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Prior to the emergence of the sliding filament model, contraction theories had been in abundance. In the absence of the kinds of structural and biochemical information available today, it has been a simple matter to speculate about the possible ways in which tension generation and shortening might occur. The advent of the sliding filament model had an immediate impact on these theories; within several years they fell by the wayside, and attention was redirected towards mechanisms by which the filaments might be driven to slide by one another. In terms of identifying the driving mechanism, the pivotal observa tion was the electron micrographic indentification of cross-bridges extending from the thick filaments. It was quite naturally assumed that such bridges, which had the ability to split ATP, were the molecular motors, i.e., that they were the sites of mechanochemical transduction. Out of this presumption grew the cross-bridge model. in which filament sliding is presumed to be driven by the cyclic interaction of cross-bridges with complementary actin sites located along the thin filaments.
This valuable resource provides a systematic account of the biochemistry of smooth muscle contraction. As a comprehensive guide to this rapidly growing area of research, it covers the structure and characteristic properties of contractile and regulatory proteins, with special emphasis on their predicted function in the live muscle. Also included in this book are intermediate filament proteins, and desmin and vimentin, whose function in smooth muscle is unknown; and several enzymes involved in the phosphorylation-dephosphorylation of contractile and other proteins.
This volume presents the proceedings of a muscle symposium, which was held as the Fourth Fujihara seminar on October 28 - November 1, 2002, at Hakone, Japan. This volume covers all fields of muscle biology, from molecules to humans. This book provides information about recent progress of muscle research as well as the problems that remain to be investigated. This volume will stimulate muscle investigators to design and perform novel experiments to clarify the mysteries in muscle contraction.
This volume presents the proceedings of a muscle symposium, which was supported by the grant from the Fujihara Foundation of Science to be held as the Fourth Fujihara Seminar on October 28 -November 1, 2002, at Hakone, Japan. The Fujihara Seminar covers all fields of natural science, while only one proposal is granted every year. It is therefore a great honor for me to be able to organize this meeting. Before this symposium, I have organized muscle symposia five times, and published the proceedings: " Cross-bridge Mechanism in Muscle Contraction (University of Tokyo Press, 1978), "Contractile Mechanisms in Muscle" (plenum, 1984); "Molecular Mechanisms of Muscle Contraction" (plenum, 1988); "Mechanism of MyofIlament Sliding in Muscle contraction" (plenum, 1993); "Mechanisms of Work Production and Work Absorption in Muscle" (plenum, 1998). As with these proceedings, this volume contains records of discussions made not only after each presentation but also during the periods of General Discussion, in order that general readers may properly evaluate each presentation and the up-to-date situation of this research field. It was my great pleasure to have Dr. Hugh Huxley, a principal discoverer of the sliding fIlament mechanism in muscle contraction, in this meeting. On my request, Dr. Huxley kindly gave a special lecture on his monumental discovery of myofIlament-lattice structure by X-ray diffraction of living skeletal muscle. I hope general readers to learn how a breakthrough in a specific research field can be achieved.
Vascular Smooth Muscle: Metabolic, Ionic, and Contractile Mechanisms addresses the vascular smooth muscle function by describing plasma lipoprotein structure, synthesis, and transport in relation to the concepts of altered vascular smooth muscle lipid metabolism leading to the genesis of atherosclerotic disease. This book is organized into six chapters and begins with an introduction to the complexities of energy metabolism and how metabolic events can be correlated with a simultaneous quantitative assessment of smooth muscle mechanics and the contractile machinery at the molecular level. The next two chapters offer the reader a view of smooth muscle membrane properties in terms of the distribution, transport, and metabolic control of electrolytes and specific aspects of ion conductance and electrical activity. This text also explains how smooth muscle cells regulate their contractile activity through regulation of calcium ion fluxes and the interaction, at the molecular level, of calcium ions with regulatory proteins associated with the contractile apparatus. Reference is made to the relation of possible anomalies in cellular or subcellular smooth muscle metabolic and/or ionic events to the bases of certain types of vascular disease. A chapter that examines the events leading to vascular pathology in the form of atherogenesis concludes the book. This book is intended for researchers and clinicians engaged in the study of smooth muscle and related areas.
