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Movement is one of the significant features of living beings. Animals and

plants exhibit a wide range of movements. Streaming of protoplasm in

the unicellular organisms like Amoeba is a simple form of movement.

Movement of cilia, flagella and tentacles are shown by many organisms.

Human beings can move limbs, jaws, eyelids, tongue, etc. Some of the

movements result in a change of place or location. Such voluntary

movements are called locomotion. Walking, running, climbing, flying,

swimming are all some forms of locomotory movements. Locomotory

structures need not be different from those affecting other types of

movements. For example, in Paramoecium, cilia helps in the movement of

food through cytopharynx and in locomotion as well. Hydra can use its

tentacles for capturing its prey and also use them for locomotion. We use

limbs for changes in body postures and locomotion as well. The above

observations suggest that movements and locomotion cannot be studied

separately. The two may be linked by stating that all locomotions are

movements but all movements are not locomotions.

Methods of locomotion performed by animals vary with their habitats

and the demand of the situation. However, locomotion is generally for

search of food, shelter, mate, suitable breeding grounds, favourable

climatic conditions or to escape from enemies/predators.

20.1 TYPES OF MOVEMENT

Cells of the human body exhibit three main types of movements, namely,

amoeboid, ciliary and muscular.

OCOMOTION AND

OVEMENT

HAPTER

20.1 Types of

Movement

20.2 Muscle

20.3 Skeletal System

20.4 Joints

20.5 Disorders of

Muscular and

Skeletal System

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Some specialised cells in our body like macrophages and leucocytes

in blood exhibit amoeboid movement. It is effected by pseudopodia formed

by the streaming of protoplasm (as in Amoeba). Cytoskeletal elements

like microfilaments are also involved in amoeboid movement.

Ciliary movement occurs in most of our internal tubular organs which

are lined by ciliated epithelium. The coordinated movements of cilia in

the trachea help us in removing dust particles and some of the foreign

substances inhaled alongwith the atmospheric air. Passage of ova through

the female reproductive tract is also facilitated by the ciliary movement.

Movement of our limbs, jaws, tongue, etc, require muscular movement.

The contractile property of muscles are effectively used for locomotion

and other movements by human beings and majority of multicellular

organisms. Locomotion requires a perfect coordinated activity of muscular,

skeletal and neural systems. In this chapter, you will learn about the

types of muscles, their structure, mechanism of their contraction and

important aspects of the skeletal system.

20.2 MUSCLE

You have studied in Chapter 8 that the cilia and flagella are the outgrowths

of the cell membrane. Flagellar movement

helps in the swimming of

spermatozoa, maintenance of water current in the canal system of sponges

and in locomotion of Protozoans like Euglena. Muscle is a specialised

tissue of mesodermal origin. About 40-50 per cent of the body

weight of a human adult is contributed by muscles. They have

special properties like excitability, contractility, extensibility and

elasticity. Muscles have been classified using different criteria,

namely location, appearance and nature of regulation of their

activities. Based on their location, three types of muscles are

identified : (i) Skeletal (ii) Visceral and (iii) Cardiac.

Skeletal muscles are closely associated with the skeletal components

of the body. They have a striped appearance under the microscope and

hence are called striated muscles. As their activities are under the

voluntary control of the nervous system, they are known as voluntary

muscles too. They are primarily involved in locomotory actions and

changes of body postures.

Visceral muscles are located in the inner walls of hollow visceral organs

of the body like the alimentary canal, reproductive tract, etc. They do not

exhibit any striation and are smooth in appearance. Hence, they are called

smooth muscles (nonstriated muscle). Their activities are not under the

voluntary control of the nervous system and are therefore known as

involuntary muscles. They assist, for example, in the transportation of food

through the digestive tract and gametes through the genital tract.

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muscle fibre is lined by the plasma membrane called sarcolemma

enclosing the sarcoplasm. Muscle fibre is a syncitium as the sarcoplasm

contains many nuclei. The endoplasmic reticulum, i.e., sarcoplasmic

reticulum of the muscle fibres is the store house of calcium ions. A

characteristic feature of the muscle fibre is the presence of a large number

of parallelly arranged filaments in the sarcoplasm called myofilaments or

myofibrils. Each myofibril has alternate dark and light bands on it. A

detailed study of the myofibril has established that the striated appearance

is due to the distribution pattern of two important proteins – Actin and

Myosin. The light bands contain actin and is called I-band or Isotropic

band, whereas the dark band called ‘A’ or Anisotropic

band contains

As the name suggests, Cardiac muscles are the muscles of heart.

