Biology:Acetylcholinesterase inhibitor

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Short description: Drugs that inhibit acetylcholinesterase
Acetylcholine
Acetylcholinesterase
Acetylcholinesterase inhibition

Acetylcholinesterase inhibitors (AChEIs) also often called cholinesterase inhibitors,[1] inhibit the enzyme acetylcholinesterase from breaking down the neurotransmitter acetylcholine into choline and acetate,[2] thereby increasing both the level and duration of action of acetylcholine in the central nervous system, autonomic ganglia and neuromuscular junctions, which are rich in acetylcholine receptors.[2] Acetylcholinesterase inhibitors are one of two types of cholinesterase inhibitors; the other being butyryl-cholinesterase inhibitors.[2] Acetylcholinesterase is the primary member of the cholinesterase enzyme family.[3]

Acetylcholinesterase inhibitors are classified as reversible, irreversible, or quasi-irreversible (also called pseudo-irreversible).[4][5]

Mechanism of action

Organophosphates

Organophosphates like TEPP and sarin inhibit cholinesterases, enzymes that hydrolyze the neurotransmitter acetylcholine.

The active centre of cholinesterases feature two important sites, namely the anionic site and the esteratic site. After the binding of acetylcholine to the anionic site of the cholinesterase, the acetyl group of acetylcholine can bind to the esteratic site. Important amino acid residues in the esteratic site are a glutamate, a histidine, and a serine. These residues mediate the hydrolysis of the acetylcholine.

The hydrolysis of acetylcholine, catalyzed by cholinesterase at the esteratic site[6]

At the esteratic site the acetylcholine is cleaved, which results in a free choline moiety and an acetylated cholinesterase. This acetylated state requires hydrolysis to regenerate itself.[6][7]

Inhibitors like TEPP modify the serine residue in the esteratic site of the cholinesterase.

The phosphorylation mechanism by which cholinesterases are inhibited. The organophosphate binds first to the serine residue in the esteratic site of the cholinesterase and after transformation to a phosphate molecule, it binds the histidine residue. This results in occupation of the esteratic site and inhibition of the cleaving activity of the cholinesterase.[6]

This phosphorylation inhibits the binding of the acetyl group of the acetylcholine to the esteratic site of the cholinesterase. Because the acetyl group can't bind the cholinesterase, the acetylcholine can't be cleaved. Therefore, the acetylcholine will remain intact and will accumulate in the synapses. This results in continuous activation of acetylcholine receptors, which leads to the acute symptoms of TEPP poisoning.[8] The phosphorylation of cholinesterase by TEPP (or any other organophosphate) is irreversible. This makes the inhibition of the cholinesterase permanent.[6][7]

The cholinesterase gets irreversible phosphorylated according to the following reaction scheme

[math]\ce{ E + PX <=> E-PX ->[k_3] EP + X }[/math]

In this reaction scheme the E indicates the cholinesterase, PX the TEPP molecule, E–PX the reversible phosphorylated cholinesterase, k3 the reaction rate of the second step, EP the phosphorylated cholinesterase and X the leaving group of the TEPP.

The irreversible phosphorylation of the cholinesterase occurs in two steps. In the first step the cholinesterase gets reversibly phosphorylated. This reaction is very fast. Then the second step takes place. The cholinesterase forms a very stable complex with TEPP, in which TEPP is covalently bound to the cholinesterase. This is a slow reaction. But after this step the cholinesterase is irreversibly inhibited.[6]

The time dependent irreversible inhibition of the cholinesterase can be described by the following equation.[6]

[math]\displaystyle{ \ln \frac E {E_0} = \frac{k_3 t}{1 + \frac{K_I} I} }[/math]

In this formula, E is the remaining enzyme activity, E0 is the initial enzyme activity, t is the time interval after mixing of the cholinesterase and the TEPP, KI is the dissociation constant for cholinesterase-TEPP complex (E–PX) and I is the TEPP concentration.

The reaction mechanism and the formula above are both also compatible for other organophosphates. The process occurs in the same way.

