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Anticholinergic

Anticholinergics (anticholinergic agents) are substances that block the action of the neurotransmitter called acetylcholine (ACh) at synapses in the central and peripheral nervous system.[1][2]

These agents inhibit the parasympathetic nervous system by selectively blocking the binding of ACh to its receptor in nerve cells. The nerve fibers of the parasympathetic system are responsible for the involuntary movement of smooth muscles present in the gastrointestinal tract, urinary tract, lungs, sweat glands, and many other parts of the body.[3]

In broad terms, anticholinergics are divided into two categories in accordance with their specific targets in the central and peripheral nervous system and at the neuromuscular junction:[3] antimuscarinic agents, and antinicotinic agents (ganglionic blockers, neuromuscular blockers).[4]

The term "anticholinergic" is typically used to refer to antimuscarinics which competitively inhibit the binding of ACh to muscarinic acetylcholine receptors; such agents do not antagonize the binding at nicotinic acetylcholine receptors at the neuromuscular junction, although the term is sometimes used to refer to agents which do so.[3][5]

Medical uses edit

Anticholinergic drugs are used to treat a variety of conditions:

Anticholinergics generally have antisialagogue effects (decreasing saliva production), and most produce some level of sedation, both being advantageous in surgical procedures.[8][9]

Until the beginning of the 20th century anticholinergic drugs were widely used to treat psychiatric disorders.[10]

Physiological effects edit

Clinically the most significant feature is delirium, particularly in the elderly, who are most likely to be affected by the toxidrome.[3]

Side effects edit

Long-term use may increase the risk of both cognitive and physical decline.[14][15] It is unclear whether they affect the risk of death generally.[14] However, in older adults they do appear to increase the risk of death.[16]

Possible effects of anticholinergics include:

Possible effects in the central nervous system resemble those associated with delirium, and may include:

  • Confusion
  • Disorientation
  • Agitation
  • Euphoria or dysphoria
  • Respiratory depression
  • Memory problems[19]
  • Inability to concentrate
  • Wandering thoughts; inability to sustain a train of thought
  • Incoherent speech
  • Irritability
  • Mental confusion (brain fog)
  • Wakeful myoclonic jerking
  • Unusual sensitivity to sudden sounds
  • Illogical thinking
  • Photophobia
  • Visual disturbances[citation needed]
    • Periodic flashes of light
    • Periodic changes in visual field
    • Visual snow
    • Restricted or "tunnel vision"
  • Visual, auditory, or other sensory hallucinations
    • Warping or waving of surfaces and edges
    • Textured surfaces
    • "Dancing" lines; "spiders", insects; form constants
    • Lifelike objects indistinguishable from reality
    • Phantom smoking
    • Hallucinated presence of people not actually there (e.g. shadow people)
  • Rarely: seizures, coma, and death
  • Orthostatic hypotension (severe drop in systolic blood pressure when standing up suddenly) and significantly increased risk of falls in the elderly population.[20]

Older patients are at a higher risk of experiencing CNS side effects.

Toxicity edit

An acute anticholinergic syndrome is reversible and subsides once all of the causative agents have been excreted. Reversible acetylcholinesterase inhibitor agents such as physostigmine can be used as an antidote in life-threatening cases. Wider use is discouraged due to the significant side effects related to cholinergic excess including seizures, muscle weakness, bradycardia, bronchoconstriction, lacrimation, salivation, bronchorrhea, vomiting, and diarrhea. Even in documented cases of anticholinergic toxicity, seizures have been reported after the rapid administration of physostigmine. Asystole has occurred after physostigmine administration for tricyclic antidepressant overdose, so a conduction delay (QRS > 0.10 second) or suggestion of tricyclic antidepressant ingestion is generally considered a contraindication to physostigmine administration.[21]

Pharmacology edit

Anticholinergics are classified according to the receptors that are affected:

Examples edit

Examples of common anticholinergics:

Antidotes edit

Physostigmine is one of only a few drugs that can be used as an antidote for anticholinergic poisoning. Nicotine also counteracts anticholinergics by activating nicotinic acetylcholine receptors. Caffeine (although an adenosine receptor antagonist) can counteract the anticholinergic symptoms by reducing sedation and increasing acetylcholine activity, thereby causing alertness and arousal.

