Essay about Muscles Are th Engine of the Body

Skeletal Muscle Structure.The cells of skeletal muscles are long fiber-like structures. They contain many nuclei and are subdivided into smaller structures called myofibrils. Myofibrils are composed of 2 kinds of myofilaments. The thin filaments are made of 2 strands of the protein actin and one strand of a regulatory protein coiled together. The thick filaments are staggered arrays of myosin molecules.

contraction, and this reduction in tension production is the cause of the loss of strength. Her muscles are actually

Smooth muscle contraction occurs when calcium is present in the smooth muscle cell and binds onto calmodulin to activate myosin light chain kinase (Wilson et al., 2002). Phosphorylation of myosin light chains result in myosin ATPase activity thus cross-bridge cycling occurs causing the muscle to contract (Horowitz et al., 1996). There are two known models of excitation and contraction in smooth muscle, electromechanical coupling (EMC) and pharmomechanical coupling

As a result of the contractions in the Muscle- Skeletal Longitudinal Section cells and the Muscle- Skeletal Cross Section cells, it allows your muscle to be able to contract in response to nerve stimuli. This means that the movements of most of these muscles are not involuntary, you can control them. Therefore, once the stimulation stops, the muscles relax.

For muscle to contract, actin and myosin filaments need to slide past each other, causing the sarcomere to shorten in length . Each myosin filament has a protruding bulbous head, which can bind with the binding sites on the

Rationale, Significance and Hypothesis. An extrinsic factor, which exerts a dominant influence on skeletal muscle fiber phenotype, is the nervous system. Buller et al. (1960) elegantly demonstrated the plastic nature of skeletal muscle fibers in response to changes in innervation type. Later, Lφmo and Westgaard (Lφmo and Westgaard, 1974; Westgaard and Lφmo, 1988) demonstrated that depolarization of muscle with specific patterns and frequencies of electrical activity are sufficient to cause changes in mature muscle fiber phenotypes. However, how myofibrillar gene expression and structural organization is affected by the frequency of impulses during activity, the amount of activity over time, or other characteristics of patterned activity is essentially unknown. To answer these questions will require the isolation and study of subsets of muscle-specific proteins in relation to different electrical activation patterns in vivo, an issue that cannot be easily addressed in preparations currently used in the study of muscle development and maintenance. However, using novel in vivo approaches can, in part, circumvent this difficulty.

A muscle twitch is the fasciculation , or "muscle twitch", is a small, local, involuntary muscle contraction and relaxation visible under the skin.

Actin and myosin are contractile proteins that are essential for muscle contraction (Powers). A contraction is triggered by a series of events called the crossbridge cycle. In a muscle fiber, the functional unit of contraction is called a sarcomere (Powers). A sarcomere contains myofibrils, which consist of actin and myosin myofilaments. The sarcomere shortens when myosin heads and thick myofilaments form crossbridges with actin molecules and thin myofilaments. The formation of a crossbridge is initiated when calcium ions released from the sarcoplasmic reticulum bind to troponin. An action potential triggers this release of these ions. The binding of calcium ions causes troponin to change shape. Tropomyosin moves away from the myosin binding cites on actin, allowing the myosin head to bind actin and form a crossbridge. When ATP on the myosin head has not been hydrolyzed yet, the myosin head is inactivated, or in the uncocked position. The myosin head has to be activated before a crossbridge cycle can begin (Powers). This occurs when ATP binds to the myosin head and is hydrolyzed to Adenosine Diphosphate (ADP) and an inorganic phosphate. The enzyme that breaks this ATP down is called myosin ATPase, which is located on the myosin head. The energy from the hydrolysis activates the myosin head putting it into the cocked position. The activated myosin head binds to actin forming a crossbridge. Then inorganic

Actin and myosin filaments can be found in skeletal muscle and are the smallest units that form a sarcomere, which is the smallest contractile unit in muscle (Baechle, 2008). The Sliding Filament Theory states that the actin filaments slide inward on the myosin filaments, pulling on the boundaries of the sarcomere, causing it to shorten the muscle fiber, also known as a concentric muscular contraction (Baechle, 2008). The Sliding Filament Theory is composed of five steps: the “Resting Phase”, the “Excitation-Contraction Coupling Phase”, the “Contraction Phase”, the “Recharge Phase”, and the “Relaxation Phase” (Baechle, 2008). During the Resting Phase, the actin and myosin filaments are lined up with no cross-bridge binding of the two filaments. During the Excitation-Contraction Coupling Phase, Calcium is released from the sarcoplasmic reticulum and binds to troponin, causing a shift in tropomyosin where the binding cites are exposed (Baechle, 2008). When the binding cites are exposed, the myosin cross-bridge head attaches to actin. During the Contraction Phase, ATP bonds break, releasing energy that is used to allow the myosin head to flex, causing the actin filaments to move toward the M-bridge. During the Recharge Phase, there is a continuous repetition of the Excitation-Contraction Coupling Phase and the Contraction Phase in order to produce muscular

Individual muscles are made up of individual muscle fibers and these fibers can be further organized into a motor unit grouped within each muscle. A motor unit is simply a bundle of grouped muscle fibers. When you want to move the brain instantaneously sends a signal or impulse through the spinal cord that reaches the motor unit. Muscle fibers are cells like the basic building block of the muscle. There are a few different types of muscle fibers, each are designed for a specific type of muscle activity. Some muscle fibers are good for endurance exercises, other work best for the short bursts. Each muscle fiber is a single cell. Each cell consists of a structure.

In the presence of the biochemical adenosine triphosphate (ATP), the myosin and actin fibres would slide past each other, effectively shortening the muscle. (Huxley).

You have probably heard some self-made expert say that building muscle quickly is not possible, only through the use of performance enhancing drugs. However, build muscle quickly is easier than most people think; you just need to know some concepts and techniques that can make it happen. You see, many people fall into the trap of listening to others about what is possible or not, and don’t ask any questions to those statements at all. The fast muscle building is possible, and this is the first thing you need to realize when going through this article.

To fully understand the events taking place and the data collected, a brief but thorough review of muscles on a physiological level is needed. Muscles are responsible for producing force and motion in the both the external world and within the body. Locomotion of the body and its organs is achieved via the contraction of three types of muscles: skeletal muscle, cardiac muscle, and smooth muscle. Our lab focuses on the effects of stimulation of skeletal muscle and more specifically, the relationship between a motor neuron and muscle contraction.

This is because once a contraction has started, the action potential has already fired, stimularing the muscle fibers. Once they

form of myosin ATP and are not very good at delivering calcium to the muscle