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DIURETICS
by
SROTA DAWN.
B.PHARM(3RD YEAR)
Definition: A diuretic can be
defined as a chemical that
increases the rate of urine
formation.
The PRIMARY ACTION: Direct
inhibition of Na+ transport along
one or more of the four major
anatomical sites.
4 major
sites of
nephron:
SITE 1 : The “PCT”
SITE 2 : The thick
ascending limb of
“HENLE’s LOOP”
SITE 3 : The “DCT”
SITE4:The“collecting
tubule &
cortical collecting
Tubule”
SITE OF
ACTION
TYPE OF
DIURETICS
EXAMPLES
1. SITE 
DIURETICS
Carbonic anhydrase
inhibitors
Acetazolamide
, methazolamide
, dichlorphenamide
etc.
2. SITE 
DIURETICS
Loop diuretics organomercurals,furos
emide,bumetanide,azo
semideetc
3. SITE 
DIURETICS
Thiazide & thiazide like
diuretics
Chlorthiazide,
benzthiazide,
hydrochlorthiazide etc.
4. SITE 
DIURETICS
Potassium-sparing
diuretics
Spironolactones
Triamterene,amiloride
5.OTHERS Osmotic diuretics Mannitol, Isosorbide,
glycerol
SITE 1 DIURETICS:
CARBONIC
ANHYDRASE INHIBITORS
MOA:INHIBITION OF
CAase
1. intracellularly
2. In luminal brush
border
effects:
reabsorption of
Na+,HNO3-
Seondary effect:
 excretion of K+
USE:
1.Glaucoma
2.Promote exeretion of
weakly acidic drug
3. In epilepsy
4. Acute mountain
sickness
ADR:
1. metabolic acidosis
2.hypokalemia
3.20%  in GFR
4.sulphonamide associat
ed hypersensitivity reactions.
SITE 2 DIURETICS:
HIGH- CEILING Or LOOP DIURETICS
MOA:
1.Inhibit the 1Na+/1K+/2Cl-
cotransport system
EFFECTS:
Reabsorption of Na+, K+,C l-
Use:
1.edemacardiac,hepatic,renal
2.Acute pulmonary edema
associated with CHF
3.HYPERCALCAEMIA & Renal
calcium stones
ADR:
1.Sulfnamoyl moiety associated
hypersensitivity reactions
2.Hypokalemia intensifies the
Toxicity of cardiac glycosidesSITE 2: Henle's loop
SITE 3 DIURETICS:
THIAZIDE DIURETICS
MOA:
All of these diuretics block the
Na+ reabsorption by inhibiting
The LUMINAL MEMBRANE
bound Na+/Cl- cotransport
system
Effects:
Naturetic,chloruretic,saluretic,
kaluretic& weak
bicarbonaturetic
Use:
1.edema associated CHF
2.hypertension(uncomplicated)
ADR:
1.Hypersensitivity reaction
2.Hypokalemia
3.cardiac output
SITE 4 : COLLECTING TUBULE&
CORTICAL COLLECTING TUBULE
SITE 4 DIURETICS:
POTASSIUM SPARING
DIURETICS
MOA:
SPIROLACTONEs:
inhibit reabsorption of Na+ by
compititively inhibiting the actions
of ALDOSTERONE
OTHERS:
Plug the Na+ channels of
Luminal membrane
EFFECTS:
Na+,Cl- exeretion without
Concomitant increase in
urinary excretion rate of K+
USE:
1.Combination therapy with
site 2&3 diuretics
2.Mild edema associated CHF
3.HYPERTENSION
OTHERS:
MANNITOL:
High luminal fluid concentration of mannitol create an
osmotic effect .this effect prevents the reabsorption of
Water.
Use:
Used in hospital setting to keep the nephrons open.
Decrease CSF volume & pressure.
THANK YOU

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Diuretics by srota dawn

  • 2. Definition: A diuretic can be defined as a chemical that increases the rate of urine formation. The PRIMARY ACTION: Direct inhibition of Na+ transport along one or more of the four major anatomical sites.
  • 3. 4 major sites of nephron: SITE 1 : The “PCT” SITE 2 : The thick ascending limb of “HENLE’s LOOP” SITE 3 : The “DCT” SITE4:The“collecting tubule & cortical collecting Tubule”
  • 4. SITE OF ACTION TYPE OF DIURETICS EXAMPLES 1. SITE  DIURETICS Carbonic anhydrase inhibitors Acetazolamide , methazolamide , dichlorphenamide etc. 2. SITE  DIURETICS Loop diuretics organomercurals,furos emide,bumetanide,azo semideetc 3. SITE  DIURETICS Thiazide & thiazide like diuretics Chlorthiazide, benzthiazide, hydrochlorthiazide etc. 4. SITE  DIURETICS Potassium-sparing diuretics Spironolactones Triamterene,amiloride 5.OTHERS Osmotic diuretics Mannitol, Isosorbide, glycerol
  • 5. SITE 1 DIURETICS: CARBONIC ANHYDRASE INHIBITORS MOA:INHIBITION OF CAase 1. intracellularly 2. In luminal brush border effects: reabsorption of Na+,HNO3- Seondary effect:  excretion of K+ USE: 1.Glaucoma 2.Promote exeretion of weakly acidic drug 3. In epilepsy 4. Acute mountain sickness ADR: 1. metabolic acidosis 2.hypokalemia 3.20%  in GFR 4.sulphonamide associat ed hypersensitivity reactions.
  • 6. SITE 2 DIURETICS: HIGH- CEILING Or LOOP DIURETICS MOA: 1.Inhibit the 1Na+/1K+/2Cl- cotransport system EFFECTS: Reabsorption of Na+, K+,C l- Use: 1.edemacardiac,hepatic,renal 2.Acute pulmonary edema associated with CHF 3.HYPERCALCAEMIA & Renal calcium stones ADR: 1.Sulfnamoyl moiety associated hypersensitivity reactions 2.Hypokalemia intensifies the Toxicity of cardiac glycosidesSITE 2: Henle's loop
  • 7. SITE 3 DIURETICS: THIAZIDE DIURETICS MOA: All of these diuretics block the Na+ reabsorption by inhibiting The LUMINAL MEMBRANE bound Na+/Cl- cotransport system Effects: Naturetic,chloruretic,saluretic, kaluretic& weak bicarbonaturetic Use: 1.edema associated CHF 2.hypertension(uncomplicated) ADR: 1.Hypersensitivity reaction 2.Hypokalemia 3.cardiac output
  • 8. SITE 4 : COLLECTING TUBULE& CORTICAL COLLECTING TUBULE SITE 4 DIURETICS: POTASSIUM SPARING DIURETICS MOA: SPIROLACTONEs: inhibit reabsorption of Na+ by compititively inhibiting the actions of ALDOSTERONE OTHERS: Plug the Na+ channels of Luminal membrane EFFECTS: Na+,Cl- exeretion without Concomitant increase in urinary excretion rate of K+ USE: 1.Combination therapy with site 2&3 diuretics 2.Mild edema associated CHF 3.HYPERTENSION
  • 9. OTHERS: MANNITOL: High luminal fluid concentration of mannitol create an osmotic effect .this effect prevents the reabsorption of Water. Use: Used in hospital setting to keep the nephrons open. Decrease CSF volume & pressure.