Mitochondria: The Dynamic Organelle
The term mihondrion is derived from Latin, with mitos meaning thread and chondrion meaning granules. Indeed, under the light microscope, mihondria often appear as rods or granules within the cytoplasm. For decades after initial visualization of mihondria by light microscopy, mihondrial function remained clouded. However, with the development of differential centri- gation and electron microscopy, it was discovered that a chief function of the mihondria was the generation of ATP for the remainder of the cell. For many years, the energy generating function of the mihondria was considered the primary, if not the sole function of the mihondria. During that period, inves- gators attempted to obtain information on the mechanism of ATP synthesis and the regulation of electron transport. In the first chapter of the book, Dr. Hassinen summarizes those studies, providing clear pictures on the transformation of reducing equivalents into a proton gradient and the mechanism by which the F F 1 0 ATPase utilizes the proton gradient to generate ATP. He also summarizes the key regulatory steps of the citric acid cycle, which is the major source of reducing equivalents for the electron transport chain. In the heart, most of the carbon that feeds into the citric acid cycle is derived from fatty acid metabolism. Although fatty acid utilization provides most of the ATP for contraction, a proper balance must be maintained between the utilization of fatty acids and that of glucose. In the second chapter, Drs.
1101680816
Mitochondria: The Dynamic Organelle
The term mihondrion is derived from Latin, with mitos meaning thread and chondrion meaning granules. Indeed, under the light microscope, mihondria often appear as rods or granules within the cytoplasm. For decades after initial visualization of mihondria by light microscopy, mihondrial function remained clouded. However, with the development of differential centri- gation and electron microscopy, it was discovered that a chief function of the mihondria was the generation of ATP for the remainder of the cell. For many years, the energy generating function of the mihondria was considered the primary, if not the sole function of the mihondria. During that period, inves- gators attempted to obtain information on the mechanism of ATP synthesis and the regulation of electron transport. In the first chapter of the book, Dr. Hassinen summarizes those studies, providing clear pictures on the transformation of reducing equivalents into a proton gradient and the mechanism by which the F F 1 0 ATPase utilizes the proton gradient to generate ATP. He also summarizes the key regulatory steps of the citric acid cycle, which is the major source of reducing equivalents for the electron transport chain. In the heart, most of the carbon that feeds into the citric acid cycle is derived from fatty acid metabolism. Although fatty acid utilization provides most of the ATP for contraction, a proper balance must be maintained between the utilization of fatty acids and that of glucose. In the second chapter, Drs.
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Mitochondria: The Dynamic Organelle

Mitochondria: The Dynamic Organelle

Mitochondria: The Dynamic Organelle

Mitochondria: The Dynamic Organelle

Paperback(Softcover reprint of hardcover 1st ed. 2007)

$219.99 
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Overview

The term mihondrion is derived from Latin, with mitos meaning thread and chondrion meaning granules. Indeed, under the light microscope, mihondria often appear as rods or granules within the cytoplasm. For decades after initial visualization of mihondria by light microscopy, mihondrial function remained clouded. However, with the development of differential centri- gation and electron microscopy, it was discovered that a chief function of the mihondria was the generation of ATP for the remainder of the cell. For many years, the energy generating function of the mihondria was considered the primary, if not the sole function of the mihondria. During that period, inves- gators attempted to obtain information on the mechanism of ATP synthesis and the regulation of electron transport. In the first chapter of the book, Dr. Hassinen summarizes those studies, providing clear pictures on the transformation of reducing equivalents into a proton gradient and the mechanism by which the F F 1 0 ATPase utilizes the proton gradient to generate ATP. He also summarizes the key regulatory steps of the citric acid cycle, which is the major source of reducing equivalents for the electron transport chain. In the heart, most of the carbon that feeds into the citric acid cycle is derived from fatty acid metabolism. Although fatty acid utilization provides most of the ATP for contraction, a proper balance must be maintained between the utilization of fatty acids and that of glucose. In the second chapter, Drs.

Product Details

ISBN-13: 9781441924186
Publisher: Springer New York
Publication date: 11/24/2010
Series: Advances in Biochemistry in Health and Disease , #2
Edition description: Softcover reprint of hardcover 1st ed. 2007
Pages: 359
Product dimensions: 6.10(w) x 9.25(h) x 0.24(d)

About the Author

Dr. Stephen W. Schaffer is a professor at the University of South Alabama. He is a member of the editorial board of Molecular and Cellular Biochemistry.

Dr. M.-Saadeh Suleiman is a professor at the University of Bristol, UK. His research includes investigating the role of metabolites and ionic species in myocardial protection, with special emphasis on amino acids, mihondria, Ca2+ loading and reactive oxygen species.

Table of Contents

Mihondrial Metabolism.- Regulation of Mihondrial Respiration in Heart Muscle.- Regulation of Fatty Acid Oxidation of the Heart.- Regulation of Mihondrial Fuel Handling by the Peroxisome Proliferator-Activated Receptors.- Molecular Structure of the Mihondrial Citrate Transport Protein.- Regulation of Pyruvate and Amino Acid Metabolism.- Amino Acids and the Mihondria.- The Dynamic Nature of the Mihondria.- Mechanotransduction of Shear-stress at the Mihondria.- Mihondria as Initiators of Cell Signaling.- Formation of Reactive Oxygen Species in Mihondria.- Mihondrial Calcium: Role in the Normal and Ischaemic/Reperfused Myocardium.- Mihondrial Ion Channels.- Mihondria as Initiators of Cell Death.- The Mihondrial Permeability Transition Pore – from Molecular Mechanism to Reperfusion Injury and Cardioprotection.- The Apoptotic Mihondrial Pathway – Modulators, Interventions and Clinical Implications.- The Role of Mihondria in Necrosis Following Myocardial Ischemia-Reperfusion.- Mihondria as Modulators of Cell Death.- Mihondria and Their Role in Ischemia/Reperfusion Injury.- Mihondrial DNA Damage and Repair.
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