Sunday, January 4, 2026

Respiratory Movements

 



Respiratory Movements

Introduction

Respiration occurs in two phases namely

·       inspiration

·       expiration

During inspiration, thoracic cage enlarges and lungs expand so that air enters the lungs easily. During expiration, the thoracic cage and lungs decrease in size and attain the preinspiratory position so that air leaves the lungs easily.

During normal quiet breathing-

-inspiration is the active process  

-expiration is the passive process

MUSCLES OF RESPIRATION

Anatomically respiratory muscles are of two types:

1. Inspiratory muscles

2. Expiratory muscles.

However, functionally respiratory muscles are generally classified into two types:

1. Primary or major respiratory muscles, which are responsible for change in size of thoracic cage during normal quiet breathing

2. Accessory respiratory muscles that help primary respiratory muscles during forced respiration.

Inspiratory Muscles

Muscles involved in inspiratory movements are known as inspiratory muscles.

Primary inspiratory muscles

Primary inspiratory muscles are the diaphragm, which is supplied by phrenic nerve (C3 to C5) and external intercostal muscles, supplied by intercostal nerves (T1 to T11).

Pump handle movement

Contraction of external intercostal muscles causes elevation of these ribs and upward and forward movement of sternum. This movement is called pump handle movement. It increases anteroposterior diameter of the thoracic cage.

Bucket handle movement

Simultaneously, the central portions of these ribs (arches of ribs) move upwards and outwards to a more horizontal position. This movement is called bucket handle

movement and it increases the transverse diameter of thoracic cage.

Lower Costal Series

Lower costal series includes seventh to tenth pair of ribs. Movement of lower costal series increases the transverse diameter of thoracic cage by bucket handle movement.

Bucket handle movement

Lower costal series of ribs also show bucket handle movement by swinging outward and upward. This movement increases the transverse diameter of the thoracic cage.

Eleventh and twelfth pairs of ribs are the floating ribs. These ribs are not involved in changing the size of thoracic cage.

Diaphragm

Movement of diaphragm increases the vertical diameter of thoracic cage. Normally, before inspiration the diaphragm is dome shaped with convexity facing upwards. During inspiration, due to the contraction, muscle fibers are shortened. But the central tendinous portion is drawn downwards so the diaphragm is flattened. Flattening of diaphragm increases the vertical diameter of the thoracic cage.

Movements of Lungs

During inspiration, due to the enlargement of thoracic cage, the negative pressure is increased in the thoracic cavity. It causes expansion of the lungs. During expiration,

the thoracic cavity decreases in size to the preinspiratory position. Pressure in the thoracic cage also comes back to the preinspiratory level. It compresses the lung tissues so that, the air is expelled out of lungs.

Accessory inspiratory muscles

Sternocleidomastoid, scalene, anterior serrati, elevators of scapulae and pectorals are the accessory inspiratory muscles.

Expiratory Muscles

Primary expiratory muscles

Primary expiratory muscles are the internal intercostal muscles, which are innervated by intercostal nerves.

Accessory expiratory muscles

Accessory expiratory muscles are the abdominal muscles.

Movements of Thoracic Cage

Inspiration causes enlargement of thoracic cage. Thoracic cage enlarges because of increase in all diameters, viz. anteroposterior, transverse and vertical diameters.

Anteroposterior and transverse diameters of thoracic cage are increased by the elevation of ribs. Vertical diameter is increased by the descent of diaphragm.

In general, change in the size of thoracic cavity occurs because of the movements of four units of structures:

1. Thoracic lid

2. Upper costal series

3. Lower costal series

4. Diaphragm.

1. Thoracic Lid

Thoracic lid is formed by manubrium sterni and the first pair of ribs. It is also called thoracic operculum. Movement of thoracic lid increases the anteroposterior diameter of thoracic cage. Due to the contraction of scalene muscles, the first ribs move upwards to a more horizontal position. This increases the anteroposterior diameter of upper thoracic cage.

2. Upper Costal Series

Upper costal series is constituted by second to sixth pair of ribs. Movement of upper costal series increases the anteroposterior and transverse diameter of the

thoracic cage.

Movement of upper costal series is of two types:

a)    Pump handle movement

b)    Bucket handle movement.

Collapsing Tendency of Lungs

Lungs are under constant threat to collapse even in resting conditions because of certain factors.

Factors Causing Collapsing Tendency of Lungs

Two factors are responsible for the collapsing tendency of lungs:

1. Elastic property of lung tissues: Elastic tissues of lungs show constant recoiling tendency and try to collapse the lungs

2. Surface tension: It is the tension exerted by the fluid secreted from alveolar epithelium on the surface of alveolar membrane. Fortunately, there are some factors, which save the lungs from collapsing.

