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Stress, Trauma and Synaptic Plasticity

Record Type:	Language materials, printed : Monograph/item
Title/Author:	Stress, Trauma and Synaptic Plasticity/ by Maxwell Bennett, Jim Lagopoulos.
Author:	Bennett, Maxwell.
other author:	Lagopoulos, Jim.
Description:	XXXIII, 231 p. 47 illus., 18 illus. in color.online resource. :
Contained By:	Springer Nature eBook
Subject:	Neurosciences. -
Online resource:	https://doi.org/10.1007/978-3-319-91116-8
ISBN:	9783319911168

Stress, Trauma and Synaptic Plasticity
Bennett, Maxwell.

Stress, Trauma and Synaptic Plasticity[electronic resource] /by Maxwell Bennett, Jim Lagopoulos. - 1st ed. 2018. - XXXIII, 231 p. 47 illus., 18 illus. in color.online resource.

Grey matter changes in the brain following stress and trauma -- Synaptic changes responsible for grey matter changes in the brain of animal models following stress -- Identification of the core neural network subserving PTSD in animal models and their modulation -- Modulation of the core neural network in stress: the role of Brain Derived Neurotrophic Factor & LTP -- Modulation of the core neural network in stress: the role of Endocannabinoids & LTD -- Functioning of the core neural network in fear and extinction -- Modulation of the core synaptic network in extinction: the role of Brain Derived Neurotrophic Factor -- Appendix 1: F-actin determination of dendritic spine integrity -- Appendix 2: Regulation of NMDA receptors. .

This book provides detailed insights into the cellular and molecular alterations that occur in the brain following stress and trauma. The changes to the grey matter in certain areas of the brain are similar in stressed humans and animals, with the most likely basis for these changes being the degeneration of synaptic connections. In the book’s initial sections, the reader will learn about the core network of synaptic connections that are affected by stress and trauma disorders. These connections are chiefly modulated by dopamine, serotonin and Brain Derived Neurotrophic Factor (BDNF). In subsequent chapters, the NMDA-receptor-mediated plasticity of these synapses is discussed, with particular attention paid to how glucocorticoids can interfere with the function of BDNF and thereby affect the synapse’s physical stability. The book concludes by integrating the observations made in the previous sections so as to present plausible hypotheses regarding the identity of the networks, synapses and molecular pathways that promote fear and extinction. Providing an up-to-date overview of the mechanisms of synaptic plasticity and physiological changes in the stressed and traumatized brain, this book will appeal to researchers, clinicians and students in the neurosciences.

ISBN: 9783319911168

Standard No.: 10.1007/978-3-319-91116-8doiSubjects--Topical Terms:

593561
Neurosciences.

LC Class. No.: RC321-580

Dewey Class. No.: 612.8

Stress, Trauma and Synaptic Plasticity
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520 $a This book provides detailed insights into the cellular and molecular alterations that occur in the brain following stress and trauma. The changes to the grey matter in certain areas of the brain are similar in stressed humans and animals, with the most likely basis for these changes being the degeneration of synaptic connections. In the book’s initial sections, the reader will learn about the core network of synaptic connections that are affected by stress and trauma disorders. These connections are chiefly modulated by dopamine, serotonin and Brain Derived Neurotrophic Factor (BDNF). In subsequent chapters, the NMDA-receptor-mediated plasticity of these synapses is discussed, with particular attention paid to how glucocorticoids can interfere with the function of BDNF and thereby affect the synapse’s physical stability. The book concludes by integrating the observations made in the previous sections so as to present plausible hypotheses regarding the identity of the networks, synapses and molecular pathways that promote fear and extinction. Providing an up-to-date overview of the mechanisms of synaptic plasticity and physiological changes in the stressed and traumatized brain, this book will appeal to researchers, clinicians and students in the neurosciences.
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