WordNet

used in treatment of Alzheimers disease and glaucoma

Wikipedia preview

出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2015/09/14 22:10:06」(JST)

wiki en

Physostigmine (also known as eserine from éséré, the West African name for the Calabar bean) is a parasympathomimetic alkaloid, specifically, a reversible cholinesterase inhibitor. It occurs naturally in the Calabar bean.

The chemical was synthesized for the first time in 1935 by Percy Lavon Julian and Josef Pikl. It is available in the U.S. under the trade names Antilirium and Isopto Eserine, and as eserine salicylate and eserine sulfate. Today, physostigmine is most commonly used for its medicinal value but before its discovery by western medicine in 1846 it was much more prevalent as a poison. Physostigmine has an LD50 of 3 mg/kg in mice.

Pharmacology

Physostigmine acts by interfering with the metabolism of acetylcholine. It is a covalent (reversible - bond hydrolyzed and released) inhibitor of acetylcholinesterase, the enzyme responsible for the breakdown of acetylcholine in the synaptic cleft of the neuromuscular junction.^[1] It indirectly stimulates both nicotinic and muscarinic acetylcholine receptors.

Synthesis

Julian's synthesis of physostigmine

Physostigmine has two chiral carbon atoms. Therefore, attention needs to be paid to the synthesis of the correct diastereomers. The 71 syntheses of physostigmine yield 33 racemic mixtures and 38 products of a single enantiomer. The first total synthesis of physostigmine was achieved by Julian and Piki in 1935.^[2] The main goal of Julian’s physostigmine synthesis was to get the intermediate key compound, l-eseroline (compound 10 in the diagram to the left). Then, this compound would be easily converted to physostigmine. In one of his earlier works^[3] Julian synthesized the ring of physostigmine from starting material 1-methyl-3-formyl oxindole, which was discovered by Friedlander. However, he faced the problems that the starting material was expensive, and the reduction of a nitrile to an amine (similar to the reaction of compound 6 to given compound 7 in the diagram) with sodium and alcohol did not result in good yield. In his second work “Studies in the Indole Series III,” he had improved the yield of amine from nitrile significantly by using palladium and hydrogen. Although he succeeded in the synthesis of the target chemical, the route had several drawbacks. First, the chemical resolution of compound 8 is unreliable, and the chemical resolution of d,l-eserethole gives optically pure enantiomers after eight recrystallizations of its tartrate salt. Second, the reaction of compound 8 to give compound 9 requires a large amount of Na. In the years since this initial work, many other groups have used a variety of approaches to overcome these problems.

Biosynthesis

Physostigmine biosynthesis is proposed from tryptamine methylation and post-heterocyclization catalyzed by an unknown enzyme:

Clinical uses

Physostigmine is used to treat glaucoma, Alzheimer's disease, and delayed gastric emptying. It has been shown to improve short term memory.^[4] Recently, it has begun to be used in the treatment of orthostatic hypotension.

Because it is a tertiary amine, it can cross the blood–brain barrier, and physostigmine salicylate is used to treat the central nervous system effects of atropine, scopolamine, and other anticholinergic drug overdoses.

Physostigmine is the antidote of choice for Datura stramonium poisoning. It is also an antidote for Atropa belladonna poisoning, the same as for atropine.^[5] It has been also used as an antidote for poisoning with GHB,^[6] but is poorly effective and often causes additional toxicity, so is not a recommended treatment.^[7]

Bioactivity

Physostigmine functions as an acetylcholinesterase inhibitor. Its mechanism is to prevent the hydrolysis of acetylcholine by acetylcholinesterase at the transmitted sites of acetylcholine. This inhibition enhances the effect of acetylcholine, making it useful for the treatment of cholinergic disorders and myasthenia gravis. More recently, physostigmine has been used to improve the memory of Alzheimer's patients due to its potent anticholinesterase activity.^{[medical citation needed]} However, its drug form, physostigmine salicylate, has poor bioavailability.

Physostigmine also has a miotic function, causing pupillary constriction. It is useful in treating mydriasis. Physostigmine also increases outflow of the aqueous humor in the eye, making it useful in the treatment of glaucoma.