Psychoactive uses edit

When a significant amount of an anticholinergic is taken into the body, a toxic reaction known as acute anticholinergic syndrome may result. This may happen accidentally or intentionally as a consequence of either recreational or entheogenic drug use, though many users find the side effects to be exceedingly unpleasant and not worth the recreational effects they experience. In the context of recreational use, anticholinergics are often called deliriants.[23]

Plant sources edit

The most common plants containing anticholinergic alkaloids (including atropine, scopolamine, and hyoscyamine among others) are:

Use as a deterrent edit

Several narcotic and opiate-containing drug preparations, such as those containing hydrocodone and codeine are combined with an anticholinergic agent to deter intentional misuse.[31] Examples include Hydromet/Hycodan (hydrocodone/homatropine), Lomotil (diphenoxylate/atropine) and Tussionex (hydrocodone polistirex/chlorpheniramine). However, it is noted that opioid/antihistamine combinations are used clinically for their synergistic effect in the management of pain and maintenance of dissociative anesthesia (sedation) in such preparations as Meprozine (meperidine/promethazine) and Diconal (dipipanone/cyclizine), which act as strong anticholinergic agents.[32]

References edit

  1. ^ "Anticholinergics", Anticholinergic Agents, Bethesda (MD): National Institute of Diabetes and Digestive and Kidney Diseases, 2012, PMID 31643610, retrieved 2020-03-23, Anticholinergics have antisecretory activities and decrease nasal and bronchial secretions, salivation, lacrimation, sweating and gastric acid production, and can be used to decrease secretions in allergic and inflammatory diseases. Anticholinergics relax smooth muscle in the gastrointestinal tract, bladder and lung and can be used for gastrointestinal, urological or respiratory conditions associated with spasm and dysmotility.
  2. ^ Clinical Pharmacology [database online]. Tampa, FL: Gold Standard, Inc.; 2009. Drugs with Anticholinergic Activity. Prescriber's Letter 2011; 18 (12):271233.
  3. ^ a b c d e Migirov, A; Datta, AR (2020), "article-17683", Physiology, Anticholinergic Reaction, This book is distributed under the terms of the Creative Commons Attribution 4.0 International License, which permits use, duplication, adaptation, distribution, and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, a link is provided to the Creative Commons license, and any changes made are indicated., Treasure Island (FL): StatPearls Publishing, PMID 31536197, retrieved 2020-03-24
  4. ^ Sharee A. Wiggins; Tomas Griebling. . Landon Center on Aging. Archived from the original on 2011-09-27. Retrieved 2011-07-09.
  5. ^ Su, Mark; Goldman, Matthew. Traub, Stephen J.; Burns, Michele M.; Grayzel, Jonathan (eds.). "Anticholinergic poisoning". UpToDate. Retrieved 2020-03-24.
  6. ^ "NERVE AGENTS". fas.org. Retrieved 2020-07-27.
