Mitochondrial Inhibitors and Neurodegenerative Disorders (Hardcover, 2000 ed.)

Mitochondria have long been the Rodney Dangerfield of cellular organelles. Believed to be the remnants of bacterial infection of eukaryotic cells eons ago, the mitochondrion evolved a symbiotic relationship in which it dutifully served as the efficient source of A TP for cell function. The extraordinary dependence of cells on the energy provided by mito chondrial oxidative metabolism of glucose, especially through critical organs such as the heart and brain, is underlined by the fatal consequences of toxins that interfere with the mitochondrial electron transport system. Consistent with their ancestry, the mitochondria have their own DNA that encodes many but not all of their proteins. The mitochon dria and their genes come from the mother via the ovum since sperm do not possess mitochondria. This extranuclear form of inheritance derived exclusively from the female side has proven to be a powerful tool for tracing the evolution by the number of base substitutions in mtDNA. That mitochondrial gene mutations might be a source of human dis ease became evident a decade ago with the characterization of a group of multisystem disorders, typically involving the nervous system, which are transmitted from mother to child. Specific point mutations in mtDNA have been associated with the different syndromes."

General

Imprint:	HumanaPress
Country of origin:	United States
Series:	Contemporary Neuroscience
Release date:	October 1999
First published:	2000
Editors:	Paul R Sanberg • Hitoo Nishino • Cesario V. Borlongan
Dimensions:	235 x 155 x 19mm (L x W x T)
Format:	Hardcover
Pages:	314
Edition:	2000 ed.
ISBN-13:	978-0-89603-805-9
Categories:	Books > Medicine > Clinical & internal medicine > Neurology & clinical neurophysiology Books > Science & Mathematics > Biology, life sciences > Biochemistry > General
LSN:	0-89603-805-X
Barcode:	9780896038059

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