The respiratory system is situated in the thorax, and is responsible for gaseous exchange between the
circulatory system and the outside world. Air is taken in via the upper airways (the nasal cavity, pharynx
and larynx) through the lower airways (trachea,primary bronchi and bronchial tree) and into the small
bronchioles and alveoli within the lung tissue.
The lungs are divided into lobes; The left lung is composed of the upper lobe, the lower lobe and the
lingula (a small remnant next to the apex of the heart), the right lung is composed of the upper, the
middle and the lower lobes.
Mechanics of Breathing
To take a breath in, the external intercostal muscles contract, moving the ribcage up and out. The
diaphragm moves down at the same time, creating negative pressure within the thorax. The lungs are
held to the thoracic wall by the pleural membranes, and so expand outwards as well. This creates
negative pressure within the lungs, and so air rushes in through the upper and lower airways.
Expiration is mainly due to the natural elasticity of the lungs, which tend to collapse if they are not held
against the thoracic wall. This is the mechanism behind lung collapse if there is air in the pleural space
( pneumothorax).
Each branch of the bronchial tree eventually sub-divides to form very narrow terminal bronchioles,
which terminate in the alveoli. There are millions of alveloi in each lung, and these are the areas
responsible for gaseous exchange, presenting a massive surface area for exchange to occur over.
Each alveolus is very closely associated with a network of capillaries containing deoxygenated blood
from the pulmonary artery. The capillary and alveolar walls are very thin, allowing rapid exchange of
gases by passive diffusion along concentration gradients.
CO2 moves into the alveolus as the concentration is much lower in the alveolus than in the blood, and
O2 moves out of the alveolus as the continuous flow of blood through the capillaries prevents saturation
of the blood with O2 and allows maximal transfer across the membrane.
The larynx receives air from the laryngopharynx. It consists of several pieces of cartilage that are
joined by membranes and ligaments.
The epiglottis, the first piece of cartilage of the larynx, is a flexible flap covers the glottis, the
upper region of the larynx, during swallowing toprevent the entrance of food.
The thyroid cartilage protects the front of the larynx. A forward projection of this cartilage
appears as the Adam's apple (anatomically known as the laryngeal prominence).
The paired arytenoid cartilages in the rear are horizontally attached to thethyroid cartilage in the
front by folds of mucous membranes. The upper vestibular folds (false vocal cords) contain
muscle fibers that bring the folds together and allow the breath to be held during periods of
muscular pressure on the thoracic cavity (straining while defecating or lifting a heavy object, for
example). The lower vocal folds (true vocal cords) contain elastic ligaments that vibrate when
skeletal muscles move them into the path of outgoing air. Various sounds, including speech, are
produced in this manner.
The cricoid cartilage, the paired cuneiform cartilages, and the paired corniculate cartilages are
the remaining cartilages supporting the larynx.
The trachea (windpipe) is a flexible tube, 10 to 12 cm (4 inches) long and 2.5 cm (1 inch) in
diameter.
The mucosa is the inner layer of the trachea. It contains mucus-producing goblet cells and
pseudostratified ciliated epithelium. The movement of the cilia sweeps debris away from the
lungs toward the pharynx.
The submucosa is a layer of areolar connective tissue that surrounds the mucosa.
Hyaline cartilage forms 16 to 20 C-shaped rings that wrap around the submucosa. The rigid rings
prevent the trachea from collapsing during inspiration.
The adventitia is the outermost layer of the trachea. It consists of areolar connective tissue.
The primary bronchi are two tubes that branch from the trachea to the left and right lungs.
Inside the lungs, each primary bronchus divides repeatedly into branches of smaller diameters,
forming secondary (lobar) bronchi, tertiary (segmental) bronchi, and numerous orders of
bronchioles (1 mm or less in diameter), including terminal bronchioles (0.5 mm in diameter) and
microscopic respiratory bronchioles. The wall of the primary bronchi is constructed like the
trachea, but as the branches of the tree get smaller, the cartilaginous rings and the mucosa are
replaced by smooth muscle.
Alveolar ducts are the final branches of the bronchial tree. Each alveolar duct has enlarged,
bubblelike swellings along its length. Each swelling is called an alveolus. Some adjacent alveoli
are connected by alveolar pores.
The respiratory membrane consists of the alveolar and capillary walls. Gas exchange occurs
across this membrane. Characteristics of this membrane follow:
Type I cells are thin, squamous epithelial cells that constitute the primary cell type of the
alveolar wall. Oxygen diffusion occurs across these cells.
Type II cells are cuboidal epithelial cells that are interspersed among the type I cells. Type II cells
secrete pulmonary surfactant (a phospholipid bound to a protein) that reduces the surface
tension of the moisture that covers the alveolar walls. A reduction in surface tension permits
oxygen to diffuse more easily into the moisture. A lower surface tension also prevents the
moisture on opposite walls of an alveolus or alveolar duct from cohering and causing the minute
airway to collapse.
Alveolar macrophage cells (dust cells) wander among the other cells of the alveolar wall,
removing debris and microorganisms.
A thin epithelial basement membrane forms the outer layer of the alveolar wall.
A dense network of capillaries surrounds each alveolus. The capillary walls consist of endothelial
cells surrounded by a thin basement membrane. The basement membranes of the alveolus and
the capillary are often so close that they fuse.
Predisposing Factor: Precipitating Factor
Aspiration of microbes
Failure of defenses
Pathophysiology of PCAP
Increase capillary permeability
Engulfing of Antigen
Edema Exudate formation
Activation of B-cells
Release of antibodies
Antigen-Antibody reaction
Accumulation of mucus
Vaso-congestion
Productive cough
Consolidation of lung
Effector T-cells destroy
antigen
Increase respiration
Hyperthermia