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Activation of the Extrinsic and Intrinsic Apoptotic Pathways in Cerebellum of Kindled Rats

Authors :
Verónica Custodio
Cristina Trejo
Emmanuel González
Cesar Mendoza
Leonardo Hernández
Carmen Rubio
Carlos Paz
Moisés Rubio-Osornio
Source :
The Cerebellum. 18:750-760
Publication Year :
2019
Publisher :
Springer Science and Business Media LLC, 2019.

Abstract

The purpose of this study is to determine the activation of the extrinsic and intrinsic apoptotic pathways in the cerebellum of rats exposed to amygdaloid electrical kindling. Western blot analyses were carried out for caspase-8 and caspase-9, Bid, Bax, and Bcl-2 in the cerebellum and immunohistochemistry of Bid, Bax, cytochrome C, and VDAC (voltage-dependent anion channels) in the cerebellar cortex of Wistar male rats with 0, 15, and 45 kindling stimulations. In the experimental group of 45 stimuli, we observed an increase in protein activation of caspase-9 and truncated Bid and Bax, in addition to a decrease in expression of pro-caspase-8 and the anti-apoptotic protein Bcl-2, determined by Western blot. Moreover, we observed a cytosolic immunopositivity for cytochrome C and a mitochondrial immunolocalization for truncated Bid and Bax in the group of 45 stimuli. In this work, we found an increase of caspase-8, a cysteine-protease that can activate caspase-3 triggering extrinsic apoptosis by signaling of death receptors. However, it also can activate the intrinsic pathway releasing Bid, which performs mitochondrial translocation of Bax, inactivating Bcl-2 and allowing the release of cytochrome C through the opening of the mitochondrial permeability transition pore, promoting the activation of caspase-9 which activates caspase-3, the main executor caspase of apoptosis. Therefore, it is concluded that there is an activation of the intrinsic and extrinsic apoptotic pathways in the cerebellum of rats exposed to the kindling model. Apoptosis signaling pathways can be analyzed as an important developing object of research about the epileptic activity. Graphical Abstract.

Details

ISSN :
14734230 and 14734222
Volume :
18
Database :
OpenAIRE
Journal :
The Cerebellum
Accession number :
edsair.doi.dedup.....6262e66ac6cd389594d551bb612025d5