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A novel biosensor with high signal‐to‐noise ratio for real‐time measurement of dopamine levels in vivo
Fast‐scan cyclic voltammetry (FSCV) is an established method for measuring dopamine (DA) levels in the brain in real time. However, it is difficult to discriminate DA from other monoamines such as serotonin (5‐hydroxytryptamine, 5‐HT) and norepinephrine (NE). We report a novel DA‐specific biosensor...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5873456/ https://www.ncbi.nlm.nih.gov/pubmed/29090830 http://dx.doi.org/10.1002/jnr.24193 |
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author | Ishida, Akimasa Imamura, Atsushi Ueda, Yoshitomo Shimizu, Takeshi Marumoto, Ryosuke Jung, Cha‐Gyun Hida, Hideki |
author_facet | Ishida, Akimasa Imamura, Atsushi Ueda, Yoshitomo Shimizu, Takeshi Marumoto, Ryosuke Jung, Cha‐Gyun Hida, Hideki |
author_sort | Ishida, Akimasa |
collection | PubMed |
description | Fast‐scan cyclic voltammetry (FSCV) is an established method for measuring dopamine (DA) levels in the brain in real time. However, it is difficult to discriminate DA from other monoamines such as serotonin (5‐hydroxytryptamine, 5‐HT) and norepinephrine (NE). We report a novel DA‐specific biosensor consisting of a carbon‐fiber electrode coated with an ion‐exchange membrane, a layer containing monoamine oxidase B, and a cellulose membrane. We performed FSCV using the probe to monitor the amount of DA in vitro and in vivo. First, we measured currents in vitro in phosphate‐buffered saline as we added one micromole each of DA, 5‐HT, and NE. The results confirmed that the biosensor selectively detected DA. Next, we implanted the probe in the striatum of male rats to investigate whether it could selectively detect changes in the DA content in vivo. The probe detected both the tonic change induced by methamphetamine administration and the phasic change induced by electrical stimulation of the medial forebrain bundle. In contrast, the electrode in the 6‐hydroxydopamine–lesioned striatum did not respond to systemic selective serotonin or serotonin/norepinephrine reuptake inhibitors, confirming its selectivity. Furthermore, the probe in the striatum could still detect changes in the DA level 1 week after electrode implantation. The results suggest that the novel biosensor can measure real‐time changes in DA levels in vivo with a relatively high signal‐to‐noise ratio. |
format | Online Article Text |
id | pubmed-5873456 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-58734562018-03-31 A novel biosensor with high signal‐to‐noise ratio for real‐time measurement of dopamine levels in vivo Ishida, Akimasa Imamura, Atsushi Ueda, Yoshitomo Shimizu, Takeshi Marumoto, Ryosuke Jung, Cha‐Gyun Hida, Hideki J Neurosci Res Research Articles Fast‐scan cyclic voltammetry (FSCV) is an established method for measuring dopamine (DA) levels in the brain in real time. However, it is difficult to discriminate DA from other monoamines such as serotonin (5‐hydroxytryptamine, 5‐HT) and norepinephrine (NE). We report a novel DA‐specific biosensor consisting of a carbon‐fiber electrode coated with an ion‐exchange membrane, a layer containing monoamine oxidase B, and a cellulose membrane. We performed FSCV using the probe to monitor the amount of DA in vitro and in vivo. First, we measured currents in vitro in phosphate‐buffered saline as we added one micromole each of DA, 5‐HT, and NE. The results confirmed that the biosensor selectively detected DA. Next, we implanted the probe in the striatum of male rats to investigate whether it could selectively detect changes in the DA content in vivo. The probe detected both the tonic change induced by methamphetamine administration and the phasic change induced by electrical stimulation of the medial forebrain bundle. In contrast, the electrode in the 6‐hydroxydopamine–lesioned striatum did not respond to systemic selective serotonin or serotonin/norepinephrine reuptake inhibitors, confirming its selectivity. Furthermore, the probe in the striatum could still detect changes in the DA level 1 week after electrode implantation. The results suggest that the novel biosensor can measure real‐time changes in DA levels in vivo with a relatively high signal‐to‐noise ratio. John Wiley and Sons Inc. 2017-11-01 2018-05 /pmc/articles/PMC5873456/ /pubmed/29090830 http://dx.doi.org/10.1002/jnr.24193 Text en © 2017 The Authors Journal of Neuroscience Research Published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Articles Ishida, Akimasa Imamura, Atsushi Ueda, Yoshitomo Shimizu, Takeshi Marumoto, Ryosuke Jung, Cha‐Gyun Hida, Hideki A novel biosensor with high signal‐to‐noise ratio for real‐time measurement of dopamine levels in vivo |
title | A novel biosensor with high signal‐to‐noise ratio for real‐time measurement of dopamine levels in vivo |
title_full | A novel biosensor with high signal‐to‐noise ratio for real‐time measurement of dopamine levels in vivo |
title_fullStr | A novel biosensor with high signal‐to‐noise ratio for real‐time measurement of dopamine levels in vivo |
title_full_unstemmed | A novel biosensor with high signal‐to‐noise ratio for real‐time measurement of dopamine levels in vivo |
title_short | A novel biosensor with high signal‐to‐noise ratio for real‐time measurement of dopamine levels in vivo |
title_sort | novel biosensor with high signal‐to‐noise ratio for real‐time measurement of dopamine levels in vivo |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5873456/ https://www.ncbi.nlm.nih.gov/pubmed/29090830 http://dx.doi.org/10.1002/jnr.24193 |
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