DIURETICS

Dr. Hiwa K. Saaed

PhD Pharmacology & Toxicology

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 Diuretics:
• mainly promotes the excretion of the
(Na+), (Cl-) or (HCO3-) and water,
• the net result being:
– Increase the urine flow,
– change urine pH
– change the ionic composition of the urine and
blood.
 Drugs used in renal disorders
I. drugs that modify salt excretion:
A. PCT: carbonic anhydrase inhibitors
B. TAL: loop diuretics
C. DCT: thiazides
D. CCT; K-spairing diuretics
E. Osmotic diuretics; manitol
II. Drugs that modify water excretion
A. Osmotic diuretics: manitol
B. ADH agonists: desmopressin
C. ADH antagonists: conivaptan, demeclocycline, lithium
 Diuretics:
Diuretics are very effective in the treatment of:

• Edema: CHF, pregnancy, & nutritional

• nephrotic syndrome
• diabetes insipidus
• hypertension
• cirrhosis of liver
• and also lower the intracellular and CSF
pressure.

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 Introduction
• Kidney: 1.3 million nephron each
• Glomerular filtration:
– Receive 25% of cardiac output
– Filtration rate: 100-120 ml/minute
– 180 L of glomerular filtrate/day
• Tubular reaborption:
– Reabsorption of 99% of glomerular filtrate  only + 1
ml/min excreted as urine
– 1.5 L/day of urine.
• Tubular secretion

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The excretion by kidney is dependent on: glomerular
filtration, tubular reabsorption and tubular secretion.

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 Introduction
• Proximal tubules:
– Reabsorption of 60-70% Na+
– Permeable to water  isotonic urine
– Isosmotic reabsorption of amino acids, glucose, cations
• Loop of Henle:
– Thin descending limb: most active water reabsorption
– Thick ascending limb:
• Reabsorption of Na+,
• Water impermeable  diluting segment
• Distal tubules:
– Na+ reabsorption
• Collecting duct: selectively water permeable
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 Diuretic Drug Groups
• the diuretics acting in these segments each have
different MOA ? b the mechanism for reabsorption
of salt & water different in each 4 segments,
• Most diuretics act from the luminal site of the
membrane & must be present in the urine:
– They are filtered at the glomerulus
– some are also sec by the weak acid sec in the proximal
tubule,
– an exception is the aldosterone receptor antagonist
enter CCT from basolateral side.

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Electrolyte Transport and Site of Action of Diuretics
Site and Mechanisms of Actions of Diuretics
Diuretics Site of Action Mechanism

Osmotic Diuretic 1. Proximal tubules Inhibition of water and Na+

2. Loop of Henle reabsorption
3. Collecting duct

Carbonic Anhydrase Proximal tubules Inhibition of bicarbonate

Inhibitor (CA-I) reabsorption
Loop Diuretic Loop of Henle Inhibition of Na+, K+, Cl-
(thick ascending limb) cotransport
Thiazide Early distal tubule Inhibition of Na+, Cl-
cotransport
K+ sparing diuretics Late distal tubule Inhibition of Na+
Collecting duct reabsorption and K+ secretion

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 Carbonic Anhydrase Inhibitor
Acetazolamide (S derivatives)

Mechanism of Actions
• Kidney: self limited diuresis 2-3 days
– Carbonic anhydrase catalyzes : CO2+H2O H2CO3
– H+ ion produced by the breakdown of H2CO3, exchanged
for Na+ & is also combined with HCO3- in the lumen of
the PCT
– Inhibition of Bicarbonate (HCO3-) reabsorption
– Reduces Na+-H+-exchange  NaHCO3 is excreted along
with H2O

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Mechanism of Action of CA-I

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 Adverse Effects and Contraindications
• Metabolic acidosis
• Renal stones (Phosphate and Calcium stone)
• Renal potassium wasting; (NaHCO3- ) enhances K+
secretion
• Diuresis is self limiting within 2-3 days?