  7. ^ Nair, V. Priya; Hunter, Jennifer M. (2004-10-01). "Anticholinesterases and anticholinergic drugs". Continuing Education in Anaesthesia, Critical Care & Pain. 4 (5): 164–168. doi:10.1093/bjaceaccp/mkh045. ISSN 1743-1816.
  8. ^ Page 592 in: Cahalan, Michael D.; Barash, Paul G.; Cullen, Bruce F.; Stoelting, Robert K. (2009). Clinical Anesthesia. Hagerstwon, MD: Lippincott Williams & Wilkins. ISBN 978-0-7817-8763-5.
  9. ^ Barash, Paul G. (2009). Clinical Anesthesia. Lippincott Williams & Wilkins. ISBN 9780781787635. from the original on 20 February 2017. Retrieved 8 December 2014.
  10. ^ Bangen, Hans: Geschichte der medikamentösen Therapie der Schizophrenie. Berlin 1992, ISBN 3-927408-82-4
  11. ^ "ATROPINE- atropine sulfate solution/ drops". DailyMed. 2017-11-20. Retrieved 2020-03-28.
  12. ^ "MYDRIACYL- tropicamide solution/ drops". DailyMed. 2019-12-13. Retrieved 2020-03-28.
  13. ^ "MYDRIACYL- tropicamide solution/ drops". DailyMed. 2019-12-13. Retrieved 2020-03-28.
  14. ^ a b Fox, C; Smith, T; Maidment, I; Chan, WY; Bua, N; Myint, PK; Boustani, M; Kwok, CS; Glover, M; Koopmans, I; Campbell, N (September 2014). "Effect of medications with anti-cholinergic properties on cognitive function, delirium, physical function and mortality: a systematic review". Age and Ageing. 43 (5): 604–15. doi:10.1093/ageing/afu096. PMID 25038833.
  15. ^ Andre, L; Gallini, A; Montastruc, F; Montastruc, JL; Piau, A; Lapeyre-Mestre, M; Gardette, V (29 August 2019). "Association between anticholinergic (atropinic) drug exposure and cognitive function in longitudinal studies among individuals over 50 years old: a systematic review". European Journal of Clinical Pharmacology. 75 (12): 1631–1644. doi:10.1007/s00228-019-02744-8. PMID 31468067. S2CID 201675824.
  16. ^ Ruxton, K; Woodman, RJ; Mangoni, AA (2 March 2015). "Drugs with anticholinergic effects and cognitive impairment, falls and all-cause mortality in older adults: A systematic review and meta-analysis". British Journal of Clinical Pharmacology. 80 (2): 209–20. doi:10.1111/bcp.12617. PMC 4541969. PMID 25735839.
  17. ^ Falk, N; Cole, A; Meredith, TJ (15 March 2018). "Evaluation of Suspected Dementia". American Family Physician. 97 (6): 398–405. PMID 29671539.
  18. ^ Gray SL, Anderson ML, Dublin S, Hanlon JT, Hubbard R, Walker R, et al. (March 2015). "Cumulative use of strong anticholinergics and incident dementia: a prospective cohort study". JAMA Internal Medicine. 175 (3): 401–407. doi:10.1001/jamainternmed.2014.7663. PMC 4358759. PMID 25621434.
  19. ^ Talan, Jamie (July–August 2008). . Neurology Now. 4 (4): 10–11. doi:10.1097/01.NNN.0000333835.93556.d1. Archived from the original on 2019-06-26. Retrieved 26 June 2019.
  20. ^ "Lifeline Learning Center". Lifeline.theonlinelearningcenter.com. Archived from the original on 12 July 2012. Retrieved 8 December 2014.
  21. ^ Rosen, Peter, John A. Marx, Robert S. Hockberger, and Ron M. Walls. Rosen's Emergency Medicine: Concepts and Clinical Practice. 8th ed. Philadelphia, PA: Mosby Elsevier, 2014.
