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Muscles as Molecular and Metabolic Machines [Mīkstie vāki]

  • Formāts: Paperback / softback, 176 pages, height x width: 234x156 mm, weight: 454 g, 14 equations; 4 Tables, black and white
  • Sērija : Routledge Revivals
  • Izdošanas datums: 14-Dec-2020
  • Izdevniecība: CRC Press
  • ISBN-10: 0367227800
  • ISBN-13: 9780367227807
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  • Formāts: Paperback / softback, 176 pages, height x width: 234x156 mm, weight: 454 g, 14 equations; 4 Tables, black and white
  • Sērija : Routledge Revivals
  • Izdošanas datums: 14-Dec-2020
  • Izdevniecība: CRC Press
  • ISBN-10: 0367227800
  • ISBN-13: 9780367227807
Citas grāmatas par šo tēmu:
First published in 1994, this book explores the paradigm of muscles as molecular and metabolic machines in which all structures and functions are exquisitely integrated and matched to each other. The analysis begins with a standard reductionist approach-reviewing the integrated machine parts. The key working components of the complete muscle machine are proteins (soluble, organelle, or membrane localized), and a conservative count indicates that today more than 100 such machine parts are known, essentially all occurring as cell specific isoforms. Random assortment of these machine parts or protein isoforms could generate an astronomical number of "muscle machines" and an equally enormous number of muscle fiber types. The question is, why aren't such large numbers ever seen?
To attack this problem, the reductionist approach is complemented with an integrationist/adaptational one. Evidence is presented that the more highly specialized the muscle type, the further one moves from the above extreme; in the most highly specialized muscles, typically only one fiber type is found. It is argued that instead of random assortment of isoforms or machine parts, only specific and often unique combinations can work in appropriate fashion. A few established examples of this fundamental principle are reviewed, but emphasis is placed on the fact that we know dreadfully little about why this is so and what kinds of further studies are needed. The issue of why the very large numbers of fiber types theoretically possible are never even approximately realized has never before been addressed. Indeed, it is rarely recognized. Muscles as Molecular and Metabolic Machines is the first work of its kind on the subject.

Recenzijas

"Muscles as Molecular and Metabolic Machines is a marvelous reference for the clinician with an inquiring mind who enjoys searching the frontiers of knowledge in the biomolecular and metabolic pathways in muscle...The writing is clearly superior scholarship and reflects the author's more than 30 years of biomolecular research on metabolic pathways of the marvelous machine called muscle."

