Loop diuretics

47,729views

Loop diuretics

MRCP revision

MRCP revision

Acute intermittent porphyria
Autoimmune hemolytic anemia
Glucose-6-phosphate dehydrogenase (G6PD) deficiency
Sickle cell disease (NORD)
Alpha-thalassemia
Beta-thalassemia
Anemia of chronic disease
Iron deficiency anemia
Sideroblastic anemia
Aplastic anemia
Immune thrombocytopenia
Polycythemia vera (NORD)
Antiphospholipid syndrome
Antithrombin III deficiency
Factor V Leiden
Protein C deficiency
Protein S deficiency
Hemophilia
Vitamin K deficiency
Disseminated intravascular coagulation
Heparin-induced thrombocytopenia
Von Willebrand disease
Hemolytic-uremic syndrome
Thrombotic thrombocytopenic purpura
Paroxysmal nocturnal hemoglobinuria
Myelodysplastic syndromes
Myelofibrosis (NORD)
Acute leukemia
Chronic leukemia
Hodgkin lymphoma
Non-Hodgkin lymphoma
Neuroblastoma
5-alpha-reductase deficiency
Androgen insensitivity syndrome
Congenital adrenal hyperplasia
Kallmann syndrome
Thyroglossal duct cyst
Pancreatic neuroendocrine neoplasms
Zollinger-Ellison syndrome
Multiple endocrine neoplasia
Carcinoid syndrome
Hyperparathyroidism
Hypoparathyroidism
Hyperprolactinemia
Pituitary adenoma
Prolactinoma
Delayed puberty
Premature ovarian failure
Constitutional growth delay
Growth hormone deficiency
Hypopituitarism
Hypoprolactinemia
Pituitary apoplexy
Sheehan syndrome
Diabetes insipidus
Syndrome of inappropriate antidiuretic hormone secretion (SIADH)
Thyroid eye disease (NORD)
Thyroid storm
Toxic multinodular goiter
Euthyroid sick syndrome
Postpartum thyroiditis
Riedel thyroiditis
Subacute granulomatous thyroiditis
Thyroid cancer
Bacillus cereus (Food poisoning)
Campylobacter jejuni
Clostridium difficile (Pseudomembranous colitis)
Escherichia coli
Helicobacter pylori
Listeria monocytogenes
Salmonella (non-typhoidal)
Salmonella typhi (typhoid fever)
Shigella
Staphylococcus aureus
Vibrio cholerae (Cholera)
Yersinia enterocolitica
Coxsackievirus
Cytomegalovirus
Herpes simplex virus
Mumps virus
Ascending cholangitis
Gallstone ileus
Alcohol-associated liver disease
Alpha 1-antitrypsin deficiency
Budd-Chiari syndrome
Cholestatic liver disease
Cirrhosis
Gilbert's syndrome
Hemochromatosis
Hepatic encephalopathy
Viral hepatitis
Jaundice
Non-alcoholic fatty liver disease
Portal hypertension
Primary biliary cholangitis
Primary sclerosing cholangitis
Reye syndrome
Wilson disease
Acute pancreatitis
Chronic pancreatitis
Pancreatic pseudocyst
Hirschsprung disease
Intussusception
Ischemic colitis
Microscopic colitis
Necrotizing enterocolitis
Protein losing enteropathy
Short bowel syndrome (NORD)
Small bowel bacterial overgrowth syndrome
Small bowel ischemia and infarction
Tropical sprue
Volvulus
Whipple's disease
