Metoprolol

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Metoprolol
Metoprolol structure.svg
Clinical data
Pronunciation /mɛˈtprlɑːl/, /mɛtˈprlɑːl/
Trade names Lopressor, Metolar XR, others
AHFS/Drugs.com Monograph
MedlinePlus a682864
License data
  • US FDAMetoprolol
Pregnancy
category
  • AU: C
  • US: C (Risk not ruled out)
Routes of
administration
By mouth, IV
Drug class Beta blocker
ATC code
Legal status
Legal status
  • In general: ℞ (Prescription only)
Pharmacokinetic data
Bioavailability 50% (single dose)[1]
70% (repeated administration)[2]
Protein binding 12%
Metabolism Liver via CYP2D6, CYP3A4
Elimination half-life 3–7 hours
Excretion Kidney
Identifiers
CAS Number
  • 51384-51-1 ☑Y
PubChem CID
  • 4171
IUPHAR/BPS
  • 553
DrugBank
  • DB00264 ☑Y
ChemSpider
  • 4027 ☑Y
UNII
  • GEB06NHM23
KEGG
  • D02358 ☑Y
ChEBI
  • CHEBI:6904 ☑Y
ChEMBL
  • CHEMBL13 ☑Y
ECHA InfoCard 100.048.603
Chemical and physical data
Formula C15H25NO3
Molar mass 267.37 g·mol−1
3D model (JSmol)
  • Interactive image
Chirality Racemic mixture
Melting point 120 °C (248 °F)
  (verify)

Metoprolol, marketed under the tradename Lopressor among others, is a medication of the selective β1 receptor blocker type.[3] It is used to treat high blood pressure, chest pain due to poor blood flow to the heart, and a number of conditions involving an abnormally fast heart rate.[3] It is also used to prevent further heart problems after myocardial infarction and to prevent headaches in those with migraines.[3]

Metoprolol is sold in formulations that can be taken by mouth or given intravenously.[3] The medication is often taken twice a day.[3] The extended-release formulation is taken once per day.[3] Metoprolol may be combined with hydrochlorothiazide (a diuretic) in a single tablet.[3]

Common side effects include trouble sleeping, feeling tired, feeling faint, and abdominal discomfort.[3] Large doses may cause serious toxicity.[4][5] Risk in pregnancy has not been ruled out.[3][6] It appears to be safe in breastfeeding.[7] Greater care is required with use in those with liver problems or asthma.[3] Stopping this drug should be done slowly to decrease the risk of further health problems.[3]

Metoprolol was first made in 1969.[8] It is on the World Health Organization's List of Essential Medicines, the most important medications needed in a basic health system.[9] It is available as a generic drug.[3] In 2013, metoprolol was the 19th-most prescribed medication in the United States.[10]

Medical uses

Metoprolol is used for a number of conditions, including hypertension, angina, acute myocardial infarction, supraventricular tachycardia, ventricular tachycardia, congestive heart failure, and prevention of migraine headaches.[11]

Due to its selectivity in blocking the beta1 receptors in the heart, metoprolol is also prescribed for off-label use in performance anxiety, social anxiety disorder, and other anxiety disorders.

Available forms

Metoprolol is sold in formulations that can be taken by mouth or given intravenously.[3] The medication is often taken twice a day.[3] The extended-release formulation is taken once per day.[3] Metoprolol may be combined with hydrochlorothiazide (a diuretic) in a single tablet.[3]

Adverse effects

Side effects, especially with higher doses, include dizziness, drowsiness, fatigue, diarrhea, unusual dreams, trouble sleeping, depression, and vision problems. Metoprolol may also reduce blood flow to the hands or feet, causing them to feel numb and cold; smoking may worsen this effect.[17] Due to the high penetration across the blood-brain barrier, lipophilic beta blockers such as propranolol and metoprolol are more likely than other less lipophilic beta blockers to cause sleep disturbances such as insomnia and vivid dreams and nightmares.[18]