Furthermore, certain organophosphates can cause OPIDN, organophosphate-induced delayed polyneuropathy. This is a disease, which is characterized by degeneration of axons in the peripheral and central nervous system. This disease will show a few weeks after contamination with the organophosphate. It is believed that the neuropathy target esterase (NTE) is affected by the organophosphate which induces the disease. However, there are no references found, which indicate that TEPP is one of the organophosphates that can cause OPIDN.[9]

Uses

Acetylcholinesterase inhibitors:[6]

  • Occur naturally as venoms and poisons (e.g., onchidal)
  • Are used as weapons (nerve agents)
  • Are used medicinally:
    • To treat myasthenia gravis, where they are used to increase neuromuscular transmission.
    • To treat glaucoma
    • To treat postural tachycardia syndrome
    • As an antidote to anticholinergic poisoning
    • To reverse the effect of non-depolarising muscle relaxants
    • To treat neuropsychiatric symptoms of diseases such as Alzheimer's disease, particularly apathy
    • To increase chances of lucid dreaming (by prolonging REM sleep)[10]
    • To treat Alzheimer's disease, the Lewy body dementias and Parkinson's disease. In these neurodegenerative conditions AChEIs are primarily used to treat the cognitive (memory and learning deficits mostly) symptoms of dementia. These symptoms are attenuated due to the role of acetylcholine in cognition in the CNS. There is some evidence to suggest that AChEIs may attenuate psychotic symptoms (especially visual hallucinations) in Parkinson's disease.[11]
    • To treat cognitive impairments in patients with schizophrenia. There is some evidence to suggest efficacy in treating positive, negative and affective symptoms.[12][13][14]
    • As a treatment for autism and to increase the percentage of rapid eye movement sleep in autistic children, in line with the mechanism by which they encourage lucid dreaming.[15][16]
  • Are used as insecticides (e.g., malathion):

Guideline recommendations

The clinical guidelines for medication management in people with dementia recommend trialing an AChE inhibitor for people with early- to mid-stage dementia. These guidelines, known as the Medication Appropriateness Tool for Comorbid Health conditions in Dementia (MATCH-D), suggest that these medicines are at least considered.[18][failed verification]

Side effects

Potential side effects of acetylcholinesterase inhibitors[19][20]
mild – generally diminishes potentially serious

Some major effects of cholinesterase inhibitors:

  • Actions on the parasympathetic nervous system, (the parasympathetic branch of the autonomic nervous system) may cause bradycardia, hypotension, hypersecretion, bronchoconstriction, GI tract hypermotility, and decrease intraocular pressure, increase lower esophageal sphincter (LES) tone
  • Cholinergic crisis.
  • Actions on the neuromuscular junction may result in prolonged muscle contraction.[21]
  • The effects of neostigmine on postoperative nausea and vomiting are controversial and there is not a clear linkage in clinical practice, however, there is good evidence to support the reduction in risk when anticholinergic agents are administered.[22]

Administration of reversible cholinesterase inhibitors is contraindicated with those that have urinary retention due to urethral obstruction.

Overdose

Hyperstimulation of nicotinic and muscarinic receptors.[4]

Titration phase

When used in the central nervous system to alleviate neurological symptoms, such as rivastigmine in Alzheimer's disease, all cholinesterase inhibitors require doses to be increased gradually over several weeks, and this is usually referred to as the titration phase. Many other types of drug treatments may require a titration or stepping up phase. This strategy is used to build tolerance to adverse events or to reach a desired clinical effect.[20] This also prevents accidental overdose and is therefore recommended when initiating treatment with drugs that are extremely potent and/or toxic (drugs with a low therapeutic index).

Examples

Reversible inhibitor

Compounds which function as reversible competitive or noncompetitive inhibitors of cholinesterase are those most likely to have therapeutic uses. These include:

Comparison table

Comparison of reversible acetylcholinesterase inhibitors
Inhibitor Duration Main site of action Clinical use Adverse effects
Edrophonium short (10 min.)[31] neuromuscular junction[31] diagnosis of myasthenia gravis[31]
Neostigmine medium (1–2 hrs.)[31] neuromuscular junction[31] visceral[31]
Physostigmine medium (0.5–5 hrs.)[31] postganglionic parasympathetic[31] treat glaucoma (eye drops)[31]
Pyridostigmine medium (2–3 hrs.)[31] neuromuscular junction[31]
Dyflos long[31] postganglionic parasympathetic[31] historically to treat glaucoma (eye drops)[31] toxic[31]
Echothiophate (irreversible) long[31] postganglionic parasympathetic[31] treat glaucoma (eye drops)[31] systemic effects[31]
Parathion (irreversible) long[31] none[31] toxic[31]

Quasi-irreversible inhibitor

Compounds which function as quasi-irreversible inhibitors of cholinesterase are those most likely to have use as chemical weapons or pesticides.



