Gaseous Exchange
RESPIRATORY ORGANS
OF COCKROACH TRACHEAL SYSTEM
Cockroach has
evolved a special type of invaginated respiratory system called Tracheal system,
especially adopted for terrestrial mode of life and high metabolic rate of
insects.
STRUCTURAL CONSTITUENTS OF TRACHEAL SYSTEM
1. TRACHEA
2. SPIRACLES
3. TRACHEOLES
1.TRACHEA
Tracheal system
consists of number of internal tube called Trachea which are the connection
between the spiracles and tracheal fluid.
2. SPIRACLES
Laterally, trachea
open outside the body through minute, slit like pores called as spiracles.
There are 2 pairs
of spiracles on lateral side of cockroach.
2 lie in thoracic
segments and 8 in first abdominal segments.
3. TRACHEOLES
On the other side,
trachea ramify throughout the body into fine branches or tracheols.
Tracheoles, finally end as blind, fluid filled fine branches which are attached with cells of tissue.
Tracheoles, finally end as blind, fluid filled fine branches which are attached with cells of tissue.
Both the trachea
and tracheoles are lined internally by thin layer of cuticle.
MECHANISM OF RESPIRATION “INFLOW OF OXYGEN”
The cockroach takes
in air directly from the atmosphere into the trachea through spiracles. This
air diffuses directly into fluid filled tracheoles through which diffuses into
the cells of tissues. Hence the blood vascular system of cockroach is devoid of
haemoglobin.
OUTFLOW OF CARBONDIOXIDE
Removal of CO2 from
cells of body is largely depended upon plasma of blood, which takes up CO2 for
its ultimate removal through body surface via the cuticle.
RESPIRATORY SYSTEM
OF FISH
MAIN RESPIRATORY ORGAN
In fish, main
respiratory organs are “Gills”. They are out growth of pharynx and lie
internally with in the body so that they are protected from mechanical
injuries.
INTERNAL STRUCTURE OF GILLS
Each gill is highly
vascularized structure. It is composed of
1. Filaments
2. Gill bar or Gill
arch
3. Lamella
1. FILAMENTS
Each gill is
composed of two rows of hundreds of filaments, which are arranged in V-shape.
2. GILL BAR OR GILL ARCH
Filaments are
supported by a cartilage or a long curved bone the gill bar or gill arch.
3. LAMELLA
Lamella is a plate
like structure which is formed by infolding of filaments. Lamella greatly
increase the surface area of the gill. Each lamella is provided by a dense
network of capillaries.
OPERCULUM (IN BONY FISHES)
Gills are covered
on each side by gill cover called “operculum”
MECHANISM OF VENTILATION
In bony fishes,
ventilation is brought about by combined effect of mouth and operculum.
§ Water is drawn into the mouth. It passes over the gills through
pharynx and ultimately exists at the back of operculum through open operculur
valve.
§ Water is moved over the gills in a continuous unidirectional
flow by maintaining a lower pressure in operculur cavity than in buccopharynx
cavity.
COUNTER CURRENT FLOW OF WATER AND BLOOD
Gaseous exchange is
facilitated in gills due to counter current flow of H2O and blood.
In the capillaries
of each lamella, blood flows in direction opposite to the movement of water
across the gill. Thus the most highly oxygenated blood is brought to water that
is just entering the gills and has even high O2 content than the blood. As the
H2O flows over the gills, gradually loosing its oxygen to the blood, it
encounter the blood that is also increasingly low in oxygen. In this way a
gradient is establishment which encourages the oxygen to move from water to
blood
IMPORTANCE
Counter current
flow is very effective as it enables the fish to extract upto 80–90% of the
oxygen from water that flows over the gills.
RESPIRATORY SYSTEM
OF MAN
MAIN FUNCTION OF RESPIRATION
The main function
of respiratory system is inflow of O2 from the atmosphere to the body and
removal of CO2 from body to the atmosphere.