• AE: Drowsiness, paresthesia, disorientation, renal stone

(in case of urine alkalinization)
Contraindication
– Liver cirrhosis (CA-I inhibits conversion of NH3 to NH4)
 NH3 increased  encephalopathy

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 Indications of CA-I
• Glaucoma (Eye: not self limiting effect)
– Orally acetazolamide
– Topically dorzolamide, brinzolamide
• Prevent mountain sickness (high altitude) sickness
inhibit sec of bicarbonate by the choroid plexus;
Acidosis of the CSF results in hyperventilation
• Urinary alkalinization: preventing uric acid and
cystine stones
• Used for their diuretic effect only if edema is
accompanied by significant Metabolic alkalosis
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 Thiazides
• Hydrochlorothiazide (prototype), Chlorothiazide,
Bendroflumethiazide, Chlorthalidone, Metolazone,
Indapamide
• All are sulfonamide derivatives, t1/2 6-12 hrs
Mechanism of Actions
– Thiazides are secreted by proximal tubules but works
in DCT
– Inhibit Na+-Cl- symporter from the lumen to tubular
cells  increase Na+, Cl- excretion (and water)
– Some thiazides have weak CA-I effect

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Mechanism of Action of Thiazide

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 Effects on Electrolytes
• Increases Na+ and Cl- excretion
• Hypokalemic metabolic alkalosis; K+ excretion
also increase associated w/ increased Na+ in
distal tubules.
• Inhibits uric acid secretion hyperuricemia
and gout
• Decreases Ca2+ excretion
 tends to increase plasma Ca++
 Retards osteoporotic process
• Increases Mg2+ excretion

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 Adverse Effects

– Hypo K+  Increased risk of digitalis toxicity

– Hypo Na+, Hypo Mg++
– Hyperuricemia  caution in gout arthritis
– Hyperglycemia and hypercholesterolemia 
not favorable for DM and dyslipidemia
(although not contraindicated)
– (Indapamid has less effects on lipid and uric acid)
– Hypercalcemia (long-term)  good for elderly
– Sexual dysfunction
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 Interactions
• Increases the risk of arrhythmia when combined
w/ digitalis, quinidine and other antiarrhythmias
• Reduces efficacy of anticoagulant and uricosuric
• Reduces the efficacy oral antidiabetics
• NSAID reduce the efficacy of thiazide

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 Indications of Thiazides
• Hypertension (single drug or in combination)
• Chronic, mild- heart failure
• Edema (loop diuretic is preferable)
• Nephrogenic Diabetes insipidus
• Prevention of Ca++ excretion in osteoporosis and
calcium nephrolithiasis

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 Loop Diuretics
• Furosemide, torasemide, bumetanide: Are sulfonamide
derivatives
• ethacrynic acid is a phenoxyacetic acid derivative
• Site of action: thick ascending limb of Henle
• Mechanism:
– Loop diuretics should be excreted into the
lumen
– Inhibits Na+, K+, 2Cl- symporter  significantly
increases the excretion of Na+, K+, Cl-
– Osmotic gradient for water reabsorption is also
decreased  increasing water excretion
– Ca2+ and Mg2+ are excreted as well.
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Mechanism of Action of Loop Diuretic

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 Interactions

• Concomitant use w/ aminoglycoside or cisplatin

increases the risk of nephrotoxicity and
ototoxicity
• PGs are important in maintaining GF; NSAID
reduces the effects of diuretics
• Probenecid reduces the effects of diuretics by
inhibiting its secretion into the lumen.

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 Indications
• Congestive heart failure (1st line drug)
• Acute pulmonary edema
• Edema due to renal failure, nephrotic syndrome,
ascites
• Hypercalcemia (that induced by malignancy)
• Severe hypertension
• Force diuresis during drug/chemical intoxication
(drug that excreted through the kidney in active
form)

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 Adverse effects
• Hypovolemic metabolic alkalosis
• Ototoxicity
• Typical sulfonamide allergy

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 Potassium Sparing Diuretics

1. Na+ channel inhibitor (Amiloride, triamterene)

 Inhibit Na+ reabsorption  Na+ excretion
 Reduced K+ secretion  K+ retention
2. Aldosterone antagonist (Spironolactone,
eplerenone) Steroid derivatives
– Aldosterone induces the expression of Na/K-
ATPase and Na+ channel
– Spironolactone and eplerenone blocks aldosterone
receptor  reduces Na+ reabsorption and K+
secretion
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Potassium Sparing Diuretics
 Potassium Sparing Diuretics
• Potassium sparing diuretic has a weak diuretic
action
• Usually used in combination w/ other diuretic:
– Potentiation of diuretic and antihypertensive effects
– Prevents hypokalemia
• Spironolactone is metabolized to its active
metabolite, canrenone.
• Long term use of spironolactone can prevent
myocardial hypertrophy and myocardial fibrosis

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 Adverse Effects
Spironolactone
• Hyperkalemia
• Antiandrogenic effect
» gynecomastia,
» decrease of libido, impotence,
» menstrual disturbance.

