کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2493532 1115511 2012 11 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Neuropeptide Y promotes neurogenesis and protection against methamphetamine-induced toxicity in mouse dentate gyrus-derived neurosphere cultures
موضوعات مرتبط
علوم زیستی و بیوفناوری علم عصب شناسی علوم اعصاب رفتاری
پیش نمایش صفحه اول مقاله
Neuropeptide Y promotes neurogenesis and protection against methamphetamine-induced toxicity in mouse dentate gyrus-derived neurosphere cultures
چکیده انگلیسی

Methamphetamine (METH) is a psychostimulant drug of abuse that causes severe brain damage. However, the mechanisms responsible for these effects are poorly understood, particularly regarding the impact of METH on hippocampal neurogenesis. Moreover, neuropeptide Y (NPY) is known to be neuroprotective under several pathological conditions. Here, we investigated the effect of METH on dentate gyrus (DG) neurogenesis, regarding cell death, proliferation and differentiation, as well as the role of NPY by itself and against METH-induced toxicity. DG-derived neurosphere cultures were used to evaluate the effect of METH or NPY on cell death, proliferation or neuronal differentiation. Moreover, the role of NPY and its receptors (Y1, Y2 and Y5) was investigated under conditions of METH-induced DG cell death. METH-induced cell death by both apoptosis and necrosis at concentrations above 10 nM, without affecting cell proliferation. Furthermore, at a non-toxic concentration (1 nM), METH decreased neuronal differentiation. NPY's protective effect was mainly due to the reduction of glutamate release, and it also increased DG cell proliferation and neuronal differentiation via Y1 receptors. In addition, while the activation of Y1 or Y2 receptors was able to prevent METH-induced cell death, the Y1 subtype alone was responsible for blocking the decrease in neuronal differentiation induced by the drug. Taken together, METH negatively affects DG cell viability and neurogenesis, and NPY is revealed to be a promising protective tool against the deleterious effects of METH on hippocampal neurogenesis.


► METH induces cell death by both necrosis and apoptosis in DG cell cultures.
► NPY prevents METH-induced apoptosis by activation of both Y1 and Y2 receptors.
► NPY inhibited glutamate release triggered by METH.
► NPY is proproliferative and proneurogenic in DG cultures via Y1 receptor activation.
► NPY prevents METH-induced decrease of neurogenesis via Y1 receptor activation.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Neuropharmacology - Volume 62, Issue 7, June 2012, Pages 2413–2423
نویسندگان
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