Autoimmune hepatitis
Celiac disease
Eosinophilic esophagitis (NORD)
Benign liver tumors
Hepatocellular adenoma
Hepatocellular carcinoma
Familial adenomatous polyposis
Juvenile polyposis syndrome
Peutz-Jeghers syndrome
Gastric cancer
Abdominal hernias
Achondroplasia
Developmental dysplasia of the hip
Muscular dystrophy
Osteomalacia and rickets
Osteoporosis
Paget disease of bone
Gout
Osteoarthritis
Compartment syndrome
Ankylosing spondylitis
Dermatomyositis
Juvenile idiopathic arthritis
Limited systemic sclerosis (CREST syndrome)
Mixed connective tissue disease
Polymyositis
Psoriatic arthritis
Raynaud phenomenon
Reactive arthritis
Rheumatoid arthritis
Sjogren syndrome
Systemic lupus erythematosus
Septic arthritis
Spondylitis
Baker cyst
Bursitis
Polymyalgia rheumatica
Temporomandibular joint dysfunction
Transient synovitis
Bone tumors
Fibromyalgia
Sciatica
Carpal tunnel syndrome
Rotator cuff tear
Prions (Spongiform encephalopathy)
Adenovirus
Eastern and Western equine encephalitis virus
Epstein-Barr virus (Infectious mononucleosis)
HIV (AIDS)
JC virus (Progressive multifocal leukoencephalopathy)
Lymphocytic choriomeningitis virus
Measles virus
Poliovirus
Rabies virus
Varicella zoster virus
West Nile virus
Cerebral palsy
Neurofibromatosis
Tuberous sclerosis
Erb-Duchenne palsy
Creutzfeldt-Jakob disease
Neurogenic bladder
Treponema pallidum (Syphilis)
Vitamin B12 deficiency
Acoustic neuroma (schwannoma)
Glaucoma
Amyloidosis
Focal segmental glomerulosclerosis (NORD)
Membranous nephropathy
Minimal change disease
Renal tubular acidosis
Nephroblastoma (Wilms tumor)
Non-urothelial bladder cancers
Transitional cell carcinoma
Renal cell carcinoma
Urinary incontinence
Renal cortical necrosis
Nephrotic syndromes: Pathology review
Renal tubular defects: Pathology review
Renal tubular acidosis: Pathology review
Cardiac preload
Bacillus anthracis (Anthrax)
Bacteroides fragilis
Bordetella pertussis (Whooping cough)
Corynebacterium diphtheriae (Diphtheria)
Coxiella burnetii (Q fever)
Francisella tularensis (Tularemia)
Moraxella catarrhalis
Bacterial epiglottitis
Laryngomalacia
Bronchodilators: Beta 2-agonists and muscarinic antagonists
Bronchodilators: Leukotriene antagonists and methylxanthines
Cytomegalovirus infection after transplant (NORD)
Graft-versus-host disease
Post-transplant lymphoproliferative disorders (NORD)
Transplant rejection
Anaphylaxis
Food allergy
Type I hypersensitivity
Hemolytic disease of the newborn
Pemphigus vulgaris
Type II hypersensitivity
Serum sickness
Type III hypersensitivity
Contact dermatitis
Type IV hypersensitivity
Atopic dermatitis
Lichen planus
Psoriasis
Erythema multiforme
Stevens-Johnson syndrome
Bullous pemphigoid
Acne vulgaris
Skin cancer

