Verapamil

Summary

Verapamil, sold under various trade names,[1] is a calcium channel blocker medication used for the treatment of high blood pressure, angina (chest pain from not enough blood flow to the heart), and supraventricular tachycardia.[7] It may also be used for the prevention of migraines and cluster headaches.[8][9] It is given by mouth or by injection into a vein.[7]

Verapamil
Clinical data
Pronunciation/vɛˈræpəmɪl/
ve-RAP-ə-mil
Trade namesIsoptin, Calan, others[1]
AHFS/Drugs.comMonograph
MedlinePlusa684030
License data
Pregnancy
category
Routes of
administration
By mouth, intravenous
Drug classCalcium channel blocker
ATC code
Legal status
Legal status
Pharmacokinetic data
Bioavailability35.1%
MetabolismLiver
Elimination half-life2.8–7.4 hours[6]
ExcretionKidney: 11%
Identifiers
  • (RS)-2-(3,4-Dimethoxyphenyl)-5-{[2-(3,4-dimethoxyphenyl)ethyl](methyl)amino}-2-(propan-2-yl)pentanenitrile
CAS Number
  • 52-53-9 checkY
PubChem CID
  • 2520
IUPHAR/BPS
  • 2406
DrugBank
  • DB00661 checkY
ChemSpider
  • 2425 checkY
UNII
  • CJ0O37KU29
KEGG
  • D02356 checkY
  • as HCl: D00619 checkY
ChEBI
  • CHEBI:9948 checkY
ChEMBL
  • ChEMBL6966 checkY
CompTox Dashboard (EPA)
  • DTXSID9041152 Edit this at Wikidata
ECHA InfoCard100.000.133 Edit this at Wikidata
Chemical and physical data
FormulaC27H38N2O4
Molar mass454.611 g·mol−1
3D model (JSmol)
  • Interactive image
ChiralityRacemic mixture
  • N#CC(c1cc(OC)c(OC)cc1)(CCCN(CCc2ccc(OC)c(OC)c2)C)C(C)C
  • InChI=1S/C27H38N2O4/c1-20(2)27(19-28,22-10-12-24(31-5)26(18-22)33-7)14-8-15-29(3)16-13-21-9-11-23(30-4)25(17-21)32-6/h9-12,17-18,20H,8,13-16H2,1-7H3 checkY
  • Key:SGTNSNPWRIOYBX-UHFFFAOYSA-N checkY
  (verify)

Common side effects include headache, low blood pressure, nausea, and constipation.[7] Other side effects include allergic reactions and muscle pains.[10] It is not recommended in people with a slow heart rate or heart failure.[10] It is believed to cause problems for the fetus if used during pregnancy.[2] It is in the non–dihydropyridine calcium channel blocker family of medications.[7]

Verapamil was approved for medical use in the United States in 1981.[7][11] It is on the World Health Organization's List of Essential Medicines.[12][13] Verapamil is available as a generic medication.[7] Long acting formulations exist.[10] In 2021, it was the 196th most commonly prescribed medication in the United States, with more than 2 million prescriptions.[14][15]

Medical uses edit

Verapamil is used for controlling ventricular rate in supraventricular tachycardia (SVT) and migraine headache prevention.[16]

Verapamil is also used for the treatment of angina (chronic stable, vasospastic or Prinzmetal variant), unstable angina (crescendo, preinfarction), and for the prevention of paroxysmal supraventricular tachycardia (PSVT).[17]

Verapamil is a class-IV antiarrhythmic and more effective than digoxin in controlling ventricular rate.[18] Verapamil is not listed as a first line antihypertensive agent by the guidelines provided by JAMA in JNC-8.[19] However, it may be used to treat hypertension if patient has co-morbid atrial fibrillation or other types of arrhythmia.[20][21]

Verapamil is also used intra-arterially to treat cerebral vasospasm.[22] Verapamil is used to treat the condition cluster headache.[23] Tentative evidence supports the use of verapamil topically to treat plantar fibromatosis.[24]

Verapamil use in people with recent onset type-1 diabetes may improve pancreatic beta cell function. In a meta-analysis involving data from 2 randomized controlled trials (113 patients with recent onset type-1 diabetes), Dutta et al. demonstrated use of verapamil over 1 year was associated with significantly higher C-peptide area under the curve levels at 1-year [MD 0.27 nmol/L (95%CI: 0.19-0.35); P < 0.01]. Higher C-peptide levels means better pancreatic insulin production and beta cell function.[25]

Contraindications edit

Use of verapamil is generally avoided in people with severe left ventricular dysfunction, hypotension (systolic blood pressure less than 90 mm Hg), cardiogenic shock, and hypersensitivity to verapamil.[4] It is also contraindicated in people with atrial flutter or fibrillation and an existing accessory tract such as in Wolff-Parkinson-White syndrome.[26][4]

Side effects edit

The most common side effect of verapamil is constipation (7.3%). While the definite mechanism by which Verapamil causes constipation has not been studied, studies have been conducted to rule out mechanisms of actions that might yield this adverse effect. In a study conducted by The National Library of Medicine titled, "Effect of Verapamil on the Human Intestinal Transit", the study found that verapamil does not have an effect on upper GI transit but rather in the colon.[27]

