diuretics-.......230820182724-a873df81.pptx

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1. Diuretics Dr. Rajendra Kumar Clinical Pharmacologist Email: [email protected]

2. THIAZIDES DIURETICS The thiazides are the most widely used diuretics. They are sulfonamide derivatives. All thiazides affect the distal convoluted tubule, and all have equal maximum diuretic effects, differing only in potency. Thiazides are sometimes called “low ceiling diuretics,” because increasing the dose above normal therapeutic doses does not promote further diuretic response. Ex: Chlorothiazide DIURIL, SODIUM DIURIL Chlorthalidone THALITONE Hydrochlorothiazide (HCTZ) MICROZIDE Indapamide Metolazone ZAROXOLYN

3. Mechanism of Action Increased excretion of Na + and Cl - Loss of K + : ( Because thiazides increase Na+ in the filt ate arriving at the distal tubule, more K+ is also exchanged for Na+, resulting in a continual loss of K+ from the body with prolonged use of these drugs.) Loss of Mg 2+ : ( Magnesium deficiency requiring supplementation can occur with chronic use of thiazide diuretics, particularly in elderly patients. The mechanism for the magnesuria is not understood.) Decreased Urinary Calcium excretion Reduced peripheral vascular resistance: ( An initial reduction in blood pressure results from a decrease in blood volume and, therefore, a decrease in cardiac output. With continued therapy, volume recovery occurs. However, there are continued antihypertensive effects, resulting from reduced peripheral vascular resistance caused by relaxation of arteriolar smooth muscle. How these agents induce vasodilation is unknown.)

4. Pharmacokinetics Orally administered Poor absorption Onset of action in ~ 1 hour Wide range of t ½ amongst different thiazides, longer than loop diuretics Free drug enters tubules by filtration and by organic acid secretion

5. Therapeutic Uses Hypertension Heart failure Hypercalciuria: prevent excess Ca 2+ excretion to form stones in ducts Osteoporosis Treatment of Li + toxicity Diabetes insipidus

6. Side Effects/ Adverse Effects Potassium depletion: Hypokalemia is the most frequent problem with the thiazide diuretics, and it can predispose patients who are taking digoxin to ventricular arrhythmias. Thiazides decrease the intravascular volume, resulting in activation of the renin–angiotensin–aldosterone system. Low-sodium diets blunt the potassium depletion caused by thiazide diuretics. Hyponatremia Hyperuricemia Volume depletion: This can cause orthostatic hypotension or light-headedness. Hypercalcemia Hyperglycemia: Therapy with thiazides can lead to glucose intolerance, possibly due to impaired release of insulin and tissue uptake of glucose. New-onset diabetes has been reported more often with thiazides than with other antihypertensive agents.

7. LOOP/ HIGH-CEILING DIURETICS (Inhibitors of Na + -K + -2Cl ¯ Cotransport) The major site of action is the thick ascending limb of Loop of Henle (TAL), therefore, called loop diuretics. Ex: Bumetanide Ethacrynic acid EDECRIN Furosemide LASIX Torsemide DEMADEX

8. Mechanism of action Loop diuretics inhibit the cotransport of Na + /K + /2Cl − in the luminal membrane in the ascending limb of the loop of Henle. Therefore, reabsorption of these ions is decreased. The loop diuretics may increase renal blood flow, possibly by enhancing prostaglandin synthesis. NSAIDs inhibit renal prostaglandin synthesis and can reduce the diuretic action of loop diuretics. [Note: Unlike thiazides, loop diuretics increase the Ca 2+ content of urine. In patients with normal serum Ca 2+ concentrations, hypocalcemia does not result, because Ca 2+ is reabsorbed in the distal convoluted tubule.]

9. Pharmacokinetics Orally administered Rapid absorption Rapid onset of action Bound to plasma proteins: displaced by warfarin and Clofibrate Duration of action is relatively brief (2 to 4 hours), allowing patients to predict the window of diuresis. They are secreted into urine.

