The Muscular System Skeletal muscle consists of numerous muscle cells called Muscle fibers. Muscle fiber terminology and characteristics Sarcolemma = plasma.

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Presentation transcript:

The Muscular System Skeletal muscle consists of numerous muscle cells called Muscle fibers. Muscle fiber terminology and characteristics Sarcolemma = plasma membrane of the muscle cell Highly invaginated by transverse tubules (T tubules) that permeate the cell. Sarcoplasma = cytoplasm of the muscle cell Contains calcium-storing sarcoplasmic reticulum Specialized endoplasmic reticulum of a muscle cell

The Muscular System Muscle fiber terminology and characteristics Muscle cells are multinucleated Nearly the entire volume of the cell is filled with numerous, long myofibrils. Two types of filaments Actin Thin filaments consisting of two strands arranged in a double helix Troponin and Tropomyosin = molecules that cover special binding sites on actin.

The Muscular System Two types of filaments Myosin Thick filaments Each myosin filament forms a protruding head at one end. Actin and myosin are parallel and arranged side by side. Striated appearance produced from overlapping filaments Each repeating unit of the pattern is called a sarcomere. Each sacromere is separted by a Z-line, to which the actin filaments are attached Myosin filaments are located between the actin, unattached to the Z-line.

The Muscular System Muscle contraction: sliding-filament model ATP binds to a myosin head and forms ADP + Pi When ATP binds to a myosin head, it is converted to ADP + Pi, which remains attached to the myosin head. Ca++ exposes the binding sites on the actin filaments Ca++ binds to the troponin molecule causing tropomyosin to expose positions on the actin filament for the attachment of myosin heads.

The Muscular System Muscle contraction: sliding-filament model 3. Cross bridges between myosin heads and actin filaments form. 1. When attachment sites on the actin are exposed, the myosin heads bind to actin to form cross bridges. 4. ADP and Pi are released and sliding motion of actin results. 1. The attachment of cross bridges between myosin and actin causes the release of ADP and Pi. This, in turn, causes a change in shape of the myosin head, which generates a sliding movement of the actin toward the center of the sarcomere. 2. This pulls the two Z-lines together, contracting the muscle fiber.

The Muscular System Muscle contraction: sliding-filament model 5. ATP causes the cross bridges to unbind. 1. When a new ATP molecule attaches to the myosin head, the cross bridge between the actin and myosin breaks, returning the myosin head to its unattached position Without the addition of a new ATP molecule, the cross bridges remain attached to the actin filaments. This is why corpses are stiff.

The Muscular System Neuromuscular junctions Synapses between neurons and muscles Muscle contraction is stimulated through the following steps: Action potential generates release of acetylcholine. Action potential generated on sacrolemma and throughout the T-tubules Receptors on the sacrolemma initiate a depolarization event and action potential. The action potential travels along the sacrolemma throughout the transverse system of tubules.

The Muscular System Muscle contraction is stimulated through the following steps: Sacroplasmic reticulum releases Ca++. Myosin cross bridges form. The Ca++ released by the sacroplasmic reticulum binds to troponin molecules on the actin helix, promoting tropomyosin molecules to expose binding sites for myosin cross-bridge formation. If ATP is available, muscle contraction begins.

The Muscular System Humans and other vertebrates have three kinds of muscles Skeletal muscle Attached to bones and causes movement of body Smooth muscle Lines the walls of blood vessels and digestive tract No striation No T-tubules, therefore, contraction is controlled and relatively slow. Cardiac muscle Striated Highly branched with cells connected by gap junctions Generates its own action potential, which spreads rapidly throughout muscle tissue by electrical synapses across gap junctions.