Many cardiac muscle cells assemble in a branching pattern to form a

cardiac muscle. Based on appearance, cardiac muscles are striated. They

are involuntary in nature as the nervous system does not control their

activities directly.

Let us examine a skeletal muscle in detail to understand the structure

and mechanism of contraction. Each organised skeletal muscle in our

body is made of a number of muscle bundles or fascicles held together

by a common collagenous connective tissue layer called fascia. Each

muscle bundle contains a number of muscle fibres (Figure 20.1). Each

Fascicle

(muscle bundle)

Muscle fibre

(muscle cell)

Sarcolemma

Blood capillary

Figure 20.1 Diagrammatic cross sectional view of a muscle showing muscle bundles

and muscle fibres

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myosin. Both the proteins are arranged as rod-like structures, parallel to

each other and also to the longitudinal axis of the myofibrils. Actin

filaments are thinner as compared to the myosin filaments, hence are

commonly called thin and thick filaments respectively. In the centre of

each ‘I’ band is an elastic fibre called ‘Z’ line which bisects it. The thin

filaments are firmly attached to the ‘Z’ line. The thick filaments in the

‘A’ band are also held together in the middle of this band by a thin fibrous

membrane called ‘M’ line. The ‘A’ and ‘I’ bands are arranged alternately

throughout the length of the myofibrils. The portion of the myofibril

between two successive ‘Z’ lines is considered as the functional unit of

contraction and is called a sarcomere (Figure 20.2). In a resting state, the

edges of thin filaments on either side of the thick filaments partially overlap

the free ends of the thick filaments leaving the central part of the thick

filaments. This central part of thick filament, not overlapped by thin

filaments is called the ‘H’ zone.

Figure 20.2 Diagrammatic representation of (a) anatomy of a muscle fibre showing

a sarcomere (b) a sarcomere

(a)

(b)

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20.2.1 Structure of Contractile Proteins

Each actin (thin) filament is made of two ‘F’ (filamentous) actins

helically wound to each other. Each ‘F’ actin is a polymer of monomeric

‘G’ (Globular) actins. Two filaments of another protein, tropomyosin

also run close to the ‘F’ actins throughout its length. A complex protein

Troponin is distributed at regular intervals on the tropomyosin. In the

resting state a subunit of troponin masks the active binding sites for

myosin on the actin filaments (Figure 20.3a).

Each myosin (thick) filament is also a polymerised protein. Many

monomeric proteins called Meromyosins (Figure 20.3b) constitute one

thick filament. Each meromyosin has two important parts, a globular

head with a short arm and a tail, the former being called the heavy

meromyosin (HMM) and the latter, the light meromyosin (LMM). The HMM

component, i.e.; the head and short arm projects outwards at regular

distance and angle from each other from the surface of a polymerised myosin

filament and is known as cross arm. The globular head is an active ATPase

enzyme and has binding sites for ATP and active sites for actin.

Figure 20.3 (a) An actin (thin) filament (b) Myosin monomer (Meromyosin)

Actinbindingsites

ATPbindingsites

Head

Crossarm

(a)

(b)

20.2.2 Mechanism of Muscle Contraction

Mechanism of muscle contraction is best explained by the sliding filament

theory which states that contraction of a muscle fibre takes place by the

sliding of the thin filaments over the thick filaments.

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Muscle contraction is initiated by a signal sent by the central nervous

system (CNS) via a motor neuron. A motor neuron alongwith the muscle

fibres connected to it constitute a motor unit. The junction between a

motor neuron and the sarcolemma of the muscle fibre is called the

neuromuscular junction or motor-end plate. A neural signal reaching

this junction releases a neurotransmitter (Acetyl choline) which generates

an action potential in the sarcolemma. This spreads through the muscle

fibre and causes the release of calcium ions into the sarcoplasm. Increase

in Ca

level leads to the binding of calcium with a subunit of troponin on

actin filaments and thereby remove the masking of active sites for myosin.