  22. ^ a b c d e "[113] How well do you know your anticholinergic (antimuscarinic) drugs? | Therapeutics Initiative". Therapeutics Initiative. 10 September 2018. Retrieved 20 September 2018.
  23. ^ a b Bersani, F. S.; Corazza, O.; Simonato, P.; Mylokosta, A.; Levari, E.; Lovaste, R.; Schifano, F. (2013). "Drops of madness? Recreational misuse of tropicamide collyrium; early warning alerts from Russia and Italy". General Hospital Psychiatry. 35 (5): 571–3. doi:10.1016/j.genhosppsych.2013.04.013. PMID 23706777.
  24. ^ Carroll FI, Blough BE, Mascarella SW, Navarro HA, Lukas RJ, Damaj MI (2014). "Bupropion and Bupropion Analogs as Treatments for CNS Disorders". Emerging Targets & Therapeutics in the Treatment of Psychostimulant Abuse. Advances in Pharmacology. Vol. 69. pp. 177–216. doi:10.1016/B978-0-12-420118-7.00005-6. ISBN 9780124201187. PMID 24484978.
  25. ^ Dwoskin, Linda P. (29 January 2014). Emerging Targets & Therapeutics in the Treatment of Psychostimulant Abuse. Elsevier Science. pp. 177–216. ISBN 978-0-12-420177-4. from the original on 20 March 2017.
  26. ^ Tasman, Allan; Kay, Jerald; Lieberman, Jeffrey A.; First, Michael B.; Maj, Mario (11 October 2011). Psychiatry. John Wiley & Sons. ISBN 978-1-119-96540-4. from the original on 20 March 2017.
  27. ^ Damaj, M. I.; Flood, P; Ho, K. K.; May, E. L.; Martin, B. R. (2004). "Effect of Dextrometorphan and Dextrorphan on Nicotine and Neuronal Nicotinic Receptors: In Vitro and in Vivo Selectivity". Journal of Pharmacology and Experimental Therapeutics. 312 (2): 780–5. doi:10.1124/jpet.104.075093. PMID 15356218. S2CID 149958.
  28. ^ Lee, Jun-Ho; Shin, Eun-Joo; Jeong, Sang Min; Kim, Jong-Hoon; Lee, Byung-Hwan; Yoon, In-Soo; Lee, Joon-Hee; Choi, Sun-Hye; Lee, Sang-Mok; Lee, Phil Ho; Kim, Hyoung-Chun; Nah, Seung-Yeol (2006). "Effects of dextrorotatory morphinans on α3β4 nicotinic acetylcholine receptors expressed in Xenopus oocytes". European Journal of Pharmacology. 536 (1–2): 85–92. doi:10.1016/j.ejphar.2006.02.034. PMID 16563374.
  29. ^ Hernandez, S. C.; Bertolino, M; Xiao, Y; Pringle, K. E.; Caruso, F. S.; Kellar, K. J. (2000). "Dextromethorphan and Its Metabolite Dextrorphan Block α3β4 Neuronal Nicotinic Receptors". The Journal of Pharmacology and Experimental Therapeutics. 293 (3): 962–7. PMID 10869398.
  30. ^ Shytle, RD; Penny, E; Silver, AA; Goldman, J; Sanberg, PR (Jul 2002). "Mecamylamine (Inversine): an old antihypertensive with new research directions". Journal of Human Hypertension. 16 (7): 453–7. doi:10.1038/sj.jhh.1001416. PMID 12080428.
  31. ^ "NIH DailyMed – Hydromet Syrup". Dailymed.nlm.nih.gov. from the original on 2011-05-23. Retrieved 2008-08-17.
  32. ^ Zacny, James P. (2003). "Characterizing the subjective, psychomotor, and physiological effects of a hydrocodone combination product (Hycodan) in non-drug-abusing volunteers". Psychopharmacology. 165 (2): 146–156. doi:10.1007/s00213-002-1245-5. PMID 12404072. S2CID 7835794.

