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ROLE OF KIDNEY IN BLOOD
AND ACID BASE BALANCE
ROLE OF
KIDNEY IN
BLOOD AND
ACID-BASE
BALANCE
IMPORTANT ROLE MAINTANENCE
OF ACID BASE
BALANCE
EXCRETING
RETAINING
H+
Hco3 -
Metabolic activities in the body produce
large quantity of acids (with lot of
hydrogen ions), which threaten to
push the body towards acidosis.
ACIDIC IN NATURE
PH 4.5 to 8.0
However, kidneys prevent this by two
ways:
Reabsorption of bicarbonate
ions (HCO3 )
Secretion of hydrogen ions (H+).
It is called filtered load of HCO3 –.
Excretion of this much HCO3 – in urine will
affect the acid-base balance of body fluids.
So, HCO3 – must be taken back from the
renal tubule by reabsorption.
4,320 mEq
of HCO3 –
FILTERED
Reabsorption of filtered HCO3 – occurs by
the secretion of H+ in the renal tubules.
About 4,380 mEq of H+ appear every day in
the renal tubule by means of filtration and
secretion.
Not all the H+ are excreted in urine.
Out of 4,380 mEq, about 4,280 to 4,330
mEq of H+ is utilized for the reabsorption of
filtered HCO3–
Only the remaining 50 to 100 mEq is
excreted.
 It results in the acidification of urine.
•Secretion of H+ into the renal tubules occurs by the
formation of carbonic acid.
•The carbonic acid is formed with the help of an
enzyme carbonic anhydrase.
•The carbonic acid immediately dissociates into H+
and HCO3 –
H+ is secreted into the lumen of proximal
convoluted tubule, distal convoluted tubule
and collecting duct.
Distal convoluted tubule and collecting duct
have a special type of cells called
intercalated cells (I cells) that are involved
in handling hydrogen and bicarbonate ions.
Secretion of H+ occurs by two
pumps:
Sodium-hydrogen
antiport pump
ATP-driven
proton pump.
SODIUM-HYDROGEN ANTIPORT PUMP
When sodium ion (Na+) is reabsorbed from the
tubular fluid into the tubular cell, H+ is secreted from
the cell into the tubular fluid in exchange for Na+.
The sodium hydrogen antiport pump present in the
tubular cellsis responsible for the exchange of Na+
and H+.
This type of sodium-hydrogen counter transport
occurs predominantly in distal convoluted tubule
ATP-DRIVEN PROTON PUMP
This is an additional pump for H+ secretion
in distal convoluted tubule and collecting
duct.
This pump operates by energy from ATP.
REMOVAL OF HYDROGEN IONS AND
ACIDIFICATION OF URINE
Excretion of H+ occurs by three
mechanisms:
Bicarbonate mechanism
Phosphate mechanism
Ammonia mechanism
BICARBONATE MECHANISM
All the filtered HCO3 – in the renal tubules is
reabsorbed.
About 80% of it is reabsorbed in proximal
convoluted tubule 15% in Henle loop and 5%
in distal convoluted tubule and collecting duct.
The reabsorption of HCO3 – utilizes the H+
secreted into the renal tubules.
„
H+ secreted into the renal tubule,
combines with filtered HCO3 – forming
carbonic acid (H2CO3).
Carbonic acid dissociates into carbon
dioxide and water in thepresence of
carbonic anhydrase. Carbon dioxide
and water enter the tubular cell.
In the tubular cells, carbon dioxide combines with
water to form carbonic acid.
It immediately dissociates into H+ and HCO3 –.
HCO3 – from the tubular cell enters the interstitium.
Simultaneously Na+ is reabsorbed from
the renal tubule under the influence of aldosterone.
HCO3 – combines with Na+ to form sodium
bicarbonate(NaHCO3).
Now, the H+ is secreted into the tubular
lumen from the cell in exchange for Na+ (Fig. 54.1).
Thus, for every hydrogen ion secreted into lumen of
tubule, one bicarbonate ion is reabsorbed from the
tubule. In this way, kidneys conserve the HCO3 –.
The reabsorption of filtered HCO3 – is an important
factor in maintaining pH of the body fluids.
PHOSPHATE MECHANISM
In the tubular cells, carbon dioxide combines with
water to form carbonic acid.
It immediately dissociates into H+ and HCO3 –.
HCO3 – from the tubular cell enters the
interstitium.
Simultaneously, Na+ is reabsorbed from renal tubule
under the influence of aldosterone.
Na+ enters the interstitium and combines with HCO3
–.
