Sarcomeres - MCAT Biological and Biochemical Foundations of Living Systems

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Duchenne Muscular Dystrophy is an X-linked recessive genetic disorder, resulting in the loss of the dystrophin protein. In healthy muscle, dystrophin localizes to the sarcolemma and helps anchor the muscle fiber to the basal lamina. The loss of this protein results in progressive muscle weakness, and eventually death.

In the muscle fibers, the effects of the disease can be exacerbated by auto-immune interference. Weakness of the sarcolemma leads to damage and tears in the membrane. The body’s immune system recognizes the damage and attempts to repair it. However, since the damage exists as a chronic condition, leukocytes begin to present the damaged protein fragments as antigens, stimulating a targeted attack on the damaged parts of the muscle fiber. The attack causes inflammation, fibrosis, and necrosis, further weakening the muscle.

Studies have shown that despite the severe pathology of the muscle fibers, the innervation of the muscle is unaffected.

A healthy muscle will have the most contractile force when                     .

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Answer

When a muscle is shortened, the force decreases as the filaments slide past one another and lose room to form new cross-bridges. When a muscle is lengthened, there is less filament overlap which leads to fewer cross-bridges. Stretching a muscle before contracting it will not affect the force produced, nor will shortening a muscle before lengthening it. Titin is a protein responsible for some of the elastic properties of muscle, but is not involved in force production.

At rest, the muscle has the potential to form the maximum number of cross-bridges, resulting in the maximum amount of force production. For further review, go over the length-tension curve for a muscle fiber.

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