Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/4728
Title: Neuropeptide Y can rescue neurons from cell death following the application of an excitotoxic insult with kainate in rat organotypic hippocampal slice cultures
Authors: Xapelli, S. 
Silva, A. P. 
Ferreira, R. 
Malva, J. O. 
Keywords: Glutamate receptors; Neurodegeneration; Neuroprotection
Issue Date: 2007
Citation: Peptides. 28:2 (2007) 288-294
Abstract: In the present work we investigated the neuroprotective role of neuropeptide Y (NPY) after an excitotoxic insult in rat organotypic hippocampal slice cultures. Exposure of 2 week-old rat hippocampal slice cultures to 12 [mu]M kainate (KA) for 24 h induced neuronal death in dentate gyrus (DG) granular cell layer, CA1 and CA3 pyramidal cell layers, as quantified by cellular propidium iodide (PI) uptake. The activation of Y1 or Y2 receptors 30 min after starting the exposure to the excitotoxic insult with kainate resulted in neuroprotection by reducing the PI uptake in DG, CA1 and CA3 cell layers. The use of Y1 or Y2 receptors antagonists, BIBP3226 (1 [mu]M) or BIIE0246 (1 [mu]M), resulted in the loss of the neuroprotection induced by the activation of Y1 or Y2 receptors, respectively, in all hippocampal subfields. Taken together these results suggest that activation of NPY Y1 or Y2 receptors activates neuroprotective pathways that are able to rescue neurons from excitotoxic cell death.
URI: https://hdl.handle.net/10316/4728
DOI: 10.1016/j.peptides.2006.09.031
Rights: openAccess
Appears in Collections:FMUC Medicina - Artigos em Revistas Internacionais

Files in This Item:
File Description SizeFormat
file1cc70f50d99d46e88577cc568a3bd38d.pdf671.08 kBAdobe PDFView/Open
Show full item record

SCOPUSTM   
Citations

31
checked on Nov 17, 2022

WEB OF SCIENCETM
Citations 50

30
checked on May 2, 2023

Page view(s)

332
checked on Apr 9, 2024

Download(s) 50

524
checked on Apr 9, 2024

Google ScholarTM

Check

Altmetric

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.