Dose giornaliera: 3 capsule
Numero di dosi per scatola: 20
Quantita per dose
Vinpocetina
45 mg
Altri ingredienti:Gomma acacia, Crusca di riso.
Ogni capsula contiene 15 mg di vinpocetina di qualità farmaceutica.
Consigli di utilizzo
Prendere due otre capsule per giorno, in due o tre volte, aumentando progressivamente le assunzioni. La dose di mantenimento generalmente raccomandata è di 30 mg per giorno.
4.9/5 • 15 recensioni
Descrizione
5.0 / 5
Qualità
5.0 / 5
Rapporto qualità-prezzo
4.6 / 5
Recensioni 15
Eccellente
93 %
Buono
7%
Medio
0%
Scarso
0%
Pessimo
0%
Filippo2020-02-22
ottimo prodotto consegna in tempi rapidi
Bausani2019-12-20
Ottimo prodotto. Risultati ottenuti
Bausani2019-03-14
Prodotto consigliato dal reparto oculistico di Prato. Ottimi risultati
Gina2020-07-23
POUR MOI CELA ME CONVIENT PUISQUE JE REPASSE UNE COMMANDE
PEREZ CASTRO Valle2020-05-15
Empezar a tomarlas , y en pocos días los despistes y la falta de concentración, desaparecen.
WETTERMAN Ingrid2020-04-01
Nunca antes he tenido la memoria y concentración que tengo ahora. Todo es más fácil, el trabajo sobre todo pero también la vida diaria.
BLANCO Azucena2020-01-29
Usado para la prescripcion para la que esta destinado y en la posologia adecuada Esta presentacion de Vimpocetine de Supersmart es excelente . No tengo duda en recomendarla .
poitrimol ingrid2019-07-17
GENIAL ANTIOXYDANT
Nanie732019-07-15
Je fais la cure depuis quelques mois , je ne peux pas donner d'avis , c'est trop récent .
ROGOWSKI Odette2019-07-02
efficace ,
Gina2019-06-18
pour moi c'est très bon et bien
Bibliografia
Kiss B, Szpomy L. On the possible role of central monoaminergic systems in the central nervous systems actions of vinpocetine. Drug Dev Res. 1988;14:263–79.
Shibuya T, Sato K. Effects of vinpocetine on experimental brain ischemia, histological study of brain monoamines. Igaku No Ayumi. 1986;139:217–9.
Nicholson CD. Pharmacology of nootropics and metabolically active compounds in relation to their use in dementia. Psychopharmacology (Berl) 1990;101:147–59
Patyar, S., Prakash, A., Modi, M., Medhi, B., 2011. Role of vinpocetine in cerebrovascular diseases. Pharmacol. Rep. 63, 618–628.
Bonoczk, P., Gulyas, B., Adam-Vizi, V., Nemes, A., Karpati, E., Kiss, B., Kapas, M., Szantay, C., Koncz, I., Zelles, T., Vas, A., 2000. Role of sodium channel inhibition in neuroprotection: effect of vinpocetine. Brain Res. Bull. 53, 245–254.
Zhang, L., Yang, L., 2015. Anti-inflammatory effects of vinpocetine in atherosclerosis and ischemic stroke: a review of the literature. Molecules 20, 335–347.
Szilagyi, G., Nagy, Z., Balkay, L., Boros, I., Emri, M., Lehel, S., Marian, T., Molnar, T., Szakall, S., Tron, L., Bereczki, D., Csiba, L., Fekete, I., Kerenyi, L., Galuska, L., Varga, J., Bonoczk, P., Vas, A., Gulyas, B., 2005. Effects of vinpocetine on the redistribution of cerebral blood flow and glucose metabolism in chronic ischemic stroke patients: a PET study. J. Neurol. Sci. 229–230, 275–284.
Gulyas, B., Halldin, C., Sandell, J., Karlsson, P., Sovago, J., Karpati, E., Kiss, B., Vas, A., Cselenyi, Z., Farde, L., 2002a. PET studies on the brain uptake and regional distribution of [11C]vinpocetine in human subjects. Acta Neurol. Scand. 106, 325–332
Gulyas, B., Halldin, C., Sovago, J., Sandell, J., Cselenyi, Z., Vas, A., Kiss, B., Karpati, E., Farde, L., 2002b. Drug distribution in man: a positron emission tomography study after oral administration of the labelled neuroprotective drug vinpocetine. Eur. J. Nucl. Med. Mol. Imaging 29, 1031–1038.
Deshmukh, R., Sharma, V., Mehan, S., Sharma, N., Bedi, K.L., 2009. Amelioration of intracerebroventricular streptozotocin induced cognitive dysfunction and oxidative stress by vinpocetine – a PDE1 inhibitor. Eur. J. Pharmacol. 620, 49–56.
Herrera-Mundo, N., Sitges, M., 2013. Vinpocetine and alpha-tocopherol prevent the increase in DA and oxidative stress induced by 3-NPA in striatum isolated nerve endings. J. Neurochem. 124, 233–240
Giachini, F.R., Lima, V.V., Carneiro, F.S., Tostes, R.C., Webb, R.C., 2011. Decreased cGMP level contributes to increased contraction in arteries from hypertensive rats: role of phosphodiesterase 1. Hypertension 57, 655–663.
Jeon, K.-I., Xu, X., Aizawa, T., Lim, J.H., Jono, H., Kwon, D.-S., Abe, J.-I., Berk, B.C., Li, J.- D., Yan, C., 2010. Vinpocetine inhibits NF-kappaB-dependent inflammation via an IKK-dependent but PDE-independent mechanism. Proc. Natl. Acad. Sci. USA 107, 9795–9800.
Medina, A.E., 2010. Vinpocetine as a potent antiinflammatory agent. Proc. Natl. Acad. Sci. USA 107, 9921–9922.
Lohmann A, Dingler E, Sommer W, et al. Bioavailability of vinpocetine and interference of the time of application with food intake. Arzneimittelforschung. 1992;42:914-917.
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