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Galantamine

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Galantamine is a type of acetylcholinesterase inhibitor. It is an alkaloid extracted from the bulbs and flowers of Galanthus nivalis (common snowdrop), Galanthus caucasicus (Caucasian snowdrop), Galanthus woronowii (Voronov's snowdrop), and other members of the family Amaryllidaceae, such as Narcissus (daffodil), Leucojum aestivum (snowflake), and Lycoris including Lycoris radiata (red spider lily).[5] It can also be produced synthetically.

Galantamine
Clinical data
Trade namesRazadyne, others
AHFS/Drugs.comMonograph
MedlinePlusa699058
License data
Pregnancy
category
Routes of
administration		By mouth
ATC code
Legal status
Legal status
Pharmacokinetic data
Bioavailability80–100%
Protein binding18%
MetabolismLiver partially CYP450:CYP2D6/3A4 substrate
Elimination half-life7 hours
ExcretionKidney (95%, of which 32% unchanged), fecal (5%)
Identifiers
  • (4aS,6R,8aS)-5,6,9,10,11,12-Hexahydro-3-methoxy-11-methyl-4aH-[1]benzofuro[3a,3,2-ef] [2]benzazepin-6-ol
CAS Number
PubChem CID
IUPHAR/BPS
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
PDB ligand
CompTox Dashboard (EPA)
ECHA InfoCard100.118.289 Edit this at Wikidata
Chemical and physical data
FormulaC17H21NO3
Molar mass287.359 g·mol−1
3D model (JSmol)
Melting point126.5 °C (259.7 °F)
  • O(c2c1O[C@H]4C[C@@H](O)/C=C\[C@@]43c1c(cc2)CN(C)CC3)C
  • InChI=1S/C17H21NO3/c1-18-8-7-17-6-5-12(19)9-14(17)21-16-13(20-2)4-3-11(10-18)15(16)17/h3-6,12,14,19H,7-10H2,1-2H3/t12-,14-,17-/m0/s1 checkY
  • Key:ASUTZQLVASHGKV-JDFRZJQESA-N checkY
  (verify)

Galantamine is primarily known for its potential to slow cognitive decline. It is used clinically for treating early-stage Alzheimer's disease and memory impairments, although it has had limited success with the more advanced condition of dementia.[6][7][8][9]

It works by increasing the amount of a type of neurotransmitter named acetylcholine by the inhibiting activity of an enzyme called acetylcholinesterase known for breaking down acetylcholine. This elevates and prolongs acetylcholine levels boosting acetylcholine's neuromodulatory functionality, subsequently enhancing functionality of the various cognitions that acetylcholine is involved in, such as memory processing, reasoning, and thinking.[6] Galantamine may cause serious adverse effects, such as stomach bleeding, liver injury or chest pain.[6][8]

Galantamine was isolated for the first time from bulbs of Galanthus nivalis (common snowdrop) in the Soviet Union in the 1940s.[10] The active ingredient was extracted, identified, and studied, in particular in relation to acetylcholinesterase (AChE)-inhibiting properties.[11][12] The first industrial process was developed in 1959.[13][14] However, it was not until the 1990s when full-scale synthesis was upscaled and optimized.[15]

Medical uses

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Galantamine, sold under the brand name Razadyne among others, is indicated for the treatment of mild to moderate vascular dementia and Alzheimer's disease.[6][7] The first person to extract galantamine and theorize its usefulness in medicine, was the Bulgarian chemist Dimitar Paskov in 1959. In the United States, it is approved by the Food and Drug Administration (FDA) for the treatment of mild to moderate dementia.[8][16] Galantamine may not be effective for treating mild cognitive impairment.[17]

Alzheimer's disease

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Alzheimer's disease is characterized by the impairment of cholinergic function.[6][8] One hypothesis is that this impairment contributes to the cognitive deficits caused by the disease. This hypothesis forms the basis for use of galantamine as a cholinergic enhancer in the treatment of Alzheimer's.[6][8] Galantamine inhibits acetylcholinesterase, an enzyme which hydrolyzes acetylcholine.[6][8] As a result of acetylcholinesterase inhibition, galantamine increases the availability of acetylcholine for synaptic transmission.[8] Additionally, galantamine binds to the allosteric sites of nicotinic receptors, which causes a conformational change.[18] This allosteric modulation increases the nicotinic receptor's response to acetylcholine.[8] The activation of presynaptic nicotinic receptors increases the release of acetylcholine, further increasing the availability of acetylcholine.[8] Galantamine's competitive inhibition of acetylcholinesterase and allosteric nicotinic modulation serves as a dual mechanism of action.[18]

