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Excretory System
Excretory System
PRODUCTS
AND THEIR
ELIMINATION
INTRODUCTION
● Animals accumulate ammonia, urea, uric acid, carbon
dioxide, water and ions like Na+, K+, Cl–, phosphate,
sulphate etc., either by metabolic activities or by other
means like excess ingestion. These substances have to be
removed totally or partially.
● Ammonia, urea and uric acid are the major forms of
nitrogenous waste excreted by the animals.
INTRODUCTION
Kidney
s
Urete
r
Urinary
bladder Urethr
a
HUMAN EXCRETORY SYSTEM
Kidneys are reddish brown, bean shaped structures situated
between the levels of last thoracic and third lumbar vertebra
close to the dorsal inner wall of the abdominal cavity.
T12
(Thoracic
)
CONVE CONCA
X VE
L3
(Lumbar
)
HUMAN EXCRETORY SYSTEM
Dorsal surface of the kidney is attached to the dorsal abdominal
wall, so only its ventral surface is covered by peritoneum. This
type of kidney is called retro-peritoneal kidney or extra
peritoneal kidney.
Vertebral column
dorsal (T12-L3)
Abdominal Kidney
wall
Peritoneum on
ventral side of kidney
Peritoneal
cavity
Peritoneum
ventral
HUMAN EXCRETORY SYSTEM
● Each kidney of an adult human measures 10-12 cm in length, 5-7
cm in width, 2-3 cm in thickness with an average weight of 120-
170 g.
● Towards the centre of the inner concave surface of the kidney is a
notch called hilum through which blood vessels(renal artery) and
nerves enter. Whereas ureter and renal vein leave the kidney.
hilu
m renal
artery
renal
10-12 cm
vein
ureter
5-7
cm
HUMAN EXCRETORY SYSTEM
● Inner to the hilum is a broad funnel shaped space called the
renal pelvis with projections called calyces.
● The outer layer of kidney is a tough capsule. Inside the
kidney, there are two zones, an outer cortex and an inner
medulla. The medulla is divided into a few conical masses
(medullary pyramids) (8 to 12 in number) projecting into
the calyces (sing.: calyx). The cortex extends in between the
medullary pyramids as renal columns called Columns of
Bertini.
HUMAN EXCRETORY SYSTEM
Columns of
Bertini
Calyces
Renal
pelvis
Cortex
Renal capsule
Medullary pyramids
GOLDEN KEY POINTS
● Kidneys are mesodermal in origin. COMPENSATE
HYPERTROPY If one kidney is removed from the body of
human being than the other one increases in size and try to
perform the function of removed kidney also. It is an example
of regeneration method called compensate hypertropy.
POST RENAL URINARY TRACT
Urine passes from the pelvis into the ureter. Both the ureter
open through separate oblique openings into the urinary
bladder. The oblique openings prevent the backflow of urine.
Renal
pelvis
ureter
urin
e Oblique opening of ureter
(prevent the backflow of
urine)
urinary bladder
Urethr
a
POST RENAL URINARY TRACT
Externally, the bladder is lined by detrusor muscle, it is
involuntary in nature while internally the bladder is lined by
transitional epithelium or urothelium. This epithelium has
great capacity to expand so that large volume of urine can be
stored if required.
Externally, the
bladder is lined by
detrusor muscle
internally the bladder is lined
by transitional epithelium or
urothelium
POST RENAL URINARY TRACT
During act of micturition urine leaves the urinary bladder and enters the membranous
duct called Urethra.
Urethra
In In
males females
•leads to end of the penis in •into the
males vulva
•the urethra has three •Only
parts, membranous
prostatic, membranous & urethra
penile urethra respectively.
POST RENAL URINARY TRACT
POST RENAL URINARY TRACT
Opening of urinary bladder is controlled by sphincters made of
circular muscles. These normally remain contracted and
during micturition these relax to release urine.
(In rabbit a single sphincter is present while in human two
sphincters, inner involuntary & outer voluntary, are present).
Urinary
bladder
Internal
sphincter
External
sphincter
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STRUCTURE OF NEPHRON
● Each kidney has nearly one million complex tubular
structures called nephrons, which are the structural and
functional units.
● Each nephron has two parts – the Glomerulus and the
Renal tubule.
renal
tubule
Glomerulu
s
STRUCTURE OF NEPHRON
GLOMERULUS
STRUCTURE OF NEPHRON
● Glomerulus is a tuft of capillaries formed by the
afferent arteriole – a fine branch of renal artery.
Blood from the glomerulus is carried away by an
efferent arteriole.
● The renal tubule begins with a double walled cup-like
structure called Bowman’s capsule, which encloses
the glomerulus. Glomerulus alongwith Bowman’s
capsule, is called the malpighian body or renal
corpuscle.
STRUCTURE OF NEPHRON
collecting duct
STRUCTURE OF NEPHRON
The tubule continues further to form a highly coiled
network – proximal convoluted tubule (PCT). A
hairpin shaped Henle’s loop is the next part of the
tubule which has a descending and an ascending limb.
The ascending limb continues as another highly coiled
tubular region called distal convoluted tubule (DCT).
