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CHAPTER 3 Structure and Function of Muscles MUSCLE ARCHITECTURE


Specifi c muscles are often described anatomically and individually by their proximal and distal attachments. The proximal attachment is called the origin; the distal attach- ment is the insertion. Muscle origins and insertions are labeled under the assumption that the proximal attach- ment is stabilized and the distal attachment is moving toward the proximal attachment performing a concentric contraction. Understanding these attachments and the movement they produce lays the foundation for studying human kinesiology. Because humans perform movement in a variety of patterns, the distal insertion is not always moving toward a proximal origin. For instance, during the closed-chain activity of moving from a standing posi- tion to sitting, the proximal attachments of the quadriceps muscles move toward the distal attachment as the quad- riceps eccentrically lower the body. Conversely, when moving from sitting to standing, the proximal attachment of the quadriceps moves away from the distal attach- ment during a closed-chain eccentric contraction. (Refer to Chapter 1 for a review of open and closed kinetic chain movements.) This same concept of the changing relationship of proximal and distal attachments can be observed during concentric contractions. When bringing the hand toward the mouth, the distal attachment of the biceps moves toward the proximal attachment. Stabiliz- ing the forearm and bringing the shoulder toward the hand during a chin-up exercise is a reversal of action of the biceps as the proximal attachment of the biceps moves toward the distal attachment (Fig. 3.9).


FIBER ARRANGEMENT


The basic architecture of an entire muscle and its rela- tionship to function depend in part on the arrangement of the muscle fi bers in terms of their angle of orientation, physiological cross-sectional area (PCSA), and length and the total length of the muscle. The PCSA refers to the area of the muscle that is perpendicular to the orientation of muscle fi bers—its cross-sectional width—and can be increased by an increase in the number of muscle fi bers or an increase in fi ber size. Fusiform muscles have fi bers that run parallel to the long axis of the muscle and its central tendon. They tend to be spindle shaped, wider at midbelly, and tapered toward the ends. In general, fusi- form muscles tend to have longer fi ber lengths and can produce a greater range of motion at the joint compared with muscles with other architectural arrangements. The biceps brachii is an example of a fusiform muscle. Strap muscles have parallel fi bers running the length of the muscle and have more of a fl attened shape that inserts into a wide fl at tendon. The rectus abdominis is an example of a strap muscle that is segmented with tendons.


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Muscle fi bers that run at an angle to the long axis of the muscle have a pennate structure and are referred to as unipennate, bipennate, or multipennate, depending on the number of muscle fi ber groups. In this arrange- ment, fascicles fan out from a central tendon. Although the oblique orientation of pennate muscles decreases the amount of force exerted at the tendon, these muscles typically can generate larger forces than fusiform muscles because they have a greater PCSA of muscle fi bers. There is a direct relationship between the cross-sectional area and the muscle’s ability to generate tension. As a rule, the greater a muscle’s width, the greater its ability to produce force compared with a muscle of similar length with a smaller width. The quadriceps at the knee joint is an example of a muscle with a pennate structure. Figure 3.10 shows examples of the various types of muscle architecture.


FIBER TYPE


Muscles are also classifi ed according to how they func- tion metabolically and mechanically. The three primary types of muscle fi bers are type I (slow twitch), type IIA (intermediate twitch), and type IIX (fast twitch). Type I muscle fi bers tend to have a slower contraction rate and are fatigue resistant. These fi bers are considered pos- tural muscles because they can sustain contractions for long periods of time to help the body maintain posi- tions against gravity. They are also activated during low- resistance, high-repetition movements associated with aerobic activity. Type II muscle fi bers contract at faster rates for shorter periods of time and produce more force than type I muscle fi bers. The body relies on type II fi bers to produce larger movements against greater loads than those encountered by type I fi bers. Type II fi bers have a greater capability to produce power but fatigue more quickly than type I fi bers. Skeletal muscles throughout the body are composed of all of the muscle fi ber types to provide both postural stability and mobility. The vastus lateralis consists of 50% type I and 50% type II fi bers, although it can vary from 5% to 90%, depending on the person’s genotype. Table 3.3 compares the characteristics and function of each muscle fi ber type.


MUSCLE CONNECTIVE TISSUE


Connective tissue plays a role in muscle function by pro- viding support and structure and by reinforcing the inter- nal forces produced by the contractile components of muscle when opposing external forces. The entire muscle houses extracellular connective tissue composed mainly of collagen and elastin. This noncontractile connective tissue is considered the passive component of a muscle, providing both support and elasticity to the muscular system. Epimysium is tough connective tissue that sur- rounds the entire muscle and is resistant to stretch. It


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