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Study · Not a test of the peptide alone · 2016

1 result

[PHARMACOLOGICAL CORRECTION OF RED BLOOD CELL MEMBRANE LIPID SPECTRUM IN PATIENTS WITH CHRONIC CEREBRAL ISCHEMIA ON THE BACKGROUND OF HYPERTENSIVE DISEASE.]

Shul'ginova AA, Laskov VB, Konoplya AI, Karaulov AV

Eksperimental'naia i klinicheskaia farmakologiia1 Jan 2016Cited by 1 (Europe PMC)

PMID29782737 (opens in a new tab)PepBankPUB-29782737

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 study1

No result from this study comes from a test of the peptide.

Studies that did not test the peptide alone1

In this study, Cerebrolysin 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 Cerebrolysin.

  1. 01HumanNot a test of Cerebrolysin aloneOther designEfficacy outcome

    In hypertensive patients with chronic cerebral ischemia, cerebrolysin with mexidol produced the least erythrocyte lipid profile correction among the reported regimens.

    In plain wordsIn hypertensive patients with cerebral ischemia, cerebrolysin with mexidol corrected red cell membrane lipids less than the other reported regimens.

    Outcome
    DecreaseErythrocyte membrane lipid profile correction
    Study

    n: not reported in source

    Comparator
    Actovegin with cereton and emoxypine with piracetam
    Outcome group
    Lipids · Cardiovascular

    Source sentences

    Summary
    while the minimum ef- fect was produced by a combination of cerebrolysin (2152 mg concentrated complex of peptides from pig brain, intravenous drip in 100.0 mL of 0.9% sodium chloride solution) and mexidol (250 mg of 2-ethyl-6-methyl-3-hydroxypyridine succinate intravenous bolus).
    1 context sentence
    Summary · context
    The combination of emoxypine (40 mg of 3-hydroxy-6-methyl-2-ethylpyridine, intramuscularly) and piracetam (1000 mg of 2-oxo-I-pyrrolidine-acetamide intravenous bolus) gave intermediate results.

    In this study, Cerebrolysin 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 Cerebrolysin.

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

    14 Oct 2026, 05:02 UTC

    Study results updated

  2. Version 1

    14 Oct 2026, 01:46 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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