This volume describes the current state of our knowledge on the neurobiology of muscle fatigue, with consideration also given to selected integrative cardiorespiratory mechanisms. Our charge to the authors of the various chapters was twofold: to provide a systematic review of the topic that could serve as a balanced reference text for practicing health-care professionals, teaching faculty, and pre-and postdoctoral trainees in the biomedi cal sciences; and to stimulate further experimental and theoretical work on neurobiology. Key issues are addressed in nine interrelated areas: fatigue of single muscle fibers, fatigue at the neuromuscular junction, fatigue of single motor units, metabolic fatigue studied with nuclear magnetic resonance, fatigue of the segmental motor system, fatigue involving suprasegmental mechanisms, the task dependency of fatigue mechanisms, integrative (largely cardiorespiratory) systems issues, and fatigue of adapted systems (due to aging, under-and overuse, and pathophysiology). The product is a volume that provides compre of processes that operate from the forebrain to the contractile proteins.
It is now widely recognized that fundamental progress in science is made not in a continuous manner but in a stepwise manner. In the field of the molecular mechanism of contraction in striated muscle, the stepwise progress was achieved by three great investigators in 1940's and 1950's. In the early 1940's, Albert Szent-Gyorgyi and his associates showed biochemically that muscle contraction is essentially an interaction between actin and myosin coupled with ATP hydrolysis. Then, in the 1950's, Hugh E. Huxley together with Jean Hanson demonstrated that striated muscle is composed of a hexagonal lattice of two kinds of interdigtating myofilaments consisting of action and myosin respectively, and made a monumental discovery that muscle contraction results from the relative sliding between the actin and myosin filaments. Andrew F. Huxley, who also participated in the discovery of the sliding filament mechanism of muscle contraction was attributed to the attachment-detachment cycle between the cross-bridges extending from the myosin filament and the complementary sites on the actin filament. After the above stepwise progress, however, muscle research appears to have entered into a period of so-called 'normal science' where detailed knowledge has been accumulating around the well established 'central dogmas' but without fundamental progress. More specifically, most experiments on muscle contraction mechanisms have been designed, carried out and interpreted on the basis of the Huxley's 1957 and the Huxley-Simmons' 1971 contraction models, as well as the kinetic scheme of actomyosin ATPase; but the molecular mechanism of contraction still remains to be a matter for debate and speculation. For further fundamental progress in this field of research, we feel it necessary to reconsider the validity of these dogmas and to interpret the results more freely. In 1978, one of us (H.S.) organized a symposium in Tokyo based on the above idea, and we published the proceedings under the title of "Cross-bridge Mechanism in Muscle Contraction" (ed. H. Sugi and G.H. Pollack, University of Tokyo Press/University Park Press, 1979). The unusual interest of muscle physiologists in this symposium encouraged us to organize a second symposium on muscle contraction in Seattle in 1982, and proceedings was again published under the title of "Contractile Mechanisms in Muscle" (ed. G.H. Pollack and H. Sugi, Plenum Publishing Corporation, 1984). We were again very much encouraged by the intense interest of the people at the symposium as well as by readers of the proceedings, and became convinced that the symposia of this kind would greatly accelerate the progress in this field. The present symposium was organized by one of us (H.S.) as the third "Cross-bride" symposium. Though most papers are concerned, as in the previous two symposia, with experiments on intact and demembranated muscle fibers and isolated myofibrils, where the three-Dimensional muofilament-lattice structures have been preserved, the results are frequently discussed in connection with the kinetics of actomyosin ATPase, reflecting the recent development of experimental methods connecting physiology and biochemistry. It has also become possible to obtain direct information about the orientation and configuration of the cross-bridges as various stages during muscle contraction.
Editions previous to this one had R.D. Keynes and David J. Aidley as primary and secondary authors.