COMPONENTS OF RESPIRATORY SYSTEM
(1) PAIRED LUNGS
The respiratory
(gas exchange) organs.
(2) AIR PASSAGE WAYS
Which conduct the
air
(3) THORACIC CAVITY
Which lodges the
lungs
(4) INTERCOSTAL MUSCLES AND DIAPHRAGM
Which decreases and
increase the diameters of thoracic cavity
(5) RESPIRATORY CONTROL CENTRES
Areas in brain
which control the respiration.
DETAILS OF COMPONENTS
+ THORACIC CAVITY
Paired lungs with
in the pleural sacs are situated in the thoracic cavity. Separating the
thoracic cavity from the abdominal cavity is a dome-shaped musculo-tendinuous
partition called as Diaphragm.
BOUNDARIES OF CAVITY
Thoracic cavity is
supported by bony cage (thoracic cage) which is made up of
§ Sternum -> in front
§ Vertebral column -> at the back
§ 12 pairs of ribs -> on each side
§ Ribs are supported by Intercostal muscles
FUNCTION
Increase in thoracic cavity diameter is responsible for inspiration. While decrease in diameter is responsible for expiration.
Increase in thoracic cavity diameter is responsible for inspiration. While decrease in diameter is responsible for expiration.
AIR PASSAGE WAYS
Air is drawn into
the lungs by inter-connected system of branching ducts called as “Respiratory
tract” or “Respiratory passage ways”
Air passage ways
consists of
AIR CONDUCTING ZONE(which only
conducts the air)
1. Nostrils
2. Nasal Cavity
3. Pharynx
(nasopharynx and oropharynx)
4. Larynx
5. Trachea
6. Bronchi
7. Bronchioles
(also called terminal Branchioles)
RESPIRATORY ZONE(Where gaseous
exchange takes place)
8. Respiratory
Bronchioles
9. Alveolar duct
10. Alveolar sacs
or alveoli
GENERAL FUNCTIONS OF CONDUCTING AIR PASSAGES
1. Conduction of
air from atmosphere to the lungs
2. Humidification
of inhaled dry air.
3. Warming /
cooling of air to body temp.
4. The injurious
particles are entrapped by mucous and removed by ciliary
movements.
5. Lymphoid tissues of pharynx provide immunological functions
5. Lymphoid tissues of pharynx provide immunological functions
6. Cartilages
prevent the passages from collapse but are not present in Bronchioles which
remains expanded by same pressure that expand the alveoli.
CONDUCTING ZONE
1. NASAL CAVITY
Atmospheric air
enters the respiratory tract through a pair of openings called external nares
(Nostrils), which lead separately into nasal cavity. Nasal cavity opens into
naso pharynx through posterior nares (choanae).
Nasal cavity is lined internally by Pseudostratified columnar ciliated epithelium containing mucous secreting cells.
Hairs, sweat and sebaceous glands are also present.
Nasal cavity is lined internally by Pseudostratified columnar ciliated epithelium containing mucous secreting cells.
Hairs, sweat and sebaceous glands are also present.
SPECIALIZED FUNCTIONS
§
Warming of air
§
Humidification or moistening of air
§
Filteration of air with the help of
hairs
§
All these together called as Air
conditioning function of upper respiratory passages
§
Olfaction ( sense of smell)
2. PHARYNX
Air enters from
Nasal cavity into pharynx through internal nostrils. The openings of nostrils
are guarded by soft palate. It is internally lined by Pseudostratified ciliated
epithelium, mucous glands are also present.
FUNCTION
Pharynx is responsible for conduction of air as well as food
Pharynx is responsible for conduction of air as well as food
3. LARYNX (VOICE BOX)
Pharynx leads air
into larynx through an opening called glottis. Glottis is guarded by flap of
tissue called epiglottis. During swallowing, soft palate and epiglottis close
the nostrils opening and glottis respectively so that food is prevented to go
either into nasal cavity or glottis. Larynx, a small chamber consists of pair
of vocal cords
FUNCTION
During speech, vocal cords move medially and their vibration produce sound
During speech, vocal cords move medially and their vibration produce sound
4. TRACHEA (WIND PIPE)
Larynx leads the
air into a flexible air duct or trachea. It bears C-shaped tracheal cartilages
which keep its lumen patent during inspiration. Its internal lining is
pseudostratified columnar ciliated epithelium containing mucous secreting
goblet cells.