Arthur J. Nelson, JOSPT, 23(5), May 1996

Chapter 1 Framework
1(12)
The Setting
1(3)
Isoform Machinery for Speeding Up Information Transfer
4(1)
Troponin C Isoforms in Speeding Up Contractile Function
5(1)
Coadaptation of Energy Demand and Energy Supply Pathways
6(4)
Coadaptation and Metabolic Isozymes: the LDH Archetype
10(1)
Coadaptation and Emergent Properties
11(2)
Chapter 2 Nerve-to-Muscle Signals
13(18)
How the Signals Get There
13(1)
What Are Channels?
14(1)
Acetylcholine: the Signal to Go
15(1)
ACh Release Depends Upon Ca++ Channels
15(1)
ACh-Induced Depolarization Depends on End-Plate Channels
16(1)
Structure of End-Plate Channels
17(2)
End-Plate Channel Isoforms
19(1)
Localization of End-Plate Channels
19(1)
Synaptic Transmission Time
20(1)
Muscle (and Nerve) Action Potentials Depend on Na+ and K+ Channels
21(1)
Structure of Na+ Channels
21(1)
Na+ Channel Isoforms
22(2)
Localization of Na+ Channels
24(1)
Isoforms of Delayed Rectifier K+ Channels
24(1)
Excitation-Contraction Coupling
25(3)
Ca++ Channel Isoforms
28(1)
E-C Coupling in Fast- and Slow-Twitch Muscles
29(1)
Facilitating Role of Calsequestrin
30(1)
Chapter 3 Design of Nerve-to-Muscle Information Systems
31(10)
Introduction
31(1)
Channels Are Extremely Efficient Catalysts
31(2)
Channel Densities Are Usually Rather Low
33(1)
Channel Densities May Be Adjusted Upward
34(1)
Design Criteria for Presynaptic Signaling Processes
35(1)
Design Criteria for Postsynaptic Signal Transduction
36(1)
Design Criteria for Na+ Channel Functions
37(1)
Design Criteria for TT and SR Ca++ Channels
38(1)
Overall Design Principles for Nerve-to-Muscle Information Flow Systems
39(2)
Chapter 4 Energy Demand of Muscle Machines
41(18)
Introduction
41(1)
The Sarcomere: the Basic Contractile Unit
42(1)
Sliding Filament Model of Contraction
43(1)
Taking Myosin Apart to Identify Functional Domains
44(1)
Globular and Filamentous Forms of Actin
45(1)
ATPase Coupling with Filament Movement
45(2)
Troponin and Tropomyosin Mediate Ca++ Regulation of Muscle Contraction
47(2)
Adaptable vs. Conservative Aspects of Contractile Components
49(3)
Myosin Isoforms: Patterns and Distribution
49(1)
Actin Isoforms
50(1)
Tropomyosin Isoforms
51(1)
Troponin Isoforms
51(1)
Co-occurrence of Specific Contractile Isoforms
51(1)
Excitation-Contraction (EC) Coupling: Decoupling of Ca+4 Channel and Ca+ 4 Pump Functions of the SR
52(1)
Ca++ Pump Isoform
52(1)
Co-occurrence of Contractile and Regulatory Protein Isoforms
52(1)
Role of Actomyosin ATPase in Adaptation of Muscle Function
53(1)
In Solution, Actomyosin ATPases Are Highly Adapted Catalysts
53(1)
Diffusion Limitation of Enzyme Function Can Be Circumvented
54(1)
The Contractile Cycle as a Channeled Reaction Sequence
55(2)
Evidence For Preferential Access To and From Actomyosin ATPase
57(1)
Minimizing Ca++ Diffusion-Based Limits
57(2)
Chapter 5 Return to the Precontraction State
59(10)
Introduction
59(1)
Ca++ ATPase and Sarcoplasmic Reticulum (SR) Structure
59(1)
Ca++ ATPase Catalytic Cycle
60(1)
Model of Ca+t ATPase Structure
61(1)
Two Ca++ ATPase Genes: Two (or More) Ca++ ATPase Isoforms
62(1)
Two Ca++ ATPases: Differences and Homologies
62(1)
Coadaptation and Design Properties of SR Ca++ ATPases
62(1)
Na+K+ ATPase and the Na+ Pump
63(1)
Na+K+ ATPase Catalytic Cycle
64(1)
Na+K+ ATPase Structure
64(1)
Minimal Design Criteria for Na+K4 ATPase as an Ion Pump
65(1)
Na+ Pump Isoforms Based on a and B Subunit Polymorphism
65(1)
Functional Significance of Na+ Pump Isoforms
66(1)