See also

References

  1. ↑ "Medications for treating people with dementia". https://www.england.nhs.uk/wp-content/uploads/2018/01/dg-medications-for-treating-people-with-dementia.pdf. 
  2. ↑ 2.0 2.1 2.2 English, Brett A.; Webster, Andrew A. (2012). "Acetylcholinesterase and its Inhibitors". Primer on the Autonomic Nervous System. Elsevier. pp. 631–633. doi:10.1016/b978-0-12-386525-0.00132-3. ISBN 978-0-12-386525-0. 
  3. ↑ Seth (2009-11-18). "23". Textbook Of Pharmacology. Elsevier India. p. III.87. ISBN 978-8131211588. "Anaesthesia: Cholinesterase inhibitors are likely to exaggerate succinylcholine-type muscle relaxation during anaesthesia. 5. Genitourinary system: It may ..." 
  4. ↑ 4.0 4.1 "Acetylcholinesterase inhibitors: pharmacology and toxicology". Current Neuropharmacology (Bentham Science Publishers Ltd.) 11 (3): 315–35. May 2013. doi:10.2174/1570159x11311030006. PMID 24179466. 
  5. ↑ "Acetylcholinesterase inhibitors in Alzheimer's disease". British Journal of Clinical Pharmacology 48 (4): 471–80. October 1999. doi:10.1046/j.1365-2125.1999.00026.x. PMID 10583015. 
  6. ↑ 6.0 6.1 6.2 6.3 6.4 6.5 6.6 "Acetylcholinesterase inhibitors: pharmacology and toxicology". Current Neuropharmacology 11 (3): 315–35. May 2013. doi:10.2174/1570159X11311030006. PMID 24179466. 
  7. ↑ 7.0 7.1 O'Brien, Richard D. (2013-10-22) (in en). Toxic Phosphorus Esters: Chemistry, Metabolism, and Biological Effects. Elsevier. ISBN 978-1-4832-7093-7. https://books.google.com/books?id=fRUlBQAAQBAJ. 
  8. ↑ Roberts, Stephen M.; James, Robert C.; Williams, Phillip L. (2014-12-08) (in en). Principles of Toxicology: Environmental and Industrial Applications. John Wiley & Sons. ISBN 978-1-118-98248-8. https://books.google.com/books?id=RZTVBQAAQBAJ. 
  9. ↑ "Organophosphate-induced delayed polyneuropathy". Toxicological Reviews 24 (1): 37–49. 2005-01-01. doi:10.2165/00139709-200524010-00003. PMID 16042503. 
  10. ↑ Yuschak, Thomas (2006). Advanced Lucid Dreaming: The Power of Supplements. Lulu. ISBN 978-1430305422. 
  11. ↑ Maudsley Prescribing Guidelines in Psychiatry (11th ed.). West Sussex: Wiley-Blackwell. 2012. ISBN 978-0-47-097948-8. 
  12. ↑ "Acetylcholinesterase inhibitors for schizophrenia". The Cochrane Database of Systematic Reviews 1 (1): CD007967. January 2012. doi:10.1002/14651858.CD007967.pub2. PMID 22258978. 
  13. ↑ "Adjunctive pharmacotherapy for cognitive deficits in schizophrenia: meta-analytical investigation of efficacy". The British Journal of Psychiatry 203 (3): 172–8. September 2013. doi:10.1192/bjp.bp.111.107359. PMID 23999481. 
  14. ↑ "Cholinesterase inhibitors as adjunctive therapy in patients with schizophrenia and schizoaffective disorder: a review and meta-analysis of the literature". CNS Drugs 24 (4): 303–17. April 2010. doi:10.2165/11530260-000000000-00000. PMID 20297855. 
  15. ↑ "An open label trial of donepezil for enhancement of rapid eye movement sleep in young children with autism spectrum disorders". Journal of Child and Adolescent Psychopharmacology 21 (4): 353–7. August 2011. doi:10.1089/cap.2010.0121. PMID 21851192. 
  16. ↑ "Safety and efficacy of donepezil in children and adolescents with autism: neuropsychological measures". Journal of Child and Adolescent Psychopharmacology 21 (1): 43–50. February 2011. doi:10.1089/cap.2010.0024. PMID 21309696. 