FUNCTION
Conduction of air
Due to mucous and upward beating of cilia, any residues of dust and germs are pushed outside the trachea towards the pharynx.
Conduction of air
Due to mucous and upward beating of cilia, any residues of dust and germs are pushed outside the trachea towards the pharynx.
5. BRONCHI
“At its lower end,
trachea bifurcates into two smaller branches called Principle Bronchi↑ which leads the air into lung of its side. They are also
supported by C-shaped cartilage rings upto the point where they enter the
lungs”.
In all areas of trachea and bronchi, not occupied by cartilage plates, the walls are composed mainly of smooth muscles.
In all areas of trachea and bronchi, not occupied by cartilage plates, the walls are composed mainly of smooth muscles.
6. BRONCHIOLES
On entering the
lungs, each bronchus divide repeatidly. As the bronchi become smaller, U-shaped
bars of cartilage are replaced by irregular plates of cartilages. The smallest
bronchi divide and give rise to Bronchioles (less than 1.5 mm in diameter).
7. TERMINAL BRONCHIOLES
Bronchioles divide
and give rise to terminal bronchioles (less than 1 mm in diameter). Walls
possess no cartilages and are almost entirely the smooth muscles. These are the
smalled airways without alveoli.
RESPIRATORY ZONE
In this zone of
respiratory tract, gaseous exchange between capillary blood and air takes
place.
1. RESPIRATORY BRONCHIOLES
Terminal
bronchioles show delicate outpouchings from their walls, which explains the
name Respiratory Bronchioles (less than 0.5 mm in diameter). They bear the
pulmonary alveoli.
2. ALVEOLAR DUCTS AND SACS
Each respiratory
bronchioles terminates at a tiny hollow sac like alveolar duct that lead into
tabular passages with numerous thin walled out pouchings called Alveolar sacs.
3. PULMONARY ALVEOLI
The alveolar sacs
consists of several alveoli openings into a single chamber. Alveoli are the
site of exchange of respiratory gases so they are considered as Respiratory
surfaces of lungs. Each alveolus is surrounded by a network of blood
capillaries.
INTERNAL STRUCTURE OF ALVEOLI
The alveolar lining
cells consists of
1. Type I cells
2. Type II cells
They are also
called pneumocytes.
“Bifurcation of
trachea is called Carina”.
TYPE I PNEUMOCYTES
Squamous shaped
cells which form the epithelial lining of alveoli
TYPE II PNEUMOCYTES
Irregular and
cuboidal shaped cells which secretes a substance called Surfactant
SURFACTANT
The internal area
of an alveoli is provided with a thin layer of fluid called as Surfactant
secreted by type II cells.
FUNCTION OF SURFACTANT
1. It reduces the
internal surface tension of alveoli which prevent it collapsing during
expiration.
2. It increases the
compliance.
3. It stabilize the
alveoli.
4. It also helps to
keep the alveoli dry.
LUNGS
Lungs are paired,
soft, spongy, elastic and highly vascularized structures, which occupy most of
thoracic cavity. In child they are pink, but with age they become dark and
mottled due to inhalation of dust.
RIGHT LUNG
Partitioned into 3
lobes by two fissures.
LEFT LUNG
Divided into 2
lobes by one fissures.
PLEURAL MEMBRANES
Each lung is
enclosed by two thin membranes called as Visceral and parietal pleural
membranes.
PLEURAL CAVITY
In between the
membranes there is a narrow cavity, the pleural cavity filled with pleural
fluid which acts as lubricant.
FUNCTION OF CAVITY
1. Cardinal
function is to exchange gases.