Other side effects include dizziness (3.3%), nausea (2.7%), low blood pressure (2.5%), and headache 2.2%. Other side effects seen in less than 2% of the population include: edema, congestive heart failure, pulmonary edema, diarrhea, fatigue, elevated liver enzymes, shortness of breath, low heart rate, atrioventricular block, rash and flushing.[4] Along with other calcium channel blockers, verapamil is known to induce gingival enlargement.[28]

Overdose edit

Acute overdose is often manifested by nausea, weakness, slow heart rate, dizziness, low blood pressure, and abnormal heart rhythms. Plasma, serum, or blood concentrations of verapamil and norverapamil, its major active metabolite, may be measured to confirm a diagnosis of poisoning in hospitalized patients or to aid in the medicolegal investigation of fatalities. Blood or plasma verapamil concentrations are usually in a range of 50–500 μg/L in persons on therapy with the drug, but may rise to 1–4 mg/L in acute overdose patients and are often at levels of 5–10 mg/L in fatal poisonings.[29][30]

Mechanism of action edit

Verapamil's mechanism in all cases is to block voltage-dependent calcium channels.[4] In cardiac pharmacology, calcium channel blockers are considered class-IV antiarrhythmic agents. Since calcium channels are especially concentrated in the sinoatrial and atrioventricular nodes, these agents can be used to decrease impulse conduction through the AV node, thus protecting the ventricles from atrial tachyarrhythmias. Verapamil is also a Kv voltage gated potassium channel blocker.[31]

Calcium channels are also present in the smooth muscle lining blood vessels. By relaxing the tone of this smooth muscle, calcium channel blockers dilate the blood vessels. This has led to their use in treating high blood pressure and angina pectoris. The pain of angina is caused by a deficit in oxygen supply to the heart.

Calcium channel blockers like verapamil dilate the coronary blood vessels, which increases the supply of blood and oxygen to the heart. They also cause dilatation of systemic peripheral vessels as well, causing a reduction in the workload of the heart. Thereby reducing myocardial oxygen consumption.[4]

Cluster headaches edit

Preventive therapy with verapamil is believed to work because it has an effect on the circadian rhythm and on CGRPs. As CGRP-release is controlled by voltage-gated calcium channels.[32]

Pharmacokinetic details edit

More than 90% of verapamil is absorbed when given orally,[4] but due to high first-pass metabolism, bioavailability is much lower (10–35%). It is 90% bound to plasma proteins and has a volume of distribution of 3–5 L/kg. It takes 1 to 2 hours to reach peak plasma concentration after oral administration.[4] It is metabolized in the liver to at least 12 inactive metabolites (though one metabolite, norverapamil, retains 20% of the vasodilatory activity of the parent drug). As its metabolites, 70% is excreted in the urine and 16% in feces; 3–4% is excreted unchanged in urine. This is a nonlinear dependence between plasma concentration and dosage. Onset of action is 1–2 hours after oral dosage. Half-life is 5–12 hours (with chronic dosages). It is not cleared by hemodialysis. It is excreted in human milk. Because of the potential for adverse reaction in nursing infants, nursing should be discontinued while verapamil is administered.[medical citation needed]

Verapamil has been reported to be effective in both short-term[33] and long-term treatment of mania and hypomania.[34] Addition of magnesium oxide to the verapamil treatment protocol enhances the antimanic effect.[35]

Veterinary use edit

Intra-abdominal adhesions are common in rabbits following surgery. Verapamil can be given postoperatively in rabbits which have suffered trauma to abdominal organs to prevent formation of these adhesions.[36][37][38] Such effect was not documented in another study with ponies.[39]

Uses in cell biology edit

Verapamil inhibits the ATP-binding cassette (ABC) transporter family of proteins found in stem cells and has been used to study cancer stem cells (CSC) within head and neck squamous cell carcinomas.[40]

Verapamil is also used in cell biology as an inhibitor of drug efflux pump proteins such as P-glycoprotein and other ABC transporter proteins.[41][40] This is useful, as many tumor cell lines overexpress drug efflux pumps, limiting the effectiveness of cytotoxic drugs or fluorescent tags. It is also used in fluorescent cell sorting for DNA content, as it blocks efflux of a variety of DNA-binding fluorophores such as Hoechst 33342. Radioactively labelled verapamil and positron emission tomography can be used with to measure P-glycoprotein function.[medical citation needed]

References edit

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  2. ^ a b "Verapamil Use During Pregnancy". Drugs.com. 18 November 2019. Retrieved 26 March 2020.
  3. ^ "Securon SR - Summary of Product Characteristics (SmPC)". (emc). 17 May 2017. Retrieved 26 March 2020.
  4. ^ a b c d e f g h "Calan- verapamil hydrochloride tablet, film coated". DailyMed. 17 December 2019. Retrieved 26 March 2020.
  5. ^ Human Medicines Evaluation Division (14 October 2020). "Active substance(s): verapamil" (PDF). List of nationally authorised medicinal products. European Medicines Agency.
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