anticholinergic, cholinergic, blocking, drugs, cholinergic, blocking, drugs, confused, with, anti, cholinesterase, anticholinergic, agents, substances, that, block, action, neurotransmitter, called, acetylcholine, synapses, central, peripheral, nervous, system. For cholinergic blocking drugs see Cholinergic blocking drugs Not to be confused with Anti cholinesterase Anticholinergics anticholinergic agents are substances that block the action of the neurotransmitter called acetylcholine ACh at synapses in the central and peripheral nervous system 1 2 These agents inhibit the parasympathetic nervous system by selectively blocking the binding of ACh to its receptor in nerve cells The nerve fibers of the parasympathetic system are responsible for the involuntary movement of smooth muscles present in the gastrointestinal tract urinary tract lungs sweat glands and many other parts of the body 3 In broad terms anticholinergics are divided into two categories in accordance with their specific targets in the central and peripheral nervous system and at the neuromuscular junction 3 antimuscarinic agents and antinicotinic agents ganglionic blockers neuromuscular blockers 4 The term anticholinergic is typically used to refer to antimuscarinics which competitively inhibit the binding of ACh to muscarinic acetylcholine receptors such agents do not antagonize the binding at nicotinic acetylcholine receptors at the neuromuscular junction although the term is sometimes used to refer to agents which do so 3 5 Contents 1 Medical uses 1 1 Physiological effects 2 Side effects 2 1 Toxicity 3 Pharmacology 4 Examples 4 1 Antidotes 5 Psychoactive uses 6 Plant sources 7 Use as a deterrent 8 ReferencesMedical uses editAnticholinergic drugs are used to treat a variety of conditions Dizziness including vertigo and motion sickness related symptoms Extrapyramidal symptoms a potential side effect of antipsychotic medications Gastrointestinal disorders e g peptic ulcers diarrhea pylorospasm diverticulitis ulcerative colitis nausea and vomiting Genitourinary disorders e g cystitis urethritis and prostatitis Insomnia although usually only on a short term basis Respiratory disorders e g asthma chronic bronchitis and chronic obstructive pulmonary disease COPD Sinus bradycardia due to a hypersensitive vagus nerve Organophosphate based nerve agent poisoning such as VX sarin tabun and soman atropine is favoured in conjunction with an oxime usually pralidoxime 6 7 Anticholinergics generally have antisialagogue effects decreasing saliva production and most produce some level of sedation both being advantageous in surgical procedures 8 9 Until the beginning of the 20th century anticholinergic drugs were widely used to treat psychiatric disorders 10 Physiological effects edit Delirium often with hallucinations and delusions indistinguishable from reality Ocular symptoms from eye drops mydriasis pupil dilation and acute angle closure glaucoma in those with shallow anterior chamber 11 12 13 Anhidrosis dry mouth dry skin Fever Constipation Tachycardia Urinary retention Cutaneous vasodilation 3 Clinically the most significant feature is delirium particularly in the elderly who are most likely to be affected by the toxidrome 3 Side effects editLong term use may increase the risk of both cognitive and physical decline 14 15 It is unclear whether they affect the risk of death generally 14 However in older adults they do appear to increase the risk of death 16 Possible effects of anticholinergics include Poor coordination Dementia 17 18 Decreased mucus production in the nose and throat consequent dry sore throat Dry mouth with possible acceleration of dental caries Cessation of sweating consequent decreased epidermal thermal dissipation leading to warm blotchy or red skin Increased body temperature Pupil dilation consequent sensitivity to bright light photophobia Loss of accommodation loss of focusing ability blurred vision cycloplegia Double vision Increased heart rate Tendency to be easily startled Urinary retention Urinary incontinence while sleeping Diminished bowel movement sometimes ileus decreases motility