Ethosuximide Explained

Ethosuximide, sold under the brand name Zarontin among others, is a medication used to treat absence seizures. It may be used by itself or with other antiseizure medications such as valproic acid. Ethosuximide is taken by mouth.[1]

Ethosuximide is usually well tolerated.[2] Common side effects include loss of appetite, abdominal pain, diarrhea, and feeling tired.[1] Serious side effects include suicidal thoughts, low blood cell levels, and lupus erythematosus.[1] [2] It is unclear if it has adverse effects on the fetus during pregnancy.[1] Ethosuximide is in the succinimide family of medications. Its mechanism of action is thought to be due to antagonism of the postsynaptic T-type voltage-gated calcium channel.[3]

Ethosuximide was approved for medical use in the United States in 1960.[4] It is on the World Health Organization's List of Essential Medicines.[5] Ethosuximide is available as a generic medication.[1], its availability was limited in many countries, with concerns about price fixing in the United States.[6]

Medical uses

Ethosuximide is approved for absence seizures, and is considered the first choice medication for treating them, in part because it lacks the idiosyncratic hepatotoxicity of the alternative anti-absence drug, valproic acid.

Adverse effects

As with other anticonvulsants, ethosuximide carries a warning about use during pregnancy. Although a causal relationship with birth defects has not be established, the potential for harm to the baby is weighed against the known harm caused by a mother having even minor seizures.[1]

Central nervous system

Common

Rare

Gastrointestinal

Genitourinary

Blood

The following can occur with or without bone marrow loss:

Skin

Eyes

Drug interactions

Valproates can either decrease or increase the levels of ethosuximide; however, combinations of valproates and ethosuximide had a greater protective index than either drug alone.

It may elevate serum phenytoin levels.

Mechanism of action

The mechanism by which ethosuximide affects neuronal excitability includes block of T-type calcium channels, and may include effects of the drug on other classes of ion channel. The primary finding that ethosuximide is a T-type calcium channel blocker gained widespread support, but initial attempts to replicate the finding were inconsistent. Subsequent experiments on recombinant T-type channels in cell lines demonstrated conclusively that ethosuximide blocks all T-type calcium channel isoforms. Significant T-type calcium channel density occurs in dendrites of neurons, and recordings from reduced preparations that strip away this dendritic source of T-type calcium channels may have contributed to reports of ethosuximide ineffectiveness.

In March 1989, Coulter, Huguenard and Prince showed that ethosuximide and dimethadione, both effective anti-absence agents, reduced low-threshold Ca2+ currents in T-type calcium channels in freshly removed thalamic neurons. In June of that same year, they also found the mechanism of this reduction to be voltage-dependent, using acutely dissociated neurons of rats and guinea pigs; it was also noted that valproic acid, which is also used in absence seizures, did not do that. The next year, they showed that anticonvulsant succinimides did this and that the pro-convulsant ones did not. The first part was supported by Kostyuk et al. in 1992, who reported a substantial reduction in current in dorsal root ganglia at concentrations ranging from 7 μmol/L to 1 mmol/L.

That same year, however, Herrington and Lingle found no such effect at concentrations of up to 2.5 mmol/L. The year after, a study conducted on human neocortical cells removed during surgery for intractable epilepsy, the first to use human tissue, found that ethosuximide had no effect on Ca2+ currents at the concentrations typically needed for a therapeutic effect.

In 1998, Slobodan M. Todorovic and Christopher J. Lingle of Washington University reported a 100% block of T-type current in dorsal root ganglia at 23.7 ± 0.5 mmol/L, far higher than Kostyuk reported. That same year, Leresche et al. reported that ethosuximide had no effect on T-type currents, but did decrease noninactivating Na+ current by 60% and the Ca2+-activated K+ currents by 39.1 ± 6.4% in rat and cat thalamocortical cells. It was concluded that the decrease in Na+ current is responsible for the anti-absence properties.