2. Phagocytosis of
air borne particles
3. Temperature
regulation
4. Removal of water
5. Maintainence of
acid-base balance (by elemination of CO2)
6. Acts as
Reservoir of blood.
BREATHING
DEFINITION
“Breathing is the process of taking in (inspiration or inhalation) and giving out of air (expiration or exhalation) from the atmosphere up to the respiratory surface and vice versa”
“Breathing is the process of taking in (inspiration or inhalation) and giving out of air (expiration or exhalation) from the atmosphere up to the respiratory surface and vice versa”
TYPES OF BREATHING
There are two types
of Breathing
Negative pressure
Breathing
Positive pressure
Breathing
NEGATIVE PRESSURE BREATHING
Normal breathing in
man is termed as negative pressure breathing in which air is drawn into the
lungs due to negative pressure (decrease in pressure in thoracic cavity in
relation to atmospheric pressure).
POSITIVE PRESSURE BREATHING
“In this kind of
breathing, lungs are actively inflated during inspiration under
positive pressure
from cycling valve”.
EXAMPLES
Frog uses positive pressure breathing.
Frog uses positive pressure breathing.
PHASES OF BREATHING
1. INSPIRATION OR
INHALATION
2. EXPIRATION OR
EXHALATION
(1) INSPIRATION
DEFINITION
“Inspiration is an energy consuming process in which air is drawn into the lungs due to negative pressure in thoracic cavity”
“Inspiration is an energy consuming process in which air is drawn into the lungs due to negative pressure in thoracic cavity”
MECHANISM
During inspiration volume of thoracic cavity increases which creates a pressure (intra thoracic) that sucks the air into the lungs.
During inspiration volume of thoracic cavity increases which creates a pressure (intra thoracic) that sucks the air into the lungs.
INCREASE IN VOLUME OF THORACIC
CAVITY
Volume of thoracic
cavity increases due to
1. Inc. in
Anterio-posterior diameter
2. Inc. in Vertical
diamter.
INCREASE IN
ANTERIO-POSTERIOR DIAMETER During contraction of external intercostals muscle,
the ribs as well as the sternum move upward and outward, which causes the
increase in anterior-posterior diameter of thoracic cavity.
INCREASE IN VERTICAL DIAMETER
Vertical diameter
of thoracic cavity inc. due to Contraction (descent) of
Diaphragm which
makes it flat.
As a consequence
thoracic cavity enlarges and the pressure is developed inside the thoracic
cavity and ultimately in the lungs. So the air through the respiratory tract
rushes into the lungs upto the alveoli where gaseous exchange occurs.
(2)EXPIRATION
DEFINITION
“It is reserve of inspiration. The passive process in which air is given out of lung due to increased pressure in thoracic cavity is called “Expiration”
“It is reserve of inspiration. The passive process in which air is given out of lung due to increased pressure in thoracic cavity is called “Expiration”
MECHANISM
During expiration, elastic recoil of pulmonary alveoli and of the thoracic wall expels the air from the lungs.
During expiration, elastic recoil of pulmonary alveoli and of the thoracic wall expels the air from the lungs.
DECREASE IN VOLUME OF THORACIC
CAVITY
Volume of thoracic
cavity ↓ due to
1. DECREASE IN
ANTERIO-POSTERIOR DIAMETER
2. DECREASE IN
VERTICAL DIAMETER
(1) DECREASE IN
ANTERIO-POSTERIOR DIAMETER
It is caused by
relaxation of external intercostals muscles and contraction of internal
intercostals muscles which moves the ribs and sternum inward and downward.
(2) DECREASE IN VERTICAL
DIAMETER
It is caused by
relaxation of diapharagm which makes it dome shaped thus reducing the volume of
thoracic cavity.
As a consequence, the lungs are compressed so the air along with water vapours is exhaled outside through respiratory passage.
As a consequence, the lungs are compressed so the air along with water vapours is exhaled outside through respiratory passage.
