2003
DOI: 10.1002/14651858.cd003119
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Vinpocetine for cognitive impairment and dementia

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Cited by 107 publications
(102 citation statements)
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“…The brain pathway for ascending (fusion) CFF is highly differ from descending (flickering) CFF pathway, the flickering neurotransmitter is mainly noradrenalin while the neurotransmitter for fusion is mainly dopamine and serotonin [18] , this explain the significant effect of vinpocetine on flickering CFF and insignificant effect on the ascending CFF in our study.…”
Section: Discussionmentioning
confidence: 50%
“…The brain pathway for ascending (fusion) CFF is highly differ from descending (flickering) CFF pathway, the flickering neurotransmitter is mainly noradrenalin while the neurotransmitter for fusion is mainly dopamine and serotonin [18] , this explain the significant effect of vinpocetine on flickering CFF and insignificant effect on the ascending CFF in our study.…”
Section: Discussionmentioning
confidence: 50%
“…Most studies performed in animal models used doses between 10 and 20 mg/kg [14,15]. These doses translated to humans would result in approximately 1,000 mg, which would be roughly a 20-fold increase in the current doses used in clinicaltrials [16][17][18].…”
Section: Discussionmentioning
confidence: 99%
“…Винпоцетин ингибирует активность натриевых каналов в нервной ткани, что является основным механизмом фармакологических агентов с нейропротективными свойствами. Это свойство винпоцетина продемонстри-ровано в том числе в экспериментах эффективной бло-кады накопления натрия в нейронах, уменьшении зоны реперфузионного повреждения и нивелировании токси-ческого воздействия окислительного стресса в результа-те аноксии [12]. Показано, что винпоцетин защищает нейроны от токсичности глутамата и N-метил-d-аспартата (NMDA) [13], с чем также связаны его нейро-протективные свойства.…”
Section: стадияunclassified