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Study · In vitro (cells) · 2014

8 results

Neuroprotective effect of novel cognitive enhancer noopept on AD-related cellular model involves the attenuation of apoptosis and tau hyperphosphorylation.

Ostrovskaya RU, Vakhitova YV, Kuzmina USh, Salimgareeva MKh, Zainullina LF, Gudasheva TA, Vakhitov VA, Seredenin SB

Journal of biomedical science6 Aug 2014Cited by 17 (Europe PMC)

Summary

BackgroundNoopept (N-phenyl-acetyl-L-prolylglycine ethyl ester) was constructed as a dipeptide analog of the standard cognition enhancer, piracetam. Our previous experiments have demonstrated the cognition restoring effect of noopept in several animal models of Alzheimer disease (AD). Noopept was also shown to prevent ionic disbalance, excitotoxicity, free radicals and pro-inflammatory cytokines accumulation, and neurotrophine deficit typical for different kinds of brain damages, including AD. In this study, we investigated the neuroprotective action of noopept on cellular model of AD, Aβ 25-35-induced toxicity in PC12 cells and revealed the underlying mechanisms.ResultsThe neuroprotective effect of noopept (added to the medium at 10 μM concentration, 72 hours before Аβ 25-35) was studied on Аβ 25-35-induced injury (5 μM for 24 h) in PC12 cells. The ability of drug to protect the impairments of cell viability, calcium homeostasis, ROS level, mitochondrial function, tau phosphorylation and neurite outgrowth caused by Аβ 25-35 were evaluated. Following the exposure of PC12 cells to Аβ 25-35 an increase of the level of ROS, intracellular calcium, and tau phosphorylation at Ser396 were observed; these changes were accompanied by a decrease in cell viability and an increase of apoptosis. Noopept treatment before the amyloid-beta exposure improved PC12 cells viability, reduced the number of early and late apoptotic cells, the levels of intracellular reactive oxygen species and calcium and enhanced the mitochondrial membrane potential. In addition, pretreatment of PC12 cell with noopept significantly attenuated tau hyperphosphorylation at Ser396 and ameliorated the alterations of neurite outgrowth evoked by Аβ25-35.ConclusionsTaken together, these data provide evidence that novel cognitive enhancer noopept protects PC12 cell against deleterious actions of Aβ through inhibiting the oxidative damage and calcium overload as well as suppressing the mitochondrial apoptotic pathway. Moreover, neuroprotective properties of noopept likely include its ability to decrease tau phosphorylation and to restore the altered morphology of PC12 cells. Therefore, this nootropic dipeptide is able to positively affect not only common pathogenic pathways but also disease-specific mechanisms underlying Aβ-related pathology.
CC BYText from Europe PMC. Highlighted sentences are the source of results.

Results from this study8

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

  1. 01LabIn vitro (cells)Efficacy outcome

    In amyloid-beta-exposed PC12 cells, Noopept pretreatment improved viability.

    In plain wordsIn amyloid-beta-exposed cells, Noopept pretreatment improved cell viability compared with amyloid-beta exposure without Noopept.

    Outcome
    IncreaseCell viability
    Study

    n: not reported in source

    PC12 cells exposed to amyloid-beta 25-35
    Comparator
    Amyloid-beta exposure without Noopept
    Outcome group
    Neuroprotection · Nervous system and cognition
    Studied dose
    10 μM · 72 hours before Аβ 25-35As given in this study.

    Source sentences

    Summary
    Noopept treatment before the amyloid-beta exposure improved PC12 cells viability, reduced the number of early and late apoptotic cells, the levels of intracellular reactive oxygen species and calcium and enhanced the mitochondrial membrane potential.
    1 context sentence
    Summary · context
    The neuroprotective effect of noopept (added to the medium at 10 μM concentration, 72 hours before Аβ 25-35) was studied on Аβ 25-35-induced injury (5 μM for 24 h) in PC12 cells.
  2. 02LabIn vitro (cells)Efficacy outcome

    In amyloid-beta-exposed PC12 cells, Noopept pretreatment reduced early apoptotic cells.

    In plain wordsIn amyloid-beta-exposed cells, Noopept pretreatment reduced early apoptotic cells compared with amyloid-beta exposure without Noopept.

