Acetazolamide

Acetazolamide

Clinical data
Trade names	Diamox, Diacarb, others
AHFS/Drugs.com	Monograph
Pregnancy category	AU: B3 US: C (Risk not ruled out)
Routes of administration	by mouth or intravenous
ATC code	S01EC01 (WHO)
Legal status
Legal status	AU: S4 (Prescription only) CA: ℞-only UK: POM (Prescription only) US: ℞-only
Pharmacokinetic data
Protein binding	70–90%[1]
Metabolism	None[1]
Elimination half-life	2–4 hours[1]
Excretion	Urine (90%)[1]
Identifiers
IUPAC name N-(5-Sulfamoyl-1,3,4-thiadiazol-2-yl)acetamide
CAS Number	216665-38-2 Y
PubChem CID	1986
IUPHAR/BPS	6792
DrugBank	DB00819 Y
ChemSpider	1909 Y
UNII	SW1TF3RGAH
KEGG	D00218 Y
ChEBI	CHEBI:27690 Y
ChEMBL	ChEMBL20 Y
PDB ligand	AZM (PDBe, RCSB PDB)
CompTox Dashboard (EPA)	DTXSID7022544
ECHA InfoCard	100.000.400
Chemical and physical data
Formula	C4H6N4O3S2
Molar mass	222.24 g·mol−1
3D model (JSmol)	Interactive image
Melting point	258 to 259 °C (496 to 498 °F)
SMILES NS(=O)(=O)c1nnc(s1)NC(=O)C
InChI InChI=1S/C4H6N4O3S2/c1-2(9)6-3-7-8-4(12-3)13(5,10)11/h1H3,(H2,5,10,11)(H,6,7,9) Y Key:BZKPWHYZMXOIDC-UHFFFAOYSA-N Y
(verify)

Acetazolamide, sold under the trade name Diamox among others, is a medication used to treat glaucoma, epilepsy, altitude sickness, periodic paralysis, idiopathic intracranial hypertension (raised brain pressure of unclear cause), and heart failure.^[2][3] It may be used long term for the treatment of open angle glaucoma and short term for acute angle closure glaucoma until surgery can be carried out,^[4] it is taken by mouth or injection into a vein.^[2]

Common side effects include numbness, ringing in the ears, loss of appetite, vomiting, and sleepiness,^[2] it is not recommended in those with significant kidney problems, liver problems, or who are allergic to sulfonamides.^[2][4] Acetazolamide is in the diuretic and carbonic anhydrase inhibitor families of medication,^[2] it works by decreasing the amount of hydrogen ions and bicarbonate in the body.^[2]

Acetazolamide came into medical use in 1952,^[5] it is on the World Health Organization's List of Essential Medicines, which lists the safest and most effective medicines needed in a health system.^[6] Acetazolamide is available as a generic medication;^[2] the wholesale cost in the developing world is about US$1.40–16.93 per month.^[7] In the United States the wholesale cost is about US$125.34 per month.^[8]

Medical uses[edit]

It is used in the treatment of glaucoma, drug-induced edema, heart failure-induced edema, epilepsy and in reducing intraocular pressure after surgery,^[9][10] it has also been used in the treatment of altitude sickness,^[11] Ménière's disease, increased intracranial pressure and neuromuscular disorders.^[12]

In epilepsy, the main use of acetazolamide is in menstrual-related epilepsy and as an add on to other treatments in refractory epilepsy,^[9][13] it has been demonstrated in drug trials to relieve symptoms associated with dural ectasia in individuals with Marfan's Syndrome.^[14] A 2012 review and meta-analysis found that there was "limited supporting evidence" but that acetazolamide "may be considered" for the treatment of central (as opposed to obstructive) sleep apnea.^[15]

It has also been used to prevent methotrexate-induced kidney damage by alkalinalizing the urine, hence speeding up methotrexate excretion by increasing its solubility in urine.^[12][16] There is some evidence to support its use to prevent hemiplegic migraine.^[17]

High altitude sickness[edit]

In the treatment of mountain sickness, acetazolamide forces the kidneys to excrete bicarbonate, the conjugate base of carbonic acid. By increasing the amount of bicarbonate excreted in the urine, the blood becomes more acidic;^[12] as the body equates acidity of the blood to its CO₂ concentration, artificially acidifying the blood fools the body into thinking it has an excess of CO₂, and it excretes this imaginary excess CO₂ by deeper and faster breathing, which in turn increases the amount of oxygen in the blood.^[18][19] Acetazolamide is not an immediate cure for acute mountain sickness; rather, it speeds up part of the acclimatization process which in turn helps to relieve symptoms.^[20] Acetazolamide is still effective if started early in the course of mountain sickness; as prevention, it is started one day before travel to altitude and continued for the first 2 days at altitude.^[21]

Pregnancy and lactation[edit]

Acetazolamide is pregnancy category B3 in Australia, which means that studies in rats, mice and rabbits in which acetazolamide was given intravenously or orally caused an increased risk of fetal malformations, including defects of the limbs.^[10] Despite this, there is insufficient evidence from studies in humans to either support or discount this evidence.^[10]

Limited data are available on the effects of nursing mothers taking acetazolamide. Therapeutic doses create low levels in breast milk and are not expected to cause problems in infants.^[22]

Side effects[edit]

Common adverse effects of acetazolamide include the following: paraesthesia, fatigue, drowsiness, depression, decreased libido, bitter or metallic taste, nausea, vomiting, abdominal cramps, diarrhea, black feces, polyuria, kidney stones, metabolic acidosis and electrolyte changes (hypokalemia, hyponatremia).^[9] Whereas less common adverse effects include Stevens–Johnson syndrome, anaphylaxis and blood dyscrasias.^[9]

Contraindications[edit]

Contraindications include:^[10]

• Hyperchloremic acidosis
• Hypokalemia (low blood potassium)
• Hyponatremia (low blood sodium)
• Adrenal insufficiency
• Impaired kidney function
• Hypersensitivity to acetazolamide or other sulfonamides.
• Marked liver disease or impairment of liver function, including cirrhosis because of the risk of development of hepatic encephalopathy. Acetazolamide decreases ammonia clearance.