The DCTs of many nephrons open into a straight tube
called collecting duct, many of which converge and open
into the renal pelvis through medullary pyramids in the
calyces.
Renal Cortex & Medulla
Malpighian
2 corpuscles are located Malpighian corpuscles are located
close
. to the kidney surface. at the junction of cortex and
medulla.
Their
3 loop of Henle are mostly The loop of Henle of these
confined
. to cortex and a very small nephrons are long, dipping deep
part of it runs in the medulla. down into the medulla.
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MECHANISM OF URINE FORMATION
Venous
Urine formation involves Peritubular return
three main processes namely capillary
Glomerular filtration
Reabsorption
Tubular secretion Efferent
Arteriole Interstitial
Glo fluid
mer
fi ur
ular
lt in
r
capil e
Afferent at 1. Reabsorpti1. Tubular
lary
Arteriole e on secretion
1. Glomerul
ar
MECHANISM OF URINE FORMATION
Capsular hydrostatic
pressure 10-18 mm of Hg
MECHANISM OF URINE FORMATION
The amount of the filtrate formed by the kidneys per minute is
called glomerular filtration rate (GFR). GFR in a healthy
individual is approximately 125 ml/minute, i.e., 180 litres per day
!
MECHANISM OF URINE FORMATION
2. Tubular Reabsorption
A comparison of the volume of the filtrate formed per day
(180 litres per day) with that of the urine released (1.5
litres), suggest that nearly 99 per cent of the filtrate has
to be reabsorbed by the renal tubules. This process is
called reabsorption.
The tubular epithelial cells in different segments of nephron
perform this either by active or passive mechanisms. For
example, substances like glucose, amino acids, Na+, etc.,
in the filtrate are reabsorbed actively whereas the
nitrogenous wastes are absorbed by passive transport.
Reabsorption of water also occurs passively in the initial
segments of the nephron.
MECHANISM OF URINE FORMATION
MECHANISM OF URINE FORMATION
3. Tubular
Secretion
During urine formation, the tubular cells secrete substances
like H+, K+ and ammonia into the filtrate. Tubular
secretion is also an important step in urine formation as it
helps in the maintenance of ionic and acid base balance of
body fluids.
MECHANISM OF URINE FORMATION
FUNCTION OF THE TUBULES
Proximal Convoluted Tubule
(PCT)
Maximum reabsorption
Descending
limb Ascending limb
of loop of of loop of Henle
Henle
Thick part – Simple Cuboidal
Thick part – Simple Cuboidal
Thin part – Simple Squamous
Thin part – Simple Squamous
Collecting
Duct
Ciliated Cuboidal
Epithelium
Concentration of urine
allows passage of small
amounts of urea into the
medullary interstitium
to keep up the osmolarity
FUNCTION OF THE TUBULES
Collecting Duct: This long duct extends from the cortex
of the kidney to the inner parts of the medulla. Large
amounts of water could be reabsorbed from this
region to produce a concentrated urine.
Ascending Ascending
Vasa Recta LOH
Descending
Descending
Vasa Recta
LOH
Medulla
MECHANISM OF CONCENTRATION OF THE
FILTRATE
MECHANISM OF CONCENTRATION OF THE
● FILTRATE
This gradient is mainly caused by NaCl and urea.
● Similarly, small amounts of urea enter the thin segment of the ascending limb of
Henle’s loop which is transported back to the interstitium by the collecting
tubule. The above described transport of substances facilitated by the special
arrangement of Henle’s loop and vasa recta is called the counter current
mechanism.
Drop in live
blood r
pressure
Angiotensinoge
JG cell release n
Angiotensin lung
Angiotensin- s
renin l Converting
Enzyme
Angiotensin- (ACE)
ll
Hypothalamus Cardio Adrenal
Vascular Cortex
SystemAldosterone
(Mineralocorticoid kidne
Vasoconstrictio
n
) y
Thirst and Salt and water
drinking Elevate retention
blood
pressure
REGULATION OF KIDNEY FUNCTION
1) Renin Angiotensinogen Aldosterone
System
The JGA plays a complex regulatory role. A fall in glomerular
blood flow/glomerular blood pressure/GFR can activate the JG
cells to release renin which converts angiotensinogen in blood to
angiotensin I and further to angiotensin II. Angiotensin II, being
a powerful vasoconstrictor, increases the glomerular blood
pressure and thereby GFR.
Angiotensin II also activates the adrenal cortex to release
Aldosterone. Aldosterone causes reabsorption of Na+ and water
from the distal parts of the tubule. This also leads to an increase in
blood pressure and GFR. This complex mechanism is generally
known as the Renin-Angiotensin mechanism.
REGULATION OF KIDNEY FUNCTION
1) ANF
Mechanism
An increase in blood flow to the atria of the heart can cause the
release of Atrial Natriuretic Factor (ANF). ANF can cause
vasodilation (dilation of blood vessels) and thereby decrease the
blood pressure. ANF mechanism, therefore, acts as a check on
the renin-angiotensin mechanism.