via the vagus nerve Increased intraocular pressure dangerous for people with narrow angle glaucoma Possible effects in the central nervous system resemble those associated with delirium and may include Confusion Disorientation Agitation Euphoria or dysphoria Respiratory depression Memory problems 19 Inability to concentrate Wandering thoughts inability to sustain a train of thought Incoherent speech Irritability Mental confusion brain fog Wakeful myoclonic jerking Unusual sensitivity to sudden sounds Illogical thinking Photophobia Visual disturbances citation needed Periodic flashes of light Periodic changes in visual field Visual snow Restricted or tunnel vision Visual auditory or other sensory hallucinations Warping or waving of surfaces and edges Textured surfaces Dancing lines spiders insects form constants Lifelike objects indistinguishable from reality Phantom smoking Hallucinated presence of people not actually there e g shadow people Rarely seizures coma and death Orthostatic hypotension severe drop in systolic blood pressure when standing up suddenly and significantly increased risk of falls in the elderly population 20 Older patients are at a higher risk of experiencing CNS side effects Toxicity edit An acute anticholinergic syndrome is reversible and subsides once all of the causative agents have been excreted Reversible acetylcholinesterase inhibitor agents such as physostigmine can be used as an antidote in life threatening cases Wider use is discouraged due to the significant side effects related to cholinergic excess including seizures muscle weakness bradycardia bronchoconstriction lacrimation salivation bronchorrhea vomiting and diarrhea Even in documented cases of anticholinergic toxicity seizures have been reported after the rapid administration of physostigmine Asystole has occurred after physostigmine administration for tricyclic antidepressant overdose so a conduction delay QRS gt 0 10 second or suggestion of tricyclic antidepressant ingestion is generally considered a contraindication to physostigmine administration 21 Pharmacology editAnticholinergics are classified according to the receptors that are affected Antimuscarinic agents operate on the muscarinic acetylcholine receptors The majority of anticholinergic drugs are antimuscarinics Antinicotinic agents operate on the nicotinic acetylcholine receptors The majority of these are non depolarising skeletal muscle relaxants for surgical use that are structurally related to curare Several are depolarizing agents Examples editExamples of common anticholinergics Antimuscarinic agents Antipsychotics clozapine quetiapine 22 Atropine Benztropine Biperiden Chlorpheniramine Certain SSRIs Paroxetine 22 Dicyclomine Dicycloverine Dimenhydrinate 22 Diphenhydramine 22 Doxepin Doxylamine Flavoxate Glycopyrronium late Hyoscyamine Ipratropium Orphenadrine Oxitropium Oxybutynin 22 Promethazine Propantheline bromide Scopolamine Solifenacin Tolterodine Tiotropium Tricyclic antidepressants 28 compounds with numerous trade names citation needed Trihexyphenidyl Tropicamide 23 Umeclidinium Antinicotinic agents Bupropion Ganglion blocker 24 25 26 Dextromethorphan Cough suppressant and ganglion blocker 27 28 29 Doxacurium Nondepolarizing skeletal muscular relaxant Hexamethonium Ganglion blocker Mecamylamine Ganglion blocker and occasional smoking cessation aid 30 Tubocurarine Nondepolarizing skeletal muscular relaxant Antidotes edit Physostigmine is one of only a few drugs that can be used as an antidote for anticholinergic poisoning Nicotine also counteracts anticholinergics by activating nicotinic acetylcholine receptors Caffeine although an adenosine receptor antagonist can counteract the anticholinergic symptoms by reducing sedation and increasing acetylcholine activity thereby causing alertness and arousal Psychoactive uses editWhen a significant amount of an anticholinergic is taken into the body a toxic reaction known as acute anticholinergic syndrome may result This may happen accidentally or intentionally as a consequence of either recreational or entheogenic drug use though many users find the side effects