    Outcome
    DecreaseEarly apoptosis
    Study

    n: not reported in source

    PC12 cells exposed to amyloid-beta 25-35
    Comparator
    Amyloid-beta exposure without Noopept
    Outcome group
    Neuroprotection · Nervous system and cognition
    Studied dose
    10 μM · 72 hours before Аβ 25-35As given in this study.

    Source sentences

    Summary
    Noopept treatment before the amyloid-beta exposure improved PC12 cells viability, reduced the number of early and late apoptotic cells, the levels of intracellular reactive oxygen species and calcium and enhanced the mitochondrial membrane potential.
    1 context sentence
    Summary · context
    The neuroprotective effect of noopept (added to the medium at 10 μM concentration, 72 hours before Аβ 25-35) was studied on Аβ 25-35-induced injury (5 μM for 24 h) in PC12 cells.
  3. 03LabIn vitro (cells)Efficacy outcome

    In amyloid-beta-exposed PC12 cells, Noopept pretreatment reduced late apoptotic cells.

    In plain wordsIn amyloid-beta-exposed cells, Noopept pretreatment reduced late apoptotic cells compared with amyloid-beta exposure without Noopept.

    Outcome
    DecreaseLate apoptosis
    Study

    n: not reported in source

    PC12 cells exposed to amyloid-beta 25-35
    Comparator
    Amyloid-beta exposure without Noopept
    Outcome group
    Neuroprotection · Nervous system and cognition
    Studied dose
    10 μM · 72 hours before Аβ 25-35As given in this study.

    Source sentences

    Summary
    Noopept treatment before the amyloid-beta exposure improved PC12 cells viability, reduced the number of early and late apoptotic cells, the levels of intracellular reactive oxygen species and calcium and enhanced the mitochondrial membrane potential.
    1 context sentence
    Summary · context
    The neuroprotective effect of noopept (added to the medium at 10 μM concentration, 72 hours before Аβ 25-35) was studied on Аβ 25-35-induced injury (5 μM for 24 h) in PC12 cells.
  4. 04LabIn vitro (cells)Efficacy outcome

    In amyloid-beta-exposed PC12 cells, Noopept pretreatment reduced intracellular reactive oxygen species.

    In plain wordsIn amyloid-beta-exposed cells, Noopept pretreatment reduced reactive oxygen species compared with amyloid-beta exposure without Noopept.

    Outcome
    DecreaseIntracellular reactive oxygen species
    Study

    n: not reported in source

    PC12 cells exposed to amyloid-beta 25-35
    Comparator
    Amyloid-beta exposure without Noopept
    Outcome group
    Neuroprotection · Nervous system and cognition
    Studied dose
    10 μM · 72 hours before Аβ 25-35As given in this study.

    Source sentences

    Summary
    Noopept treatment before the amyloid-beta exposure improved PC12 cells viability, reduced the number of early and late apoptotic cells, the levels of intracellular reactive oxygen species and calcium and enhanced the mitochondrial membrane potential.
    1 context sentence
    Summary · context
    The neuroprotective effect of noopept (added to the medium at 10 μM concentration, 72 hours before Аβ 25-35) was studied on Аβ 25-35-induced injury (5 μM for 24 h) in PC12 cells.
  5. 05LabIn vitro (cells)Efficacy outcome

    In amyloid-beta-exposed PC12 cells, Noopept pretreatment reduced intracellular calcium.

    In plain wordsIn amyloid-beta-exposed cells, Noopept pretreatment reduced intracellular calcium compared with amyloid-beta exposure without Noopept.

    Outcome
    DecreaseIntracellular calcium
    Study

    n: not reported in source

    PC12 cells exposed to amyloid-beta 25-35
    Comparator
    Amyloid-beta exposure without Noopept
    Outcome group
    Receptor activity and mechanism · Nervous system and cognition
    Studied dose
    10 μM · 72 hours before Аβ 25-35As given in this study.

