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PKCε and cardioprotection : an exploration of putative mechanisms

Includes bibliographical references.

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Bibliographic Details
Main Author: McCarthy, Joy
Other Authors: Essop, Faadiel
Format: Thesis
Language:English
Published: Department of Medicine 2014
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access_status_str Open Access
author McCarthy, Joy
author2 Essop, Faadiel
author_browse Essop, Faadiel
McCarthy, Joy
author_facet Essop, Faadiel
McCarthy, Joy
author_sort McCarthy, Joy
collection Thesis
description Includes bibliographical references.
format Thesis
id oai:open.uct.ac.za:11427/3429
institution University of Cape Town (South Africa)
language eng
last_indexed 2026-06-10T12:32:36.207Z
license_str Not specified — see source repository
provenance_str_mv Harvested via OAI-PMH from UCTD — University of Cape Town Open Access Repository
publishDate 2014
publishDateRange 2014
publishDateSort 2014
publisher Department of Medicine
publisherStr Department of Medicine
record_format dspace
source_str UCTD — University of Cape Town Open Access Repository
spelling oai:open.uct.ac.za:11427/3429 PKCε and cardioprotection : an exploration of putative mechanisms McCarthy, Joy Essop, Faadiel Opie, Lionel H Medicine Includes bibliographical references. Recent studies have investigated the underlying regulatory mechanisms that may explain the cardioprotective role of PKCε. Sub-proteome analysis has identified interactions between activated PKCε and various mitochondrial proteins, which orchestrate mitochondrial homeostasis, including proteins governing mitochondrial oxidative phosphorylation, electron transfer, ion transport and control of mitochondrial permeability transition (MPT). MPT disruption is regarded as a key step in the initiation of an apoptotic cascade. However, brief pore opening may be beneficial in triggering the generation of small amounts of protective reactive oxygen species (ROS) and restoring calcium homeostasis. PKCε also interacts with adenine nucleotide translocases (ANTs), inner mitochondrial membrane proteins essential for ATP production and an integral component of the permeability transition pore. An augmented capacity to generate ATP would fundamentally enhance resilience to ischemia. 2014-07-29T09:07:21Z 2014-07-29T09:07:21Z 2006 Doctoral Thesis Doctoral PhD http://hdl.handle.net/11427/3429 eng application/pdf Department of Medicine Faculty of Health Sciences University of Cape Town
spellingShingle Medicine
McCarthy, Joy
PKCε and cardioprotection : an exploration of putative mechanisms
thesis_degree_str Doctoral
title PKCε and cardioprotection : an exploration of putative mechanisms
title_full PKCε and cardioprotection : an exploration of putative mechanisms
title_fullStr PKCε and cardioprotection : an exploration of putative mechanisms
title_full_unstemmed PKCε and cardioprotection : an exploration of putative mechanisms
title_short PKCε and cardioprotection : an exploration of putative mechanisms
title_sort pkcε and cardioprotection an exploration of putative mechanisms
topic Medicine
url http://hdl.handle.net/11427/3429
work_keys_str_mv AT mccarthyjoy pkceandcardioprotectionanexplorationofputativemechanisms