CONTROL OF RATE OF
BREATHING
Rate of breathing can
be controlled by two modes.
VOLUNTARY CONTROL
INVOLUTARY CONTROL
VOLUNTARY CONTROL
Breathing is also
under voluntary control by CEREBRAL CORTEX
EXAMPLES
We can hold our breath for short time or can breath faster and deeper at our will.
We can hold our breath for short time or can breath faster and deeper at our will.
INVOLUNTARY CONTROL
Mostly, rate of
breathing is controlled automatically. This is termed as Involuntary control
which is maintained by coordination of respiratory and cardio-vascular system.
TWO MODES OF
INVOLUNTARY CONTROL
A. NERVOUS CONTROL
(through respiratory centers in brain)
B CHEMICAL CONTROL (through chemoreceptors)
B CHEMICAL CONTROL (through chemoreceptors)
(A) NERVOUS CONTROL
§ Control of rate of breathing by nervous control is through the
Respiratory centers in Medulla oblongata which are sensory to the changes in
Conc. of CO2 and H+ present in the cerebro-spiral fluid (CSF).
RESPIRATORY CENTRES IN MEDULLA
Two center are
present
(1) DORSAL GROUP OF NEURONS
Medulla contains a
dorsal group (Inspiratory group) of neurons responsible for inspiration
FUNCTION
In response to increase conc. of CO2 and H+ (decreased pH), it sends impulses to the intercostals muscles to increase the breathing rate
In response to increase conc. of CO2 and H+ (decreased pH), it sends impulses to the intercostals muscles to increase the breathing rate
(2) VENTRAL GROUP OF NEURONS
Another area in the
medulla is ventral (expiratory) group of neurons.
FUNCTION
It inhibits the dorsal group and mainly responsible for expiration
It inhibits the dorsal group and mainly responsible for expiration
(B) CHEMICAL CONTROL
Chemical control of
rate of breathing is through chemoreceptors.
LOCATION OF CHEMORECEPTORS
AORTIC BODIES
CAROTID BODIES
AORTIC BODIES
The peripheral
chemoreceptors which are located above and below the arch of aorta are called
Aortic bodies. It sends impulses to medulla through Vagus nerve.
CAROTID BODIES
Chemoreceptors
which are located at the bifurcation of carotid arteries are called Carotid
bodies. It sends impulses to medulla through Glossopharyngeal nerve.
FUNCTION
Inc. in concentration of CO2 and H+ in blood are basic stimuli to increase the rate of breathing which are monitered by these chemoreceptors and then send the impulses to medulla oblongata which produce action potential in inspiratory muscles.
Inc. in concentration of CO2 and H+ in blood are basic stimuli to increase the rate of breathing which are monitered by these chemoreceptors and then send the impulses to medulla oblongata which produce action potential in inspiratory muscles.
DISORDERS OF
RESPIRATORY TRACT
(1) LUNG CANCER (BRONCHIAL CARCINOMA)
CAUSES
§ Smoking is a major risk factor either acitively or passively.
§ Asbestos, nickel, radioactive gases are associated with
increased risk of bronchial cascinoma
PHYSIOLOGICAL
EFFECTS
+ LOSS OF CILIA
The toxic contents
of smoke such as nicotine and SO2 cause the gradual loss of cilia of
epithelical cells so that dust and germ are settled inside the lungs.
+ ABNORMAL GROWTH OF MUCOUS GLANDS
Tumor arises by
uncontrolled and abnormal growth of bronchial epithelium mucous glands. The
growth enlarges and some times obstruct a large bronchus.
The tumours cells can spread to other structures causing cancer.
The tumours cells can spread to other structures causing cancer.
SYMPTOMS
§
Cough- due to irritation
§
Breath lessness – due to obstruction.