10. Therapeutic uses The loop diuretics are the drugs of choice for acute pulmonary edema & Chronic peripheral edema caused from heart failure or renal impairment. Chronic Renal failure or Nephrosis Hypertension Hypercalcemia Acute and chronic hyperkalemia

11. Adverse Effects Ototoxicity: Reversible or permanent hearing loss may occur with loop diuretics, particularly when used in conjunction with other ototoxic drugs (for example, aminoglycoside antibiotics). Ethacrynic acid is the most likely to cause deafness. Hyperuricemia: Furosemide and ethacrynic acid compete with uric acid for the renal secretory systems, thus blocking its secretion and, in turn, causing or exacerbating gouty attacks. Acute hypovolemia: Loop diuretics can cause a severe and rapid reduction in blood volume, with the possibility of hypotension, shock, and cardiac arrhythmias. Potassium depletion: The heavy load of Na + presented to the collecting tubule results in increased exchange of tubular Na + for K + , leading to the possibility of hypokalemia. The loss of K + from cells in exchange for H + leads to hypokalemic alkalosis. Use of potassium-sparing diuretics or supplementation with K + can prevent the development of hypokalemia. Hypomagnesemia: Chronic use of loop diuretics combined with low dietary intake of Mg 2+ can lead to hypomagnesemia, particularly in the elderly. This can be corrected by oral supplementation.

12. POTASSIUM-SPARING DIURETICS Potassium-sparing diuretics act in the collecting tubule to inhibit Na + reabsorption and K + excretion. These drugs should be avoided in patients with renal dysfunction because of the increased risk of hyperkalemia. Within this class, there are drugs with two distinct mechanisms of action: aldosterone antagonists and sodium channel blockers. Ex: Amiloride MIDAMOR Eplerenone INSPRA Spironolactone ALDACTONE Triamterene DYRENIUM

13. Mechanism of action Spironolactone is a synthetic steroid that antagonizes aldosterone at intracellular cytoplasmic receptor sites rendering the spironolactone–receptor complex inactive. It prevents translocation of the receptor complex into the nucleus of the target cell, ultimately resulting in a failure to produce mediator proteins that normally stimulate the Na + /K + -exchange sites of the collecting tubule. Thus, a lack of mediator proteins prevents Na + reabsorption and, therefore, K + and H + secretion. Eplerenone is another aldosterone receptor antagonist, which has actions comparable to those of spironolactone, although it may have fewer endocrine effects than spironolactone

14. Pharmacokinetics Both spironolactone and eplerenone are absorbed after oral administration and are significantly bound to plasma proteins. Spironolactone is extensively metabolized and converted to several active metabolites. The metabolites, along with the parent drug, are thought to be responsible for the therapeutic effects. Spironolactone is a potent inhibitor of P-glycoprotein, and eplerenone is metabolized by cytochrome P450 3A4.

15. Therapeutic Use Diuretic Secondary Hyperaldosteronism Heart failure Resistant hypertension Ascites Polycystic ovary syndrome Nephrotic syndrome

16. Side effects/ Adverse effects Spironolactone can cause Gastric upset. Gynecomastia in male patients & Menstrual irregularities in female patients. Because it chemically resembles some of the sex steroids. Hyperkalemia, Nausea Lethargy Mental confusion can occur. Potassium-sparing diuretics should be used with caution with other medications that can induce hyperkalemia, such as angiotensin-converting enzyme inhibitors and potassium supplements.

