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Brain Histamine N-Methyltransferase As a Possible Target of Treatment for Methamphetamine Overdose

Stereotypical behaviors induced by methamphetamine (METH) overdose are one of the overt symptoms of METH abuse, which can be easily assessed in animal models. Currently, there is no successful treatment for METH overdose. There is increasing evidence that elevated levels of brain histamine can atten...

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Autores principales: Kitanaka, Junichi, Kitanaka, Nobue, Hall, F. Scott, Uhl, George R., Takemura, Motohiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Libertas Academica 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4777238/
https://www.ncbi.nlm.nih.gov/pubmed/26966348
http://dx.doi.org/10.4137/DTI.S38342
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author Kitanaka, Junichi
Kitanaka, Nobue
Hall, F. Scott
Uhl, George R.
Takemura, Motohiko
author_facet Kitanaka, Junichi
Kitanaka, Nobue
Hall, F. Scott
Uhl, George R.
Takemura, Motohiko
author_sort Kitanaka, Junichi
collection PubMed
description Stereotypical behaviors induced by methamphetamine (METH) overdose are one of the overt symptoms of METH abuse, which can be easily assessed in animal models. Currently, there is no successful treatment for METH overdose. There is increasing evidence that elevated levels of brain histamine can attenuate METH-induced behavioral abnormalities, which might therefore constitute a novel therapeutic treatment for METH abuse and METH overdose. In mammals, histamine N-methyltransferase (HMT) is the sole enzyme responsible for degrading histamine in the brain. Metoprine, one of the most potent HMT inhibitors, can cross the blood–brain barrier and increase brain histamine levels by inhibiting HMT. Consequently, this compound can be a candidate for a prototype of drugs for the treatment of METH overdose.
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spelling pubmed-47772382016-03-10 Brain Histamine N-Methyltransferase As a Possible Target of Treatment for Methamphetamine Overdose Kitanaka, Junichi Kitanaka, Nobue Hall, F. Scott Uhl, George R. Takemura, Motohiko Drug Target Insights Review Stereotypical behaviors induced by methamphetamine (METH) overdose are one of the overt symptoms of METH abuse, which can be easily assessed in animal models. Currently, there is no successful treatment for METH overdose. There is increasing evidence that elevated levels of brain histamine can attenuate METH-induced behavioral abnormalities, which might therefore constitute a novel therapeutic treatment for METH abuse and METH overdose. In mammals, histamine N-methyltransferase (HMT) is the sole enzyme responsible for degrading histamine in the brain. Metoprine, one of the most potent HMT inhibitors, can cross the blood–brain barrier and increase brain histamine levels by inhibiting HMT. Consequently, this compound can be a candidate for a prototype of drugs for the treatment of METH overdose. Libertas Academica 2016-03-02 /pmc/articles/PMC4777238/ /pubmed/26966348 http://dx.doi.org/10.4137/DTI.S38342 Text en © 2016 the author(s), publisher and licensee Libertas Academica Ltd. This is an open-access article distributed under the terms of the Creative Commons CC-BY-NC 3.0 License.
spellingShingle Review
Kitanaka, Junichi
Kitanaka, Nobue
Hall, F. Scott
Uhl, George R.
Takemura, Motohiko
Brain Histamine N-Methyltransferase As a Possible Target of Treatment for Methamphetamine Overdose
title Brain Histamine N-Methyltransferase As a Possible Target of Treatment for Methamphetamine Overdose
title_full Brain Histamine N-Methyltransferase As a Possible Target of Treatment for Methamphetamine Overdose
title_fullStr Brain Histamine N-Methyltransferase As a Possible Target of Treatment for Methamphetamine Overdose
title_full_unstemmed Brain Histamine N-Methyltransferase As a Possible Target of Treatment for Methamphetamine Overdose
title_short Brain Histamine N-Methyltransferase As a Possible Target of Treatment for Methamphetamine Overdose
title_sort brain histamine n-methyltransferase as a possible target of treatment for methamphetamine overdose
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4777238/
https://www.ncbi.nlm.nih.gov/pubmed/26966348
http://dx.doi.org/10.4137/DTI.S38342
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