Factors Preventing Collapsing Tendency of Lungs

In spite of elastic property of lungs and surface tension in the alveoli of lungs, the collapsing tendency of lungs is prevented by two factors:

1. Intrapleural pressure: It is the pressure in the pleural cavity, which is always negative (see below). Because of negativity, it keeps the lungs expanded and prevents the collapsing tendency of lungs produced by the elastic tissues.

2. Surfactant: It is a substance secreted in alveolar epithelium. It reduces surface tension and prevents the collapsing tendency produced by surface tension.

Surfactant

Surfactant is a surface acting material or agent that is responsible for lowering the surface tension of a fluid. Surfactant that lines the epithelium of the alveoli in lungs

is known as pulmonary surfactant and it decreases the surface tension on the alveolar membrane.

Source of secretion of pulmonary surfactant

Pulmonary surfactant is secreted by two types of cells:

1. Type II alveolar epithelial cells in the lungs, which are called surfactant secreting alveolar cells or pneumocytes. Characteristic feature of these cells is the presence of microvilli on their alveolar surface.

2. Clara cells, which are situated in the bronchioles. These cells are also called bronchiolar exocrine cells.

Chemical Composition of surfactant

Surfactant is a lipoprotein complex formed by lipids especially phospholipids, proteins and ions.

1. Phospholipids: Phospholipids form about 75% of the surfactant. Major phospholipid present in the surfactant is dipalmitoylphosphatidylcholine (DPPC).

2. Other lipids: Other lipid substances of surfactant are triglycerides and phosphatidylglycerol (PG).

3. Proteins: Proteins of the surfactant are called specific surfactant proteins. There are four main surfactant proteins, called SPA, SPB, SPC and SPD.

SPA and SPD are hydrophilic, while SPB and SPC are hydrophobic. Surfactant proteins are vital components of surfactant and the surfactant becomes inactive in the absence of proteins.

4. Ions: Ions present in the surfactant are mostly calcium ions.

Formation of surfactant

Type II alveolar epithelial cells and Clara cells have a special type of membrane bound organelles called lamellar bodies, which form the intracellular source of surfactant. Laminar bodies contain surfactant phospholipids and surfactant proteins. These materials are synthesized in endoplasmic reticulum and stored in laminar bodies. By means of exocytosis, lipids and proteins of lamellar bodies are released into surface fluid lining the alveoli. Here, in the presence of surfactant proteins and

calcium, the phospholipids are arranged into a lattice (meshwork) structure called tubular myelin. Tubular myelin is in turn converted into surfactant in the form of a film that spreads over the entire surface of alveoli. Most of the surfactant is absorbed into the type II alveolar cells, catabolized and the products are loaded into lamellar bodies for recycling.

Factors necessary for the formation and spreading of surfactant

Formation of surfactant requires many substances. Formation of tubular myelin requires DPPC, PG and the hydrophobic proteins, SPB and SPC. Formation of surfactant film requires SPB, SPC and PG. Type II alveolar epithelial cells occupy only about 5% of alveolar surface. However, the surfactant must spread over the entire alveolar surface. It is facilitated by PG and calcium ions. Glucocorticoids play important role in the formation of surfactant.

Functions of surfactant

1. Surfactant reduces the surface tension in the alveoli of lungs and prevents collapsing tendency of lungs.

Surfactant acts by the following mechanism:

1. Phospholipid molecule in the surfactant has two portions. One portion of the molecule is hydrophilic. This portion dissolves in water and lines the alveoli. Other portion is hydrophobic and it is directed towards the alveolar air. This surface of the phospholipid along with other portion spreads over the alveoli and reduces the surface tension. SPB and SPC play active role in this process.

2. Surfactant is responsible for stabilization of the alveoli, which is necessary to withstand the collapsing tendency.

3. It plays an important role in the inflation of lungs after birth. In fetus, the secretion of surfactant begins after the 3rd month. Until birth, the lungs are solid and not expanded. Soon after birth, the first breath starts because of the stimulation of

respiratory centers by hypoxia and hypercapnea. Although the respiratory movements are attempted by the infant, the lungs tend to collapse repeatedly. And, the presence of surfactant in the alveoli prevents the lungs from collapsing.

4. Another important function of surfactant is its role in defense within the lungs against infection and inflammation. Hydrophilic proteins SPA and SPD

destroy the bacteria and viruses by means of opsonization. These two proteins also control the formation of inflammatory mediators.

Effect of deficiency of surfactant – respiratory distress syndrome

Absence of surfactant in infants, causes collapse of lungs and the condition is called respiratory distress syndrome or hyaline membrane disease. Deficiency of surfactant occurs in adults also and it is called adult respiratory distress syndrome (ARDS). In addition, the deficiency of surfactant increases the susceptibility for bacterial and viral infections.


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