to be exceedingly unpleasant and not worth the recreational effects they experience In the context of recreational use anticholinergics are often called deliriants 23 Plant sources editThe most common plants containing anticholinergic alkaloids including atropine scopolamine and hyoscyamine among others are Atropa belladonna deadly nightshade Brugmansia species Datura species Garrya species Hyoscyamus niger henbane Mandragora officinarum mandrake Use as a deterrent editSeveral narcotic and opiate containing drug preparations such as those containing hydrocodone and codeine are combined with an anticholinergic agent to deter intentional misuse 31 Examples include Hydromet Hycodan hydrocodone homatropine Lomotil diphenoxylate atropine and Tussionex hydrocodone polistirex chlorpheniramine However it is noted that opioid antihistamine combinations are used clinically for their synergistic effect in the management of pain and maintenance of dissociative anesthesia sedation in such preparations as Meprozine meperidine promethazine and Diconal dipipanone cyclizine which act as strong anticholinergic agents 32 References edit Anticholinergics Anticholinergic Agents Bethesda MD National Institute of Diabetes and Digestive and Kidney Diseases 2012 PMID 31643610 retrieved 2020 03 23 Anticholinergics have antisecretory activities and decrease nasal and bronchial secretions salivation lacrimation sweating and gastric acid production and can be used to decrease secretions in allergic and inflammatory diseases Anticholinergics relax smooth muscle in the gastrointestinal tract bladder and lung and can be used for gastrointestinal urological or respiratory conditions associated with spasm and dysmotility Clinical Pharmacology database online Tampa FL Gold Standard Inc 2009 Drugs with Anticholinergic Activity Prescriber s Letter 2011 18 12 271233 a b c d e Migirov A Datta AR 2020 article 17683 Physiology Anticholinergic Reaction This book is distributed under the terms of the Creative Commons Attribution 4 0 International License which permits use duplication adaptation distribution and reproduction in any medium or format as long as you give appropriate credit to the original author s and the source a link is provided to the Creative Commons license and any changes made are indicated Treasure Island FL StatPearls Publishing PMID 31536197 retrieved 2020 03 24 Sharee A Wiggins Tomas Griebling Urinary Incontinence Landon Center on Aging Archived from the original on 2011 09 27 Retrieved 2011 07 09 Su Mark Goldman Matthew Traub Stephen J Burns Michele M Grayzel Jonathan eds Anticholinergic poisoning UpToDate Retrieved 2020 03 24 NERVE AGENTS fas org Retrieved 2020 07 27 Nair V Priya Hunter Jennifer M 2004 10 01 Anticholinesterases and anticholinergic drugs Continuing Education in Anaesthesia Critical Care amp Pain 4 5 164 168 doi 10 1093 bjaceaccp mkh045 ISSN 1743 1816 Page 592 in Cahalan Michael D Barash Paul G Cullen Bruce F Stoelting Robert K 2009 Clinical Anesthesia Hagerstwon MD Lippincott Williams amp Wilkins ISBN 978 0 7817 8763 5 Barash Paul G 2009 Clinical Anesthesia Lippincott Williams amp Wilkins ISBN 9780781787635 Archived from the original on 20 February 2017 Retrieved 8 December 2014 Bangen Hans Geschichte der medikamentosen Therapie der Schizophrenie Berlin 1992 ISBN 3 927408 82 4 ATROPINE atropine sulfate solution drops DailyMed 2017 11 20 Retrieved 2020 03 28 MYDRIACYL tropicamide solution drops DailyMed 2019 12 13 Retrieved 2020 03 28 MYDRIACYL tropicamide solution drops DailyMed 2019 12 13 Retrieved 2020 03 28 a b Fox C Smith T Maidment I Chan WY Bua N Myint PK Boustani M Kwok CS Glover M Koopmans I Campbell N September 2014 Effect of medications with anti cholinergic properties on cognitive function delirium physical function and mortality a systematic review Age and Ageing 43 5 604 15 doi 10 1093 ageing afu096 PMID 25038833 Andre L Gallini A Montastruc F Montastruc JL Piau A Lapeyre Mestre M Gardette V 29 August 2019 Association between anticholinergic atropinic drug exposure and cognitive function in longitudinal studies among individuals over 50 years old a