دورية أكاديمية

Reduced level of synapsin I protein in the rat striatum after intraventricular administration of proteasome inhibitors: preliminary studies

التفاصيل البيبلوغرافية
العنوان: Reduced level of synapsin I protein in the rat striatum after intraventricular administration of proteasome inhibitors: preliminary studies
المؤلفون: Wójcik, S., Spodnik, J. H., Sidor-Kaczmarek, J., Moryś, J.
المساهمون: This work was supported by a Polish Ministry of Science and Higher Education grant - NN401 005735 (to SW) and by a statutory (ST-11) grant from the Polish Ministry of Science and Higher Education ST-0011/07/211.
المصدر: Folia Morphologica; Vol 74, No 4 (2015); 428-433
بيانات النشر: Via Medica
سنة النشر: 2015
المجموعة: Via Medica Journals
مصطلحات موضوعية: epoxomicin, lactacystin, MG-132, synapsin I, rat, neuronal nuclear antigen, Western blot
الوصف: Background: We have recently described changes present in nigrostriatal terminals after intraperitoneal administration of MG-132 and changes that occur in the walls of the rat lateral ventricle after intraventricular administration of MG-132, lactacystin and epoxomicin — different classes of proteasome inhibitors. Substances that inhibit ubiquitin-proteasome system (UPS) activity, are intensively studied due to their potential role as novel therapeutic strategies in the treatment of cancer and ischaemia-reperfusion injury in the brain. The aim of this study is to determine the influence of intraventricular administration of MG-132, lactacystin and epoxomicin on the level in the rat striatum synapsin I — one of the most prominent neuron-specific phosphoproteins in the brain. Materials and methods and Results: Two weeks after administration of studied proteasome inhibitors, substantial reduction (up to 80%) of synapsin I was ob­served in the rat striatum. Because neurons, and especially dopaminergic ones, are sensitive to the depletion of proteasome function, we assume that observed synapsin I decrease may reflect changes in population of striatal neurons and/or nigrostriatal terminals. Conclusions: Understanding of cellular mechanisms standing behind our findings needs further studies, and could provide valuable contribution to the discussion on the mechanisms linking UPS inhibition and survival of neurons.
نوع الوثيقة: article in journal/newspaper
وصف الملف: application/pdf; application/xhtml+xml
اللغة: English
العلاقة: https://journals.viamedica.pl/folia_morphologica/article/view/FM.2015.0103Test
DOI: 10.5603/FM.2015.0103
الإتاحة: https://doi.org/10.5603/FM.2015.0103Test
https://journals.viamedica.pl/folia_morphologica/article/view/FM.2015.0103Test
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رقم الانضمام: edsbas.DA009096
قاعدة البيانات: BASE