context
    The drug was administered intramuscularly or rectally as suppositories for 20 days.
  2. 02AnimalAnimal study (in vivo)Efficacy outcome

    In rat offspring with developmental delay, Cortexin improved motor activity in the Open Field test.

    In plain wordsIn rats with developmental delay, Cortexin improved movement in the Open Field test.

    Outcome
    IncreaseOpen Field motor activity
    Study

    ratn: not reported in source

    Developmental delay after prenatal ethanol or neonatal ischemia-hypoxia
    Outcome group
    Exercise and physical function · Nervous system and cognition
    Studied dose
    Dose not stated · intramuscular or rectal · 20 daysAs given in this study (rat).

    Source sentences

    Summary
    Administration of cortexin in all forms reduced the severity of neurological deficits as measured by mNSS scores, improved motor activity in the Open Field test, enhanced performance in the Adhesive Removal and Rotarod tests, and decreased structural changes in brain tissues.
    2 context sentences
    Summary · context
    The neurotropic properties of bovine brain cortex polypeptides were studied using two models of mental and physical developmental delays in rats: toxic CNS damage (oral administration of ethanol during the last week of pregnancy) and neonatal trauma (ischemia-hypoxia).
    Summary · context
    The drug was administered intramuscularly or rectally as suppositories for 20 days.
  3. 03AnimalAnimal study (in vivo)Efficacy outcome

    In rat offspring with developmental delay, Cortexin improved Adhesive Removal test performance.

    In plain wordsIn rats with developmental delay, Cortexin improved performance in the Adhesive Removal test.

    Outcome
    IncreaseAdhesive Removal performance
    Study

    ratn: not reported in source

    Developmental delay after prenatal ethanol or neonatal ischemia-hypoxia
    Outcome group
    Exercise and physical function · Nervous system and cognition
    Studied dose
    Dose not stated · intramuscular or rectal · 20 daysAs given in this study (rat).

    Source sentences

    Summary
    Administration of cortexin in all forms reduced the severity of neurological deficits as measured by mNSS scores, improved motor activity in the Open Field test, enhanced performance in the Adhesive Removal and Rotarod tests, and decreased structural changes in brain tissues.
    2 context sentences
    Summary · context
    The neurotropic properties of bovine brain cortex polypeptides were studied using two models of mental and physical developmental delays in rats: toxic CNS damage (oral administration of ethanol during the last week of pregnancy) and neonatal trauma (ischemia-hypoxia).
    Summary · context
    The drug was administered intramuscularly or rectally as suppositories for 20 days.
  4. 04AnimalAnimal study (in vivo)Efficacy outcome

    In rat offspring with developmental delay, Cortexin improved Rotarod performance.

    In plain wordsIn rats with developmental delay, Cortexin improved Rotarod performance.

    Outcome
    IncreaseRotarod performance
    Study

    ratn: not reported in source

    Developmental delay after prenatal ethanol or neonatal ischemia-hypoxia
    Outcome group
    Exercise and physical function · Nervous system and cognition
    Studied dose
    Dose not stated · intramuscular or rectal · 20 daysAs given in this study (rat).

    Source sentences

    Summary
    Administration of cortexin in all forms reduced the severity of neurological deficits as measured by mNSS scores, improved motor activity in the Open Field test, enhanced performance in the Adhesive Removal and Rotarod tests, and decreased structural changes in brain tissues.
    2 context sentences
    Summary · context
    The neurotropic properties of bovine brain cortex polypeptides were studied using two models of mental and physical developmental delays in rats: toxic CNS damage (oral administration of ethanol during the last week of pregnancy) and neonatal trauma (ischemia-hypoxia).
    Summary · context
    The drug was administered intramuscularly or rectally as suppositories for 20 days.
  5. 05AnimalAnimal study (in vivo)Efficacy outcome

    In rat offspring with developmental delay, Cortexin decreased structural changes in brain tissue.

    In plain wordsIn rats with developmental delay, Cortexin reduced structural brain changes.

    Outcome
    DecreaseStructural brain changes
    Study

    ratn: not reported in source

    Developmental delay after prenatal ethanol or neonatal ischemia-hypoxia
    Outcome group
    Neuroprotection · Nervous system and cognition
    Studied dose
    Dose not stated · intramuscular or rectal · 20 daysAs given in this study (rat).

    Source sentences

    Summary
    Administration of cortexin in all forms reduced the severity of neurological deficits as measured by mNSS scores, improved motor activity in the Open Field test, enhanced performance in the Adhesive Removal and Rotarod tests, and decreased structural changes in brain tissues.
    2 context sentences
    Summary · context
    The neurotropic properties of bovine brain cortex polypeptides were studied using two models of mental and physical developmental delays in rats: toxic CNS damage (oral administration of ethanol during the last week of pregnancy) and neonatal trauma (ischemia-hypoxia).
    Summary · context
    The drug was administered intramuscularly or rectally as suppositories for 20 days.
  6. 06AnimalAnimal study (in vivo)Efficacy outcome

    In rat offspring with developmental delay, Cortexin reduced neuronal damage in multiple cortical regions versus placebo.

    In plain wordsIn rats with developmental delay, Cortexin reduced damage to cortical neurons versus placebo.

    Outcome
    DecreaseNeuronal damage
    Study

    ratn: not reported in source

    Developmental delay after prenatal ethanol or neonatal ischemia-hypoxia
    Comparator
    placebo
    Outcome group
    Neuroprotection · Nervous system and cognition
    Studied dose
    Dose not stated · intramuscular or rectal · 20 daysAs given in this study (rat).

    Source sentences

    Summary
    Histological examination revealed reduced neuronal damage in multiple cortical regions, with a significant increase in normal, unchanged neurons compared to placebo groups.
    2 context sentences
    Summary · context
    The neurotropic properties of bovine brain cortex polypeptides were studied using two models of mental and physical developmental delays in rats: toxic CNS damage (oral administration of ethanol during the last week of pregnancy) and neonatal trauma (ischemia-hypoxia).
    Summary · context
    The drug was administered intramuscularly or rectally as suppositories for 20 days.
  7. 07AnimalAnimal study (in vivo)Efficacy outcome

    In rat offspring with developmental delay, Cortexin significantly increased normal unchanged neurons versus placebo.

    In plain wordsIn rats with developmental delay, Cortexin increased normal neurons versus placebo.

    Outcome
    IncreaseNormal unchanged neurons
    Study

    ratn: not reported in source

    Developmental delay after prenatal ethanol or neonatal ischemia-hypoxia
    Comparator
    placebo
    Outcome group
    Neuroprotection · Nervous system and cognition
    Studied dose
    Dose not stated · intramuscular or rectal · 20 daysAs given in this study (rat).

    Source sentences

    Summary
    Histological examination revealed reduced neuronal damage in multiple cortical regions, with a significant increase in normal, unchanged neurons compared to placebo groups.
    2 context sentences
    Summary · context
    The neurotropic properties of bovine brain cortex polypeptides were studied using two models of mental and physical developmental delays in rats: toxic CNS damage (oral administration of ethanol during the last week of pregnancy) and neonatal trauma (ischemia-hypoxia).
    Summary · context
    The drug was administered intramuscularly or rectally as suppositories for 20 days.

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

    21 Oct 2026, 18:59 UTC

    Study data updated · source update from Europe PMC

  2. Version 2

    14 Oct 2026, 05:02 UTC

    Study results updated

  3. Version 1

    14 Oct 2026, 01:46 UTC

    First added · source update from Europe PMC

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