Vilasinee Hirunpanich B.Pharm(Hon), M.Sc In Pharm (Pharmacology)

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Vilasinee Hirunpanich B.Pharm(Hon), M.Sc In Pharm (Pharmacology)

Transcript of Vilasinee Hirunpanich B.Pharm(Hon), M.Sc In Pharm (Pharmacology)

Page 1: Vilasinee Hirunpanich B.Pharm(Hon), M.Sc In Pharm (Pharmacology)

Vilasinee HirunpanichB.Pharm(Hon), M.Sc In Pharm (Pharmacology)

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Outline of diuretic drugs

Basic knowledge in anatomy and physiology

Classification of diuretics

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Classification of Diuretics

Loop Diuretics Thiazides Diuretics K+-sparing diuretics Osmotic DiureticsCarbonic anhydrase

inhibitors

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1. Loop diuretics (high ceiling diuretics)

block Na+-K+-2Cl- cotransport in the thick ascending limb of the loop of Henle

high efficacy: 25% of filtrated solute is reabsorbed

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Structure of loop diuretics

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Mechanism of action of Loop of Henle

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pharmacokinetic

Rapidly absorbedEliminate by renal secretionTorsemide (1h) is more rapidly than furosemide (Lasix) (2-3 h)

Duration 2-3 h (furosemide), 3-4 h(torsemide)

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Adverse effects

1. Fluid and electrolytes imbalance

Hyponatremia, Hypokalemia and hypomagnesia

2. H+ loss metabolic alkalosis

3. Ototoxicityethacrynic most often

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Adverse effects (cont)

4. Hyperuricemia5. Hyperglycemia6. Hypersensitivity to sulfonamide

skin rash7. Others: dehydration

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Ototoxic drugs; aminoglycoside

digitalis glycosideNSAIDsprobenecidLitiumanticoagulant

Drug interaction

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Clinical indications

1. Hypertension and CHF2. Acute pulmonary edema 3. Other edematous conditions

3. Mild hyperkalemia (simultaneous NaCl and water)

4. I-, Br- intoxication

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2.Thiazide Diuretics

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Thiazide diuretics

Sulfonamide and benzothiadiazide (thiazide) derivatives–Hydrochlorothiazide (HCTZ), indapamide, chlorthalidone, metolazone

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Mechanism of action of thiazide diuretics

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Mechanism of actions

Increase Na+, Cl-, K+, Mg2+ in urine….water retention

Some drug has vasodilator effect such as indapamide (Natrilix )

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Pharmacokinetic

Chlorothiazide is less lipid soluble and must given in large dose

Indapamide is excreted primarily by the billiary system

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Adverse effects

1.Fluid and electrolytes imbalanceHypokalemia Hyponatremia

Hypercalcemia2. hyperglycemia due toimpaired pancreatic release of

insulin3.hyperlipidemia

4.allergic reaction

5. Other: weakness, fatigability

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Drug interactionDecrease the effect of

anticoagulanturicosuric

agentsulfonylureainsulin

Increase the effect of

digitalis glycoside

lithium

Decrease the effect of thiazideNSAIDsbile acid sequesteringprobencid

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Clinical indications

Hypertension, CHF

hepatic cirrhosis

nephrolithiasis due to idiopathic hypercalcinuria

nephrogenic diabetes insipidus

Br- intoxicity

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3. K+-sparing diuretics

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K+ sparing diuretics

1. Aldosterone antagonists

2. Inhibitor of renal epithelium Na+ channel

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Aldosterone antagonist

Structure similar to aldosterone hormone

Ex.spironolactone (synthesis

steriod), eplerenone (spironolactone

analog)

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spironolactonespecific antagonist

prevent protein synthesis that required for Na+ and K+ transport

increase Na+ excretion and preserve of K+

Potentcy is low and depend on aldosterone level

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pharmacokinetic

SpironolactoneOnset and duration of action are

determined by the kinetic of aldosterone response in target tissue.

Slow onset (48 hr)Canrenone is the active

metabolized which has very long t12.than parent drug.

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Adverse effects

hyperkalemia…..life threateningEndocrine effects

-gynecomastia-hirsutism-deepening voice- decrease libido

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Pts using salicylate because inhibiting canrenone

K+

administration

coadministration with thiazide or loop diuretic for edema (additive effect)

hyperaldosteronism

contraindication

Clinical use

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2. Inhibitor of renal epithelium Na+ channel

Triamtereneamiloride

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late distal tubules and collecting ducts

block Na+ channel in the luminal membrane

increase NaCl excretion and decrease K+ excretion

Mechanism of action of K+-sparing diuretic

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Adverse effectanemia: triamterene, folic

antagonistkidney stone (triamterene is

poorly soluble)ARF (acute renal failure)(combination of triamterene and

indomethacin has been reported )

life-threatening:

hyperkalemia

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contraindication

Renal failureother K+ sparing diureticACEIK+ supplementNSIADs

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Co administration with other diuretic (additive effect)

prevent depletion of intracellular K+ store

Clinical Use

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Osmotic diuretics

Properties 1. Freely filtered at the glomerulus2. No reabsorption at the renal tubule3. No pharmacological effectsGlycerine, Isosorbide, Mannitol,

Urea site of action: Proximal tubule and

descending limb of Henle’s loop

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Structure of osmotic diuretics

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Mechanism of action

Limit water reabsorption

act as increase urine volume.

increase renal blood flow

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Pharmacokinetic

Poorly absorbed so they must be given parenterally

Mannitol is excreted by glomerular filtration within 30-60 min

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Adverse effects

1. Extracellular volume expansion

Rapidly distributed in the extracellular compartment and extract water from the intracellular compartment

2. Dehydration 3. Nausea, vomiting, headache

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Clinical Indications

1. To increase urine volume 2. Reduction of intracranial and

intraocular pressureextract water from the eye and brainGlycerine: control intraocular

pressure, pre/post operative ocular surgery

Mannitol, urea: reduce cerebral edema before/after neuro-surgery

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5. Carbonic anhydrase inhibitors

Inhibit carbonic anhydrase enzyme at proximal tubule

SO2NH2 (sulfonamide) group is essential for activity.

Acetazolamide (Diamox), dichlorophenamide, ethoxalamide, methazolamide

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Structure of carbonic anhydrase inhibitors

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Mechanism of action of carbonic anhydrase inhibitors

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1. increase the excretion of HCO3-

(Urine alkalinization, pH 8)Increase Na+, K+, secretion2. Metabolic acidosis3. eye; decrease formation of

aqueous humor4. Paresthesia, Drowsiness,

Somnolence

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Pharmacokinetic

Well absorbed after oral administration

The effect of increased of HCO3-

is apparent within 30 min.Maximal effect within 2 hPersist for 12 h after single doseExcrete by tubular secretion

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Adverse effects

1. Hypersensitivitysulfonamide derivative (fever, rashes,

bone marrow suppression)2. Renal stoneCa2+ salt are relatively insoluble at

alkaline pH.3. Metabolic acidosis and urine

alkalinization4. Renal potassium wasting 5. Others: drowsiness, paresthesia

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Clinical indications1. Glaucoma (decrease intraocular

pressure)Dorzolamide, brinzolamide

(topically use)2. Urinary alkalinizationincrease the secretion of uric

acid, weak acid drugs(aspirin)3. Metabolic acidosis4. Acute mountain sickness (24 h

before ascent)

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Loop diuretic& thiazide (different position)

K+sparing diuretic& loop diuretic or thiazide (decrease ADR)

Moduretic (amiloride + HCTZ)Dyazide (triamterene+HCTZ)

Diuretic combination