H+ is secreted into the tubular lumen from the cell in
exchange for Na+
H+, which is secreted into renal tubules, reacts
with phosphate buffer system.
It combines with sodium hydrogen phosphate to
form sodium dihydrogen phosphate.
Sodium dihydrogen phosphate is excreted in
urine.
The H+, which is added to urine in the form of
sodium dihydrogen, makes the urine acidic.
It happens mainly in distal tubule and collecting
duct because of the presence of large quantity of
sodium hydrogen phosphate in these segments
Excretion of hydrogen ions
in combination with phosphate ions
AMMONIA MECHANISM
This is the most important mechanism by which
kidneys excrete H+ and make the urine acidic.
In the tubular epithelial cells, ammonia is formed
when the amino acid glutamine is converted into
glutamic acid in the presence of the enzyme
glutaminase.
Ammonia is also formed by the deamination of
some of the amino acids such as glycine and
alanine
Ammonia (NH3) formed in tubular cells is secreted
into tubular lumen in exchange for sodium ion. Here,
it combines with H+ to form ammonium (NH4). The
tubular cell membrane is not permeable to
ammonium.
Therefore, it remains in the lumen and then excreted
into urine. Thus, H+ is added to urine in the form of
ammonium compounds resulting in acidification of
urine.
For each NH4 excreted one HCO3 – is added to
interstitial fluid.
This process takes place mostly in the proximal
convoluted tubule because glutamine is converted
into ammonia in the cells of this segment.
Thus, by excreting H+ and conserving HCO3
–, kidneys produce acidic urine and help to
maintain the acid-base balance of body fluids.
„
Excretion of hydrogen ions in combination with
ammonia
occurs when kidneys fail to excrete
metabolic acids.
occurs when kidneys excrete large
quantity of hydrogen.
Metabolic acidosis
Metabolic alkalosis
INTRODUCTION
 Blood vessels of kidneys are highly
specialized to facilitate the functions
of nephrons in the formayion of urine.
 In adults, during resting conditions
both the kidneys receive 1300 ml of
blood per minute or about 26% of the
cardiac output.
 Maximum blood supply to kidneys has
got the functional significance.
 Renal arteries suppy blood to the
kidneys.
RENAL BLOOD VESSELS
◈ Renal artery.
◈ Segmental artery.
◈ Arcuate artery.
◈ Interlobular artery
◈ Afferent arteriole.
◈ Glomerular cappilaries.
◈ Efferent arteriole.
◈ Peritubular capillaries/vasa recta.
◈ Venous system.
RENAL AUTOREGULATION
◈ Renal autoregulation is important to
maintain the glomerular filteration
rate.
◈ Blood flow to kidneys remains normal
even when the mean arterial blood
pressure very widely between 60mm
Hg and 180mm Hg.
◈ Two mechanisms,
1. Myogenic response.
2. Tubuloglomerular feedback.
SPECIAL FEATURES OF RENAL
CIRCULATION
◈ Renal arteries arise directly from the
aorta.so the high pressure in aorta
facilitates the high blood flow to the
kidneys.
◈ Whole amount of blood,which flows
to kidney has to pass through the
glomerular capillaries before entering
the venous system.
SPECIAL FEATURES OF RENAL
CIRCULATION
◈ Autoregulation of renal blood flow is
well establised.
◈ Peritubular capillaries from a low
pressure bed with a pressure of 8mm
hg to 10mm hg.this low pressure helps
tubular reabsorption.
FILTRATION IN THE GLOMERULUS
 Blood enters the glomerulus from a
branch of the renal artery.
 This blood is under high pressure.
 The capillary walls are thick.
 They are pierced with openings.
FILTRATION IN THE GLOMERULUS
 The plasma filters though the
membrane under pressure.
 Proteins do not pass.
 A membrane surrounds each capillary
of the glomerulus.
 The blood plasma is filtered at about
150 litres per day
HORMONAL REGULATION OF BP
◈ The following increases,
 Adrenaline
 Noradrenaline
 Thyroxine
 Aldosterone
 Vasopressin
 Angiotensin
 Serotonin
◈ The following decreases,
 vasoactive intestinal
polypeptide.
 Bradykinin.
 Peostaglandin.
 Histamine.
 Acetylcholine.
 Atrial Natriuretic peptide .
 Brain Natriuretic peptide.
 C – type Natriuretic
peptide.
REFERENCE :
◈ jaypee-essentials-of-medical-
physiology-6th-edition
◈ Guyton-and-Hall-Textbook-of-
Medical-Physiology-12th-Ed

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role of kindey in acid base balance

  • 1. ROLE OF KIDNEY IN BLOOD AND ACID BASE BALANCE
  • 2. ROLE OF KIDNEY IN BLOOD AND ACID-BASE BALANCE
  • 3.
