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TEERTHANKER MAHAVEER COLLEGE OF PHARMACY
TMU, MORADABAD
DIURETICS
A
PRESENTATION
FOR PARTIAL
FULLFILMENT OF
MASTER OF PHARMACY
COURSE CODE :- MPL106
(PHARMACOLOGY)
PRESENTED BY:-
MOHIT PANDEY
M.PHARM 1 SEM
(PHARMACOLOGY)
PRESENTED TO:-
DR. K.K. SHARMA
PROFESSOR
PHARMACOLOGY
INTRODUCTION
Diuretics are substances that slow renal reabsorption of water and thereby
cause diuresis (an elevated urine flow rate), which in turn reduces blood
volume.
The kidney regulates the ionic composition and volume of urine by active
reabsorption or secretion of ions and/or passive reabsorption of water.
Diuretics are drugs that increase the volume of urine excreted.
NATRIURETICS – which increase the loss of sodium in urine.
FIG:- GENERAL DIAGRAM OF KIDNEY CONSISTING OF NEPHRONS
FUNCTION OF KIDNEY
• Functional Unit :- NEPHRON
• 1.2 MILLION NEPHRON IN ONE KIDNEY
Maintain the balance of Na+ , K+, Cl- , urea , uric acid ,bicarbonate and ammonia
in the body.
Also regulate the balance between blood–body fluid.
Glomerular Filtration Rate – 120ML/MINUTE
NORMAL URINE OUTPUT = 1.5L/DAY
Urine Output – 400-500ml/day = OLIGUREA
Urine output - 3500ml/day = POLYUREA
CLASSIFICATION OF DIURETICS
HIGH CEILING / LOOP DIURETICS
• Loop diuretics include furosemide, torsemide,
azosemide, and bumetanide
• SITE OF ACTION - thick ascending limb of the
loop of Henle.
• Where 20% -30% of filtered NaCl is reabsorbed.
• Loop diuretics acts by bind to the Na-K-2Cl
cotransport protein and inhibit its action, impairing
reabsorption of Na+
, K+, and Cl- . Leads to
hypochloremia in blood.
THIAZIDE DIURETICS (MEDIUM EFFICACY)
• Thiazide diuretics are Chlorothiazide,
chlorthalidone.
• SITE OF ACTION - The thiazide diuretics
act mainly in the distal convoluted tubule to
decrease the reabsorption of Na+ by inhibition
of a Na+ /Cl- cotransporter. As a result, these
drugs increase the concentration of Na+ and
Cl− in the tubular fluid.
• Therapeutic use- hypertension , C.H.F.
• Hypercalciuria- to prevent renal stone.
• A/E- electrolyte imbalance, hypotension (due
to depletion of volume)
CARBONIC ANHYDRASE INHIBITOR
• Acetazolamide Act by suppressing the activity
of carbonic anhydrase enzyme.
• SITE OF ACTION- PROXIMAL
CONVOLUTED TUBULE.
• THERAPEUTIC USE- used to treat glaucoma
(Lowering of intraocular tension due to decreased
formation of aqueous humour (aqueous is rich
in HCO3 ¯ )
• Carbonic anhydrase catalyzes this reaction:-
CO2 + H2O ⇋ HCO3
– + H+
• Physiological of carbonic anhydrase enzyme:-
1) The acid–base homeostasis balance (by
secreting and excreting protons)
2) The bicarbonate reabsorption process.
Potassium-Sparing Diuretics
• Potassium sparing diuretics primarily acts on late distal convoluted tube and
collecting duct of the nephron.
• They act by following mechanism:-
1. By antagonizing aldosterone action-Aldosterone enhances activity of
sodium–potassium pumps results in increase secretion of K+ and
reabsorption of Na+; increases reabsorption of water, which increases blood
volume and blood pressure.
E.g. Spironolactone, Eplerenone.
2. By inhibit Na+ channel responsible for Na+ reabsorption and K+ excretion.
E.g. Amiloride, triamterene.
ALDOSTERONE ANTAGONIST
• ALDOSTERONE acts by combining with an intracellular mineralocorticoid receptor (MR) which
induces the formation of ‘aldosterone-induced proteins’ (AIPs).
• The AIPs promote Na+ reabsorption and K+ secretion.
• Aldosterone antagonist combines with MR and inhibits the formation of AIPs in a competitive manner.
• E.g. SPIRONOLACTONE
Na+ channel inhibitor
• Na+ channel inhibitor block the luminal Na+ channels and indirectly inhibit K+ excretion,
while the net excess loss of Na+ is minor, because this is only a small fraction of the total
amount of Na+ excreted in urine.
OSMOTIC DIURETICS
• E.g. - Mannitol ,a nonelectrolyte of low molecular weight.
• Pharmacologically inert , can be given to raise osmolarity of plasma and
tubular fluid. Freely filtered at the glomerulus and undergoes limited
reabsorption.
• SITE OF ACTION – PCT AND LOOP OF HENLE.
• Mannitol limit tubular water and electrolyte reabsorption.
• It acts to Expands extracellular fluid volume (because it does not enter cells,
mannitol draws water from the intracellular compartment).
REFERENCES
• Tripathi KD. Essentials of medical pharmacology. JP Medical Ltd;
2013 Sep 30.
• Whalen K. Lippincott® illustrated reviews: pharmacology. Wolters
kluwer India Pvt Ltd; 2018 Oct 25.
• Tortora GJ, Derrickson BH. Principles of anatomy and physiology.
John Wiley & Sons; 2018 May 15.
• Bell R, Mandalia R. Diuretics and the kidney. BJA education. 2022
Jun 1;22(6):216-23.
• Roush GC, Kaur R, Ernst ME. Diuretics: a review and update.
Journal of cardiovascular pharmacology and therapeutics. 2014
Jan;19(1):5-13.