Utilising the energy from ATP hydrolysis, the myosin head now binds to

the exposed active sites on actin to form a cross bridge (Figure 20.4). This

pulls the attached actin filaments towards the centre of ‘A’ band. The

‘Z’ line attached to these actins are also pulled inwards thereby causing a

shortening of the sarcomere, i.e., contraction. It is clear from the above

steps, that during shortening of the muscle, i.e., contraction, the ‘I’ bands

get reduced, whereas the ‘A’ bands retain the length (Figure 20.5). The

myosin, releasing the ADP and P

goes back to its relaxed state. A new

ATP binds and the cross-bridge is broken (Figure 20.4). The ATP is again

hydrolysed by the myosin head and the cycle of cross bridge formation

Figure 20.4 Stages in cross bridge formation, rotation of head and breaking of

cross bridge

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and breakage is repeated causing further sliding. The process continues

till the Ca

ions are pumped back to the sarcoplasmic cisternae resulting

in the masking of actin filaments. This causes the return of ‘Z’ lines back

to their original position, i.e., relaxation. The reaction time of the fibres

can vary in different muscles. Repeated activation of the muscles can lead

to the accumulation of lactic acid due to anaerobic breakdown of glycogen

in them, causing fatigue. Muscle contains a red coloured oxygen storing

pigment called myoglobin. Myoglobin content is high in some of the

muscles which gives a reddish appearance. Such muscles are called the

Red fibres. These muscles also contain plenty of mitochondria which can

utilise the large amount of oxygen stored in them for ATP production.

These muscles, therefore, can also be called aerobic muscles. On the

other hand, some of the muscles possess very less quantity of myoglobin

and therefore, appear pale or whitish. These are the White fibres. Number

of mitochondria are also few in them, but the amount of sarcoplasmic

reticulum is high. They depend on anaerobic process for energy.

Figure 20.5 Sliding-filament theory of muscle contraction (movement of the thin

filaments and the relative size of the I band and H zones)

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20.3 SKELETAL SYSTEM

Skeletal system consists of a framework of bones and a few cartilages.

This system has a significant role in movement shown by the body.

Imagine chewing food without jaw bones and walking around without

the limb bones. Bone and cartilage are specialised connective tissues.

The former has a very hard matrix due to calcium salts in it and the latter

has slightly pliable matrix due to chondroitin salts. In human beings,

this system is made up of 206 bones and a few cartilages. It is grouped

into two principal divisions – the axial and the appendicular skeleton.

Axial skeleton comprises 80 bones distributed along the main axis

of the body. The skull, vertebral column, sternum and ribs constitute

axial skeleton. The skull (Figure 20.6) is composed of two sets of bones –

cranial and facial, that totals to 22 bones. Cranial bones are 8 in number.

They form the hard protective outer covering, cranium for the brain. The

facial region is made up of 14 skeletal elements which form the front part

of the skull. A single U-shaped bone called hyoid is present at the base of

the buccal cavity and it is also included in the skull. Each middle ear

contains three tiny bones – Malleus, Incus and Stapes, collectively called

Ear Ossicles. The skull region articulates with the superior region of the

Parietal

bone

Frontal bone

Temporal

bone

Occipital

bone

Occipital

condyle

Sphenoid bone

Ethmoid bone

Lacrimal bone

Nasal bone

Zygomatic bone

Maxilla

Mandible

Hyoid bone

Figure 20.6 Diagrammatic view of human skull

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vertebral column with the help of two occipital

condyles (dicondylic skull).

Our vertebral column (Figure 20.7) is

formed by 26 serially arranged units called

vertebrae and is dorsally placed. It extends from

the base of the skull and constitutes the main

framework of the trunk. Each vertebra has a

central hollow portion (neural canal) through

which the spinal cord passes. First vertebra is

the atlas and it articulates with the occipital

condyles. The vertebral column is differentiated

into cervical (7), thoracic (12), lumbar (5), sacral

(1-fused) and coccygeal (1-fused) regions

starting from the skull. The number of cervical

vertebrae are seven in almost all mammals

including human beings. The vertebral column

protects the spinal cord, supports the head and

serves as the point of attachment for the ribs

and musculature of the back. Sternum is a

flat bone on the ventral midline of thorax.