REGULATION OF KIDNEY FUNCTION
Venous Return Blood
vessel
1. Vasodilation
o Decreased blood pressure
Atrial Atrial Natriuretic
Stretch Factor
Rt (ANF)
Atrium
Natriuria ( increase salt excretion hence water
excretion)
Blood Volume
Venous Return
Blood pressure
AUTO REGULATION OF KIDNEY FUNCTION
1) Myogenic Mechanism
An increase in blood pressure will tend to stretch the
afferent arteriole, which would be expected to increase the
blood flow to the glomerulus. The wall of the afferent
arteriole, however, responds to stretch by contraction, this
reduces the diameter of the arteriole, and therefore causes
increase in the resistance to flow. This myogenic mechanism,
thus, reduces variations in flow to the glomerulus in case of
fluctuations in blood pressure.
REGULATION OF KIDNEY FUNCTION
MICTURITION
Urine formed by the nephrons is ultimately carried to the urinary
bladder where it is stored till a voluntary signal is given by the
central nervous system (CNS). This signal is initiated by the
stretching of the urinary bladder as it gets filled with urine. In
response, the stretch receptors on the walls of the bladder send
signals to the CNS. The CNS passes on motor messages to
initiate the contraction of smooth muscles of the bladder and
simultaneous relaxation of the urethral sphincter causing the
release of urine. The process of release of urine is called
micturition and the neural mechanisms causing it is called the
micturition reflex.
MICTURITION
MICTURITION
COMPOSITION OF URINE
95% = Water
2% = Salts
2.7% = Urea
Rest 0.3% = Other materials like the Drugs, Hippuric acid, Uric
acid, Vitamin-C, Dyes etc.
GOLDEN KEY POINTS
1. Urea formation takes place in liver.
2. Urea elimination = Kidney.
3. Blood vessel with maximum urea is Hepatic vein.
4. Blood vessel with minimum urea is renal vein.
5. Amount of urea in urine depend upon protein diet.
GOLDEN KEY POINTS
1. Pale yellow colour of urine is due to the Urochrome pigment. It
is formed in the blood due to the reduction of Haemoglobin. So in
the body of a healthy animal urochrome is found in a very less
amount.
2. pH of urine = 6.
3. The specific gravity of urine is 1.01 to 1.05.
4. Ions excreted out through urine are mainly monovalent ions
e.g. Na+, K+, Cl-, HCO3-, H3O+ etc.
5. Ions removed out through faecal matter are mainly divalent
and trivalent ions e.g. Ca2+, Mg2+, CO3-2, PO4-3.
6. Substances which are completely reabsorbed are called high
threshold substances e.g. Glucose and Amino acid.
7. Substances which are not reabsorbed at all are called
athreshold substances e.g. Inulin, Sulphates, Para Amino
Hippuric Acid (PAHA).
GOLDEN KEY POINTS
1. Substances which are reabsorbed the body are demand of
variable threshold substances e.g. Electrolytes and water.
2. Substances which are less reabsorbed are called low threshold
substances e.g. Urea.
1. A healthy human excrete (on an average) 25 gm urea/day.
2. Workers in deep mine usually suffer from dehydration because
water is lost along with salt in the form of sweat.
3. Diuretic substances: Substances which increases the urine
formation are called diuretic substance e.g. tea, coffee and alcohol.
4. If glucose remain unreabsorbed from PCT than comes out through
urine. This condition is called glycosuria. Where as this disease is
called diabetes mellitus.
5. Disease caused due to deficiency of ADH or vasopressin is called
diabetes insipidus. It is characterized by more dilute urine.
ABNORMAL CONSTITUENTS OF URINE
Polyuria - Excessive urination.
Proteinuria - Presence of proteins in urine.
Albuminuri - Presence of albumin in urine, usually occurs in
a nephritis (inflammation of glomeruli), when the
size of the filtering slits enlarges and basement
membrane looses its negative charge.
Ketonuria - Presence of abnormally high ketone bodies in
urine.
Haemoglobi - Presence of haemoglobin in urine.
nuria
Haematuria - Presence of Blood/RBC in urine.
Pyuria - Presence of WBC in urine.
ROLE OF OTHER ORGANS IN EXCRETION
Other than the kidneys, lungs, liver and skin also help in the elimination of
excretory wastes.
Our lungs remove large amounts of CO2 (approximately 200ml/minute) and also
significant quantities of water every day.
Liver, the largest gland in our body, secretes bile-containing substances like
bilirubin, biliverdin, cholesterol, degraded steroid hormones, vitamins and
drugs. Most of these substances ultimately pass out alongwith digestive wastes.
The sweat and sebaceous glands in the skin can eliminate certain substances
through their secretions. Sweat produced by the sweat glands is a watery fluid
containing NaCl, small amounts of urea, lactic acid, etc. Though the primary
function of sweat is to facilitate a cooling effect on the body surface, it also helps
in the removal of some of the wastes mentioned above. Sebaceous glands
eliminate certain substances like sterols, hydrocarbons and waxes through
sebum. This secretion provides a protective oily covering for the skin.
HEMODIALYSIS
HEMODIALYSIS