Magnitude of the Postexercise Na+K+ Imbalance
66(1)
Short-Term Na+K+ ATPase Regulatory Mechanisms
66(1)
Long-Term Na+K+ ATPase Regulatory Mechanisms
67(1)
Muscle Na+K+ ATPase Functional Design Considerations
67(2)
Chapter 6 Supplying Muscle Machines with Energy
69(26)
Introduction
69(1)
Three Basic ATP-Synthesizing Pathways in Muscle
69(5)
Utilizing ATP
74(1)
The Nature of Effective Phosphagens
74(3)
Phosphagen Storage
74(1)
Utilizing Phosphagen
74(1)
Phosphagens "Buffer" ATP Content
75(1)
Phosphagen End Products
76(1)
Osmotic or Ionic Effects of Phosphagen Mobilization
76(1)
Ancillary Roles of Phosphagens
76(1)
Phosphagens: Their Pros and Cons
77(1)
Anaerobic Glycolysis
77(9)
Glycogen---An Ideal Fermentable Fuel
78(1)
ATP Yields of Anaerobic Pathways
78(1)
Turning on Anaerobic Glycolysis: Hormones and Neurotransmitters
78(2)
Turning on Anaerobic Glycolysis: Enzyme and Isozyme Function
80(2)
The Problem of Anaerobic End Products
82(1)
Upper Glycolytic Limits in Muscle: A Coadaptation Problem
83(3)
Oxidative Metabolism
86(9)
Nature of Endogenous Aerobic Fuels
87(1)
ATP Yields of Aerobic Pathways
87(1)
End Products of Aerobic Metabolism
87(2)
Nature of Exogenous Fuels of Aerobic Muscle Metabolism
89(1)
Storage Sites of Exogenous Fuels
89(1)
Flux Rates Sustainable by Exogenous Fuels
90(1)
Regulating Fluxes of Exogenous Fuels
91(2)
Coordinating Aerobic and Glycolytic Pathways
93(2)
Chapter 7 Integrating Atp Supply and Demand
95(24)
Quantifying Energy Coupling
95(1)
Energy Coupling in Anaerobically-Driven Muscles
96(1)
Human Muscle at Maximum Aerobic Work Rates
97(1)
Setting the ATP Demand: V vs S or S vs V
97(2)
Gastrocnemius of the Laboratory Rat
99(1)
Biceps and Soleus of the Laboratory Cat
99(2)
Gracilis and Gastrocnemius of the Laboratory Dog
101(1)
Gastrocnemius of the Laboratory Rabbit
101(1)
Biceps Femoris of the Greyhound---Canine Super-Athlete
102(1)
Leg Muscle of the Thoroughbred---Equine Super-Athlete
102(1)
Calf Muscle of Variably Adapted Humans
103(1)
Serving a Small Muscle Mass with a Large Cardiac Output
103(1)
Flight Muscle of Insects---Champion Animal Athletes
104(1)
Thermally Driven Change in ATP Turnover Rates
105(1)
Pathway Intermediates and the Latent Enzyme Concept
105(3)
Exogenous Control of Energy Coupling
108(1)
Oxygen Sensing in Regulation of ATP Turnover
109(6)
O2 Sensing---Possible Pathways and Mechanisms
115(1)
Controlling the Physical State of ICF
116(3)
Chapter 8 Isoform Definition of Muscle Machines
119(18)
Introduction
119(1)
Denning Muscle Fiber Types
119(2)
Nature's Fastest Oxidative Muscles: One Isoform Combination to the Exclusion of All Others?
121(3)
Fish White Muscle: An Anaerobic Type of Muscle Displaying Exceptional Compositional Homogeneity
124(1)
Sound-Producing Muscles: Structurally Homogeneous Muscles Designed for High Frequency, Not Power Output
125(2)
Rattler Muscle of the Rattlesnake
127(1)
Brain Heater Organ: A Structurally Homogeneous Muscle Designed for Thermogenesis, Not Power Output
127(3)
Electroplax: A Structurally Homogeneous Kind of Muscle Designed for Electrical Discharge, Not Power Output
130(1)
Why Muscles Specialize into So Few Different Fiber Types
130(2)
Glycolytic Function in Chronic Hypobaric Hypoxia
132(1)
Role of MDH and LDH in Chronic Hypobaric Hypoxia
132(1)
Role of LDH Isozymes in Chronic Hypobaric Hypoxia
133(1)
The Fixed Nature of the Lactate Paradox in Andean Natives
134(1)
Isoform Basis for Plasticity of Muscle Function
134(1)
The Issue of Emergent Properties
135(2)
References 137
Peter W. Hochachka