    Source sentences

    Summary
    Noopept treatment before the amyloid-beta exposure improved PC12 cells viability, reduced the number of early and late apoptotic cells, the levels of intracellular reactive oxygen species and calcium and enhanced the mitochondrial membrane potential.
    1 context sentence
    Summary · context
    The neuroprotective effect of noopept (added to the medium at 10 μM concentration, 72 hours before Аβ 25-35) was studied on Аβ 25-35-induced injury (5 μM for 24 h) in PC12 cells.
  6. 06LabIn vitro (cells)Efficacy outcome

    In amyloid-beta-exposed PC12 cells, Noopept pretreatment enhanced mitochondrial membrane potential.

    In plain wordsIn amyloid-beta-exposed cells, Noopept pretreatment increased mitochondrial membrane potential compared with amyloid-beta exposure without Noopept.

    Outcome
    IncreaseMitochondrial membrane potential
    Study

    n: not reported in source

    PC12 cells exposed to amyloid-beta 25-35
    Comparator
    Amyloid-beta exposure without Noopept
    Outcome group
    Mitochondrial function · Nervous system and cognition
    Studied dose
    10 μM · 72 hours before Аβ 25-35As given in this study.

    Source sentences

    Summary
    Noopept treatment before the amyloid-beta exposure improved PC12 cells viability, reduced the number of early and late apoptotic cells, the levels of intracellular reactive oxygen species and calcium and enhanced the mitochondrial membrane potential.
    1 context sentence
    Summary · context
    The neuroprotective effect of noopept (added to the medium at 10 μM concentration, 72 hours before Аβ 25-35) was studied on Аβ 25-35-induced injury (5 μM for 24 h) in PC12 cells.
  7. 07LabIn vitro (cells)Efficacy outcome

    In amyloid-beta-exposed PC12 cells, Noopept pretreatment attenuated tau hyperphosphorylation at Ser396.

    In plain wordsIn amyloid-beta-exposed cells, Noopept pretreatment reduced tau hyperphosphorylation at Ser396 compared with amyloid-beta exposure without Noopept.

    Outcome
    DecreaseTau hyperphosphorylation at Ser396
    Study

    n: not reported in source

    PC12 cells exposed to amyloid-beta 25-35
    Comparator
    Amyloid-beta exposure without Noopept
    Outcome group
    Neuroprotection · Nervous system and cognition
    Studied dose
    10 μM · 72 hours before Аβ 25-35As given in this study.

    Source sentences

    Summary
    In addition, pretreatment of PC12 cell with noopept significantly attenuated tau hyperphosphorylation at Ser396 and ameliorated the alterations of neurite outgrowth evoked by Аβ25-35.
    1 context sentence
    Summary · context
    The neuroprotective effect of noopept (added to the medium at 10 μM concentration, 72 hours before Аβ 25-35) was studied on Аβ 25-35-induced injury (5 μM for 24 h) in PC12 cells.
  8. 08LabIn vitro (cells)Efficacy outcome

    In amyloid-beta-exposed PC12 cells, Noopept pretreatment ameliorated alterations of neurite outgrowth.

    In plain wordsIn amyloid-beta-exposed cells, Noopept pretreatment reduced neurite growth alterations compared with amyloid-beta exposure without Noopept.

    Outcome
    DecreaseNeurite outgrowth alterations
    Study

    n: not reported in source

    PC12 cells exposed to amyloid-beta 25-35
    Comparator
    Amyloid-beta exposure without Noopept
    Outcome group
    Neuroprotection · Nervous system and cognition
    Studied dose
    10 μM · 72 hours before Аβ 25-35As given in this study.

    Source sentences

    Summary
    In addition, pretreatment of PC12 cell with noopept significantly attenuated tau hyperphosphorylation at Ser396 and ameliorated the alterations of neurite outgrowth evoked by Аβ25-35.
    1 context sentence
    Summary · context
    The neuroprotective effect of noopept (added to the medium at 10 μM concentration, 72 hours before Аβ 25-35) was studied on Аβ 25-35-induced injury (5 μM for 24 h) in PC12 cells.

AI wrote and checked these results. AI can make mistakes, so check important results against the source.

Version history

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  1. Version 2Current

    21 Oct 2026, 15:58 UTC

    Study results updated

  2. Version 1

    21 Oct 2026, 12:50 UTC

    First added · source update from Europe PMC

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