Trihexyphenidyl

Trihexyphenidyl
Names
Trade namesArtane, Parkin, Pacitane, Hexymer, others
IUPAC name
  • (RS)-1-Cyclohexyl-1-phenyl-3-(1-piperidyl)propan-1-ol
Clinical data
Drug classAntimuscarinic[1]
Main usesParkinsonism, extrapyramidal symptoms[2][1]
Side effectsDry mouth, blurry vision, nausea, dizziness[1]
WHO AWaReUnlinkedWikibase error: ⧼unlinkedwikibase-error-statements-entity-not-set⧽
Pregnancy
category
  • AU: B1
  • US: C (Risk not ruled out)
    Routes of
    use    		Oral, as tablet or elixir
    Onset of actionWithin an hour[1]
    Duration of actionUp to 12 hrs[1]
    External links
    AHFS/Drugs.comMonograph
    MedlinePlusa682160
    Legal
    License data
    Legal status
    Pharmacokinetics
    Elimination half-life3.3-4.1 hours
    Chemical and physical data
    FormulaC20H31NO
    Molar mass301.474 g·mol−1
    3D model (JSmol)
    SMILES
    • OC(c1ccccc1)(CCN2CCCCC2)C3CCCCC3
    InChI
    • InChI=1S/C20H31NO/c22-20(18-10-4-1-5-11-18,19-12-6-2-7-13-19)14-17-21-15-8-3-9-16-21/h1,4-5,10-11,19,22H,2-3,6-9,12-17H2 checkY
    • Key:HWHLPVGTWGOCJO-UHFFFAOYSA-N checkY

    Trihexyphenidyl (THP), also known as benzhexol, is a medication used to treat Parkinsonism and certain extrapyramidal symptoms that occur as a result of antipsychotic medication.[2][1] Use is not recommended in Parkinson’s disease due to side effects.[3] It is taken by mouth.[1] Onset of effects are within an hour and can last up to 12 hours.[1]

    Common side effects include dry mouth, blurry vision, nausea, and dizziness.[1] Other side effects may include misuse, anxiety, trouble sleeping, and hallucinations.[3] It is in the antimuscarinic class and works by reducing cholinergic activity in the brain.[1][3]

    Trihexyphenidyl was patented in 1948 and came into medical use in 1949.[4][1] It is on the World Health Organization's List of Essential Medicines as an alternative to biperiden.[5] It is available as a generic medication.[3] In the United Kingdom 84 tablets of 2 mg cost the NHS less than 5 pounds as of 2021.[3] In the United States it is similarly inexpensive.[6]

    Medical uses

    Trihexyphenidyl is used for the symptomatic treatment of Parkinson's disease in mono and combination therapy.[7] It is active in postencephalitic, arteriosclerotic, and idiopathic forms. The drug is also commonly used to treat extrapyramidal side effects occurring during antipsychotic treatment. It reduces the frequency and duration of oculogyric crises as well as of dyskinetic movements and spastic contractions. Trihexyphenidyl may improve psychotic depression and mental inertia frequently associated with Parkinson's disease and symptomatic problems caused by antipsychotic treatment.

    The drug cannot cure Parkinson's disease, but may alleviation of symptoms. An estimated 50 to 75% of people with Parkinson's disease will react positively and experience a 20 to 30% symptomatic improvement. To increase benefits trihexyphenidyl is often given with levodopa, other antimuscarinic or antihistaminic (e.g. diphenhydramine) agents. Combination treatment with dopaminergic agonists such as cabergoline is also possible. This is often termed a 'multidimensional approach'. It has also been prescribed for essential tremor and akathisia.[8][9]

    Dosage

    It is generally started at a dose of 1 mg per day and may be increased up to 20 mg per day.[3]

    Contraindications

    Contradindications include:[10]

    • Hypersensitivity to trihexyphenidyl
    • Narrow angle glaucoma
    • Ileus
    • Caution : People with obstructive diseases of the urogenital tract, people with a known history of seizures and those with potentially dangerous tachycardia
    • People under 18 yrs. of age should not be treated due to a lack of clinical experience.
    • People should allow a period to adjust to the dose when first starting trihexyphenidyl and when the dose has been increased or added to a regimen with other drugs because acute somnolence and accumulated fatigue can make it particularly dangerous to operate an automobile, heavy machinery etc.