17. CARBONIC ANHYDRASE INHIBITORS Acetazolamide and other carbonic anhydrase inhibitors are more often used for their other pharmacologic actions than for their diuretic effect, because they are much less efficacious than the thiazide or loop diuretics. Limited uses as diuretics Developed from sulfanilamide (caused metabolic acidosis and alkaline urine) Ex: Acetazolamide DIAMOX

18. Mechanism of action Acetazolamide inhibits carbonic anhydrase located intracellularly (cytoplasm) and on the apical membrane of the proximal tubular epithelium. The decreased ability to exchange Na + for H + in the presence of acetazolamide results in a mild diuresis. Additionally, HCO3 − is retained in the lumen, with marked elevation in urinary pH . The loss of HCO3 − causes a hyperchloremic metabolic acidosis and decreased diuretic efficacy following several days of therapy. Changes in the composition of urinary electrolytes induced by acetazolamide. Phosphate excretion is increased by an unknown mechanism. [Note: Carbonic anhydrase catalyzes the reaction of CO2 and H2O, leading to H2CO3, which spontaneously ionizes to H + and HCO3 − (bicarbonate).]

19. Pharmacokinetics Acetazolamide is well absorbed orally and excreted unchanged in urine. Action of a single dose lasts 8–12 hours. It is approximately 90% protein bound and eliminated renally by both active tubular secretion and passive reabsorption.

20. Therapeutic use Glaucoma: as adjuvant to other ocular hypotensive To alkalinize urine: for urinary tract infection or to promote excretion of certain acidic drugs. Epilepsy: as adjuvant in absence seizures when primary drugs are not fully effective; but tolerance to antiepileptic action develops. Mountain sickness Periodic paralysis.

21. Adverse Effects Metabolic acidosis (mild) Potassium depletion Renal stone formation Drowsiness Paresthesia may occur. The drug should be avoided in patients with hepatic cirrhosis, because it could lead to a decreased excretion of NH 4 + .

22. OSMOTIC DIURETICS A number of straightforward, hydrophilic chemical compounds that pass through the glomerulus, like mannitol and urea, cause some degree of diuresis. A decrease in reabsorption from filtered compounds will result in a rise in urine output. These compounds raise the osmolarity of the tubular fluid and stop more water from being absorbed, which causes osmotic diuresis. Only a tiny bit of extra salt might also be excreted. Osmotic diuretics are ineffective for treating diseases where Na + retention develops because they are used to promote water excretion rather than Na + excretion. Ex: Mannitol OSMITROL Urea [Note: Mannitol is not absorbed when given orally and should be given intravenously.]

23. Mechanism of action Osmotic diuretics are not reabsorbed. Increase osmotic pressure specifically in the proximal tubule and loop of Henle. Prevents passive reabsorption of H2O Increase H2O and Na + excretion.

24. Therapeutic use Mannitol: Drug of choice, Non-toxic, freely filtered, non re-absorbable and non-metabolized. Administered prophylactically for acute renal failure secondary to trauma, CVS disease, surgery or nephrotoxic drugs. Short-term treatment of acute glaucoma. Infused to lower intracranial pressure Urea, Glycerol and Isosorbide are less efficient can penetrate cell membranes.

25. Side Effects Increase extracellular fluid volume Cardiac failure Pulmonary edema Hypernatremia Headache Nausea Hyperkalaemia secondary to diabetes or impaired renal function

26. References W. Karen, F. Richard, Panavelil Thomas A. “Chapter 18: Diuretics, Lippincott Illustrated reviews: Pharmacology, Sixth Edition”, published by wolters kluwer Page- 241-253. Katzung Bertram G., “Chapter 15: Diuretic Agents, Basic & Clinical Pharmacology, 14 th Edition,” Published by Mc Graw Hill education, Page: 254- 275. Hall John E., Chapter 31: “Diuretics, Kidney diseases, Guyton and Hall Textbook of Medical Physiology, 12 th Edition,” published by Saunders Elsevier, Page: 397-409. Tripathi KD, “Chapter 42: Diuretics, Essentials of Medical Pharmacology, 8 th Edition,” published by The health sciences publisher, Page: 625-638. Tripathi KD, “Chapter 8: Drugs acting on Kidney, Pharmacological Classification of drugs with doses and preparations, 5 th edition,” published by Jaypee brothers medical publishers ltd, Page: 102-103.

27. THANK YOU….. Doctors