Transcript

Watch video only

Diuretics are medications that act on the kidneys to increase production of urine - and therefore, eliminates water from the body. There are 5 main types of diuretics - carbonic anhydrase inhibitors; osmotic diuretics; thiazide and thiazide-like diuretics; potassium sparing diuretics; and last but not least, loop diuretics - which we’ll get intimately acquainted with during this video.

Now, the basic unit of the kidney is called a nephron, and each nephron is made up of a glomerulus, which filters the blood. Blood enters the glomerulus with the afferent arteriole, and exits the glomerulus from the efferent arteriole. The filtered content then goes through the renal tubule, where excess waste, and molecules (such as ions and water), are removed or filtered through an exchange between the tubule and the peritubular capillaries. So the renal tubule plays a huge role in secretion and reabsorption of fluid and ions - such as sodium, potassium, and chloride - in order to maintain homeostasis, or the balance of fluid and ions in our body. The renal tubule has a few segments of its own: the proximal convoluted tubule; the U-shaped loop of Henle, with a thin descending, a thin ascending limb, and a thick ascending limb; and finally, the distal convoluted tubule, which empties into the collecting duct, which collects the urine.

Different kinds of diuretics act on different segments of the renal tubule. Now, loop diuretics - as you might have guessed - act on the loop of Henle. To be more specific, they mainly target the thick ascending limb. The thick ascending limb is impermeable to water and it is lined with cuboidal cells that have Na+K+2Cl- cotransporters on the apical surface. These transporters reabsorb sodium, potassium, and chloride from inside the thick ascending limb back into the blood. As such, they shuttle one sodium into the cell, down its concentration gradient, and that powers the movement of one potassium and two chlorides into the cell as well. Think of it as a revolving door where sodium is the guy doing all the pushing, and one potassium and two chlorides just follow him in. This way, approximately 25% of the filtered sodium is reabsorbed in the loop of Henle, mostly in the thick ascending limb. Now, on the basolateral side of the tubule cell, a Na/K ATPase uses energy in the form of ATP to pump three sodium ions into the interstitial fluid in exchange for letting two potassium ions into the cell. This helps to maintain the low sodium concentration inside the cell. Finally, both chloride and potassium move from the cell back into the lumen of the thick ascending limb, through special channels on the apical side of the cells that simply “leak” these ions passively. Funnily enough, the passive movement of potassium generates an electrochemical gradient that increases the reabsorption of calcium and magnesium through a paracellular pathway - meaning, these ions don’t use any channels, but rather they sneak between two epithelial cells and go back in the bloodstream. Now that’s a lot of activity for such a tiny cell!

Ok, now here’s where loop diuretics come into play. Just to get acquainted with our team here, there’s 4 main diuretics - 3 of them: furosemide, bumetanide and torsemide - are chemically related, in that they are sulfonamide derivatives. The last non-sulfonamide loop diuretic, ethacrynic acid, is a phenoxyacetic acid derivative.

These medications can be administered orally or intravenously, and once they’re in the bloodstream, they get secreted from the peritubular capillaries into the proximal tubule. Then, they make their way to the thick ascending limb and bind to the Na+K+2Cl- cotransporters. Loop diuretics bind to the Cl- site on the transporter and block it, so now sodium, potassium, and chloride can’t be reabsorbed into the bloodstream and they get excreted out with the urine. Other ions that depend on sodium reabsorption, like calcium and magnesium are excreted as well. Now remember, water follows where sodium goes. So this means there will be more water molecules in the lumen as well, so more urine is produced. Okay, now regarding calcium, there’s an important distinction from thiazide diuretics, which is another important class of diuretics. Loop diuretics increase calcium excretion, while thiazide diuretics decrease calcium excretion. There’s a mnemonic to help you remember this fact! “Loops lose calcium”!

Okay, now, along with inhibiting these Na+K+2Cl- cotransporters, loop diuretics also stimulate the release of prostaglandins, which dilate the afferent arteriole. As a result, they increase the renal plasma flow and they also increase the glomerular filtration rate, or GFR. However, many individuals who take loop diuretics also take non-steroidal anti-inflammatory drugs, or NSAIDs, which inhibit prostaglandin synthesis and thus, they can decrease the loop diuretics’ effect.

Ok, so the major indication for diuretics is for the management of edematous states, like heart failure, pulmonary edema, cirrhosis with ascites, or nephrotic syndrome, where fluid builds up in the extracellular space. However, they can also be used as an alternative agent for hypertension. Since these medications cause water loss through the urine, it leads to decreased plasma volume and cardiac output, resulting in lower blood pressure.

Sources

  1. "Katzung & Trevor's Pharmacology Examination and Board Review,12th Edition" McGraw-Hill Education / Medical (2018)
  2. "Rang and Dale's Pharmacology" Elsevier (2019)
  3. "Goodman and Gilman's The Pharmacological Basis of Therapeutics, 13th Edition" McGraw-Hill Education / Medical (2017)
  4. "Cellular mechanism of the action of loop diuretics on the thick ascending limb of Henle's loop" Klin Wochenschr (1983)
  5. "Cellular mechanism of action of loop diuretics: implications for drug effectiveness and adverse effects" Am J Cardiol (1986)
  6. "Loop Diuretics in Acute Kidney Injury Prevention, Therapy, and Risk Stratification" Kidney and Blood Pressure Research (2019)