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Anxiolytic-Like and Antinociceptive Effects of 2(S)-Neoponcirin in Mice
Study aims: 2(S)-neopincirin (NEO) is a constituent from of Clinopodium mexicanum, which is used in traditional Mexican herbal medicine for its tranquilizing and analgesic properties. This study investigated the anxiolytic-like, sedative and antinociceptive effects of NEO in several mice models. Mat...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6269808/ https://www.ncbi.nlm.nih.gov/pubmed/23812250 http://dx.doi.org/10.3390/molecules18077584 |
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author | Cassani, Julia Araujo, Anna G. Escalona Martínez-Vázquez, Mariano Manjarrez, Norberto Moreno, Julia Estrada-Reyes, Rosa |
author_facet | Cassani, Julia Araujo, Anna G. Escalona Martínez-Vázquez, Mariano Manjarrez, Norberto Moreno, Julia Estrada-Reyes, Rosa |
author_sort | Cassani, Julia |
collection | PubMed |
description | Study aims: 2(S)-neopincirin (NEO) is a constituent from of Clinopodium mexicanum, which is used in traditional Mexican herbal medicine for its tranquilizing and analgesic properties. This study investigated the anxiolytic-like, sedative and antinociceptive effects of NEO in several mice models. Material and methods: The anxiolytic-like effect was evaluated in the hole-board (HBT) and Open Field Tests (OFT); sedative effect was evaluated in sleeping time induced by sodium pentobarbital, and its antinociceptive actions were measured in the hot plate test. To evaluate if the GABA receptor could be involved in the anxiolytic-like effect produced by NEO, in independent experiments, the effects produced by co-administration of NEO plus muscimol (MUS) and NEO plus Pitrotoxin (PTX) were evaluated in the HBT. Results: NEO was isolated from Clinopodium mexicanum leaves. The NMR, MS and optic rotation data helped establish its identity as (2S)-5-hydroxy-4′-methoxyflavanone-7-O-{β-glucopyranosyl-(1→6)-β-rhamnoside}. NEO showed an anxiolytic-like effect and was able to counter the nociception induced by a thermal stimulus in a dose-dependent manner. PTX blocked the anxiolytic-like effect of NEO, while MUS was able to enhance it. Conclusions: The findings of present work demonstrated that NEO possesses anxiolytic-like and antinociceptive effects in mice. Such effects are not associated with changes in the locomotor activity. These results supported the notion that anxiolytic-like effect of NEO involves the participation of GABAergic system. |
format | Online Article Text |
id | pubmed-6269808 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62698082018-12-17 Anxiolytic-Like and Antinociceptive Effects of 2(S)-Neoponcirin in Mice Cassani, Julia Araujo, Anna G. Escalona Martínez-Vázquez, Mariano Manjarrez, Norberto Moreno, Julia Estrada-Reyes, Rosa Molecules Article Study aims: 2(S)-neopincirin (NEO) is a constituent from of Clinopodium mexicanum, which is used in traditional Mexican herbal medicine for its tranquilizing and analgesic properties. This study investigated the anxiolytic-like, sedative and antinociceptive effects of NEO in several mice models. Material and methods: The anxiolytic-like effect was evaluated in the hole-board (HBT) and Open Field Tests (OFT); sedative effect was evaluated in sleeping time induced by sodium pentobarbital, and its antinociceptive actions were measured in the hot plate test. To evaluate if the GABA receptor could be involved in the anxiolytic-like effect produced by NEO, in independent experiments, the effects produced by co-administration of NEO plus muscimol (MUS) and NEO plus Pitrotoxin (PTX) were evaluated in the HBT. Results: NEO was isolated from Clinopodium mexicanum leaves. The NMR, MS and optic rotation data helped establish its identity as (2S)-5-hydroxy-4′-methoxyflavanone-7-O-{β-glucopyranosyl-(1→6)-β-rhamnoside}. NEO showed an anxiolytic-like effect and was able to counter the nociception induced by a thermal stimulus in a dose-dependent manner. PTX blocked the anxiolytic-like effect of NEO, while MUS was able to enhance it. Conclusions: The findings of present work demonstrated that NEO possesses anxiolytic-like and antinociceptive effects in mice. Such effects are not associated with changes in the locomotor activity. These results supported the notion that anxiolytic-like effect of NEO involves the participation of GABAergic system. MDPI 2013-06-28 /pmc/articles/PMC6269808/ /pubmed/23812250 http://dx.doi.org/10.3390/molecules18077584 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Cassani, Julia Araujo, Anna G. Escalona Martínez-Vázquez, Mariano Manjarrez, Norberto Moreno, Julia Estrada-Reyes, Rosa Anxiolytic-Like and Antinociceptive Effects of 2(S)-Neoponcirin in Mice |
title | Anxiolytic-Like and Antinociceptive Effects of 2(S)-Neoponcirin in Mice |
title_full | Anxiolytic-Like and Antinociceptive Effects of 2(S)-Neoponcirin in Mice |
title_fullStr | Anxiolytic-Like and Antinociceptive Effects of 2(S)-Neoponcirin in Mice |
title_full_unstemmed | Anxiolytic-Like and Antinociceptive Effects of 2(S)-Neoponcirin in Mice |
title_short | Anxiolytic-Like and Antinociceptive Effects of 2(S)-Neoponcirin in Mice |
title_sort | anxiolytic-like and antinociceptive effects of 2(s)-neoponcirin in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6269808/ https://www.ncbi.nlm.nih.gov/pubmed/23812250 http://dx.doi.org/10.3390/molecules18077584 |
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