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Toxicity and Neuropharmacological Effects of Elenine

Elenine is the aglycone of elenoside, a cytotoxic arylnaphthalene lignan (NSC 644013-W/1) derived from Justicia hyssopifolia. (Family: Acanthaceae). Elenoside is a β-D-glucoside, with a similar chemical structure to etoposide, exhibiting central depressant activity. In the present study, elenine was...

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Detalles Bibliográficos
Autores principales: Navarro, Eduardo, Alonso, S. J., Navarro, R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3118537/
https://www.ncbi.nlm.nih.gov/pubmed/21716687
http://dx.doi.org/10.1155/2011/312524
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author Navarro, Eduardo
Alonso, S. J.
Navarro, R.
author_facet Navarro, Eduardo
Alonso, S. J.
Navarro, R.
author_sort Navarro, Eduardo
collection PubMed
description Elenine is the aglycone of elenoside, a cytotoxic arylnaphthalene lignan (NSC 644013-W/1) derived from Justicia hyssopifolia. (Family: Acanthaceae). Elenoside is a β-D-glucoside, with a similar chemical structure to etoposide, exhibiting central depressant activity. In the present study, elenine was given to mice and rats at doses of 10, 20, and 40 mg/kg. Acute toxicity (24 h) and general behaviour in mice was studied as well as its effects on muscular relaxant activity, locomotor activity (Varimex test), and the open-field test and were compared with 10 mg/kg of chlorpromazine. Elenine produced a reduction in the permanence time in muscular relaxant activity (traction test). Spontaneous activity was lower in the Varimex test. The ambulation and rearing were lower compared with the control group, and an increase in boluses was observed in the open-field test. Thus, it can be concluded that elenine has central sedative effects at lower doses than those used with elenoside and has a possible application in conditions of anxiety.
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spelling pubmed-31185372011-06-28 Toxicity and Neuropharmacological Effects of Elenine Navarro, Eduardo Alonso, S. J. Navarro, R. Evid Based Complement Alternat Med Research Article Elenine is the aglycone of elenoside, a cytotoxic arylnaphthalene lignan (NSC 644013-W/1) derived from Justicia hyssopifolia. (Family: Acanthaceae). Elenoside is a β-D-glucoside, with a similar chemical structure to etoposide, exhibiting central depressant activity. In the present study, elenine was given to mice and rats at doses of 10, 20, and 40 mg/kg. Acute toxicity (24 h) and general behaviour in mice was studied as well as its effects on muscular relaxant activity, locomotor activity (Varimex test), and the open-field test and were compared with 10 mg/kg of chlorpromazine. Elenine produced a reduction in the permanence time in muscular relaxant activity (traction test). Spontaneous activity was lower in the Varimex test. The ambulation and rearing were lower compared with the control group, and an increase in boluses was observed in the open-field test. Thus, it can be concluded that elenine has central sedative effects at lower doses than those used with elenoside and has a possible application in conditions of anxiety. Hindawi Publishing Corporation 2011 2011-05-26 /pmc/articles/PMC3118537/ /pubmed/21716687 http://dx.doi.org/10.1155/2011/312524 Text en Copyright © 2011 Eduardo Navarro et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Navarro, Eduardo
Alonso, S. J.
Navarro, R.
Toxicity and Neuropharmacological Effects of Elenine
title Toxicity and Neuropharmacological Effects of Elenine
title_full Toxicity and Neuropharmacological Effects of Elenine
title_fullStr Toxicity and Neuropharmacological Effects of Elenine
title_full_unstemmed Toxicity and Neuropharmacological Effects of Elenine
title_short Toxicity and Neuropharmacological Effects of Elenine
title_sort toxicity and neuropharmacological effects of elenine
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3118537/
https://www.ncbi.nlm.nih.gov/pubmed/21716687
http://dx.doi.org/10.1155/2011/312524
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