    Side effects

    Dose-dependent side effects are frequent, but typically lessen over time as the body adapts to the medication. All of the following symptoms considered, Artane has been shown to dramatically and consistently improve neurologic defects in people aged 16-86 over the course of five years.[11] People who are older or who have psychiatric conditions may become confused or develop delirium. Side effects include but are not limited to:[12]

    • Central nervous system: drowsiness, vertigo, headache, and dizziness are frequent. With high doses nervousness, agitation, anxiety, delirium, and confusion are noted. Trihexyphenidyl may be abused due to a short acting mood-elevating and euphoric effect. The normal sleep architecture may be altered (REM sleep depression). Trihexyphenidyl may lower the seizure-threshold.
    • Peripheral side effects: dry mouth, impaired sweating, abdominal discomfort, nausea, and constipation are frequent. Tachycardia or heart palpitations (fast heart rate) may be noted. Allergic reactions are rare, but may occur. Many of these peripheral symptoms, especially considering an acute increase in anxiety with various physical complaints, as well as evidence of orthostatic hypotension and tachycardia are indicative of withdrawal, especially in people with psychiatric conditions [13]
    • Eyes: trihexyphenidyl causes mydriasis with or without photophobia. It may precipitate narrow angle glaucoma or cause blurred vision.
    • Tolerance may develop during therapy which requires dose adjustments.
    • Striated musculature and weight gain.

    Trihexyphenidyl is a pregnancy category C drug. It is advised to only use with caution if benefits outweigh risks.[14]

    Overdose

    Trihexyphenidyl (THP) and other antiparkinsonian drugs are known to be substances of abuse. This is true both in abusers of other substances and in chronic schizophrenics, the latter being infrequent abusers of other drugs. Trihexyphenidyl mimics an atropine intoxication with mydriasis, dryness of mucous membranes, red face, atonic states of bowels and bladder, and hyperthermia in high doses. Central consequences are agitation, confusion, and hallucinations. An untreated overdose may be fatal, particularly in children. Premortal signs are respiratory depression and cardiac arrest. A specific antagonist is physostigmine which combines a peripheral and a central action. Carbachol can be used to treat atonic bowel and bladder. The vital functions should be monitored and stabilized. It may be necessary to treat hyperthermia with cooling blankets. Clinical case reports have repeatedly shown overdose of trihexyphenidyl alongside other substances.

    Interactions

    • Other anticholinergic drugs (e.g. spasmolytics, antihistamines, TCAs) : Side effects of trihexyphenidyl may be increased.
    • Quinidine : Increased anticholinergic action (particular on AV conduction).
    • Antipsychotics : Long term use of trihexyphenidyl may mask or increase the risk of tardive dyskinesia.
    • Pethidine (meperidine) : Central effects and side effects of pethidine may be increased.
    • Metoclopramide : Action of metoclopramide is decreased.
    • Alcohol : Risk of serious intoxication.

    Pharmacology

    The exact mechanism of action in parkinsonian syndromes is not precisely understood, but it is known that trihexyphenidyl blocks efferent impulses in parasympathetically innervated structures like smooth muscles (spasmolytic activity), salivary glands, and eyes (mydriasis). In higher doses direct central inhibition of cerebral motor centers may contribute. In very high doses central toxicity as seen in atropine overdose is noted. It binds to the M1 muscarinic receptor[15] and possibly the dopamine receptor.[16] Trihexyphenidyl is rapidly absorbed from the gastrointestinal tract. The onset of action is within 1 hour after oral dosing. The peak activity is noted after 2 to 3 hours.[17] The duration of action of one single dose is 6 to 12 hours in a dose dependent manner. It is excreted in the urine, probably as unchanged drug. More precise data in animals and humans have so far not been determined.[18][19]

    History

    Artane, or its generic form Trihexyphenidyl HCL, was approved by the FDA on June 25th, 2003 for the clinical use of all types of parkinsonism.[20] However, it has been clinically relevant in trials pertaining to Parkinson's disease since 1949.[21] Artane is an anticholinergic drug which is prescribed by doctors throughout the world. It is also abused, typically in combination with other drugs or delicate pharmaceutical agents. Prisons in Iraq were among the places where abuse was obvious, along with within communities of Iraqi soldiers.