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A presentation on DIURETICS and their potential

  • 1. TEERTHANKER MAHAVEER COLLEGE OF PHARMACY TMU, MORADABAD DIURETICS A PRESENTATION FOR PARTIAL FULLFILMENT OF MASTER OF PHARMACY COURSE CODE :- MPL106 (PHARMACOLOGY) PRESENTED BY:- MOHIT PANDEY M.PHARM 1 SEM (PHARMACOLOGY) PRESENTED TO:- DR. K.K. SHARMA PROFESSOR PHARMACOLOGY
  • 2. INTRODUCTION Diuretics are substances that slow renal reabsorption of water and thereby cause diuresis (an elevated urine flow rate), which in turn reduces blood volume. The kidney regulates the ionic composition and volume of urine by active reabsorption or secretion of ions and/or passive reabsorption of water. Diuretics are drugs that increase the volume of urine excreted. NATRIURETICS – which increase the loss of sodium in urine.
  • 3. FIG:- GENERAL DIAGRAM OF KIDNEY CONSISTING OF NEPHRONS
  • 4. FUNCTION OF KIDNEY • Functional Unit :- NEPHRON • 1.2 MILLION NEPHRON IN ONE KIDNEY Maintain the balance of Na+ , K+, Cl- , urea , uric acid ,bicarbonate and ammonia in the body. Also regulate the balance between blood–body fluid. Glomerular Filtration Rate – 120ML/MINUTE NORMAL URINE OUTPUT = 1.5L/DAY Urine Output – 400-500ml/day = OLIGUREA Urine output - 3500ml/day = POLYUREA
  • 6.
  • 7. HIGH CEILING / LOOP DIURETICS • Loop diuretics include furosemide, torsemide, azosemide, and bumetanide • SITE OF ACTION - thick ascending limb of the loop of Henle. • Where 20% -30% of filtered NaCl is reabsorbed. • Loop diuretics acts by bind to the Na-K-2Cl cotransport protein and inhibit its action, impairing reabsorption of Na+ , K+, and Cl- . Leads to hypochloremia in blood.
  • 8. THIAZIDE DIURETICS (MEDIUM EFFICACY) • Thiazide diuretics are Chlorothiazide, chlorthalidone. • SITE OF ACTION - The thiazide diuretics act mainly in the distal convoluted tubule to decrease the reabsorption of Na+ by inhibition of a Na+ /Cl- cotransporter. As a result, these drugs increase the concentration of Na+ and Cl− in the tubular fluid. • Therapeutic use- hypertension , C.H.F. • Hypercalciuria- to prevent renal stone. • A/E- electrolyte imbalance, hypotension (due to depletion of volume)
  • 9. CARBONIC ANHYDRASE INHIBITOR • Acetazolamide Act by suppressing the activity of carbonic anhydrase enzyme. • SITE OF ACTION- PROXIMAL CONVOLUTED TUBULE. • THERAPEUTIC USE- used to treat glaucoma (Lowering of intraocular tension due to decreased formation of aqueous humour (aqueous is rich in HCO3 ¯ ) • Carbonic anhydrase catalyzes this reaction:- CO2 + H2O ⇋ HCO3 – + H+ • Physiological of carbonic anhydrase enzyme:- 1) The acid–base homeostasis balance (by secreting and excreting protons) 2) The bicarbonate reabsorption process.
  • 10. Potassium-Sparing Diuretics • Potassium sparing diuretics primarily acts on late distal convoluted tube and collecting duct of the nephron. • They act by following mechanism:- 1. By antagonizing aldosterone action-Aldosterone enhances activity of sodium–potassium pumps results in increase secretion of K+ and reabsorption of Na+; increases reabsorption of water, which increases blood volume and blood pressure. E.g. Spironolactone, Eplerenone. 2. By inhibit Na+ channel responsible for Na+ reabsorption and K+ excretion. E.g. Amiloride, triamterene.
  • 11. ALDOSTERONE ANTAGONIST • ALDOSTERONE acts by combining with an intracellular mineralocorticoid receptor (MR) which induces the formation of ‘aldosterone-induced proteins’ (AIPs). • The AIPs promote Na+ reabsorption and K+ secretion. • Aldosterone antagonist combines with MR and inhibits the formation of AIPs in a competitive manner. • E.g. SPIRONOLACTONE Na+ channel inhibitor • Na+ channel inhibitor block the luminal Na+ channels and indirectly inhibit K+ excretion, while the net excess loss of Na+ is minor, because this is only a small fraction of the total amount of Na+ excreted in urine.
  • 12. OSMOTIC DIURETICS • E.g. - Mannitol ,a nonelectrolyte of low molecular weight. • Pharmacologically inert , can be given to raise osmolarity of plasma and tubular fluid. Freely filtered at the glomerulus and undergoes limited reabsorption. • SITE OF ACTION – PCT AND LOOP OF HENLE. • Mannitol limit tubular water and electrolyte reabsorption. • It acts to Expands extracellular fluid volume (because it does not enter cells, mannitol draws water from the intracellular compartment).
  • 13. REFERENCES • Tripathi KD. Essentials of medical pharmacology. JP Medical Ltd; 2013 Sep 30. • Whalen K. Lippincott® illustrated reviews: pharmacology. Wolters kluwer India Pvt Ltd; 2018 Oct 25. • Tortora GJ, Derrickson BH. Principles of anatomy and physiology. John Wiley & Sons; 2018 May 15. • Bell R, Mandalia R. Diuretics and the kidney. BJA education. 2022 Jun 1;22(6):216-23. • Roush GC, Kaur R, Ernst ME. Diuretics: a review and update. Journal of cardiovascular pharmacology and therapeutics. 2014 Jan;19(1):5-13.