In the introduction of a paper published in 2001, Dr. Juan Carlos Gomora and colleagues at the University of Virginia in Charlottesville pointed out that past studies were often done in isolated neurons that had lost most of their T-type channels. Using cloned α1G, α1H, and α1I T-type calcium channels, Gomora's team found that ethosuximide blocked the channels with an IC50 of 12 ± 2 mmol/L and that of N-desmethylmethsuximide (the active metabolite of mesuximide) is 1.95 ± 0.19 mmol/L for α1G, 1.82 ± 0.16 mmol/L for α1I, and 3.0 ± 0.3 mmol/L for α1H. It was suggested that the blockade of open channels is facilitated by ethosuximide's physically plugging the channels when current flows inward.

Stereochemistry

Ethosuximide is a chiral drug with a stereocenter. Therapeutically, the racemate, the 1: 1 mixture of ( S ) and ( R ) - isomers used.[7]

Society and culture

Cost

As of 2019 there were concerns in the United States that the price of ethosuximide was inflated by manufacturers.[8] [9]

Availability

Availability of ethosuximide is limited in many countries.[10] It was marketed under the trade names Emeside and Zarontin. However, both capsule preparations were discontinued from production, leaving only generic preparations available. Emeside capsules were discontinued by their manufacturer, Laboratories for Applied Biology, in 2005.[11] Similarly, Zarontin capsules were discontinued by Pfizer in 2007.[12] Syrup preparations of both brands remained available.

See also

Notes and References

  1. Web site: Ethosuximide. The American Society of Health-System Pharmacists. 8 December 2016. live. https://web.archive.org/web/20161221003723/https://www.drugs.com/monograph/ethosuximide.html. 21 December 2016.
  2. Book: WHO Model Formulary 2008 . 2009 . 9789241547659 . ((World Health Organization)) . Stuart MC, Kouimtzi M, Hill SR . 10665/44053 . World Health Organization . World Health Organization . free . 69, 74–75 .
  3. Huguenard . John R. . Block of T -Type Ca2+ Channels Is an Important Action of Succinimide Antiabsence Drugs . Epilepsy Currents . March 2002 . 2 . 2 . 49–52 . 10.1046/j.1535-7597.2002.00019.x . 15309165 . 320968 .
  4. Web site: Drugs@FDA: FDA-Approved Drugs . U.S. Food and Drug Administration . 29 December 2020.
  5. Book: ((World Health Organization)) . World Health Organization model list of essential medicines: 21st list 2019 . 2019 . 10665/325771 . World Health Organization . World Health Organization . Geneva . WHO/MVP/EMP/IAU/2019.06. License: CC BY-NC-SA 3.0 IGO . free .
  6. Attorney General Tong leads 44-state coalition in antitrust lawsuit against Teva Pharmaceuticals, 19 other generic drug manufacturers, 15 individuals in conspiracy to fix prices and allocate markets for more than 100 different generic drugs . 5 April 2020 . 12 May 2019 . Office of the Attorney General of the State of Connecticut.
  7. Rote Liste Service GmbH (Hrsg.): Rote Liste 2017 – Arzneimittelverzeichnis für Deutschland (einschließlich EU-Zulassungen und bestimmter Medizinprodukte). Rote Liste Service GmbH, Frankfurt/Main, 2017, Aufl. 57,, S. 182.
  8. Web site: States sue generic drug makers, claiming a conspiracy to fix prices . consumeraffairs.com . 5 April 2020 . en . 14 May 2019.
  9. News: Staff . WMBF News . South Carolina joins lawsuit against manufacturers in alleged conspiracy to fix prescription drug prices . 5 April 2020 . wmbfnews.com.
  10. Book: Hempel . Georg . Methods of Therapeutic Drug Monitoring Including Pharmacogenetics . 2019 . Elsevier . 978-0-444-64067-3 . 241 . en.
  11. Concern over ethosuximide capsule discontinuation . Pharm J . Oct 29, 2005 . 275 . 539 . 2008-08-31 . live . https://web.archive.org/web/20081013220747/http://www.pharmj.com/Editorial/20051029/news/p539ethosuximide.html . 2008-10-13 . (paywalled archive)
  12. Web site: Zarontin capsules discontinued. 2012-10-24. live. https://web.archive.org/web/20120626002021/http://www.epilepsy.org.uk/news/drugwatch/ethosuximide. 2012-06-26.