To reduce the prevalence of negative side effects associated with galantamine, such as nausea and vomiting, a dose-escalation scheme may be used.[19] The use of a dose-escalation scheme has been well accepted in countries where galantamine is used.[19] A dose-escalation scheme for Alzheimer's treatment involves a recommended starting dosage of 4 mg galantamine tablets given twice a day (8 mg/day).[6] After a minimum of 4 weeks, the dosage may then be increased to 8 mg given twice a day (16 mg/day).[6] After a minimum of 4 weeks at 16 mg/day, the treatment may be increased to 12 mg given twice a day (24 mg/day).[6] Dosage increases are based upon the assessment of clinical benefit as well as tolerability of the previous dosage.[6] If treatment is interrupted for more than three days, the process is usually restarted, beginning at the starting dosage, and re-escalating to the current dose.[6] It has been found that a dosage between 16–24 mg/day is the optimal dosage.[20]

In December 2023, the FDA approved a New Drug Application (NDA) for a pro-drug of galantamine called ALPHA-1062.[21] In July 2024, The FDA approved benzgalantamine (Zunveyl), previously known as ALPHA-1062, to treat mild-to-moderate Alzheimer's disease.[22]

Side effects

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The adverse effect profile of galantamine includes potential for allergic reaction, including hives, swelling of the face or throat, and skin rash.[6][23] Using galantamine may cause chest pain, bloody urine, stomach bleeding, and liver injury, among other side effects.[6][23] Nausea, vomiting, diarrhea, dizziness, and headache are considered common side effects.[6]

A gradual titration over more than three months may enable long-term tolerability in some people.[24]

Galantamine has a wide spectrum of interactions with other medications and medical disorders, requiring close assessment between the physician and patient.[23]

Pharmacology

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Galantamine's chemical structure contains a tertiary amine. At a neutral pH, this tertiary amine will often bond to a hydrogen, and appear mostly as an ammonium ion.[6]

Galantamine is a potent allosteric potentiating ligand of human nicotinic acetylcholine receptors (nAChRs) α4β2, α3β4, and α6β4, and chicken/mouse nAChRs α7/5-HT3 in certain areas of the brain.[6][25] By binding to the allosteric site of the nAChRs, a conformational change occurs which increases the receptors response to acetylcholine.[8] This modulation of the nicotinic cholinergic receptors on cholinergic neurons in turn causes an increase in the amount of acetylcholine released.[26] However, recent studies suggest that Galantamine does not functionally act at human nAChRs α4β2 or α7 as a positive allosteric modulator.[27][28]

Galantamine also works as a weak competitive and reversible cholinesterase inhibitor in all areas of the body.[6] By inhibiting acetylcholinesterase, it increases the concentration and thereby action of acetylcholine in certain parts of the brain. Galantamine's effects on nAChRs and complementary acetylcholinesterase inhibition make up a dual mechanism of action. It is hypothesized that this action might relieve some of the symptoms of Alzheimer's.

 
Galantamine's dual mechanism of action

Galantamine in its pure form is a white powder. The atomic resolution 3D structure of the complex of galantamine and its target, acetylcholinesterase, was determined by X-ray crystallography in 1999 (PDB code: 1DX6; see complex).[29] There is no evidence that galantamine alters the course of the underlying dementing process.[30]

Pharmacokinetics

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Absorption of galantamine is rapid and complete and shows linear pharmacokinetics. It is well absorbed with absolute oral bioavailability between 80 and 100%. It has a terminal elimination half-life of seven hours. Peak effect of inhibiting acetylcholinesterase was achieved about one hour after a single oral dose of 8 mg in some healthy volunteers.

The coadministration of food delays the rate of galantamine absorption, but does not affect the extent of absorption.[18]

Plasma protein binding of galantamine is about 18%, which is relatively low.

