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Transient Receptor Potential Canonical Channels and Brain Diseases

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Attention for Chapter 5: TRPC Channels and Programmed Cell Death
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Chapter title
TRPC Channels and Programmed Cell Death
Chapter number 5
Book title
Transient Receptor Potential Canonical Channels and Brain Diseases
Published in
Advances in experimental medicine and biology, January 2017
DOI 10.1007/978-94-024-1088-4_5
Pubmed ID
Book ISBNs
978-9-40-241086-0, 978-9-40-241088-4
Authors

Jian Zhou, Yichang Jia, Zhou, Jian, Jia, Yichang

Abstract

Neurotrophins, including nerve growth factor (NGF) and brain-derived neurotrophic factor (BDNF), bind to their high-affinity receptors to promote neuronal survival during brain development. One of the key downstream pathways is the phospholipase C (PLC) pathway, which not only plays a central role in calcium release from internal store but also in activation of TRPC channels coupled with neurotrophin receptors. TRPC channels are required for the neurotrophin-mediated neuronal protective effects. In addition, activation of TRPC channels is able to protect neurons in the absence of neurotrophin. In some circumstances, TRPC channels coupled with metabotropic glutamate receptor may mediate the excitotoxicity by calcium overload. One of the key questions in the field is the channel gating mechanisms; understanding of which would help design compounds to modulate the channel properties. The development and identification of TRPC channel agonists or blockers are promising and may unveil new therapeutic drugs for the treatment of neurodegenerative diseases and epilepsy.

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Mendeley readers

The data shown below were compiled from readership statistics for 2 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 2 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 1 50%
Student > Bachelor 1 50%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 2 100%