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Dose–Response Effect of Antibodies to S100 Protein and Cannabinoid Receptor Type 1 in Released-Active Form in the Light–Dark Test in Mice

Earlier studies have shown that combination of antibodies to S100 protein and to cannabinoid receptor type 1 in released-active form (Brizantin) may possess anxiolytic properties and decrease nicotine dependence. Released-active form of antibodies is a novel approach that permits to modify natural f...

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Autores principales: Kardash, Elena V., Ertuzun, Irina A., Khakimova, Gul'nara R., Kolyadin, Andrey N., Tarasov, Sergey A., Wagner, Stéphanie, Andriambeloson, Emile, Ivashkin, Vladimir T., Epstein, Oleg I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6043939/
https://www.ncbi.nlm.nih.gov/pubmed/30013455
http://dx.doi.org/10.1177/1559325818779752
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author Kardash, Elena V.
Ertuzun, Irina A.
Khakimova, Gul'nara R.
Kolyadin, Andrey N.
Tarasov, Sergey A.
Wagner, Stéphanie
Andriambeloson, Emile
Ivashkin, Vladimir T.
Epstein, Oleg I.
author_facet Kardash, Elena V.
Ertuzun, Irina A.
Khakimova, Gul'nara R.
Kolyadin, Andrey N.
Tarasov, Sergey A.
Wagner, Stéphanie
Andriambeloson, Emile
Ivashkin, Vladimir T.
Epstein, Oleg I.
author_sort Kardash, Elena V.
collection PubMed
description Earlier studies have shown that combination of antibodies to S100 protein and to cannabinoid receptor type 1 in released-active form (Brizantin) may possess anxiolytic properties and decrease nicotine dependence. Released-active form of antibodies is a novel approach that permits to modify natural functions of the target molecule (antigen) under investigation. The aim of the present study was to evaluate the anxiolytic-like effect of Brizantin in the light–dark test in mice, according to its ability to influence the number of entries into the lit compartment and the total time spent there. Three doses of Brizantin (2.5, 5, and 10 mL/kg) were compared with diazepam (1 mg/kg), placebo, and vehicle control. Anxiolytic-like effect of the tested drug was shown to be dose dependent, with an increasing trend from 2.5 to 10 mL/kg. Brizantin in its highest dose significantly increased studied behavioral parameters, although its effect was less pronounced than that of the reference drug diazepam (1 mg/kg).
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spelling pubmed-60439392018-07-16 Dose–Response Effect of Antibodies to S100 Protein and Cannabinoid Receptor Type 1 in Released-Active Form in the Light–Dark Test in Mice Kardash, Elena V. Ertuzun, Irina A. Khakimova, Gul'nara R. Kolyadin, Andrey N. Tarasov, Sergey A. Wagner, Stéphanie Andriambeloson, Emile Ivashkin, Vladimir T. Epstein, Oleg I. Dose Response Original Article Earlier studies have shown that combination of antibodies to S100 protein and to cannabinoid receptor type 1 in released-active form (Brizantin) may possess anxiolytic properties and decrease nicotine dependence. Released-active form of antibodies is a novel approach that permits to modify natural functions of the target molecule (antigen) under investigation. The aim of the present study was to evaluate the anxiolytic-like effect of Brizantin in the light–dark test in mice, according to its ability to influence the number of entries into the lit compartment and the total time spent there. Three doses of Brizantin (2.5, 5, and 10 mL/kg) were compared with diazepam (1 mg/kg), placebo, and vehicle control. Anxiolytic-like effect of the tested drug was shown to be dose dependent, with an increasing trend from 2.5 to 10 mL/kg. Brizantin in its highest dose significantly increased studied behavioral parameters, although its effect was less pronounced than that of the reference drug diazepam (1 mg/kg). SAGE Publications 2018-06-26 /pmc/articles/PMC6043939/ /pubmed/30013455 http://dx.doi.org/10.1177/1559325818779752 Text en © The Author(s) 2018 http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Article
Kardash, Elena V.
Ertuzun, Irina A.
Khakimova, Gul'nara R.
Kolyadin, Andrey N.
Tarasov, Sergey A.
Wagner, Stéphanie
Andriambeloson, Emile
Ivashkin, Vladimir T.
Epstein, Oleg I.
Dose–Response Effect of Antibodies to S100 Protein and Cannabinoid Receptor Type 1 in Released-Active Form in the Light–Dark Test in Mice
title Dose–Response Effect of Antibodies to S100 Protein and Cannabinoid Receptor Type 1 in Released-Active Form in the Light–Dark Test in Mice
title_full Dose–Response Effect of Antibodies to S100 Protein and Cannabinoid Receptor Type 1 in Released-Active Form in the Light–Dark Test in Mice
title_fullStr Dose–Response Effect of Antibodies to S100 Protein and Cannabinoid Receptor Type 1 in Released-Active Form in the Light–Dark Test in Mice
title_full_unstemmed Dose–Response Effect of Antibodies to S100 Protein and Cannabinoid Receptor Type 1 in Released-Active Form in the Light–Dark Test in Mice
title_short Dose–Response Effect of Antibodies to S100 Protein and Cannabinoid Receptor Type 1 in Released-Active Form in the Light–Dark Test in Mice
title_sort dose–response effect of antibodies to s100 protein and cannabinoid receptor type 1 in released-active form in the light–dark test in mice
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6043939/
https://www.ncbi.nlm.nih.gov/pubmed/30013455
http://dx.doi.org/10.1177/1559325818779752
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