Metabolism

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Approximately 75% of a dose of galantamine is metabolised in the liver. In vitro studies have shown that hepatic CYP2D6 and CYP3A4 are involved in galantamine metabolism. Within 24 hours of intravenous or oral administration approximately 20% of a dose of galantamine will be excreted unreacted in the urine.[18]

In humans, several metabolic pathways for galantamine exist.[25] These pathways lead to the formation of a number of different metabolites.[25] One of the metabolites that may result can be formed through the glucuronidation of galantamine.[25] Additionally, galantamine may undergo oxidation or demethylation at its nitrogen atom, forming two other possible metabolites.[25] Galantamine can undergo demethylation at its oxygen atom, forming an intermediate which can then undergo glucuronidation or sulfate conjugation.[25] Lastly, galantamine may be oxidized and then reduced before finally undergoing demethylation or oxidation at its nitrogen atom, or demethylation and subsequent glucuronidation at its oxygen atom.[25]

 
Metabolic pathways of galantamine

Drug interactions

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Since galantamine is metabolized by CYP2D6 and CYP3A4, inhibiting either of these isoenzymes will increase the cholinergic effects of galantamine.[18] Inhibiting these enzymes may lead to adverse effects.[18] It was found that paroxetine, an inhibitor of CYP2D6, increased the bioavailability of galantamine by 40%.[18] The CYP3A4 inhibitors ketoconazole and erythromycin increased the bioavailability of galantamine by 30% and 12%, respectively.[18]

Extraction and synthesis

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Main article: Galantamine total synthesis

Since the alkaloid is isolated from botanical sources containing low amounts (0.1%) by weight, extraction yields are low.[31] Although galantamine can be produced from natural resources, it also has many industrial syntheses, such as by Janssen, Ortho-McNeil Pharmaceutical, Shire, and Takeda Pharmaceutical Company.[32]

Research

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Organophosphate poisoning

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The toxicity of organophosphates results primarily from their action as irreversible inhibitors of acetylcholinesterase.[33] Inhibiting acetylcholinesterase causes an increase in acetylcholine, as the enzyme is no longer available to catalyze its breakdown.[33] In the peripheral nervous system, acetylcholine accumulation can cause an overstimulation of muscarinic receptors followed by a desensitization of nicotinic receptors.[33] This leads to severe skeletal muscle fasciculations (involuntary contractions).[33] The effects on the central nervous system include anxiety, restlessness, confusion, ataxia, tremors, seizures, cardiorespiratory paralysis, and coma.[33] As a reversible acetylcholinesterase inhibitor, galantamine has the potential to serve as an effective organophosphate poisoning treatment by preventing irreversible acetylcholinesterase inhibition.[33] Additionally, galantamine has anticonvulsant properties which may make it even more desirable as an antidote.[33]

Research supported in part by the US Army has led to a US patent application for the use of galantamine and/or its derivatives for treatment of organophosphate poisoning.[33] The indications for use of galantamine in the patent application include poisoning by nerve agents "including but not limited to soman, sarin, and VX, tabun, and Novichok agents". Galantamine was studied in the research cited in the patent application for use along with the well-recognized nerve agent antidote atropine. According to the investigators, an unexpected synergistic interaction occurred between galantamine and atropine in an amount of 6 mg/kg or higher. Increasing the dose of galantamine from 5 to 8 mg/kg decreased the dose of atropine needed to protect experimental animals from the toxicity of soman in dosages 1.5 times the dose generally required to kill half the experimental animals.[34]

Autism

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Galantamine given in addition to risperidone to autistic children has been shown to improve some of the symptoms of autism such as irritability, lethargy, and social withdrawal.[35] Additionally, the cholinergic and nicotinic receptors are believed to play a role in attentional processes.[36] Some studies have noted that cholinergic and nicotinic treatments have improved attention in autistic children.[36] As such, it is hypothesized that galantamine's dual action mechanism might have a similar effect in treating autistic children and adolescents.[36]

Anesthesia

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Galantamine may have some limited use in reducing the side-effects of anesthetics ketamine and diazepam. In one study, a control group of patients were given ketamine and diazepam and underwent anesthesia and surgery.[37] The experimental group was given ketamine, diazepam, and nivalin (of which the active ingredient is galantamine).[37] The degree of drowsiness and disorientation of the two groups was then assessed 5, 10, 15, 30 and 60 minutes after surgery.[37] The group that had taken nivalin were found to be more alert 5, 10, and 15 minutes after the surgery.[37]

