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Psychotropic Effects of an Alcoholic Extract from the Leaves of Albizia zygia (Leguminosae-Mimosoideae)
BACKGROUND: Albizia zygia is used in Ghanaian traditional medicine for the management of mental disorders. The present study tested the hypothesis that an extract of the leaves of Albizia zygia (AZE) may possess antipsychotic and antidepressant properties. METHOD: The novelty- and apomorphine-induce...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5646350/ https://www.ncbi.nlm.nih.gov/pubmed/29234443 http://dx.doi.org/10.1155/2017/9297808 |
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author | Amoateng, Patrick Osei-Safo, Dorcas Kukuia, Kennedy Kwami Edem Adjei, Samuel Akure, Obed Awintuma Agbemelo-Tsomafo, Constance Adu-Poku, Shirley Nyarko Agyeman-Badu, Kenneth Yaw |
author_facet | Amoateng, Patrick Osei-Safo, Dorcas Kukuia, Kennedy Kwami Edem Adjei, Samuel Akure, Obed Awintuma Agbemelo-Tsomafo, Constance Adu-Poku, Shirley Nyarko Agyeman-Badu, Kenneth Yaw |
author_sort | Amoateng, Patrick |
collection | PubMed |
description | BACKGROUND: Albizia zygia is used in Ghanaian traditional medicine for the management of mental disorders. The present study tested the hypothesis that an extract of the leaves of Albizia zygia (AZE) may possess antipsychotic and antidepressant properties. METHOD: The novelty- and apomorphine-induced locomotor and rearing behaviours of AZE in mice were explored in an open-field observational test system. The effects of AZE in apomorphine-induced cage climbing test, extract-induced catalepsy, and haloperidol-induced catalepsy on mice were also investigated. Lastly, the forced swimming and tail suspension tests in mice were employed to screen the possible antidepressant effects of AZE. RESULTS: AZE (100–3000 mg/kg) showed signs of central nervous system (CNS) depression under observation, with no lethality, 24 h after treatment in mice. AZE (100–1000 mg/kg) produced a significant decrease in the frequency of novelty- and apomorphine-induced locomotor activities in mice. The extract also significantly decreased the frequency and duration of apomorphine-induced climbing activities in mice. AZE, while failing to produce any cataleptic event in naïve mice, significantly enhanced haloperidol-induced catalepsy at a dose of 1000 mg/kg. However, AZE did not produce any significant antidepressant effects in the test models employed. CONCLUSION: The extract of Albizia zygia exhibited an antipsychotic-like activity in mice. |
format | Online Article Text |
id | pubmed-5646350 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-56463502017-12-11 Psychotropic Effects of an Alcoholic Extract from the Leaves of Albizia zygia (Leguminosae-Mimosoideae) Amoateng, Patrick Osei-Safo, Dorcas Kukuia, Kennedy Kwami Edem Adjei, Samuel Akure, Obed Awintuma Agbemelo-Tsomafo, Constance Adu-Poku, Shirley Nyarko Agyeman-Badu, Kenneth Yaw Evid Based Complement Alternat Med Research Article BACKGROUND: Albizia zygia is used in Ghanaian traditional medicine for the management of mental disorders. The present study tested the hypothesis that an extract of the leaves of Albizia zygia (AZE) may possess antipsychotic and antidepressant properties. METHOD: The novelty- and apomorphine-induced locomotor and rearing behaviours of AZE in mice were explored in an open-field observational test system. The effects of AZE in apomorphine-induced cage climbing test, extract-induced catalepsy, and haloperidol-induced catalepsy on mice were also investigated. Lastly, the forced swimming and tail suspension tests in mice were employed to screen the possible antidepressant effects of AZE. RESULTS: AZE (100–3000 mg/kg) showed signs of central nervous system (CNS) depression under observation, with no lethality, 24 h after treatment in mice. AZE (100–1000 mg/kg) produced a significant decrease in the frequency of novelty- and apomorphine-induced locomotor activities in mice. The extract also significantly decreased the frequency and duration of apomorphine-induced climbing activities in mice. AZE, while failing to produce any cataleptic event in naïve mice, significantly enhanced haloperidol-induced catalepsy at a dose of 1000 mg/kg. However, AZE did not produce any significant antidepressant effects in the test models employed. CONCLUSION: The extract of Albizia zygia exhibited an antipsychotic-like activity in mice. Hindawi 2017 2017-10-03 /pmc/articles/PMC5646350/ /pubmed/29234443 http://dx.doi.org/10.1155/2017/9297808 Text en Copyright © 2017 Patrick Amoateng et al. https://creativecommons.org/licenses/by/4.0/ 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 Amoateng, Patrick Osei-Safo, Dorcas Kukuia, Kennedy Kwami Edem Adjei, Samuel Akure, Obed Awintuma Agbemelo-Tsomafo, Constance Adu-Poku, Shirley Nyarko Agyeman-Badu, Kenneth Yaw Psychotropic Effects of an Alcoholic Extract from the Leaves of Albizia zygia (Leguminosae-Mimosoideae) |
title | Psychotropic Effects of an Alcoholic Extract from the Leaves of Albizia zygia (Leguminosae-Mimosoideae) |
title_full | Psychotropic Effects of an Alcoholic Extract from the Leaves of Albizia zygia (Leguminosae-Mimosoideae) |
title_fullStr | Psychotropic Effects of an Alcoholic Extract from the Leaves of Albizia zygia (Leguminosae-Mimosoideae) |
title_full_unstemmed | Psychotropic Effects of an Alcoholic Extract from the Leaves of Albizia zygia (Leguminosae-Mimosoideae) |
title_short | Psychotropic Effects of an Alcoholic Extract from the Leaves of Albizia zygia (Leguminosae-Mimosoideae) |
title_sort | psychotropic effects of an alcoholic extract from the leaves of albizia zygia (leguminosae-mimosoideae) |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5646350/ https://www.ncbi.nlm.nih.gov/pubmed/29234443 http://dx.doi.org/10.1155/2017/9297808 |
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