(2)TUBERCLOSIS (KOCH’S DISEASE)(INFECTIOUS DISEASE OF LUNG)
CAUSE
Caused by a Bacterium called as “MYCOBECTERIUM TUBERCLOSIS”
Caused by a Bacterium called as “MYCOBECTERIUM TUBERCLOSIS”
PHYSIOLOGICAL EFFECTS
§ Tuber Bacili causes
§ Invasion of infected region by macrophages
§ Fibrosis of lungs thus reducing the total amount of functional
lung tissues
These effects cause
§ Increased work during breathing
§ Reduced vital and breathing capacity
§ Difficulty in diffusion of air from alveolar air into blood.
SYMPTOMS
§
Coughing (some time blood in sputum)
§
Chest pair
§
Shortness of breath
§
Fever
§
Sweating at night
§
Weight loss
§
Poor apetite
PREVENTION
A live vaccine (BCG) provides protection against tuberclosis.
A live vaccine (BCG) provides protection against tuberclosis.
3.COPD-(CHRONIC OBSTRUCTIVE PULMONARY DISEASE)
They include
A. Emphysema
B. Asthma
(3-A)EMPHYSEMA
CAUSES
It is a chronic infection caused by inhaling Smoke and other toxic substances such as Nitrogen dioxide and Sulphur dioxide
It is a chronic infection caused by inhaling Smoke and other toxic substances such as Nitrogen dioxide and Sulphur dioxide
PHYSIOLOGICAL EFFECTS
§
Long infection – Irritants deranges
the normal protective mechanisms such as loss of cilia, excess mucus secretion causing
obstruction of air ways
§
Elasticity of lung is lost
§
Residual volume increases while vital
capacity decreases.
§
Difficulty in expiration due to
obstruction
§
Entrapment of air in alveoli
§
All these together cause the marked
destruction of as much as 50-80% of alveolar walls.
§
Loss of alveolar walls reduces the
ability of lung to oxygenate the blood and remove the CO2
§
Oxygen supply to body tissues
especially brain decreases.
SYMPTOMS
§
Victim’s breathing becomes labored
day by day.
§
Patient becomes depressed, irritable
and sluggish.
§
Concentration of CO2 increases which
may cause death.
(3-B) ASTHAMA
“Respiratory tract
disorder in which there are recurrent attacks of breathlessness,
characteristically accompanied by wheezing when breathing out.”
CAUSES
It is usually caused by Allergic hypersensitivity to the plant pollens, dust, animal fur or smoke or in older person may be due to common cough.
Heridity is major factor in development of Asthma.
It is usually caused by Allergic hypersensitivity to the plant pollens, dust, animal fur or smoke or in older person may be due to common cough.
Heridity is major factor in development of Asthma.
PHYSIOLOGICAL EFFECTS
§
Localized edema in walls of small
bronchioles.
§
Secretion of thick mucus.
§
Spastic Contraction of bronchial
smooth muscles (so the resistance in air flow increases).
§
Residual volume of lung increases due
to difficulty in expiration.
§
Thoracic cavity becomes permanently
enlarged.
SYMPTOMS
§
The asthmatic patient usually can
inspire quite adequately but has great difficulty in expiring.
LUNG CAPACITIES
1. TOTAL AVERAGE LUNG CAPACITY
DEFINITION
“It is the maximum volume in which the lung can be expanded with
greatest possible inspiratory efforts.”
Or
“Total lung capacity is the combination of residual volume and vital
capacity.
VALUE
Total lung capacity = 5000 cm3 or 5 lit of air.
Total lung capacity = 5000 cm3 or 5 lit of air.
2. TIDAL VOLUME
“The amount of air
which a person takes in and gives out during normal breathing is called Tidal
Volume.”
VALUE
450cm3 to 500 cm3 (1/2 litre)
450cm3 to 500 cm3 (1/2 litre)
3. INSPIRATORY
RESERVE VOLUME
DEFINITION
‘“Amount of air inspired with a maximum inspiratory effort in excess of tidal volume.”
‘“Amount of air inspired with a maximum inspiratory effort in excess of tidal volume.”
