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Anxiolytic-like effect of Urena lobata (L.) in swiss albino mice
Anxiety disorders are general and psychological problems that are also linked to symptoms of depression. This study aimed to investigate the anxiolytic-like effects of Urena lobata L. (MEUL) methanolic extract in different behavioral paradigms in Swiss albino mice. For this, after an oral acute toxi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Berlin Heidelberg
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7817066/ http://dx.doi.org/10.1186/s40816-021-00249-5 |
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author | Islam, Muhammad Torequl Riaz, Thoufiqul Alam Ayatollahi, Seyed Abdulmajid Sharifi-Rad, Javad |
author_facet | Islam, Muhammad Torequl Riaz, Thoufiqul Alam Ayatollahi, Seyed Abdulmajid Sharifi-Rad, Javad |
author_sort | Islam, Muhammad Torequl |
collection | PubMed |
description | Anxiety disorders are general and psychological problems that are also linked to symptoms of depression. This study aimed to investigate the anxiolytic-like effects of Urena lobata L. (MEUL) methanolic extract in different behavioral paradigms in Swiss albino mice. For this, after an oral acute toxicity study, adult male mice were treated with MEUL (250 and 500 mg/kg, p.o.) and/or diazepam (2 mg/kg, i.p.), and subjected to a number of behavioral studies. In the open-field test, the number of square field cross, grooming, and rearing, was counted, while in the light/dark and swing test, the time spent in the dark portion and number of swings was calculated, respectively. Additionally, the phytochemical analysis was also done. Results reveal that the MEUL possesses alkaloids, glycosides, flavonoids, phenols, saponins, terpenes (including triterpenes), gums, and reducing sugars. MEUL showed a significant (p < 0.05) anxiolytic-like effect in experimental animals, where it’s dose-dependently modulated the test parameters in an open-field test. The MEUL also increased the light residence time and the number of swings in a dose-dependent manner. A dose of 500 mg/kg of MEUL caused the highest calming effect when combined with the experimental animals’ diazepam group. Taken together, findings expand an understanding of the impact of U. lobata on the central nervous system and show that this plant may be useful for the treatment of disorders associated with anxiety. |
format | Online Article Text |
id | pubmed-7817066 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-78170662021-01-21 Anxiolytic-like effect of Urena lobata (L.) in swiss albino mice Islam, Muhammad Torequl Riaz, Thoufiqul Alam Ayatollahi, Seyed Abdulmajid Sharifi-Rad, Javad Clin Phytosci Original Contribution Anxiety disorders are general and psychological problems that are also linked to symptoms of depression. This study aimed to investigate the anxiolytic-like effects of Urena lobata L. (MEUL) methanolic extract in different behavioral paradigms in Swiss albino mice. For this, after an oral acute toxicity study, adult male mice were treated with MEUL (250 and 500 mg/kg, p.o.) and/or diazepam (2 mg/kg, i.p.), and subjected to a number of behavioral studies. In the open-field test, the number of square field cross, grooming, and rearing, was counted, while in the light/dark and swing test, the time spent in the dark portion and number of swings was calculated, respectively. Additionally, the phytochemical analysis was also done. Results reveal that the MEUL possesses alkaloids, glycosides, flavonoids, phenols, saponins, terpenes (including triterpenes), gums, and reducing sugars. MEUL showed a significant (p < 0.05) anxiolytic-like effect in experimental animals, where it’s dose-dependently modulated the test parameters in an open-field test. The MEUL also increased the light residence time and the number of swings in a dose-dependent manner. A dose of 500 mg/kg of MEUL caused the highest calming effect when combined with the experimental animals’ diazepam group. Taken together, findings expand an understanding of the impact of U. lobata on the central nervous system and show that this plant may be useful for the treatment of disorders associated with anxiety. Springer Berlin Heidelberg 2021-01-20 2021 /pmc/articles/PMC7817066/ http://dx.doi.org/10.1186/s40816-021-00249-5 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Original Contribution Islam, Muhammad Torequl Riaz, Thoufiqul Alam Ayatollahi, Seyed Abdulmajid Sharifi-Rad, Javad Anxiolytic-like effect of Urena lobata (L.) in swiss albino mice |
title | Anxiolytic-like effect of Urena lobata (L.) in swiss albino mice |
title_full | Anxiolytic-like effect of Urena lobata (L.) in swiss albino mice |
title_fullStr | Anxiolytic-like effect of Urena lobata (L.) in swiss albino mice |
title_full_unstemmed | Anxiolytic-like effect of Urena lobata (L.) in swiss albino mice |
title_short | Anxiolytic-like effect of Urena lobata (L.) in swiss albino mice |
title_sort | anxiolytic-like effect of urena lobata (l.) in swiss albino mice |
topic | Original Contribution |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7817066/ http://dx.doi.org/10.1186/s40816-021-00249-5 |
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