There are 12 pairs of ribs. Each rib is a

thin flat bone connected dorsally to the

vertebral column and ventrally to the sternum.

It has two articulation surfaces on its dorsal

end and is hence called bicephalic. First seven

pairs of ribs are called true ribs. Dorsally, they

are attached to the thoracic vertebrae and

ventrally connected to the sternum with the

help of hyaline cartilage. The 8

, 9

and 10

pairs of ribs do not articulate directly with the

sternum but join the seventh rib with the help

of hyaline cartilage. These are called

vertebrochondral (false) ribs. Last 2 pairs (11

and 12

) of ribs are not connected ventrally

and are therefore, called floating ribs. Thoracic

vertebrae, ribs and sternum together form the

rib cage (Figure 20.8).

The bones of the limbs alongwith their

girdles constitute the appendicular skeleton.

Each limb is made of 30 bones. The bones of

the hand (fore limb) are humerus, radius and

Cervical vertebra

Intervertebral

disc

Sacrum

Coccyx

Thoracic

vertebra

Lumbar

vertebra

Figure 20.7 Vertebral column (right lateral view)

Figure 20.8 Ribs and rib cage

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Figure 20.9 Right pectoral girdle and upper

arm. (frontal view)

ulna, carpals (wrist bones – 8 in number),

metacarpals (palm bones – 5 in number) and

phalanges (digits – 14 in number) (Figure

20.9). Femur (thigh bone – the longest bone),

tibia and fibula, tarsals (ankle bones – 7 in

number), metatarsals (5 in number) and

phalanges (digits – 14 in number) are the

bones of the legs (hind limb) (Figure 20.10). A

cup shaped bone called patella cover the knee

ventrally (knee cap).

Pectoral and Pelvic girdle bones help in

the articulation of the upper and the lower limbs

respectively with the axial skeleton. Each

girdle is formed of two halves. Each half of

pectoral girdle consists of a clavicle and a

scapula (Figure 20.9). Scapula is a large

triangular flat bone situated in the dorsal part

of the thorax between the second and the

seventh ribs. The dorsal, flat, triangular body

of scapula has a slightly elevated ridge called

the spine which projects as a flat, expanded

process called the acromion. The clavicle

articulates with this. Below the acromion is a

depression called the glenoid cavity which

articulates with the head of the humerus to

form the shoulder joint. Each clavicle is a long

slender bone with two curvatures. This bone

is commonly called the collar bone.

Pelvic girdle consists of two coxal bones

(Figure 20.10). Each coxal bone is formed by

the fusion of three bones – ilium, ischium and

pubis. At the point of fusion of the above bones

is a cavity called acetabulum to which the thigh

bone articulates. The two halves of the pelvic

girdle meet ventrally to form the pubic

symphysis containing fibrous cartilage.

20.4 JOINTS

Joints are essential for all types of movements

involving the bony parts of the body.

Locomotory movements are no exception to

Figure 20.10 Right pelvic girdle and lower limb

bones (frontal view)

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this. Joints are points of contact between bones, or between bones and

cartilages. Force generated by the muscles is used to carry out movement

through joints, where the joint acts as a fulcrum. The movability at these

joints vary depending on different factors. Joints have been classified into

three major structural forms, namely, fibrous, cartilaginous and synovial.

Fibrous joints do not allow any movement. This type of joint is shown

by the flat skull bones which fuse end-to-end with the help of dense fibrous

connective tissues in the form of sutures, to form the cranium.

In cartilaginous joints, the bones involved are joined together with

the help of cartilages. The joint between the adjacent vertebrae in the

vertebral column is of this pattern and it permits limited movements.

Synovial joints are characterised by the presence of a fluid filled synovial

cavity between the articulating surfaces of the two bones. Such an arragement

allows considerable movement. These joints help in locomotion and many

other movements. Ball and socket joint (between humerus and pectoral

girdle), hinge joint (knee joint), pivot joint (between atlas and axis), gliding

joint (between the carpals) and saddle joint (between carpal and metacarpal

of thumb) are some examples.

20.5 DISORDERS OF MUSCULAR AND SKELETAL SYSTEM

Myasthenia gravis: Auto immune disorder affecting neuromuscular

junction leading to fatigue, weakening and paralysis of skeletal muscle.