  • 4. IMPORTANT ROLE MAINTANENCE OF ACID BASE BALANCE EXCRETING RETAINING H+ Hco3 -
  • 5. Metabolic activities in the body produce large quantity of acids (with lot of hydrogen ions), which threaten to push the body towards acidosis. ACIDIC IN NATURE PH 4.5 to 8.0
  • 6. However, kidneys prevent this by two ways: Reabsorption of bicarbonate ions (HCO3 ) Secretion of hydrogen ions (H+).
  • 7. It is called filtered load of HCO3 –. Excretion of this much HCO3 – in urine will affect the acid-base balance of body fluids. So, HCO3 – must be taken back from the renal tubule by reabsorption. 4,320 mEq of HCO3 – FILTERED
  • 8. Reabsorption of filtered HCO3 – occurs by the secretion of H+ in the renal tubules. About 4,380 mEq of H+ appear every day in the renal tubule by means of filtration and secretion.
  • 9. Not all the H+ are excreted in urine. Out of 4,380 mEq, about 4,280 to 4,330 mEq of H+ is utilized for the reabsorption of filtered HCO3– Only the remaining 50 to 100 mEq is excreted.  It results in the acidification of urine.
  • 10. •Secretion of H+ into the renal tubules occurs by the formation of carbonic acid. •The carbonic acid is formed with the help of an enzyme carbonic anhydrase. •The carbonic acid immediately dissociates into H+ and HCO3 –
  • 11. H+ is secreted into the lumen of proximal convoluted tubule, distal convoluted tubule and collecting duct. Distal convoluted tubule and collecting duct have a special type of cells called intercalated cells (I cells) that are involved in handling hydrogen and bicarbonate ions.
  • 12. Secretion of H+ occurs by two pumps: Sodium-hydrogen antiport pump ATP-driven proton pump.
  • 13. SODIUM-HYDROGEN ANTIPORT PUMP When sodium ion (Na+) is reabsorbed from the tubular fluid into the tubular cell, H+ is secreted from the cell into the tubular fluid in exchange for Na+. The sodium hydrogen antiport pump present in the tubular cellsis responsible for the exchange of Na+ and H+. This type of sodium-hydrogen counter transport occurs predominantly in distal convoluted tubule
  • 14. ATP-DRIVEN PROTON PUMP This is an additional pump for H+ secretion in distal convoluted tubule and collecting duct. This pump operates by energy from ATP.
  • 15. REMOVAL OF HYDROGEN IONS AND ACIDIFICATION OF URINE Excretion of H+ occurs by three mechanisms: Bicarbonate mechanism Phosphate mechanism Ammonia mechanism
  • 16. BICARBONATE MECHANISM All the filtered HCO3 – in the renal tubules is reabsorbed. About 80% of it is reabsorbed in proximal convoluted tubule 15% in Henle loop and 5% in distal convoluted tubule and collecting duct. The reabsorption of HCO3 – utilizes the H+ secreted into the renal tubules. „
  • 17. H+ secreted into the renal tubule, combines with filtered HCO3 – forming carbonic acid (H2CO3). Carbonic acid dissociates into carbon dioxide and water in thepresence of carbonic anhydrase. Carbon dioxide and water enter the tubular cell.
  • 18. In the tubular cells, carbon dioxide combines with water to form carbonic acid. It immediately dissociates into H+ and HCO3 –. HCO3 – from the tubular cell enters the interstitium. Simultaneously Na+ is reabsorbed from the renal tubule under the influence of aldosterone. HCO3 – combines with Na+ to form sodium bicarbonate(NaHCO3). Now, the H+ is secreted into the tubular lumen from the cell in exchange for Na+ (Fig. 54.1).
  • 19. Thus, for every hydrogen ion secreted into lumen of tubule, one bicarbonate ion is reabsorbed from the tubule. In this way, kidneys conserve the HCO3 –. The reabsorption of filtered HCO3 – is an important factor in maintaining pH of the body fluids.
  • 20.
