Striated muscle is the most common muscle type in the vertebrate body. This book describes in molecular terms the components and intracellular events responsible for the contraction and relaxation of striated muscle. The topic is introduced with a discussion of motile systems occurring throughout the biological world and their relation to the highly specialised contractile system of muscle. Professor Perry then goes on to discuss the mechanochemical process and the regulatory roles of calcium, I filament proteins and phosphorylation. The book ends with an examination of the role of dystrophin and its implications in Duchenne muscular dystrophy, the most common form of muscle disease. Molecular Mechanisms in Striated Muscle will provide an important source of information and current theory for researchers and postgraduate students in muscle physiology, biochemistry and medicine.

Molecular Control Mechanisms in Striated Muscle Contraction addresses the molecular mechanisms by which contraction of heart and skeletal muscles is regulated, as well as the modulation of these mechanisms by important (patho)physiological variables such as ionic composition of the myoplasm and phosphorylations of contractile and regulatory proteins. For the novice, this volume includes chapters that summarize current understanding of excitation-contraction coupling in striated muscles, as well as the compositions and structures myofibrillar thick and thin filaments. For the expert, this volume presents detailed pictures of current understanding of the mechanisms underlying the CA2+ regulation of contraction in heart and skeletal muscles and discusses important directions for future investigation.

The book is a collection of original research and review articles addressing the intriguing field of the cellular and molecular players involved in muscle homeostasis and regeneration. One of the most ambitious aspirations of modern medical science is the possibility of regenerating any damaged part of the body, including skeletal muscle. This desire has prompted clinicians and researchers to search for innovative technologies aimed at replacing organs and tissues that are compromised. In this context, the papers, collected in this book, addressing a specific aspects of muscle homeostasis and regeneration under physiopathologic conditions, will help us to better understand the underlying mechanisms of muscle healing and will help to design more appropriate therapeutic approaches to improve muscle regeneration and to counteract muscle diseases.

There has been a lot of debate concerning the nature of the molecular mechanism that produces filament sliding and muscle shortening. This book presents the different kinds of structural and mechanical evidence in favour of the swinging of myosin heads on actin during the contractile cycle.