VALUE
200 cm3 or 2 lit. (Average value)
200 cm3 or 2 lit. (Average value)
4. EXPIRATORY RESERVE VOLUME
DEFINITION
“Amount of air expelled by an active expiratory effort after passive expirations.”
“Amount of air expelled by an active expiratory effort after passive expirations.”
VALUE
1000 cm3 or 1 litre.
1000 cm3 or 1 litre.
5. VITAL CAPACITY
DEFINITION
“After an extra deep breath, the maximum volume of air inspired and
expired is called Vital capacity.”
Or
“It is the combination of inspiratory reserve volume, expiratory
reserve volume and tidal volume.”
VALUE
Averages about 4 litre.
Averages about 4 litre.
6. RESIDUAL VOLUME
DEFINITION
“Amount of air which remains in lung after maximum expiratory effort is
called Residual volume.”
VALUE
Approximately 1 litre or 1000 cm3.
Approximately 1 litre or 1000 cm3.
IMPORTANCE OF LUNG CAPACITY
§
Residual volume prevent the lung from
collapsing completely.
§
Responsible for gaseous exchange in
between breathing.
§
It is not stagnant since inspired air
mixes with it each time.
§
Aging or Emphysema, etc can increase
the residual volume at the expense of vital capacity.
HAEMOGLOBIN
INTRODUCTION
“Haemoglobin is an iron containing respiratory pigment present in the red blood cells of vertebrates and responsible for their red colour.”
“Haemoglobin is an iron containing respiratory pigment present in the red blood cells of vertebrates and responsible for their red colour.”
STRUCTURE
Haemoglobin
consists of
1. Heme
2. Protein (globin
like chains)
1. HEME
One Haemoglobin
molecule consists of 4 molecules of Heme. Each Heme molecule contains an iron
(Fe++) binding pocket. Thus one molecule of Haemoglobin can combine with 4 iron
atoms.
2. GLOBIN
Each Hb molecule contains
four globin like chains (Two α chains and Two β chains).
ROLE OF HB DURING
RESPIRATION
Two major functions
are performed by Hb.
1. Transport of O2
from lung to tissues.
2. Transport of CO2
from tissues to lungs.
1. “TRANSPORT OF O2 FROM LUNGS TO TISSUES”
“Nearly 97% of O2
is transported from the lungs to the tissues in
combination with
Hb.”
ATTACHMENT OF O2 WITH HB
It is the iron of
Hb molecule which reversibly binds with oxygen. One Hb molecule can bind 4
molecules of O2. Thus due to Hb, blood could carry 70 times more oxygen than
plasma.
MECHANISM OF TRANSPORT
§
Due to high O2 concentration in
alveolar air, the O2 moves from air to the venous blood where O2 concentration
is low.
§
It combines loosely with Hb to form
Oxyhemo Globin.
§
In this form, O2 is carried to the
tissues where due to low oxygen concentration in tissues, oxy Hb dissociates
releasing oxygen, which enters in tissues.
Whole process can
be represented by following equation.
2. “TRANSPORT OF CO2 FROM TISSUES TO LUNGS”
“Haemoglobin is
also involved in 35% of transport of CO2 from tissues to alveolar blood
capillaries in alveoli.”
ATTACHMENT OF CO2 WITH HB
CO2 binds
reversibly with NH2 group of Hb to form loose compound called “Carboamino
Haemoglobin.”
MECHANISM OF TRANSPORT
§
Carbon dioxide due to its higher
concentration in tissue diffuses out into the blood where it combines with Hb
to form Carboamino Hb.
§
In the alveoli it breaks and CO2
diffuses out into the Alveoli from where it is expired.
MYOGLOBIN
INTRODUCTION
“Myoglobin is a heme protein, smaller than Hb, found in muscles and giving red colour to them.
“Myoglobin is a heme protein, smaller than Hb, found in muscles and giving red colour to them.
STRUCTURE
Myoglobin consists
of one heme molecule and one globin chain. It can combine with one iron (Fe++)
atom and can carry one molecule of O2.
