DIURETICS - Universitas Indonesiastaff.ui.ac.id/.../nafrialdi.phd/material/intl-diuretics.pdf ·...
Transcript of DIURETICS - Universitas Indonesiastaff.ui.ac.id/.../nafrialdi.phd/material/intl-diuretics.pdf ·...
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DIURETICSDIURETICS
NAFRIALDINAFRIALDI
Departement of Pharmacology FKUIDepartement of Pharmacology FKUI
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IntroductionIntroduction• Kidney: 1.3 million nephron eachKidney: 1.3 million nephron each• Glomeruli: Glomeruli:
– Receive 25% of cardiac outputReceive 25% of cardiac output– Filtration rate: 100-120 ml/minuteFiltration rate: 100-120 ml/minute
• Tubules: Tubules: – Reabsorption of 99% of glomerular filtrate Reabsorption of 99% of glomerular filtrate
only only ++ 1 ml/min. excreted as urin 1 ml/min. excreted as urin– SecretionSecretion
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Introduction• Proximal tubuls:
– Reabsorption of 65% Na+ – Permeable to water isotonic urine
• Loop of Henle– Thick decending limb: most active water reabsorption – Thin ascending limb– Thick ascending limb:
• Reabsorption of Na+, • Water impermeable diluting segment
• Distal tubules : – Na+ reabsorption
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Electrolyte Transport and Site of Action of Diuretics
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Site and Mechanisms of Actions of Diuretics
Diuretics Site of Action Mechanism
Osmotic Diuretic 1. Proximal tubules2. Loop of Henle3. Collecting duct
Inhibition of water and Na+ reabsorption
Carbonic Anhydrase Inhibitor (CA-I)
Proximal tubules Inhibition of bicarbonate reabsorption
Loop Diuretic Loop of Henle (thick ascending limb)
Inhibition of Na+, K+, Cl- cotransport
Thiazide Early distal tubule Inhibition of Na+, Cl- cotransport
Potassium sparing diuretics
Late distal tubuleCollecting duct
Inhibition of Na+ reabsorption and K+ secretion
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Osmotic Diuretics
• Mannitol, urea, glycerine, isosorbide• Properties of osmotic diuretics:
– Freely filtrated by glomerulus– Negligible tubular reabsorption– Chemically inert– Usually non metabolized
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Mechanism of Action
• OD is filtrated and increases osmotic pressure in tubular lumen
• Hence, increases excretion of water and electrolytes
• Almost all of electrolyte are excreted: Na+, K+, Ca++, Mg++, HCO3
-, phosphate
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Pharmacokinetics• Mannitol and urea:
– Not absorbed from GI tract intravenous• Glycerine and isosorbide:
– Can be administered orally• Metabolism:
– glycerine 80% metabolized– mannitol 20%– Urea, isosorbide: not metabolized
• Excretion: renal
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Indications• Glaucoma (rare)• Brain edema
– mannitol and urea are given before and after brain surgery
• Disequilibrium syndrome after hemodialysis
• Prophylaxis of ATN (acute tubular necrosis) due to contrast media, surgery, and trauma.
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Adverse Effects• Innitial increase of plasma volume
potentially dangerous in heart failure and lung edema
• Hypo Na+ headache, nausea, vomitus• Hypovolemia• Hypersensitivity reaction• Vein thrombosis, pain if extravasation (urea)• Hyperglycemia, glycosuria (glycerine)
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Contraindications
• Renal failure and anuria
• Lung edema
• Dehydration
• Intracranial hemorrhage, except before craniotomy
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Carbonic Anhydrase Inhibitor Acetazolamide, Dichlorphenamide, Metazolamide
Mecanism of Actions• Kidney:
– Inhibition of Bicarbonate (HCO3-) reabsorption – Reduces Na-H-exchange NaHCO3 is excreted
along w/ H2O • Eye:
– Inhibits formation of aqueous humor decreases intra ocular pressure
• CNS: anti convulsive effects– due to pH decrease – direct effect
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Mechanism of Action of CA-I
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Indications of CA-I• Glaucoma • Epilepsi: limited usage• Acute mountain sickness• Familial periodic paralysis• Urinary alkalinization: preventing uric acid
and cystine stones• Metabolic alkalosis
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Adverse Effects and Contraindications
• Metabolic acidosis• Renal stones (Phosphate and Calsium
stone)• Renal potassium wasting (NaHCO3
- enhances K+ secretion)
• Drawsiness, parestesia, disorientationContraindication
– Liver cirrhosis (CA-I inhibits conversion of NH3 to NH4) NH3 increased
– Renal failure (↑ risk of metabolic acidosis)
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Preparatrions
• Acetazolamide (Diamox®):– Tablet 125 and 250 mg– Doses: 250-1000 mg/day
• Dichlorphenamide: tablet 50 mg (1-4 times daily)
• Metazolamide: tablet 25 and 50 mg (1-4 times daily)
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Thiazides• Hydrochlorothiazide (HCT), Chlorothiazide, Bendroflumethiazide,
Clortalidone, Metolazone, Indapamide)
• Mechanism of Actions– Thiazides are secreted by proximal tubules
but works in distal convoluted tubules– 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
THIAZIDES
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Thiazides
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Effects on Electrolytes• Increases Na+ and Cl- excretion• K+ excretion also increase associated w/
