利尿剂英文

Diuretics,Yanna Wu Ph.D., M.D.Associate ProfessorDepartment of PharmacologySchool of Basic MedicineTianjin Medical UniversityEmail: ,1,introduction,Diuretics act on renal tubules, promote the production ofurine are used to treat edema and unedema diseases (hypertension, heart failure, renal failure, and cirrhosis),2,Physiology of Kidneys,Process of urine formation,180 L filtrate,1-2 L final urine,99%,nephron,renal corpuscle,3,Reabsorption of tubules and collecting tubes,Proximal convoluted tubules NaHCO3 (Na+, HCO3-) are reabsorbed epithelium is permeable to ions and water, and permit passive flow in either direction - Na+ reabsorption is accompanied by passive absorption of waterCarbonic anhydrase inhibitors (acetazolamide) reduce Na+-H+ exchange, in turn, sodium reabsorption is decreased,4,Na+-K+-ATPase,Na+-H+-exchanger,Carbonic anhydrase,diffuses,Na+-HCO3- symporter,basolateral membrane,apical membrane,bicarbonate,Carbonic acid,Carbon dioxide,5,Reabsorption of tubules and collecting tubes,thick ascending limb of Henles Loop Na+/K+/2Cl- cotransport system water is impermeable at this segment, tubular fluid is hypotonic with respect to plasma as it enters the distal convoluted tubule (diluted) inhibitors of Na+/K+/2Cl- symporter block its function, increase excretion of Na+, K+, Cl-, Mg2+, Ca2+,6,apical membrane,Basolateral membrane,Na+/K+/2Cl- cotransport system,lumen-positive electrical potential,Na+-K+-ATPase,interstitial fluid,7,dilution function and concentration function,In the thick ascending limb, large amount of ions are reabsorbed, but water is impermeable at this segment, as a result, the tubular fluid becomes dilutedilution functionAt the same time, the reabsorption of ions at this limb produces a hypertonic renal medulla. When the urine pass through the collecting duct, the hypertonic interstitial fluid sucks water out of the tubules, thereby the tubular fluid becomes concentrationconcentration function,8,Reabsorption of tubules and collecting tubes,Distal convoluted tubuleNa+/Cl- symporterboth parathormone and calcitriol increase Ca2+ reabsorption further dilutedthis segment is in the cortical part, the hypertonic state of renal medulla is not affected,9,Cl-,apical membrane,Basolateral membrane,interstitial fluid,Parathormonecalcitriol,Na+/Cl- symporter,10,Reabsorption of tubules and collecting tubes,late distal tubules and collecting tubules Na+/K+ exchange reabsorption of Na+ and its coupled secretion of K+ is regulated by aldosterone absorption of water is regulated by antidiuretic hormone (ADH)Promotes collecting tubules permeable to watermodulates the concentration of final urine,11,lumen-negative electrical potential,all these agents are K+-sparing diuretics,12,Classification of Diuretics,High efficacy diureticsModerate efficacy diuretics Low efficacy diuretics,13,Classification of Diuretics,High efficacy diureticsModerate efficacy diuretics Low efficacy diuretics,14,High efficacy diuretics,Furosemide, bumetanide, ethacrynic acid have their major action on the ascending limb of the loop of Henle loop diuretics,15,Pharmacokinetics,absorbed rapidly by oral administration. Bioavailability is 50-70%. If given iv, the effects of furosemide response within 5 mins, duration time 2-3 hrs. 50-60 L of urine excretion within 24 hours after using large doses of furosemide. Protein binding rate is 95%. t1/2 1 hr, which may be prolonged to 10 hr in renal dysfunction.,16,Mechanism of action,inhibit the Na+/K+/2Cl- cotransporter in the thick ascending limb of the loop of Henle reabsorption of Na+, Cl-, Ca2+ and Mg2+ are decreasedsecretion of K+ is increasedthe most efficacious of the diuretic drugs the ascending limb accounts for the reabsorption of 25%-30% of filtered NaCldownstream sites are not able to compensate for this increased Na+ load,17,apical membrane,Basolateral membrane,Na+/K+/2Cl- cotransport system,lumen-positive electrical potential,Na+-K+-ATPase,interstitial fluid,18,Pharmacological effects,Diuretic activity Diuretic activity is rapid, strong and shortLarge amounts of Na+, Cl-, K+, Ca2+ and Mg2+ are excreted and Cl- loss is more than Na+ in urine,Relative changes in the composition of urine induced by loop diuretics,19,Pharmacological effects,Decrease renal vascular resistance, increase renal blood flow redistribution of blood flow within the renal cortex Increase renin release large volume depletion reflexly activate the sympathetic nervous system and stimulate the intrarenal baroreceptor mechanism induces renal prostaglandins synthesis in the kidney,20,Pharmacological effects,Relieve pulmonary congestion and reduce left ventricular filling pressures increase systemic venous capacitance in congestive heart failure patient Inhibit electrolyte transport in inner ear alternate the electrolyte composition of endolymph, contribute to drug induced ototoxity,21,Clinical Uses,emergency situationsacute pulmonary edema and brain edemabumetanide or furosemide is first choice Serious edema edema of nephrotic syndrome, nephrosis; ascites of liver cirrhosis edema patients who do not respond to salt restrictions or thiazidesChronic congestive heart failure to minimize venous and pulmonary congestion,22,Clinical Uses,Hyperkalemia Acute or chronic renal failure increase the rates of urine flow and enhance K+ excretion in acute renal failureconvert oliguric renal failure to nonoliguric failureAcute hypercalcemia Hypertension crisis Detoxication,23,Side effects,Electrolyte disturbancehypokalemia, hyponatremia, hypomagnesemia, hypochloremic metabolic alkalosisinduce cardiac arrhythmias potassium-sparing diuretics or dietary supplementation