• Megaloblastic anemia: Triamterene (folate

antagonist)

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 INDICATIONS
• Antihypertension:
– In combination w/ other antihypertensives
– To increase the effect and to prevent hypokalemia
– Aldosteronism (that occur in cirrhosis)
CONTRAINDICATIONS/PRECAUTIONS
• Conditions that prone to hyperkalemia:
– Renal failure
– Should never be combined with ACE-inhibition, ARB,
NSAID, K+ supplementation

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 Osmotic Diuretics (OD)
• Mannitol (prototype),
• Others rarely used: urea, glycerin, isosorbide
• Properties of osmotic diuretics:
– Freely filtrated by glomerulus
– Negligible tubular reabsorption
– Chemically inert
– Usually non metabolized

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 Pharmacokinetics
• Mannitol and urea: intravenous
• Glycerin and isosorbide: Can be administered
orally
• Metabolism:
– glycerin 80% metabolized
– mannitol 20%
– Urea, isosorbide: not metabolized
• Excretion: renal

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 Mechanism of Action
• OD is filtrated and increases osmotic pressure in
tubular lumen
• Hence, increases excretion of water and
electrolytes (Na+, K+, Ca++, Mg++, HCO3-,
phosphate) ↑volume of urine & rate of urine flow
through the tubule
• Mannitol can also reduce brain volume and
intracranial pressure by osmotically extracting
water from the tissue into the blood
• A similar effect occurs in the eye
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 Indications
• Glaucoma (rare) ↓IOP
• Brain edema ↓brain volume & pressure
– mannitol and urea are given before and after
brain surgery
• Disequilibrium syndrome after hemodialysis
• Solute overload in sever hemolysis and
rhabdomyolysis
• Prophylaxis of ATN (acute tubular necrosis) due
to contrast media, surgery, and trauma.
– NaCl 0.45% can also be used

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 Adverse Effects
• Removal of water from the I.C compartments 
Initial increase of plasma volume  potentially
dangerous in heart failure and pulmonary
edema  Hypo Na+  headache, nausea,
vomiting
• Water exc.  Hypovolemia  hypernatremia
• Hypersensitivity reaction
• Vein thrombosis, pain if extravasation (urea)
• Hyperglycemia, glycosuria (glycerin)

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 Antidiuretic Hormone (ADH) Agonists and Antagonists

• ADH & Desmopressin are ADH Agonists

• Peptides must be given parenterally(rapid degradation by
trypsin)
• Secretion of ADH increase in response to:
–  Plasma osmolarity
– Hypovolemia, hypotension (bleeding, dehydration)

• Demeclocycline and conivaptan are ADH

antagonists
• Lithium has ADH antagonist effect but never used
for this purpose

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 Mechanism of Action
• Works in ascending limb of Henle’s loop and
collecting ducts
• Two kind of receptors:
– V1: vascular smooth muscle vasoconstriction
– V2: kidney  increase water permeability of
tubular epithelium  water reabsorption

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 ADH
• ADH facilitates water reabsorption from the
collecting tubule by:
• activation of V2 receptors(coupled to GS,
stimulate AC) increase cAMP
• cause insertion of additional aquaporin AQP2
water channels into the luminal membrane in
this part of the tubule

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 ADH antagonists
• Conivaptan is an ADH inhibitor at V1a and V2
receptors
• Demeclocycline and Li inhibit the action of ADH
at some point distal to the generation of cAMP
and presumably the insertion of water channels
into the membrane.

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 Clinical uses of ADH Agonists
• ADH and desmopressin reduce urine volume
and concentrate it, are useful in Pitutary
Diabetes Insipidus (not for nephrogenic DI Rx
by salt restriction, thizides and loop diuretics)
• DI due to head trauma or brain surgery
• Gastrointestinal bleeding due to portal
hypertension (by reducing mesenteric blood
flow)

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 Clinical uses of ADH Antagonists
• Oppose the actions of ADH and other naturally
occurring peptides (certain tumors; small cell
carcinoma of the lung) that act on the same V2
receptors, significant water retention and
dangerous hyponatremia.
• Syndrome of inappropriate ADH secretion
(SIADH) can be treated with demeclocycline and
conivaptan

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 Adverse effects
• ADH, Desmopressin, water overload,
hyponatremia
• Demeclocycline: bone and teeth abnormalities
• Li: nephrogenic DI

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