    Chemistry

    Trihexyphenidyl can be synthesized in two ways, one linear and one convergent synthesis.

    In the first way, the initial 2-(1-piperidino)propiophenone is synthesized in turn by the aminomethylation of acetophenone using paraformaldehyde and piperidine in a Mannich reaction. In the second step the 2-(1-piperidino)propiophenone is reacted with cyclohexylmagnesium bromide in a Grignard reaction.[22]

    Artane linear and convergent synthesis

    Stereochemistry

    Trihexyphenidyl has a chiral center and two enantiomers. Medications are racemates.[23]

    Enantiomers

    CAS number: 40520-25-0
    CAS number: 40520-24-9

    Society and culture

    Recreational use

    In a 2008 news report, trihexyphenidyl was seen to be used for recreational purposes among Iraqi soldiers and police, among other prescription drugs. The report states that the drugs were taken to relieve combat stress.[24] Although that may be the case for some, others used Artane as a substitute or more intense version of LSD. This was especially prevalent in the 1960s, according to a report in "The New Yorker". Similarly to those in Iraqi forces, some of the appeal was that the individual may retain partial control while under the influence.[25]

    The neurologist Oliver Sacks reports using the drug recreationally in the 1960s.[26] He recalled taking "a large dose" knowing full well the drug was intended for people with Parkinson's. More recounts of Dr. Sacks' experiences - including experimentation with mescaline, psilocybin, LSD, and probably DMT[27] - have been compared in his book Hallucinations.

    Research

    Equivocal preliminary results from small studies exist for:

    References

    1. 1 2 3 4 5 6 7 8 9 10 11 "Trihexyphenidyl Monograph for Professionals". Drugs.com. Archived from the original on 3 June 2021. Retrieved 19 September 2021.
    2. 1 2 "TGA eBS - Product and Consumer Medicine Information Licence". www.ebs.tga.gov.au. Archived from the original on 2021-06-02. Retrieved 2020-08-20.
    3. 1 2 3 4 5 6 BNF (80 ed.). BMJ Group and the Pharmaceutical Press. September 2020 – March 2021. p. 431. ISBN 978-0-85711-369-6.{{cite book}}: CS1 maint: date format (link)
    4. ↑ Association, Pharmaceutical Manufacturers (1962). Review of Drugs, 1941-1961: Single Chemical Entities Introduced in the United States and Patent Status. p. 42. Archived from the original on 2021-09-22. Retrieved 2021-09-19.
    5. ↑ World Health Organization (2023). The selection and use of essential medicines 2023: web annex A: World Health Organization model list of essential medicines: 23rd list (2023). Geneva: World Health Organization. hdl:10665/371090. WHO/MHP/HPS/EML/2023.02.
    6. ↑ "Trihexyphenidyl Prices, Coupons & Patient Assistance Programs". Drugs.com. Archived from the original on 22 January 2021. Retrieved 19 September 2021.
    7. ↑ Harris MK, Shneyder N, Borazanci A, Korniychuk E, Kelley RE, Minagar A (March 2009). "Movement disorders". The Medical Clinics of North America. Common Neurologic Disorders. 93 (2): 371–88, viii. doi:10.1016/j.mcna.2008.09.002. PMID 19272514.
    8. ↑ Inada T (December 2017). "[Drug-Induced Akathisia]". Brain and Nerve = Shinkei Kenkyu No Shinpo. 69 (12): 1417–1424. doi:10.11477/mf.1416200927. PMID 29282345.
    9. ↑ Duma SR, Fung VS (April 2019). "Drug-induced movement disorders". Australian Prescriber. 42 (2): 56–61. doi:10.18773/austprescr.2019.014. PMC 6478951. PMID 31048939.
    10. ↑ "TGA eBS - Product and Consumer Medicine Information Licence". www.ebs.tga.gov.au. Archived from the original on 2021-06-02. Retrieved 2020-08-20.
    11. ↑ Doshay LJ, Constable K, Zier A (April 1954). "Five year follow-up of treatment with trihexyphenidyl (artane); outcome in four hundred eleven cases of paralysis agitans". Journal of the American Medical Association. 154 (16): 1334–6. doi:10.1001/jama.1954.02940500014005. PMID 13151847.
    12. ↑ "Trihexyphenidyl". Web MD. First Databank Inc. Archived from the original on 2018-09-16. Retrieved 2021-07-18.
    13. ↑ "Trihexyphenidyl". Toxnet. Archived from the original on 2019-06-29. Retrieved 2021-07-18.
    14. ↑ "trihexyphenidyl (Rx)". Medscape. Archived from the original on 2021-06-03. Retrieved 2021-07-18.
    15. ↑ Giachetti A, Giraldo E, Ladinsky H, Montagna E (September 1986). "Binding and functional profiles of the selective M1 muscarinic receptor antagonists trihexyphenidyl and dicyclomine". British Journal of Pharmacology. 89 (1): 83–90. doi:10.1111/j.1476-5381.1986.tb11123.x. PMC 1917044. PMID 2432979.
    16. ↑ Berke JD, Hyman SE (March 2000). "Addiction, dopamine, and the molecular mechanisms of memory". Neuron. 25 (3): 515–32. doi:10.1016/S0896-6273(00)81056-9. PMID 10774721. S2CID 14766533.
    17. ↑ "Trihexyphenidyl Hydrochloride". Drugs.com. Archived from the original on 2019-06-29. Retrieved 2021-07-18.
    18. ↑ Watson Laboratories Inc. trihexyphenidyl hydrochloride tablets, USP. prescribing information. Corona, CA; 2005 May.
    19. ↑ McEvoy GK, ed. (2006). "Trihexyphenidyl". AHFS drug information. Bethesda, MD: American Society of Health-System Pharmacists. p. 1256.
    20. ↑ Katz R, Feeney J, Ressler T, David P. "Approval Package for Application No. 6-773/36" (PDF). Access Data from the Food and Drug Association. FDA. Archived (PDF) from the original on 6 April 2021. Retrieved 8 May 2017.
    21. ↑ Doshay LJ, Constable K (August 1949). "Artane therapy for parkinsonism; a preliminary study of results in 117 cases". Journal of the American Medical Association. 140 (17): 1317–22. doi:10.1001/jama.1949.02900520003002. PMID 18137284.
    22. ↑ Weiss MJ, O'Donoghue MD (September 1957). "Synthesis of Certain 3-Hydroxy-3-phenylpropylsulfonium Salts. Sulfonium Analogs of Artane (Trihexyphenidyl) and Pathilon (Tridihexethyl Iodide)". Journal of the American Chemical Society. 79 (17): 4771–6. doi:10.1021/ja01574a048.
    23. ↑ Rote Liste Service GmbH (Hrsg.) (2017). Rote Liste 2017 – Arzneimittelverzeichnis für Deutschland (einschließlich EU-Zulassungen und bestimmter Medizinprodukte). Vol. Aufl. 57. Frankfurt/Main: Rote Liste Service GmbH. p. 224. ISBN 978-3-946057-10-9.
    24. ↑ Al-Husaini M, Goode E (2008-12-20). "Abuse of Prescription Drugs Rises Among Stressed Iraqi Soldiers". New York Times. Archived from the original on 2021-06-03. Retrieved 2021-07-18.
    25. ↑ Sacks O. "Altered States". The New Yorker. Condé Nast. Archived from the original on 5 September 2015. Retrieved 7 May 2017.
    26. ↑ Smith K (2012-10-30), "Oliver Sacks shares his hallucinations", The Guardian, Guardian, archived from the original on 2021-06-03, retrieved 2021-07-18
    27. ↑ Sacks O (2012). "Chapter 6". Hallucinations. Random House Inc.
    28. ↑ Sanger TD, Bastian A, Brunstrom J, Damiano D, Delgado M, Dure L, et al. (May 2007). "Prospective open-label clinical trial of trihexyphenidyl in children with secondary dystonia due to cerebral palsy". Journal of Child Neurology. 22 (5): 530–7. doi:10.1177/0883073807302601. PMID 17690057. S2CID 73087776.
    29. ↑ Tarnopolsky M, Alshahoumi R (November 2015). ""Complex I Deficiency". In Saneto R, Parikh S, Cohen BH (eds.). Mitochondrial Case Studies: Underlying Mechanisms and Diagnosis. Academic Press. pp. 257–64. ISBN 978-0-12-801149-2.

     This article incorporates public domain material from the United States Department of Health and Human Services document: "Toxnet:Trihexyphenidyl".

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