AN OVERVIEW OF THE URINARY SYSTEM
FUNCTIONS OF THE URINARY SYSTEM
► Remove wastes
► Regulate levels of
ions (K+, Na+, Cl -, Ca++, HPO4-2), glucose, amino acids, calcitriol (active
Vitamin D), and erythropoietin, creatinine
► Regulate blood
osmolarity
► Regulate blood volume
and pressure
► Regulate blood pH -
NH3 (ammonia, a base) and H+ (acid)
Physiological Mechanisms of the Nephron
► Glomerular filtration
► Reabsorption
► Secretion
GLOMERULAR FILTRATION
► Occurs in glomerulus
of renal corpuscle - end product is called ''filtrate"
► Passive process
► H2O (osmosis)
► Urea (diffusion)
► All particles smaller
than large proteins and blood cells (RBC, WBC platelets) are filtered (return
to blood)
REABSORPTION
(in the-P.C.T.)
► 65% of all filtrate
is reabsorbed here (H2O) - passive
► 50% of the urea
filtered is re-absorbed (because it's small) – passive
► Na+ (and K+,
SO4-3, Cl-, Ca++, PO4-3 )
►Na+ &
glucose (symport), and vitamins enter P.C.T cell by active transport
REABSORPTION (in the descending Loop of Henle)
► Impermeable to ions
► Increase in
osmolarity due to H2O reabsorption
REABSORPTION (in the ascending Loop of Henle) - Na+!!!
REABSQRPTION (in the D.C.T.)
► More Na+/Cl-
reabsorption occurs here
► Ca++
reabsorption, regulated by PTH (secreted from parathyroid glands) - PTH
increases blood Ca++
REABSORPTION (in the Collecting Duct)
► More H2O
reabsorption regulated by vasopressin (ADH), secreted by posterior pituitary
gland
► More Na+ and H2O
reabsorption regulated by aldosterone (secreted from adrenal glands)
SECRETION (in the P.C.T.)
► Deamination of glutamine
in the proximal convoluted tubule cells generates ammonia:
NH3 + H+
→ NH4+
► As
more H+ is secreted, HCO3- is reabsorbed.
► These
reactions increase during acidosis to return homeostatic balance.
SECRETION (in the D.C.T.)
►
K+ secreted in exchange for Na+ reabsorption
SECRETION (in the Collecting Duct)
► H+ secreted as
a by-product of our primary buffer system:
CO2 + H2O → H2CO3
→H+ + HCO3-
► Resulting HCO3-
can buffer blood pH.
► Amino acids are deaminated
in the PCT cells.
► The resulting ammonia binds H+ to form NH4+,
buffering urine.
REGULATION
Glomerular filtration rate (GFR)
► Controlled by
constriction/dilation of afferent arterioles
► Increased blood volume / blood pressure causes stretching of
the heart, which releases ANP - this causes
relaxation of afferent and efferent arterioles and thereby increases GFR
(↑ GFR causes less Na+
/ H2O reabsorption) thus ↓ ing blood volume and blood pressure
to normal
► Sympathetic stimulation
(NorEPI via a1 receptors) can cause vasoconstriction of afferent
arterioles (and therefore
lower GFR) - this increases blood flow to other areas.
► Decreased blood volume / blood pressure (as might be seen in
diuresis / natriuresis) causes renin release by JG
cells:
Renin
releases Angiotensin I from liver precursor
ACE
(lungs) converts AG I to AG II
AG
II stimulates constriction of afferent and efferent arterioles and thereby
decreases GFR
(↓
GFR causes more Na+ / H2O reabsorption) thus ↑-ing
blood volume and blood pressure to normal
RENTN-ANGIOTENSIN PATHWAY
► AG II stimulates adrenal
cortex to secrete aldosterone
► Aldosterone causes
increased Na+ / H2O reabsorption
► This causes increased K + excretion and an
increase in blood volume / pressure.
► AG II also stimulates ADH
release from pituitary gland
► ADH acts on collecting
duct to increase H2O reabsorption which also increases blood volume
/ pressure.
SUMMARY
₪ The
kidney filters approximately 180 L of H2O from plasma and forms 1-2
L of urine every day.
₪ Through
reabsorption of these filtered products and secretion of wastes, the kidney is
responsible for:
Regulating
pH of blood and body fluids
Maintaining
blood glucose levels
Maintaining
Ca++ homeostasis
Maintaining
electrolyte balance of ICF/ECF
Regulating
blood volume and blood pressure
Excretion of
toxins and wastes: urea, ammonia, creatinine, uric acid, drugs
₪ The
kidney is also responsible for:
Vitamin
D formation (calcitriol)
RBC
formation (erythropoietin)
₪ Regulation occurs neuronally
via sympathetic stimulation and
hormonally via renin-angiotensin pathway,
aldosterone, ADH, and ANP.