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Brain distribution of geissoschizine methyl ether in rats using mass spectrometry imaging analysis
Geissoschizine methyl ether (GM) is one of the main active ingredients responsible for ameliorating the behavioral and psychological symptoms of dementia (BPSD) in Kampo medicine yokukansan. GM is mainly metabolized into hydroxylated forms (HM-1/2). However, the brain distributions of GM and HM has...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7190722/ https://www.ncbi.nlm.nih.gov/pubmed/32350314 http://dx.doi.org/10.1038/s41598-020-63474-x |
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author | Matsumoto, Takashi Ikarashi, Yasushi Takiyama, Mikina Watanabe, Junko Setou, Mitsutoshi |
author_facet | Matsumoto, Takashi Ikarashi, Yasushi Takiyama, Mikina Watanabe, Junko Setou, Mitsutoshi |
author_sort | Matsumoto, Takashi |
collection | PubMed |
description | Geissoschizine methyl ether (GM) is one of the main active ingredients responsible for ameliorating the behavioral and psychological symptoms of dementia (BPSD) in Kampo medicine yokukansan. GM is mainly metabolized into hydroxylated forms (HM-1/2). However, the brain distributions of GM and HM has not been reported in vivo. In this study, therefore, the plasma concentrations and brain distribution of these compounds were examined in vivo using rats injected intravenously with GM. Plasma concentrations were analyzed using liquid chromatography-tandem mass spectrometry analysis and brain distribution using mass spectrometry imaging analysis. Plasma GM and HM-1 concentrations decreased in the 4 h after injection, whereas the concentration of plasma HM-2 increased at 4 h. In the 0.25 h-brain, GM signals were diffusely observed throughout the brain, including the cerebral cortex, hippocampus, striatum, thalamus, amygdala, cerebellum, and cerebral ventricle. HM signals were detected only in the ventricles of the brain at 4 h. These results suggest that plasma GM enters the brain and distributes in the parenchyma of various brain regions involved in BPSD, while plasma HM does not enter the brain parenchyma. This study is also the first to visually demonstrate the brain distribution of GM and its metabolite in vivo. |
format | Online Article Text |
id | pubmed-7190722 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-71907222020-05-05 Brain distribution of geissoschizine methyl ether in rats using mass spectrometry imaging analysis Matsumoto, Takashi Ikarashi, Yasushi Takiyama, Mikina Watanabe, Junko Setou, Mitsutoshi Sci Rep Article Geissoschizine methyl ether (GM) is one of the main active ingredients responsible for ameliorating the behavioral and psychological symptoms of dementia (BPSD) in Kampo medicine yokukansan. GM is mainly metabolized into hydroxylated forms (HM-1/2). However, the brain distributions of GM and HM has not been reported in vivo. In this study, therefore, the plasma concentrations and brain distribution of these compounds were examined in vivo using rats injected intravenously with GM. Plasma concentrations were analyzed using liquid chromatography-tandem mass spectrometry analysis and brain distribution using mass spectrometry imaging analysis. Plasma GM and HM-1 concentrations decreased in the 4 h after injection, whereas the concentration of plasma HM-2 increased at 4 h. In the 0.25 h-brain, GM signals were diffusely observed throughout the brain, including the cerebral cortex, hippocampus, striatum, thalamus, amygdala, cerebellum, and cerebral ventricle. HM signals were detected only in the ventricles of the brain at 4 h. These results suggest that plasma GM enters the brain and distributes in the parenchyma of various brain regions involved in BPSD, while plasma HM does not enter the brain parenchyma. This study is also the first to visually demonstrate the brain distribution of GM and its metabolite in vivo. Nature Publishing Group UK 2020-04-29 /pmc/articles/PMC7190722/ /pubmed/32350314 http://dx.doi.org/10.1038/s41598-020-63474-x Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Matsumoto, Takashi Ikarashi, Yasushi Takiyama, Mikina Watanabe, Junko Setou, Mitsutoshi Brain distribution of geissoschizine methyl ether in rats using mass spectrometry imaging analysis |
title | Brain distribution of geissoschizine methyl ether in rats using mass spectrometry imaging analysis |
title_full | Brain distribution of geissoschizine methyl ether in rats using mass spectrometry imaging analysis |
title_fullStr | Brain distribution of geissoschizine methyl ether in rats using mass spectrometry imaging analysis |
title_full_unstemmed | Brain distribution of geissoschizine methyl ether in rats using mass spectrometry imaging analysis |
title_short | Brain distribution of geissoschizine methyl ether in rats using mass spectrometry imaging analysis |
title_sort | brain distribution of geissoschizine methyl ether in rats using mass spectrometry imaging analysis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7190722/ https://www.ncbi.nlm.nih.gov/pubmed/32350314 http://dx.doi.org/10.1038/s41598-020-63474-x |
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