systematic review European Journal of Clinical Pharmacology 75 12 1631 1644 doi 10 1007 s00228 019 02744 8 PMID 31468067 S2CID 201675824 Ruxton K Woodman RJ Mangoni AA 2 March 2015 Drugs with anticholinergic effects and cognitive impairment falls and all cause mortality in older adults A systematic review and meta analysis British Journal of Clinical Pharmacology 80 2 209 20 doi 10 1111 bcp 12617 PMC 4541969 PMID 25735839 Falk N Cole A Meredith TJ 15 March 2018 Evaluation of Suspected Dementia American Family Physician 97 6 398 405 PMID 29671539 Gray SL Anderson ML Dublin S Hanlon JT Hubbard R Walker R et al March 2015 Cumulative use of strong anticholinergics and incident dementia a prospective cohort study JAMA Internal Medicine 175 3 401 407 doi 10 1001 jamainternmed 2014 7663 PMC 4358759 PMID 25621434 Talan Jamie July August 2008 Common Drugs May Cause Cognitive Problems Neurology Now 4 4 10 11 doi 10 1097 01 NNN 0000333835 93556 d1 Archived from the original on 2019 06 26 Retrieved 26 June 2019 Lifeline Learning Center Lifeline theonlinelearningcenter com Archived from the original on 12 July 2012 Retrieved 8 December 2014 Rosen Peter John A Marx Robert S Hockberger and Ron M Walls Rosen s Emergency Medicine Concepts and Clinical Practice 8th ed Philadelphia PA Mosby Elsevier 2014 a b c d e 113 How well do you know your anticholinergic antimuscarinic drugs Therapeutics Initiative Therapeutics Initiative 10 September 2018 Retrieved 20 September 2018 a b Bersani F S Corazza O Simonato P Mylokosta A Levari E Lovaste R Schifano F 2013 Drops of madness Recreational misuse of tropicamide collyrium early warning alerts from Russia and Italy General Hospital Psychiatry 35 5 571 3 doi 10 1016 j genhosppsych 2013 04 013 PMID 23706777 Carroll FI Blough BE Mascarella SW Navarro HA Lukas RJ Damaj MI 2014 Bupropion and Bupropion Analogs as Treatments for CNS Disorders Emerging Targets amp Therapeutics in the Treatment of Psychostimulant Abuse Advances in Pharmacology Vol 69 pp 177 216 doi 10 1016 B978 0 12 420118 7 00005 6 ISBN 9780124201187 PMID 24484978 Dwoskin Linda P 29 January 2014 Emerging Targets amp Therapeutics in the Treatment of Psychostimulant Abuse Elsevier Science pp 177 216 ISBN 978 0 12 420177 4 Archived from the original on 20 March 2017 Tasman Allan Kay Jerald Lieberman Jeffrey A First Michael B Maj Mario 11 October 2011 Psychiatry John Wiley amp Sons ISBN 978 1 119 96540 4 Archived from the original on 20 March 2017 Damaj M I Flood P Ho K K May E L Martin B R 2004 Effect of Dextrometorphan and Dextrorphan on Nicotine and Neuronal Nicotinic Receptors In Vitro and in Vivo Selectivity Journal of Pharmacology and Experimental Therapeutics 312 2 780 5 doi 10 1124 jpet 104 075093 PMID 15356218 S2CID 149958 Lee Jun Ho Shin Eun Joo Jeong Sang Min Kim Jong Hoon Lee Byung Hwan Yoon In Soo Lee Joon Hee Choi Sun Hye Lee Sang Mok Lee Phil Ho Kim Hyoung Chun Nah Seung Yeol 2006 Effects of dextrorotatory morphinans on a3b4 nicotinic acetylcholine receptors expressed in Xenopus oocytes European Journal of Pharmacology 536 1 2 85 92 doi 10 1016 j ejphar 2006 02 034 PMID 16563374 Hernandez S C Bertolino M Xiao Y Pringle K E Caruso F S Kellar K J 2000 Dextromethorphan and Its Metabolite Dextrorphan Block a3b4 Neuronal Nicotinic Receptors The Journal of Pharmacology and Experimental Therapeutics 293 3 962 7 PMID 10869398 Shytle RD Penny E Silver AA Goldman J Sanberg PR Jul 2002 Mecamylamine Inversine an old antihypertensive with new research directions Journal of Human Hypertension 16 7 453 7 doi 10 1038 sj jhh 1001416 PMID 12080428 NIH DailyMed Hydromet Syrup Dailymed nlm nih gov Archived from the original on 2011 05 23 Retrieved 2008 08 17 Zacny James P 2003 Characterizing the subjective psychomotor and physiological effects of a hydrocodone combination product Hycodan in non drug abusing volunteers Psychopharmacology 165 2 146 156 doi 10 1007 s00213 002 1245 5 PMID 12404072 S2CID 7835794 Retrieved from https en wikipedia org w index php title Anticholinergic amp oldid 1183091351, wikipedia, wiki, book, books, library,

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