  17. ↑ 17.0 17.1 Chatonnet, Arnaud; Lenfant, Nicolas; Marchot, Pascale; Selkirk, Murray E. (2017-04-05). "Natural genomic amplification of cholinesterase genes in animals". Journal of Neurochemistry (International Society for Neurochemistry (Wiley)) 142: 73–81. doi:10.1111/jnc.13990. ISSN 0022-3042. PMID 28382676. 
  18. ↑ "Medication appropriateness tool for co-morbid health conditions in dementia: consensus recommendations from a multidisciplinary expert panel". Internal Medicine Journal 46 (10): 1189–1197. October 2016. doi:10.1111/imj.13215. PMID 27527376. 
  19. ↑ Consumer Reports; Drug Effectiveness Review Project (May 2012). "Evaluating Prescription Drugs Used to Treat: Alzheimer's Disease Comparing Effectiveness, Safety, and Price". Best Buy Drugs: 2. http://www.consumerreports.org/health/resources/pdf/best-buy-drugs/AlzheimersFINAL.pdf. Retrieved 1 May 2013. , which claims Alzheimer's Association guidance as a source
  20. ↑ 20.0 20.1 "The tolerability and safety of cholinesterase inhibitors in the treatment of dementia". International Journal of Clinical Practice. Supplement (127): 45–63. June 2002. PMID 12139367. 
  21. ↑ Singh, Ravneet; Sadiq, Nazia M. (2020), "Cholinesterase Inhibitors", StatPearls (Treasure Island (FL): StatPearls Publishing), PMID 31335056, http://www.ncbi.nlm.nih.gov/books/NBK544336/, retrieved 2020-10-12 
  22. ↑ Barash, Paul G; Cullen, Bruce F; Stoelting, Robert K; Cahalan, Michael K; Stock, M Christine (15 April 2013). Clinical Anesthesia (7th ed.). pp. 552–554. ISBN 978-1-4511-4419-2. 
  23. ↑ "Inhibition of acetylcholinesterase by caffeine, anabasine, methyl pyrrolidine and their derivatives". Toxicology Letters 55 (3): 335–42. March 1991. doi:10.1016/0378-4274(91)90015-X. PMID 2003276. 
  24. ↑ "Acetylcholinesterase inhibitory, antioxidant and phytochemical properties of selected medicinal plants of the Lamiaceae family". Molecules 19 (1): 767–82. January 2014. doi:10.3390/molecules19010767. PMID 24413832. 
  25. ↑ "Inhibition of acetylcholinesterase activity by bicyclic monoterpenoids". Journal of Agricultural and Food Chemistry 53 (5): 1765–8. March 2005. doi:10.1021/jf040019b. PMID 15740071. 
  26. ↑ "In-vitro inhibition of human erythrocyte acetylcholinesterase by salvia lavandulaefolia essential oil and constituent terpenes". The Journal of Pharmacy and Pharmacology 52 (7): 895–902. July 2000. doi:10.1211/0022357001774598. PMID 10933142. 
  27. ↑ Bauer, Brent A.. "Huperzine A: Can it treat Alzheimer's?". Mayo Clinic. http://www.mayoclinic.com/health/huperzine-a/AN02022. 
  28. ↑ "Efficacy and safety of natural acetylcholinesterase inhibitor huperzine A in the treatment of Alzheimer's disease: an updated meta-analysis". Journal of Neural Transmission 116 (4): 457–65. April 2009. doi:10.1007/s00702-009-0189-x. PMID 19221692. 
  29. ↑ "Isolation of the acetylcholinesterase inhibitor ungeremine from Nerine bowdenii by preparative HPLC coupled on-line to a flow assay system". Biological & Pharmaceutical Bulletin 27 (11): 1804–9. November 2004. doi:10.1248/bpb.27.1804. PMID 15516727. 
  30. ↑ "Novel bipharmacophoric inhibitors of the cholinesterases with affinity to the muscarinic receptors M1 and M2". MedChemComm 8 (6): 1346–1359. June 2017. doi:10.1039/c7md00149e. PMID 30108847. 
  31. ↑ 31.00 31.01 31.02 31.03 31.04 31.05 31.06 31.07 31.08 31.09 31.10 31.11 31.12 31.13 31.14 31.15 31.16 31.17 31.18 31.19 31.20 31.21 31.22 31.23 31.24 Pharmacology. Edinburgh: Churchill Livingstone. 2003. p. 156. ISBN 978-0-443-07145-4. 

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