increased Na+ in distal tubules.• Inhibits uric acid secretion hyper uricemia
and gout • Decreases Ca2+ excretion (unknown
mechanism) tends to increase plasma Ca++ Delays osteoporotic process
• Increases Mg2+ excretion
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PharmacokineticsDrugs Potency T1/2 (h) Elimination
Bendroflumethiazide
10 3-3,9 30% renal70% metabolism
Chlorothiazide 0.1 1,5 renal
HCT 1 2,5 renal
Polithiazide 25 2,5 2,5 % renal75% unknown
Clortalidon 1 47 65% renal10% bile25% unknown
Indapamid 20 14 metabolism
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– Hypo K+ Increased risk of digitalis toxicity– Hypo Na+, Hypo Mg++– Hyper uricemia 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
Adverse Effects
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Interactions
• Increases the risk of arrhythmia when combined w/ digitalis, quinidine and other anti arrhythmias
• Reduces efficacy of anticoagulant and uricosuric
• NSAID reduce the efficacy of thiazide• Reduces the efficacy oral antidiabetics
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Indications of Thiazides• Hypertension (single drug or in combination)• Chronic, mild- heart failure • Edema (loop diuretic is preferable)• Diabetes insipidus (mainly nephrogenic)• Prevention of Ca++ excretion in osteoporosis and
calcium nephrolithiasis
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Loop Diuretics• Furosemide, torasemide, bumetanide, ethacrynic acid• Site of action: thick ascending limb of Ansa
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
• NSAID reduces the effects of diuretics• Probenecid reduces the effects of diuretics
by inhibiting its secretion into the lumen. • Increases the risk of arrhythmia when
combined w/ digitalis, quinidine and other anti arrhythmias
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Indications• Congestive heart failure (first line drug)• Acute pulmonary edema• Edema due to renal failure, nephrotic
syndrome, ascites• Hypercalsemia• Severe hypertension• Force diuresis during drug/chemical
intoxication (drug that excreted through the kidney in active form)
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Potassium Sparing Diuretics
1. Na+ channel inhibitor (Amiloride, triamterene) Inhibit Na+ reabsorption Na+ excretion Reduced K+ secretion K+ retention
1. Aldosterone antagonist (Spironolactone, eplerenone)
– Aldosterone induces the expression of Na/K- ATPase and Na+ channel
– Spironolactone and eplerenone blocks aldoserone receptor reduces Na+ reabsorption and K+ secretion
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1. Na+ Channel Inhibitors
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• Potassium sparing diuretic has a weak diuretic action
• Usually used in combination w/ other diuretic:– Potentiation of diuretic and anti hypertensive effects– Prevents hypokalemia
• Spironolactone is metabolized to its active metabolyte, canrenone.
• Longterm use of spironolactone can prevent myocardial hypertrophy and myocardial fibrosis
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Adverse Effects
• Hyperkalemia• Anti androgenic effect (gynecomastia,
decrease of libido, impotency, menstrual dysturbance): spironolakton
• Megaloblastic anemia : Triamteren (folate antagonist)
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INDICATIONS• Antihypertension:
– In combination w/ other anti hypertensives– To increase the effect and to prevent
hypokalemia
CONTRAINDICATIONS/PRECAUTIONS• Conditions that prone to hyperkalemia:
– Renal failure– Under treatment w/ ACE-inhibition, ARB,
NSAID, K+ supplementation
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Antidiuretic Hormone• Vasopresin• Arginin vasopresin (AVP)• Desmopresin (DDAVP, 1-deamino-8D-arginine
vasopresin) (synthetic)• Secreted by posterior hypiphysis • Secretion increase in response to:
� ↑ Plasma osmolarity (dehidrasi)– Hypovolemia, hypotension (bleeding, dehydration)
• Regulation – Osmoreceptor in the CNS (treshold of secretion 280
mOsm) – Volume receptor in left atrium and aortic arc
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Mechanism of Action• Works in ascending limb of Henle’s loop
and collecting ducts • 2 kind of receptors:
– V1: vascular smooth muscle vasoconstriction
– V2: kidney increase water permeability of tubular epithelium water reabsorption
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Indications
• Neurogenic Diabetes Insipidus (central type) (not for nephrogenic DI)
• DI due to head trauma or brain surgery • Gastrintestinal bleeding due to portal
hypertension (by reducing mesenteric blood flow)
• Von Willebrand disease (DDAVP stimulate secretion of vWF in endothelial cells)
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Adverse Effects• Hypertension• Abdominal colic due to increased peristalsis• Coronary vasoconstriction angina pectoris• Preparation:
– Pitressin for injection– Vasopresin tanat for IM injection– Intranasal powder– Lipresin (lisine-vasopresin) nasal spray– Desmopresin acetate (DDAVP): nasal drop
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Kinetics
• Not to be administered orally (rapid degradation by trypsin)
• Administration: im, iv, sc, intranasal• Half-life of ADH: 17-35 minutes• Desmopresin (DDAVP): long half-life
effective untill 48-96 h after intranasal administration.
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