Serious side effects that are advised to be reported immediately include symptoms of bradycardia (resting heart rate slower than 60 beats per minute), persistent symptoms of dizziness, fainting and unusual fatigue, bluish discoloration of the fingers and toes, numbness/tingling/swelling of the hands or feet, sexual dysfunction, erectile dysfunction, hair loss, mental/mood changes, depression, breathing difficulty, cough, dyslipidemia and increased thirst. Consuming alcohol while taking metoprolol may cause mild body rashes and is not advised.[17]

Precautions

Metoprolol may worsen the symptoms of heart failure in some patients, who may experience chest pain or discomfort, dilated neck veins, extreme fatigue, irregular breathing, an irregular heartbeat, shortness of breath, swelling of the face, fingers, feet, or lower legs, weight gain, or wheezing.[19]

This medicine may cause changes in blood sugar levels or cover up signs of low blood sugar, such as a rapid pulse rate.[19] It also may cause some people to become less alert than they are normally, making it dangerous for them to drive or use machines.[19]

Greater care is required with use in those with liver problems or asthma.[3] Stopping this drug should be done slowly to decrease the risk of further health problems.[3]

Pregnancy and breastfeeding

Risk for the fetus has not been ruled out, per being rated pregnancy category C in the United States.[3][6] Metoprolol is category C in Australia, meaning that it may be suspected of causing harmful effects on the human fetus (but no malformations).[6] It appears to be safe in breastfeeding.[7]

Overdose

Excessive doses of metoprolol can cause severe hypotension, bradycardia, metabolic acidosis, seizures, and cardiorespiratory arrest. Blood or plasma concentrations may be measured to confirm a diagnosis of overdose or poisoning in hospitalized patients or to assist in a medicolegal death investigation. Plasma levels are usually less than 200 μg/l during therapeutic administration, but can range from 1–20 mg/l in overdose victims.[20][21][22]

Pharmacology

General pharmacological principles of metoprolol:[citation needed]

  • beta-1 selective
  • moderately lipophilic
  • without intrinsic sympathomimetic activity
  • with weak membrane stabilizing activity
  • decreases heart rate, contractility, and cardiac output, therefore decreasing blood pressure

Mechanism of action

Metoprolol blocks β1 adrenergic receptors in heart muscle cells, thereby decreasing the slope of phase 4 in the nodal action potential (reducing Na+ uptake) and prolonging repolarization of phase 3 (slowing down K+ release).[23] It also suppresses the norepinephrine-induced increase in the sarcoplasmic reticulum (SR) Ca2+ leak and the spontaneous SR Ca2+ release, which are the major triggers for atrial fibrillation.[23]

Pharmacokinetics

Metoprolol has a short half-life of 3 to 7 hours, so is taken at least twice daily or as a slow-release preparation.

It undergoes α-hydroxylation and O-demethylation as a substrate of the cytochrome liver enzymes CYP2D6[24][25] and a small percentage by CYP3A4, resulting in inactive metabolites.

Chemistry

Metoprolol has a very low melting point; around 120 °C (248 °F) for the tartrate, and around 136 °C (277 °F) for the succinate. Because of this, metoprolol is always manufactured in a salt-based solution, as drugs with low melting points are difficult to work with in a manufacturing environment. The free base exists as a waxy white solid, and the tartrate salt is finer crystalline material.[citation needed]

The active substance metoprolol is employed either as metoprolol succinate or as metoprolol tartrate (where 100 mg metoprolol tartrate corresponds to 95 mg metoprolol succinate). The tartrate is an immediate-release formulation and the succinate is an extended-release formulation.[26]

Stereochemistry

Metoprolol contains a stereocenter and consists of two enantiomers. This is a racemate, i.e. a 1:1 mixture of (R)- and the (S)-form:[27]

Enantiomers of metoprolol
(R)-Metoprolol Structural Formula V1.svg
CAS-Nummer: 81024-43-3
(S)-Metoprolol Structural Formula V1.svg
CAS-Nummer: 81024-42-2