with potassium Ototoxicity hearing loss or deafness which can be potentiated by renal dysfunction or combined with another ototoxic drugs (eg, aminoglycoside antibiotics),24,Side effects,Hyperuricemia hypovolemia-associated enhancement of uric acid reabsorption in the proximal tubule OthersHyperglycemiaincrease LDL-C and decrease HDL-C in plasma,25,Interaction,first or second generation of cephalosporins potentiates ototoxicity of loop diuetics NSAIDs reduce Na+ excretion by inhibiting PGs synthesis in the kidneywarfarin is capable of competitive binding plasma protein with loop diuretics,26,Classification of Diuretics,High efficacy diuretics (loop diuretics) Moderate efficacy diuretics Low efficacy diuretics,27,Moderate efficacy diuretics,classification thiazidesHydrochlorothiazideChlorothiazideCyclopenthiazide thiazide-like diureticsChlorthalidone the most widely used diuretic drugs affect the distal tubule,28,Pharmacokinetics,All thiazides are absorbed when given orallyThey are excreted unchanged in the urine and are not effective when renal function is severely impaired HydrochlorothiazideIts renal excretion competes with uric acid,29,Mechanism of action,act mainly in the distal tubule to decrease the reabsorption of Na+ by inhibition of Na+/Cl- cotransporter on the luminal membrane increase the concentration of Na+ and Cl- in the tubule fluid acid-base balance is not usually affected,30,Cl-,apical membrane,Basolateral membrane,interstitial fluid,Parathormonecalcitriol,Na+/Cl- symporter,31,Pharmacological effects,Diuretic activity10% of filtered sodium is excreted Promote potassium excretion increase the Na+ in the filtrate arriving at the distal tubule more potassium is exchanged for sodium Enhance Ca2+ reabsorption decrease Ca2+ excretion from urine in the distal convoluted tubule,32,Pharmacological effects,Relative changes in the composition of urine induced by thiazide diuretics,33,Pharmacological effects,Hypotensive effect initial hypotensive effectsdecrease in blood volume and therefore a decrease in cardiac output continued hypotensive effectsNa+ excretion - intercellular Na+ concentration - Na+/Ca2+ exchange - intercellular Ca2+ concentration - sensitivity of blood vessel response to NA - reduced peripheral vascular resistance caused by relaxation of arteriolar smooth muscle,34,Clinical Uses,Edemamild and moderate cardiac edema (CHF) Hypertensioneither uses alone or in combination with other antihypertensive drugs Nephrolithiasis due to idiopathic hypercalciuria; osteoporosisdecrease Ca2+ in tubular fluidincrease Ca2+ in plasma,35,Clinical Uses,Diabetes insipidusUsed for the palliation of nephrogenic and pituitary diabetes insipidus. Typical symptoms: polydipsia and polyuria mechanism,36,Side effects,Electrolyte disturbanceshypokalemia, magnesium deficiency Hyperuricemia and induced gout increases absorption of uric acid and competes for the transport mechanism with uric acidHyperglycemia and hyperlipidemia decrease glucose tolerance, reduce insulin secretion and glucose utilization, aggravates preexisting diabetesincreases plasma concentrations of LDL-cholesterol, triglyeride and total cholesterol,37,Side effects,Hypovolemia over treatment, acute loss of excessive fluid leads to postural hypotension and dizzinessOthersphotosensitive, thrombocytopenia, agranulocytosis Thiazides binding with quinidine can lead to polymorphic ventricular tachycardia,38,Classification of Diuretics,High efficacy diuretics (loop diuretics) Moderate efficacy diuretics Low efficacy diuretics (K+-sparing diuretics),39,Low efficacy diuretics,act in the late distal tubules and collecting tubule to inhibit Na+ reabsorption and K+ secretionThese drugs reduce potassium secretion, so term as K+ retention diuretics or K+ sparing diuretics High efficacy and moderate efficacy diuretics increase K+ excretion, so term as K+ lossing diureticsMajor use is in combination with other diuretics to reduce sodium reabsorption and prevent potassium loss in the tubule.,40,Spironolactone,Mechanism of actionaldosterone regulate Na+ reabsorption and K+ secretion at late distal tubules and collecting ductSpironolactone is a competitive antagonist to aldosteronebind with cytoplasmic aldosterone receptorspromotes Na+ excretionblunt the K+ secretion,41,42,lumen,apical membrane,interstitial fluid,Collecting tubule,Basolateral membrane,AIP: aldosterone-induced protein; SP: spironolactone;ALD: aldosterone,Triamtereneamiloride,spironolactone,aldosterone,42,Spironolactone,Pharmacological effectsless than 2-3% of the filtered sodium is excreted effective only in the increasing status of aldosterone and ineffective for total adrenoprival animal the higher the level of endogenous aldosterone, the greater the effects of spironolactone on urinary excretion,43,Relative changes in the composition of urine induced by potassium-sparing diuretics,44,Spironolactone,Clinical UsesEdema of primary hyperaldosteronism and refractory edema associated with secondary aldosteronism (cardiac failure, hepatic cirrhosis , nephrotic syndrome, and severe ascites )in combination with other diuretics to reduce sodium reabsorption and prevent potassium loss in the tubuleinhibits renal excretion of digoxin, the dosages of digoxin need to be reduced if both drugs combined use,45,Triamterene and amiloride,Pharmacological effectsdirectly block sodium ion channels in the late distal tubules and clollecing duct, inhibit Na+ reabsorption and promote its excretion do not block the aldosterone receptorstill effective for total adrenoprival animalThe major use is in combination with other diuretics,46,47,lumen,apical membrane,interstit