Oneirogen

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Galantamine is known to have oneirogenic properties. Research has demonstrated its potential to increase dream recall, dream self-awareness and dream vividness. The enhancement of such dream properties can facilitate the induction of lucid dreams.[38][39]

References

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  27. ^ Moerke MJ, McMahon LR, Wilkerson JL (April 2020). "More than Smoke and Patches: The Quest for Pharmacotherapies to Treat Tobacco Use Disorder". Pharmacological Reviews. 72 (2): 527–557. doi:10.1124/pr.119.018028. PMC 7090325. PMID 32205338. Archived from the original on October 8, 2021. Retrieved October 24, 2020.
  28. ^ Kowal NM, Ahring PK, Liao WY, Indurti DC, Harvey BS, O'Connor SM, et al. (July 2018). "Galantamine is not a positive allosteric modulator of human α4β2 or α7 nicotinic acetylcholine receptors". British Journal of Pharmacology. 175 (14): 2911–2925. doi:10.1111/bph.14329. PMC 6016680. PMID 29669164.
  29. ^ Greenblatt HM, Kryger G, Lewis T, Silman I, Sussman JL (December 1999). "Structure of acetylcholinesterase complexed with (-)-galanthamine at 2.3 A resolution". FEBS Letters. 463 (3): 321–6. Bibcode:1999FEBSL.463..321G. doi:10.1016/S0014-5793(99)01637-3. PMID 10606746. S2CID 573270.
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  31. ^ Kim JK, Park SU (2017). "Pharmacological aspects of galantamine for the treatment of Alzheimer's disease". EXCLI Journal. 16: 35–39. doi:10.17179/excli2016-820. PMC 5318685. PMID 28337117.
  32. ^ Mucke HA (November 2015). "The case of galantamine: repurposing and late blooming of a cholinergic drug". Future Science OA. 1 (4): FSO73. doi:10.4155/fso.15.73. PMC 5137937. PMID 28031923.
  33. ^ a b c d e f g h Albuquerque EX, Pereira EF, Aracava Y, Fawcett WP, Oliveira M, Randall WR, et al. (August 2006). "Effective countermeasure against poisoning by organophosphorus insecticides and nerve agents". Proceedings of the National Academy of Sciences of the United States of America. 103 (35): 13220–5. Bibcode:2006PNAS..10313220A. doi:10.1073/pnas.0605370103. PMC 1550772. PMID 16914529.
  34. ^ Albuquerque, Edson X, Adler, Michael, Pereira, Edna F.R. (January 22, 2009). "United States Patent Application 20090023706". US Patent and Trademark Office. Archived from the original on July 13, 2020. Retrieved May 27, 2016.
  35. ^ Ghaleiha A, Ghyasvand M, Mohammadi MR, Farokhnia M, Yadegari N, Tabrizi M, et al. (July 2014). "Galantamine efficacy and tolerability as an augmentative therapy in autistic children: A randomized, double-blind, placebo-controlled trial". Journal of Psychopharmacology. 28 (7): 677–85. doi:10.1177/0269881113508830. PMID 24132248. S2CID 206491732.
  36. ^ a b c Nicolson R, Craven-Thuss B, Smith J (October 2006). "A prospective, open-label trial of galantamine in autistic disorder". Journal of Child and Adolescent Psychopharmacology. 16 (5): 621–9. doi:10.1089/cap.2006.16.621. PMID 17069550.
  37. ^ a b c d Chakalova E, Marinova M, Srebreva M, Anastasov D, Ploskov K (1987). "[Attempt to eliminate residual somnolence and disorientation with nivaline after anesthesia with ketalar and diazepam for minor obstetrical and gynecologic surgery]". Akusherstvo I Ginekologiia (in Bulgarian). 26 (3): 28–31. PMID 3631427.
  38. ^ Tan S, Fan J (June 2023). "A systematic review of new empirical data on lucid dream induction techniques". Journal of Sleep Research. 32 (3): e13786. doi:10.1111/jsr.13786. PMID 36408823.
  39. ^ Sparrow G, Hurd R, Carlson R, Molina A (August 2018). "Exploring the effects of galantamine paired with meditation and dream reliving on recalled dreams: Toward an integrated protocol for lucid dream induction and nightmare resolution". Consciousness and Cognition. 63. Elsevier BV: 74–88. doi:10.1016/j.concog.2018.05.012. PMID 29960246.
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