Diuretics | Definition | Mechanism of Action | Classes of DrugsChetan Prakash
This presentation provides knowledge about Diuretics,Role of sodium, types of urine output, General mechanism of action, Normal Physiolofy of urine formation, GFR Formation, Classes of Diuretics, diuretics abuse and recent discovery. An assignment for the subject, Advanced Pharmacology-I, 1st year M.Pharm, 1st semester.
Diuretics
Pharmacology
Katzung
Abnormalities in fluid volume and electrolyte composition are common and important clinical disorders. Drugs that block specific transport functions of the renal tubules are valuable clinical tools in the treatment of these disorders. Although various agents that increase urine volume (diuretics) have been described since antiquity, it was not until 1937 that carbonic anhydrase inhibitors were first described and not until 1957 that a much more useful and powerful diuretic agent (chlorothiazide) became available. Technically, a “diuretic” is an agent that increases urine volume, whereas a “natriuretic” causes an increase in renal sodium excretion and an “aquaretic” increases excretion of solute-free water. Because natriuretics almost always also increase water excretion, they are usually called diuretics. Osmotic diuretics and antidiuretic hormone antagonists (see Agents That Alter Water Excretion) are aquaretics that are not directly natriuretic.
Diuretics | Definition | Mechanism of Action | Classes of DrugsChetan Prakash
This presentation provides knowledge about Diuretics,Role of sodium, types of urine output, General mechanism of action, Normal Physiolofy of urine formation, GFR Formation, Classes of Diuretics, diuretics abuse and recent discovery. An assignment for the subject, Advanced Pharmacology-I, 1st year M.Pharm, 1st semester.
Diuretics
Pharmacology
Katzung
Abnormalities in fluid volume and electrolyte composition are common and important clinical disorders. Drugs that block specific transport functions of the renal tubules are valuable clinical tools in the treatment of these disorders. Although various agents that increase urine volume (diuretics) have been described since antiquity, it was not until 1937 that carbonic anhydrase inhibitors were first described and not until 1957 that a much more useful and powerful diuretic agent (chlorothiazide) became available. Technically, a “diuretic” is an agent that increases urine volume, whereas a “natriuretic” causes an increase in renal sodium excretion and an “aquaretic” increases excretion of solute-free water. Because natriuretics almost always also increase water excretion, they are usually called diuretics. Osmotic diuretics and antidiuretic hormone antagonists (see Agents That Alter Water Excretion) are aquaretics that are not directly natriuretic.
Hypolipidemic agents, also known as cholesterol-lowering drugs or antihyperlipidemic agents, are a diverse group of pharmaceuticals that are used in the treatment of high levels of fats (lipids), such as cholesterol, in the blood (hyperlipidemia). They are also called lipid-lowering drugs.
Chemistry of Anti Anginal Drugs by Professor BeubenzProfessor Beubenz
This presentation will give you an idea about the chemistry of Anti-anginal drugs along with its classification, mechanism of action & Structural Activity Relationship.
#Professor_Beubenz
For more such videos do
#Subscribe
#Share
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to the Channel Professor Beubenz
Thank You.
https://www.youtube.com/watch?v=-7yjQm4zzX8&t=1183s
Hypolipidemic agents, also known as cholesterol-lowering drugs or antihyperlipidemic agents, are a diverse group of pharmaceuticals that are used in the treatment of high levels of fats (lipids), such as cholesterol, in the blood (hyperlipidemia). They are also called lipid-lowering drugs.
Chemistry of Anti Anginal Drugs by Professor BeubenzProfessor Beubenz
This presentation will give you an idea about the chemistry of Anti-anginal drugs along with its classification, mechanism of action & Structural Activity Relationship.
#Professor_Beubenz
For more such videos do
#Subscribe
#Share
#Like
to the Channel Professor Beubenz
Thank You.
https://www.youtube.com/watch?v=-7yjQm4zzX8&t=1183s
Diuretics and antidiuretics detail STUDYNittalVekaria
diuretics and antidiuretics detail study
-diuretic are the drug which increase the urine formation and excretion.
- antidiuretic work by decrease the urine formation.
classification, mechanism of action, use ,pharmacokinetic, pharmacodynamic,adverse effect
-newer drug
-banned diuretic and antidiuretic drug
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Their dose and adverse effects
Pharmacologicaol uses
all about diuretics
the detail study of diuretics which include their drugs, use,classification of diuretics, side effect, mechanism of action, metabolism, synthesis etc. this all things are cover in this presentation.
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Classify the agents used for general anesthesia
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Improve medication adherence.
Improve dosage regimen adherence.
More effective Drug treatment.
Reduce incidence of adverse drug effect and unnecessary healthcare cost.
ADR reporting.
Improve quality of life for patient.
Raising image of Pharmacist & its profession.
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Read| The latest issue of The Challenger is here! We are thrilled to announce that our school paper has qualified for the NATIONAL SCHOOLS PRESS CONFERENCE (NSPC) 2024. Thank you for your unwavering support and trust. Dive into the stories that made us stand out!