Recently, physostigmine has been proposed as antidote for intoxication with gamma hydroxybutyrate (GHB, a potent sedative-hypnotic agent that can cause loss of consciousness, loss of muscle control, and death). Physostigmine may treat GHB by producing a nonspecific state of arousal. However, not enough scientific evidence shows physostigmine properly treats GHB toxicity. Furthermore, lower doses of GHB produce a stronger action at the GHB receptor than the GABA_B-receptor, resulting in a stimulating effect which would act synergistically with physostigmine and producing hyperstimulation when the GHB blood levels begin to drop.

Physostigmine also has other proposed uses: it could reverse undesired side effects of benzodiazepines such as diazepam, alleviating anxiety and tension. Another proposed use of physostigmine is to reverse the effects of barbiturates (any of a group of barbituric acids derived for use as sedatives or hypnotics).

History

The Calabar Bean

The Efik people, also, divided into the Akwa Ibom State for Ibibio people, of what is now on the Southern-East modern day Nigeria, were the first to come in contact with physostigmine, the active ingredient in the Calabar bean.^[8] The Calabar bean, or chopping nut, was very prevalent in Efik culture as an ordeal poison. Individuals accused of witchcraft would drink the white, milky extract of the bean, made by crushing the bean in a mortar and soaking the remains in water. If the accused died, it was considered proof of their use of witchcraft. If they lived, usually due to vomiting up the poison, then they were declared innocent and sent free.^[9]

Western Medicine's Discovery

In 1846, European missionaries arrived in what was referred to as Old Calabar, now part of Nigeria. These missionaries wrote about the use of the calabar bean as a test for witchcraft. These beans eventually made their way back to Scotland, the home of these particular missionaries, where in 1855 Robert Christison, a toxicologist, tested the toxicity of the poison on himself by eating one. He survived to document the experience. The bean was studied throughout the 1860s by a few different Edinburgh scientists; including Douglas Argyll Robertson who wrote a paper on the use of calabar bean extract on the eye and was the first to use it medicinally, and Thomas Richard Fraser who researched how to best extract the active principle, which was later determined to be physostigmine. Fraser also studied the antagonism between physostigmine and atropine incredibly rigorously, at a time when the concept of antagonism had little if any experimental support. Fraser's research is still the basis of today's knowledge about the interactions between atropine and physostigmine at many different and specific doses.^[10] Physostigmine's first use as a treatment for glaucoma was by Ludwig Laqueur in 1876. Laqueur himself suffered from glaucoma so, like Christison, he experimented on himself, although Laqueur was much more scientific and methodical in his self-treatment.

In the 1920s, Otto Loewi determined the biomechanical mechanism for the effects of physostigmine on the body. Loewi was studying how actions that we now consider to be controlled by the parasympathetic nervous system, were directed by chemicals. During his studies, Loewi discovered acetylcholine and that physostigmine acted by preventing acetylcholine inhibition. In 1936, Loewi was awarded the Nobel Prize for his work on discovering acetylcholine and biological chemical transmitters. More important discoveries surrounding physostigmine were made at Edinburgh University in 1925. Edgar Stedman and George Barger determined the structure of physostigmine using a method called chemical degradation. Percy Lavon Julian was later the first to synthesize physostigmine in 1935. English scientist Sir Robert Robinson was also working on the synthesis of physostigmine, but surprisingly Julian, a relatively unknown scientist at the time, was the successful one.^[11]

Side effects

An overdose can cause cholinergic syndrome. Other side effects may include nausea, vomiting, diarrhea, anorexia, dizziness, headache, stomach pain, sweating, dyspepsia, and seizures.^[12] The carbamate functional group readily hydrolyses in water, and in bodily conditions. The metabolite thus formed from physostigmine and some other alkaloids (e.g. cymserine) is eseroline, which research has suggested may be neurotoxic to humans.^[13] Death can result from failure of the respiratory system and paralysis of the heart.