  • 21. PHOSPHATE MECHANISM In the tubular cells, carbon dioxide combines with water to form carbonic acid. It immediately dissociates into H+ and HCO3 –. HCO3 – from the tubular cell enters the interstitium. Simultaneously, Na+ is reabsorbed from renal tubule under the influence of aldosterone. Na+ enters the interstitium and combines with HCO3 –. H+ is secreted into the tubular lumen from the cell in exchange for Na+
  • 22. H+, which is secreted into renal tubules, reacts with phosphate buffer system. It combines with sodium hydrogen phosphate to form sodium dihydrogen phosphate. Sodium dihydrogen phosphate is excreted in urine. The H+, which is added to urine in the form of sodium dihydrogen, makes the urine acidic. It happens mainly in distal tubule and collecting duct because of the presence of large quantity of sodium hydrogen phosphate in these segments
  • 23. Excretion of hydrogen ions in combination with phosphate ions
  • 24. AMMONIA MECHANISM This is the most important mechanism by which kidneys excrete H+ and make the urine acidic. In the tubular epithelial cells, ammonia is formed when the amino acid glutamine is converted into glutamic acid in the presence of the enzyme glutaminase. Ammonia is also formed by the deamination of some of the amino acids such as glycine and alanine
  • 25. Ammonia (NH3) formed in tubular cells is secreted into tubular lumen in exchange for sodium ion. Here, it combines with H+ to form ammonium (NH4). The tubular cell membrane is not permeable to ammonium. Therefore, it remains in the lumen and then excreted into urine. Thus, H+ is added to urine in the form of ammonium compounds resulting in acidification of urine. For each NH4 excreted one HCO3 – is added to interstitial fluid.
  • 26. This process takes place mostly in the proximal convoluted tubule because glutamine is converted into ammonia in the cells of this segment. Thus, by excreting H+ and conserving HCO3 –, kidneys produce acidic urine and help to maintain the acid-base balance of body fluids. „
  • 27. Excretion of hydrogen ions in combination with ammonia
  • 28. occurs when kidneys fail to excrete metabolic acids. occurs when kidneys excrete large quantity of hydrogen. Metabolic acidosis Metabolic alkalosis
  • 29.
  • 30. INTRODUCTION  Blood vessels of kidneys are highly specialized to facilitate the functions of nephrons in the formayion of urine.  In adults, during resting conditions both the kidneys receive 1300 ml of blood per minute or about 26% of the cardiac output.
  • 31.  Maximum blood supply to kidneys has got the functional significance.  Renal arteries suppy blood to the kidneys.
  • 32.
  • 33.
  • 34. RENAL BLOOD VESSELS ◈ Renal artery. ◈ Segmental artery. ◈ Arcuate artery. ◈ Interlobular artery ◈ Afferent arteriole. ◈ Glomerular cappilaries. ◈ Efferent arteriole. ◈ Peritubular capillaries/vasa recta. ◈ Venous system.
  • 35.
  • 36. RENAL AUTOREGULATION ◈ Renal autoregulation is important to maintain the glomerular filteration rate. ◈ Blood flow to kidneys remains normal even when the mean arterial blood pressure very widely between 60mm Hg and 180mm Hg. ◈ Two mechanisms, 1. Myogenic response. 2. Tubuloglomerular feedback.
  • 37. SPECIAL FEATURES OF RENAL CIRCULATION ◈ Renal arteries arise directly from the aorta.so the high pressure in aorta facilitates the high blood flow to the kidneys. ◈ Whole amount of blood,which flows to kidney has to pass through the glomerular capillaries before entering the venous system.
  • 38. SPECIAL FEATURES OF RENAL CIRCULATION ◈ Autoregulation of renal blood flow is well establised. ◈ Peritubular capillaries from a low pressure bed with a pressure of 8mm hg to 10mm hg.this low pressure helps tubular reabsorption.
  • 39. FILTRATION IN THE GLOMERULUS  Blood enters the glomerulus from a branch of the renal artery.  This blood is under high pressure.  The capillary walls are thick.  They are pierced with openings.
  • 40. FILTRATION IN THE GLOMERULUS  The plasma filters though the membrane under pressure.  Proteins do not pass.  A membrane surrounds each capillary of the glomerulus.  The blood plasma is filtered at about 150 litres per day
  • 41. HORMONAL REGULATION OF BP ◈ The following increases,  Adrenaline  Noradrenaline  Thyroxine  Aldosterone  Vasopressin  Angiotensin  Serotonin
  • 42. ◈ The following decreases,  vasoactive intestinal polypeptide.  Bradykinin.  Peostaglandin.  Histamine.  Acetylcholine.  Atrial Natriuretic peptide .  Brain Natriuretic peptide.  C – type Natriuretic peptide.
  • 43. REFERENCE : ◈ jaypee-essentials-of-medical- physiology-6th-edition ◈ Guyton-and-Hall-Textbook-of- Medical-Physiology-12th-Ed