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dc.contributor.author
Kem, William
dc.contributor.author
Soti, Ferenc
dc.contributor.author
Wildeboer, Kristin
dc.contributor.author
LeFrancois, Susan
dc.contributor.author
MacDougall, Kelly
dc.contributor.author
Wei, Dong Qing
dc.contributor.author
Chou, Kuo Chen
dc.contributor.author
Arias, Hugo Rubén

dc.date.available
2020-01-21T00:23:58Z
dc.date.issued
2006-04
dc.identifier.citation
Kem, William; Soti, Ferenc; Wildeboer, Kristin; LeFrancois, Susan; MacDougall, Kelly; et al.; The Nemertine Toxin Anabaseine and Its Derivative DMXBA (GTS-21): Chemical and Pharmacological Properties; Molecular Diversity Preservation International; Marine Drugs; 4; 3; 4-2006; 255-273
dc.identifier.issn
1660-3397
dc.identifier.uri
http://hdl.handle.net/11336/95370
dc.description.abstract
Nemertines are a phylum of carnivorous marine worms that possess a variety of alkaloidal, peptidic or proteinaceous toxins that serve as chemical defenses against potential predators. The hoplonemertines additionally envenomate their prey with a mixture of proboscis alkaloids delivered with the help of a calcareous stylet that punctures the skin of the victim. Anabaseine, the first of these alkaloids to be identified, stimulates a wide variety of animal nicotinic acetylcholine receptors (AChRs), especially the neuromuscular [e.g., α1 2β1γδ (embryogenic) or α1 2β1γε (adult)] and α7 AChRs that are inhibited by the snake peptide α-bungarotoxin. A synthetic derivative, 3-(2,4-Dimethoxybenzylidene)-Anabaseine (DMXBA; also called GTS-21), improves memory in experimental animals and humans and is currently in clinical trials to determine whether it can ameliorate cognitive problems associated with schizophrenia. Here we summarize present knowledge concerning the chemistry and mechanisms of action of these two substances (anabaseine and DMXBA) on AChRs, especially those found in the mammalian brain.
dc.format
application/pdf
dc.language.iso
eng
dc.publisher
Molecular Diversity Preservation International

dc.rights
info:eu-repo/semantics/openAccess
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.subject
ANABASEINE
dc.subject
COGNITION
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DMXBA
dc.subject
GTS-21
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NEMERTINE
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NICOTINIC RECEPTORS
dc.subject.classification
Farmacología y Farmacia

dc.subject.classification
Medicina Básica

dc.subject.classification
CIENCIAS MÉDICAS Y DE LA SALUD

dc.title
The Nemertine Toxin Anabaseine and Its Derivative DMXBA (GTS-21): Chemical and Pharmacological Properties
dc.type
info:eu-repo/semantics/article
dc.type
info:ar-repo/semantics/artículo
dc.type
info:eu-repo/semantics/publishedVersion
dc.date.updated
2019-12-18T13:56:04Z
dc.journal.volume
4
dc.journal.number
3
dc.journal.pagination
255-273
dc.journal.pais
Suiza

dc.journal.ciudad
Basilea
dc.description.fil
Fil: Kem, William. University of Florida; Estados Unidos
dc.description.fil
Fil: Soti, Ferenc. University of Florida; Estados Unidos
dc.description.fil
Fil: Wildeboer, Kristin. University of Florida; Estados Unidos
dc.description.fil
Fil: LeFrancois, Susan. University of Florida; Estados Unidos
dc.description.fil
Fil: MacDougall, Kelly. University of Florida; Estados Unidos
dc.description.fil
Fil: Wei, Dong Qing. Shanghai Jiao Tong University; China
dc.description.fil
Fil: Chou, Kuo Chen. Gordon Life Science Institute; Estados Unidos
dc.description.fil
Fil: Arias, Hugo Rubén. Western University of Health Sciences; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Matemática Bahía Blanca. Universidad Nacional del Sur. Departamento de Matemática. Instituto de Matemática Bahía Blanca; Argentina
dc.journal.title
Marine Drugs

dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3663414/
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://www.mdpi.com/1660-3397/4/3/255
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/https://doi.org/10.3390/md403255
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