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Neuropharmacological Effects of Terpenoids on Preclinical Animal Models of Psychiatric Disorders: A Review
Terpenoids are widely distributed in nature, especially in the plant kingdom, and exhibit diverse pharmacological activities. In recent years, screening has revealed a wide variety of new terpenoids that are active against different psychiatric disorders. This review synthesized the current publishe...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9495487/ https://www.ncbi.nlm.nih.gov/pubmed/36139909 http://dx.doi.org/10.3390/antiox11091834 |
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author | Mony, Tamanna Jahan Elahi, Fazle Choi, Ji Woong Park, Se Jin |
author_facet | Mony, Tamanna Jahan Elahi, Fazle Choi, Ji Woong Park, Se Jin |
author_sort | Mony, Tamanna Jahan |
collection | PubMed |
description | Terpenoids are widely distributed in nature, especially in the plant kingdom, and exhibit diverse pharmacological activities. In recent years, screening has revealed a wide variety of new terpenoids that are active against different psychiatric disorders. This review synthesized the current published preclinical studies of terpenoid use in psychiatric disorders. This review was extensively investigated to provide empirical evidence regarding the neuropharmacological effects of the vast group of terpenoids in translational models of psychiatric disorders, their relevant mechanisms of action, and treatment regimens with evidence of the safety and psychotropic efficacy. Therefore, we utilized nine (9) electronic databases and performed manual searches of each. The relevant data were retrieved from the articles published until present. We used the search terms “terpenoids” or “terpenes” and “psychiatric disorders” (“psychiatric disorders” OR “psychiatric diseases” OR “neuropsychiatric disorders” OR “psychosis” OR “psychiatric symptoms”). The efficacy of terpenoids or biosynthetic compounds in the terpenoid group was demonstrated in preclinical animal studies. Ginsenosides, bacosides, oleanolic acid, asiatic acid, boswellic acid, mono- and diterpenes, and different forms of saponins and triterpenoids were found to be important bioactive compounds in several preclinical studies of psychosis. Taken together, the findings of the present review indicate that natural terpenoids and their derivatives could achieve remarkable success as an alternative therapeutic option for alleviating the core or associated behavioral features of psychiatric disorders. |
format | Online Article Text |
id | pubmed-9495487 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-94954872022-09-23 Neuropharmacological Effects of Terpenoids on Preclinical Animal Models of Psychiatric Disorders: A Review Mony, Tamanna Jahan Elahi, Fazle Choi, Ji Woong Park, Se Jin Antioxidants (Basel) Review Terpenoids are widely distributed in nature, especially in the plant kingdom, and exhibit diverse pharmacological activities. In recent years, screening has revealed a wide variety of new terpenoids that are active against different psychiatric disorders. This review synthesized the current published preclinical studies of terpenoid use in psychiatric disorders. This review was extensively investigated to provide empirical evidence regarding the neuropharmacological effects of the vast group of terpenoids in translational models of psychiatric disorders, their relevant mechanisms of action, and treatment regimens with evidence of the safety and psychotropic efficacy. Therefore, we utilized nine (9) electronic databases and performed manual searches of each. The relevant data were retrieved from the articles published until present. We used the search terms “terpenoids” or “terpenes” and “psychiatric disorders” (“psychiatric disorders” OR “psychiatric diseases” OR “neuropsychiatric disorders” OR “psychosis” OR “psychiatric symptoms”). The efficacy of terpenoids or biosynthetic compounds in the terpenoid group was demonstrated in preclinical animal studies. Ginsenosides, bacosides, oleanolic acid, asiatic acid, boswellic acid, mono- and diterpenes, and different forms of saponins and triterpenoids were found to be important bioactive compounds in several preclinical studies of psychosis. Taken together, the findings of the present review indicate that natural terpenoids and their derivatives could achieve remarkable success as an alternative therapeutic option for alleviating the core or associated behavioral features of psychiatric disorders. MDPI 2022-09-18 /pmc/articles/PMC9495487/ /pubmed/36139909 http://dx.doi.org/10.3390/antiox11091834 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Mony, Tamanna Jahan Elahi, Fazle Choi, Ji Woong Park, Se Jin Neuropharmacological Effects of Terpenoids on Preclinical Animal Models of Psychiatric Disorders: A Review |
title | Neuropharmacological Effects of Terpenoids on Preclinical Animal Models of Psychiatric Disorders: A Review |
title_full | Neuropharmacological Effects of Terpenoids on Preclinical Animal Models of Psychiatric Disorders: A Review |
title_fullStr | Neuropharmacological Effects of Terpenoids on Preclinical Animal Models of Psychiatric Disorders: A Review |
title_full_unstemmed | Neuropharmacological Effects of Terpenoids on Preclinical Animal Models of Psychiatric Disorders: A Review |
title_short | Neuropharmacological Effects of Terpenoids on Preclinical Animal Models of Psychiatric Disorders: A Review |
title_sort | neuropharmacological effects of terpenoids on preclinical animal models of psychiatric disorders: a review |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9495487/ https://www.ncbi.nlm.nih.gov/pubmed/36139909 http://dx.doi.org/10.3390/antiox11091834 |
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