History

Metoprolol was first made in 1969.[8]

Society and culture

Metoprolol is on the World Health Organization's List of Essential Medicines, the most important medications needed in a basic health system.[9] It is available as a generic drug.[3] In 2013, metoprolol was the 19th-most prescribed medication in the United States.[28]

Legal status

Within the UK metoprolol is classified as a prescription-only drug in the beta blocker class and is regulated by the Medicines and Healthcare Products Regulatory Agency (MHRA). The MHRA is a government body set up in 2003 and is responsible for regulating medicines, medical devices, and equipment used in healthcare. The MHRA acknowledges that no product is completely risk free but takes into account research and evidence to ensure that any risks associated are minimal.[29]

The use of beta blockers such as metoprolol was approved in the US by the FDA (Food and Drug Administration) in 1967. The FDA has approved beta blockers for the treatment of cardiac arrhythmias, hypertension, migraines, and others. Prescribers may choose to prescribe beta blockers for other treatments if there is just cause even though it is not approved by the FDA. Drug manufacturers, however, are unable to advertise beta blockers for other purposes that have not been approved by the FDA. Since the FDA does not regulate the practice of medicine after the drug has been approved, it is legal to prescribe beta blockers for other treatments such as performance anxiety.[30]

Legislation

The MHRA granted the Intas Pharmaceuticals Limited Marketing Authorisation (licences) for metoprolol tartrate (50mg and 100mg tablets) for medicinal prescription only on September 23rd 2011; this was after it was established that there was no new or unexpected safety concerns and that the benefits of metoprolol tartrate were greater than the risks. Metoprolol tartrate is a generic version of Lopressor, which was licensed and authorised on June 6th 1997 to Novartis Pharmaceuticals.[31]

In sport

Metoprolol is a beta blocker and is banned by the world anti-doping agency in some sports. Beta blockers can be used to reduce heart rate and minimize tremors, which can enhance performance in sports such as archery.[32] All beta blockers are banned during and out of competition for archery and shooting.[33] In some sports such as all forms of billiards, darts, and golf, beta blockers are banned during competition only. Furthermore, any form of beta blocker is banned within riflery competitions by the National Collegiate Athletic Association.[34]

To detect if beta blockers have been used trace analysis of human urine is analysed. Uncharged drugs and/or metabolites of beta blockers can be analysed by gas-chromatography-mass spectrometry in selected ion monitoring (GC-MS-SIM). However, in modern times it is increasingly difficult to detect the presence of beta blockers used for sports doping purposes. A disadvantage to using GC-MS-SIM is that prior knowledge of the molecular structure of the target drugs/metabolites is required. Modern times have shown a variance in structures and hence novel beta blockers can go undetected.[35]

Lawsuit

In 2012, an $11 million settlement was reached with Toprol XL (time-release formula version of metoprolol) and its generic equivalent metoprolol. The lawsuit involved the pharmaceuticals companies AstraZeneca AB, AstraZeneca LP, AstraZeneca Pharmaceuticals LP, and Aktiebolaget Hassle. The claims of the lawsuit advise that the manufacturers violated antitrust and consumer protection law. Claiming that to increase profits, lower cost generic versions of Toprol XL were intentionally kept off the market. This claim was subsequently denied by the defendants.[36]

References

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  33. ^ World Anti-Doping Agency (2017). Prohibited List. Montreal: WADA’s Executive Committee.
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  36. ^ Prnewswire.com. (2018). $11 Million Settlement Reached in Lawsuit Involving the Heart Medication, Toprol XL®, and its generic equivalent, metoprolol succinate. [online] Available at: https://www.prnewswire.com/news-releases/11-million-settlement-reached-in-lawsuit-involving-the-heart-medication-toprol-xl-and-its-generic-equivalent-metoprolol-succinate-177848501.html [Accessed 4 Mar. 2018].

External links

  • U.S. National Library of Medicine: Drug Information Portal - Metoprolol
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