FUNCTION OF MYOGLOBIN
§
Myoglobin has high affinity for O2 as
compared to Haemoglobin so it binds more tightly.
§
It stores the O2 within the muscles.
§
It supplies the O2 to the muscles
when there is severe oxygen deficiency (During exercise)
It can be
represented as follows:
Mb + O2 ↔ MbO2
TRANSPORT OF GASES
Oxygen and
carbondioxide are exchanged in, Alveoli by Diffusion.
O2 TRANSPORT
Blood returning
into the lungs from all parts of body is depleted from oxygen. This
deoxygenated blood is dark maroon in colour to appear bluish through skin. It
becomes oxygenated in the lungs.
TWO FORMS OF O2 IN BLOOD
O2 is transported
in the blood in two forms:
§
Dissolved form (3%)
§
Combination with Hb (97%) ®
Oxyhaemoglobin
MECHANISM OF O2 TRANSPORT
+ DIFFUSION OF O2 FROM ALVEOLUS
INTO PULMONARY BLOOD
The air inhaled into
the lungs has high concentration of oxygen while venous blood in pulmonary
capillaries has low in concentration. Due to this difference in concentration
across the respiratory surface, oxygen diffuses into the blood flowing into
capillaries around the Alveoli. Now blood becomes oxygenated which is bright
red in colour.
+ DIFFUSION OF O2 FROM
CAPILLARIES INTO CELLS
Concentration of O2
in the arterial end of capillaries is much more greater
than concentration
of O2 in the cells. So O2 diffuses from the blood to the body cells. Since the
blood takes in oxygen much more rapidly than water. Thus it can transport
enough oxygen to the tissues to meet their demand.
CO2 TRANSPORT
Blood returning
from tissues contain excess of CO2 as a respiratory by-product, which is
eliminated from the body during expiration in the lungs.”
THREE FORMS OF CO2 IN BLOOD
§
Dissolved form (in plasma) – 5%
§
In form of HCO3- (in RBC’s) – 60%
§
In combination with Hb (Carboamino
Hb) – 35%
+ DISSOLVED FORM
Only 5% of CO2 is
transported in dissolved form in plasma. Here it combines with H2O of plasma to
form H2CO3. But this reaction is very slow as plasma does not contain Carbonic
Anhydrase to accelerate this reaction.
Reactions can be represented by following equations.
Reactions can be represented by following equations.
CO2 + H2O ↔ H2CO3
H2CO3 ↔HCO3- + H+
HCO3- + k+ ↔ KHCO3
+ IN FORM OF HCO3-
60% of CO2 is
transported in the blood in form of HCO3- in RBC’s. Here it combines with water
to form H2CO3. But this reaction occurs rapidly in
RBC’s due to presence
of Carbonic Anhydrase.
Reactions can be
represented by following equations
CO2 + H2O ↔ H2CO3
H2CO3 ↔ HCO3- + H+
HCO3- + Na+ ↔ NaHCO3
+ IN COMBINATION WITH HB
As discussed
previously in role of Hb.
MECHANISM OF CO2 TRANSPORT
+ DIFFUSION OF CO2 FROM CELLS INTO CAPILLARIES
CO2 is continuously
synthesizing in the tissues as a result of metabolism. Thus due to its higher
concentration. CO2 diffuses from the tissues into blood, which becomes
deoxygenated.
+ DIFFUSION OF CO2 FROM
PULMONARY BLOOD INTO ALVEOLUS
Blood returning from tissues contain high concentration of CO2. This blood is brought to lungs, where CO2 diffuses from the blood into alveolus where its concentration is lower.
Blood returning from tissues contain high concentration of CO2. This blood is brought to lungs, where CO2 diffuses from the blood into alveolus where its concentration is lower.
FACTORS EFFECTING THE TRANSPORT OF GASES
Following are some
factors, which influence the transport of respiratory gases across the alveolar
wall.
1. Concentration
Gradient
2. Presence of
competitor such as CO
3. Moisture
4. Surfactant
5. pH
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