References

^ Katzung, B. G.; Masters, S.; Trever, A. (2009). Basic and Clinical Pharmacology. McGraw Hill. p. 110. ISBN 978-0-07-160405-5.
^ Julian, P. L.; Pikl, J. (1935). "Studies in the Indole Series. III. On the Synthesis of Physostigmine". Journal of the American Chemical Society 57 (3): 539–544. doi:10.1021/ja01306a046.
^ Julian, P. L.; Pikl, J.; Boggess, D. (1934). "Studies in the Indole Series. II. Alkylation of 1-Methyl-3-Formyloxindole and a Synthesis of the Basic Ring Structure of Physostigmine". Journal of the American Chemical Society 56 (8): 1797–1801. doi:10.1021/ja01323a046.
^ Krus et al. 1968
^ Potter, S. O. L. (1893). A Handbook of Materia Medica, Pharmacy and Therapeutics. London: P. Blakiston's. p. 53.
^ Traub, S. J.; Nelson, L. S.; Hoffman, R. S. (2002). "Physostigmine as a treatment for gamma-hydroxybutyrate toxicity: a review". Journal of Toxicology. Clinical Toxicology 40 (6): 781–787. doi:10.1081/CLT-120015839. PMID 12475191.
^ Zvosec, D. L.; Smith, S. W.; Litonjua, R.; Westfal, R. E. (2007). "Physostigmine for gamma-hydroxybutyrate coma: inefficacy, adverse events, and review". Clinical Toxicology 45 (3): 261–265. doi:10.1080/15563650601072159. PMID 17453877.
^ Roberts, M. F.; Wink, M. (1998). Alkaloids: Biochemistry, Ecology, and Medicinal Applications. Plenum Press. p. 38. ISBN 978-1-4419-3263-1.
^ Scheindlin, S. (2010). "Episodes in the Story of Physostigmine". Molecular Interventions 10 (1): 4–5. doi:10.1124/mi.10.1.1.
^ Proudfoot, A. (2006). "The early toxicology of physostigmine: a tale of beans, great men and egos". Toxicology Review 25 (2): 99–138.
^ Scheindlin, S. (2010). "Episodes in the Story of Physostigmine". Molecular Interventions 10 (1): 5–10. doi:10.1124/mi.10.1.1.
^ Alzheimer Research Forum
^ Somani, SM; Kutty, RK; Krishna, G (1990). "Eseroline, a metabolite of physostigmine, induces neuronal cell death". Toxicology and applied pharmacology 106 (1): 28–37. doi:10.1016/0041-008X(90)90102-Z. PMID 2251681.

UpToDate Contents

全文を閲覧するには購読必要です。 To read the full text you will need to subscribe.

1. 抗コリン剤中毒 anticholinergic poisoning
2. 化学テロ：早急な認識および初回薬物治療マネージメント chemical terrorism rapid recognition and initial medical management
3. カルバマゼピン中毒 carbamazepine poisoning
4. 三環系抗うつ剤中毒 tricyclic antidepressant poisoning
5. Toxic plant ingestions and nicotine poisoning in children: Management

English Journal

Conclusive identification of the oxybutynin-hydrolyzing enzyme in human liver.

Sato Y, Miyashita A, Iwatsubo T, Usui T.SourceDrug Metabolism Research Laboratories, Drug Discovery Research, Astellas Pharma Inc., 2-1-6 Kashima, Yodogawa-ku, Osaka 532-8514, Japan. yuichiro.sato@astellas.com.
Drug metabolism and disposition: the biological fate of chemicals.Drug Metab Dispos.2012 May;40(5):902-6. Epub 2012 Jan 31.
The aim of this study was to conclusively determine the enzyme responsible for the hydrolysis of oxybutynin in human liver. Hydrolysis in human liver microsomes (HLMs) and human liver cytosol (HLC) followed Michaelis-Menten kinetics with similar K(m) values. In recombinant human carboxylesterase (CE
PMID 22293119

Theta and gamma coherence across the septotemporal axis during distinct behavioral states.