Interactions[edit]

It is possible that it might interact with:^[10]

• Amphetamines, because it increases the pH of the renal tubular urine, hence reducing the clearance of amphetamines.
• Other carbonic anhydrase inhibitors — potential for additive inhibitory effects on carbonic anhydrase and hence potential for toxicity.
• Ciclosporin, may increase plasma levels of ciclosporin.
• Antifolates such as trimethoprim, methotrexate, pemetrexed and raltitrexed.
• Hypoglycemics, acetazolamide can both increase or decrease blood glucose levels.
• Lithium, increases excretion, hence reducing therapeutic effect.
• Methenamine compounds, reduces the urinary excretion of methenamines.
• Phenytoin, reduces phenytoin excretion, hence increasing the potential for toxicity.
• Primidone, reduces plasma levels of primidone. Hence reducing anticonvulsant effect.
• Quinidine, reduces urinary excretion of quinidine, hence increasing the potential for toxicity.
• Salicylates, potential for severe toxicity.
• Sodium bicarbonate, potential for kidney stone formation.
• Anticoagulants, cardiac glycosides, may have their effects potentiated by acetazolamide.

Mechanism of action[edit]

Carbonic anhydrase (ribbon) complex with a sulfonamide inhibitor (ball-and-sticks).

Proximal convoluted tubule. Urinary space is on left.

Acetazolamide is a carbonic anhydrase inhibitor, hence causing the accumulation of carbonic acid.^[12] Carbonic anhydrase is an enzyme found in red blood cells and many other tissues that catalyses the following reaction:^[23]

H₂CO₃ ⇌ H₂O + CO₂

hence lowering blood pH, by means of the following reaction that carbonic acid undergoes:^[24]

H₂CO₃ ⇌ HCO₃⁻ + H⁺

which has a pK_a of 6.3.^[24]

The mechanism of diuresis involves the proximal tubule of the kidney; the enzyme carbonic anhydrase is found here, allowing the reabsorption of bicarbonate, sodium, and chloride. By inhibiting this enzyme, these ions are excreted, along with excess water, lowering blood pressure, intracranial pressure, and intraocular pressure. By excreting bicarbonate, the blood becomes acidic, causing compensatory hyperventilation with deep respiration (Kussmaul respiration), increasing levels of oxygen and decreasing levels of carbon dioxide in the blood.^[25]

In the eye this results in a reduction in aqueous humour.^[10]

Bicarbonate (HCO₃⁻) has a pK_a of 10.3 with carbonate (CO₃²⁻), far further from physiologic pH (7.35–7.45), and so it is more likely to accept a proton than to donate one, but it is also far less likely for it to do either, thus bicarbonate will be the major species at physiological pH.

Under normal conditions in the proximal convoluted tubule of the kidney, most of the carbonic acid (H₂CO₃) produced intracellularly by the action of carbonic anhydrase quickly dissociates in the cell to bicarbonate (HCO₃⁻) and an H⁺ ion (a proton), as previously mentioned. The bicarbonate (HCO₃⁻) exits at the basal portion of the cell via sodium (Na⁺) symport and chloride (Cl⁻) antiport and re-enters circulation, where it may accept a proton if blood pH decreases, thus acting as a weak, basic buffer. The remaining H⁺ left over from the intracellular production of carbonic acid (H₂CO₃) exits the apical (urinary lumen) portion of the cell by Na⁺ antiport, acidifying the urine. There, it may join with another bicarbonate (HCO₃⁻) that dissociated from its H⁺ in the lumen of the urinary space only after exiting the proximal convoluted kidney cells/glomerulus as carbonic acid (H₂CO₃) because bicarbonate (HCO₃⁻) itself can not diffuse across the cell membrane in its polar state. This will replenish carbonic acid (H₂CO₃) so that it then may be reabsorbed into the cell as itself or CO₂ and H₂O (produced via a luminal carbonic anhydrase). As a result of this whole process, there is a greater net balance of H⁺ in the urinary lumen than bicarbonate (HCO₃⁻), and so this space is more acidic than physiologic pH. Thus, there is an increased likelihood that any bicarbonate (HCO₃⁻) that was left over in the lumen diffuses back into the cell as carbonic acid, CO₂, or H₂O.

In short, under normal conditions, the net effect of carbonic anhydrase in the urinary lumen and cells of the proximal convoluted tubule is to acidify the urine and transport bicarbonate (HCO₃⁻) into the body. Another effect is excretion of Cl⁻ as it is needed to maintain electroneutrality in the lumen, as well as the reabsorption of Na⁺ into the body.

Thus, by disrupting this process with acetazolamide, urinary Na⁺ and bicarbonate (HCO₃⁻) are increased, and urinary H⁺ and Cl⁻ are decreased. Inversely, serum Na⁺ and bicarbonate (HCO₃⁻) are decreased, and serum H⁺ and Cl⁻ are increased. H₂O generally follows sodium, and so this is how the clinical diuretic effect is achieved, which reduces blood volume and thus preload on the heart to improve contractility and reduce blood pressure, or achieve other desired clinical effects of reduced blood volume such as reducing edema or intracranial pressure.^[26]

History[edit]

An early description of this compound (as 2-acetylamino-1,3,4-thiadiazole-5-sulfonamide) and its synthesis appears in U.S. Patent 2554816^[27]

References[edit]