Muscular dystrophy: Progressive degeneration of skeletal muscle mostly

due to genetic disorder.

Tetany: Rapid spasms (wild contractions) in muscle due to low Ca

body fluid.

Arthritis: Inflammation of joints.

Osteoporosis: Age-related disorder characterised by decreased bone mass

and increased chances of fractures. Decreased levels of estrogen is a

common cause.

Gout: Inflammation of joints due to accumulation of uric acid crystals.

SUMMARY

Movement is an essential feature of all living beings. Protoplasmic streaming, ciliary

movements, movements of fins, limbs, wings, etc., are some forms exhibited by

animals. A voluntary movement which causes the animal to change its place, is

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called locomotion. Animals move generally in search of food, shelter, mate, breeding

ground, better climate or to protect themselves.

The cells of the human body exhibit amoeboid, ciliary and muscular

movements. Locomotion and many other movements require coordinated muscular

activities. Three types of muscles are present in our body. Skeletal muscles are

attached to skeletal elements. They appear striated and are voluntary in nature.

Visceral muscles, present in the inner walls of visceral organs are nonstriated and

involuntary. Cardiac muscles are the muscles of the heart. They are striated,

branched and involuntary. Muscles possess excitability, contractility, extensibility

and elasticity.

Muscle fibre is the anatomical unit of muscle. Each muscle fibre has many

parallelly arranged myofibrils. Each myofibril contains many serially arranged

units called sarcomere which are the functional units. Each sarcomere has a central

‘A’ band made of thick myosin filaments, and two half ‘I’ bands made of thin actin

filaments on either side of it marked by ‘Z’ lines. Actin and myosin are polymerised

proteins with contractility. The active sites for myosin on resting actin filament are

masked by a protein-troponin. Myosin head contains ATPase and has ATP binding

sites and active sites for actin. A motor neuron carries signal to the muscle fibre

which generates an action potential in it. This causes the release of Ca

from

sarcoplasmic reticulum. Ca

activates actin which binds to the myosin head to

form a cross bridge. These cross bridges pull the actin filaments causing them to

slide over the myosin filaments and thereby causing contraction. Ca

are then

returned to sarcoplasmic reticulum which inactivate the actin. Cross bridges are

broken and the muscles relax.

Repeated stimulation of muscles leads to fatigue. Muscles are classified as

Red and White fibres based primarily on the amount of red coloured myoglobin

pigment in them.

Bones and cartilages constitute our skeletal system. The skeletal system is

divisible into axial and appendicular. Skull, vertebral column, ribs and sternum

constitute the axial skeleton. Limb bones and girdles form the appendicular

skeleton. Three types of joints are formed between bones or between bone and

cartilage – fibrous, cartilaginous and synovial. Synovial joints allow considerable

movements and therefore, play a significant role in locomotion.

EXERCISES

1. Draw the diagram of a sarcomere of skeletal muscle showing different regions.

2. Define sliding filament theory of muscle contraction.

3. Describe the important steps in muscle contraction.

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4. Write true or false. If false change the statement so that it is true.

(a) Actin is present in thin filament

(b) H-zone of striated muscle fibre represents both thick and thin filaments.

(d) There are 11 pairs of ribs in man.

(e) Sternum is present on the ventral side of the body.

5. Write the difference between :

(a) Actin and Myosin

(b) Red and White muscles

6. Match Column I with Column II :

Column I Column II

(a) Smooth muscle (i) Myoglobin

(b) Tropomyosin (ii) Thin filament

(d) Skull (iv) Involuntary

7. What are the different types of movements exhibited by the cells of human

body?

8. How do you distinguish between a skeletal muscle and a cardiac muscle?

9. Name the type of joint between the following:-

(a) atlas/axis

(b) carpal/metacarpal of thumb

(d) femur/acetabulum

(e) between cranial bones

(f) between pubic bones in the pelvic girdle

10. Fill in the blank spaces:

(a) All mammals (except a few) have __________ cervical vertebra.

(b) The number of phalanges in each limb of human is __________

__________ and __________.

(d) In a muscle fibre Ca

is stored in __________

(e) __________ and __________ pairs of ribs are called floating ribs.

(f) The human cranium is made of __________ bones.

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