Penley SC, Hinman JR, Sabolek HR, Escabí MA, Markus EJ, Chrobak JJ.SourceDepartment of Psychology, University of Connecticut, Storrs, Connecticut.
Hippocampus.Hippocampus.2012 May;22(5):1164-75. doi: 10.1002/hipo.20962. Epub 2011 Jul 11.
Theta (4-12 Hz) and gamma (40-100 Hz) field potentials represent the interaction of synchronized synaptic input onto distinct neuronal populations within the hippocampal formation. Theta is quite prominent during exploratory activity, locomotion, and REM sleep. Although it is generally acknowledged
PMID 21748821

Japanese Journal

Formal total synthesis of (-)-physostigmine

Asakawa Kaori,Noguchi Naoyoshi,Nakada Masahisa
Heterocycles 76(1), 183-190, 2008-09-03
NAID 40016208560

Synthesis of cycloalkanoindoles, the carba analogs of physostigmine

Kiraly Imre,Hornyanszky Gabor,Kupai Katalin [他]
Heterocycles 75(1), 43-56, 2008-01-01
NAID 40015919657

Related Pictures

★リンクテーブル★

リンク元	「コリンエステラーゼ阻害薬」「フィゾスチグミン」「フイゾスチグミン」
拡張検索	「physostigmine salicylate」

「コリンエステラーゼ阻害薬」

Physostigmine
Systematic (IUPAC) name
	(3aR,8aS)-1,3a,8-Trimethyl-1H,2H,3H,3aH,8H,8aH-pyrrolo[2,3-b]indol-5-yl N-methylcarbamate
Clinical data
Trade names	Antilirium
AHFS/Drugs.com	monograph
Pregnancy; category	AU: C; US: C (Risk not ruled out);
Legal status	US: ℞-only;
Routes of; administration	intravenous, intramuscular, ophthalmic
Pharmacokinetic data
Metabolism	Major metabolite: Eseroline
Identifiers
CAS Registry Number	57-47-6
ATC code	S01EB05 V03AB19
PubChem	CID: 5983
IUPHAR/BPS	6598
DrugBank	DB00981
ChemSpider	5763
UNII	9U1VM840SP
KEGG	D00196
ChEBI	CHEBI:27953
ChEMBL	CHEMBL94
Chemical data
Formula	C15H21N3O2
Molecular mass	275.346 g/mol
	SMILES O=C(Oc1cc2c(cc1)N([C@H]3N(CC[C@@]23C)C)C)NC ;
	InChI InChI=1S/C15H21N3O2/c1-15-7-8-17(3)13(15)18(4)12-6-5-10(9-11(12)15)20-14(19)16-2/h5-6,9,13H,7-8H2,1-4H3,(H,16,19)/t13-,15+/m1/s1 ; Key:PIJVFDBKTWXHHD-HIFRSBDPSA-N ;
(what is this?) (verify)

　　[★]

英: cholinesterase inhibitor cholinesterase inhibitors
同: 抗コリンエステラーゼ薬 anticholinesterase
関: アセチルコリン、アセチルコリン受容体、副交感神経

コリンエステラーゼ阻害薬=

アルツハイマー病の治療薬

作用機序

図：GOO.203

活性部位に結合

エドロフォニウムやドネペジルは活性化部位に結合して、酵素の機能を可逆的に失わせる (GOO.204)

エドロフォニウムは四級アミンなので腎臓より速やかに排泄され、持続時間が短い。

酵素ををカルバモイル化

フィゾスチグミンやネオスチグミンは活性化部位に位置するセリン残基のヒドロキシ基にカルバモイル基(NH₂CO-)を転移することで、機能を可逆的に失わせる (GOO.204)

酵素をリン酸化

有機リン化合物系

薬理作用

動態

適応

臨床応用

種類	疾患への適応
ムスカリン作動薬	緑内障、手術後の腸管麻痺、尿閉
コリンエステラーゼ阻害薬	緑内障、手術後の腸管麻痺、尿閉、重症筋無力症の診断・治療、アルツハイマー病
ムスカリン受容体遮断薬	鎮痙薬（消化管、胆管、尿路など）、胃・十二指腸潰瘍、散瞳薬、パーキンソン病、麻酔前投与