5. Anatomy of Renal system
Remember the nephron is the most
important part of the kidney that
regulates fluid and electrolytes.
Urine formation:
1.Glomerular filtration rate =
180L/day
2.Tubular re-absorption (around
98%)
3.Tubular secretion
Nephron
6. • How could urine output be increased ?
↑ Glomerular filtration Vs ↓ Tubular reabsorption (the most
important clinically)
o If you increase the glomerular filtriation increase tubular
reabsorption (so you cant use glomerular filtiration)
• Purpose of Using Diuretics
1. To maintain urine volume ( e.g.: renal failure)
2. To mobilize edema fluid (e.g.: heart failure,liver failure,
nephrotic syndrome)
3. To control high blood pressure.
10. Osmotic Diuretics
Pharmacologically inert, nonmetabolisable.
Freely filtered by Glomerulus.
do not interact with receptors or directly block renal
transport
activity dependent on development of osmotic pressure
Mannitol (prototype)
Urea
Glycerol
Isosorbide
11. Mechanism of Action
osmotic diuretics are not reabsorbed
increases osmotic pressure specifically in the
proximal tubule and loop of Henle
prevents passive reabsorption of H2O
osmotic force solute in lumen > osmotic force of
reabsorbed Na+
increased H2O and Na+ excretion
12. Therapeutic Uses
Mannitol
drug of choice: non-toxic, freely filtered, non-reabsorbable
and non-metabolized
administered prophylatically 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
13. Side Effects
increased extracellular fluid volume
cardiac failure
pulmonary edema
hypernatremia
hyperkalemia secondary to diabetes or
impaired renal function
headache, nausea, vomiting
14. Xanthine diuretics
Act by increasing renal Blood flow as well as by
inhibiting tubular reabsorption of Sodium.
This produces net loss of water and electrolytes
diuretic action is not much affected by changes in acid
base balance.
Theophylline is most effective.
15. Carbonic Anhydrase Inhibitors
Limited uses as diuretics
Acetazolamide
•prototype carbonic anhydrase inhibitor
•developed from sulfanilamide (caused metabolic
acidosis and alkaline urine)
16. Mechanism of Action
inhibits carbonic anhydrase in renal proximal tubule cells
carbonic anhydrase catalyzes formation of HCO3- and H+ from
H2O and CO2
inhibition of carbonic anhydrase decreases [H+] in tubule lumen
less H+ for Na+/H+
exchange
increased lumen Na+,
increased H2O
retention
Site I
17. Therapeutic Uses
used to treat chronic open-angle glaucoma
aqueous humor has high [HCO3-]
acute mountain sickness
prevention and treatment
metabolic alkalosis
sometimes epilepsy
mostly used in combination with other diuretics in
resistant patients
18. Side Effects
rapid tolerance
increased HCO3- excretion causes metabolic
acidosis
drowsiness
fatigue
CNS depression
paresthesia (pins and needles under skin)
nephrolithiasis (renal stones)
K+ wasting
19. Thiazide Diuretics
active in distal convoluted tubule
Chlorothiazide (prototype)
Hydrochlorothiazide
Chlorthalidone
Metolazone
20. Mechanism of Action
inhibit Na+ and Cl- transporter in distal convoluted
tubules
increased Na+ and Cl- excretion
weak inhibitors of carbonic anhydrase, increased
HCO3- excretion
increased K+/Mg2+
excretion
decrease Ca2+
excretion
Site III
24. Loop Diuretics
active in “loop” of Henle
Furosemide (prototype)
Bumetanide
Torsemide
Ethacrynic acid
25. Mechanism of Action
enter proximal tubule via organic acid transporter
inhibits apical Na-K-2Cl transporter in thick ascending loop of
henle
competes with Cl- binding site
enhances passive Mg2+
and Ca2+ excretion
increased K+ and H+
excretion in CCD
inhibits reabsorption of
~25% of glomerular filtrate
Site II
26. Pharmacokinetics
orally administered, rapid absorption
rapid onset of action
bound to plasma proteins: displaced by warfarin, and
clofibrate
increase toxicity of cephalosporin antibiotics and lithium
additive toxicity with other ototoxic drugs (Drug Interaction)
inhibitors of organic acid ion transport decrease potency
(i.e. probenecid, NSAID’s) (Drug Interaction)
27. Therapeutic Uses
edema: cardiac, pulmonary or renal
chronic renal failure or nephrosis
hypertension
hypercalcemia
acute and chronic hyperkalemia
29. K+ sparing diuretics
three groups
steroid aldosterone antagonists
spironolactone, eplerenone
Pteridines
triamterene
Pyrazinoylguanidines
amiloride
30. Mechanism of Action
K+ sparing diuretics function in CCD
decrease Na+ transport in collecting tubule
Triamterene/Amiloride
organic bases
secreted into lumen by
proximal tubule cells
inhibit apical Na+
channel
Spironolactone
competitive antagonist for mineralocorticoid receptor
prevents aldosterone stimulated increases in Na+
transporter expression
Site IV