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Oridonin: A Review of Its Pharmacology, Pharmacokinetics and Toxicity

Oridonin, as a natural terpenoids found in traditional Chinese herbal medicine Isodon rubescens (Hemsl.) H.Hara, is widely present in numerous Chinese medicine preparations. The purpose of this review focuses on providing the latest and comprehensive information on the pharmacology, pharmacokinetics...

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Autores principales: Li, Xiang, Zhang, Chuan-Tao, Ma, Wei, Xie, Xin, Huang, Qun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8289702/
https://www.ncbi.nlm.nih.gov/pubmed/34295243
http://dx.doi.org/10.3389/fphar.2021.645824
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author Li, Xiang
Zhang, Chuan-Tao
Ma, Wei
Xie, Xin
Huang, Qun
author_facet Li, Xiang
Zhang, Chuan-Tao
Ma, Wei
Xie, Xin
Huang, Qun
author_sort Li, Xiang
collection PubMed
description Oridonin, as a natural terpenoids found in traditional Chinese herbal medicine Isodon rubescens (Hemsl.) H.Hara, is widely present in numerous Chinese medicine preparations. The purpose of this review focuses on providing the latest and comprehensive information on the pharmacology, pharmacokinetics and toxicity of oridonin, to excavate the therapeutic potential and explore promising ways to balance toxicity and efficacy of this natural compound. Information concerning oridonin was systematically collected from the authoritative internet database of PubMed, Elsevier, Web of Science, Wiley Online Library and Europe PMC applying a combination of keywords involving “pharmacology,” “pharmacokinetics,” and “toxicology”. New evidence shows that oridonin possesses a wide range of pharmacological properties, including anticancer, anti-inflammatory, hepatorenal activities as well as cardioprotective protective activities and so on. Although significant advancement has been witnessed in this field, some basic and intricate issues still exist such as the specific mechanism of oridonin against related diseases not being clear. Moreover, several lines of evidence indicated that oridonin may exhibit adverse effects, even toxicity under specific circumstances, which sparked intense debate and concern about security of oridonin. Based on the current progress, future research directions should emphasize on 1) investigating the interrelationship between concentration and pharmacological effects as well as toxicity, 2) reducing pharmacological toxicity, and 3) modifying the structure of oridonin—one of the pivotal approaches to strengthen pharmacological activity and bioavailability. We hope that this review can provide some inspiration for the research of oridonin in the future.
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spelling pubmed-82897022021-07-21 Oridonin: A Review of Its Pharmacology, Pharmacokinetics and Toxicity Li, Xiang Zhang, Chuan-Tao Ma, Wei Xie, Xin Huang, Qun Front Pharmacol Pharmacology Oridonin, as a natural terpenoids found in traditional Chinese herbal medicine Isodon rubescens (Hemsl.) H.Hara, is widely present in numerous Chinese medicine preparations. The purpose of this review focuses on providing the latest and comprehensive information on the pharmacology, pharmacokinetics and toxicity of oridonin, to excavate the therapeutic potential and explore promising ways to balance toxicity and efficacy of this natural compound. Information concerning oridonin was systematically collected from the authoritative internet database of PubMed, Elsevier, Web of Science, Wiley Online Library and Europe PMC applying a combination of keywords involving “pharmacology,” “pharmacokinetics,” and “toxicology”. New evidence shows that oridonin possesses a wide range of pharmacological properties, including anticancer, anti-inflammatory, hepatorenal activities as well as cardioprotective protective activities and so on. Although significant advancement has been witnessed in this field, some basic and intricate issues still exist such as the specific mechanism of oridonin against related diseases not being clear. Moreover, several lines of evidence indicated that oridonin may exhibit adverse effects, even toxicity under specific circumstances, which sparked intense debate and concern about security of oridonin. Based on the current progress, future research directions should emphasize on 1) investigating the interrelationship between concentration and pharmacological effects as well as toxicity, 2) reducing pharmacological toxicity, and 3) modifying the structure of oridonin—one of the pivotal approaches to strengthen pharmacological activity and bioavailability. We hope that this review can provide some inspiration for the research of oridonin in the future. Frontiers Media S.A. 2021-07-05 /pmc/articles/PMC8289702/ /pubmed/34295243 http://dx.doi.org/10.3389/fphar.2021.645824 Text en Copyright © 2021 Li, Zhang, Ma, Xie and Huang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Li, Xiang
Zhang, Chuan-Tao
Ma, Wei
Xie, Xin
Huang, Qun
Oridonin: A Review of Its Pharmacology, Pharmacokinetics and Toxicity
title Oridonin: A Review of Its Pharmacology, Pharmacokinetics and Toxicity
title_full Oridonin: A Review of Its Pharmacology, Pharmacokinetics and Toxicity
title_fullStr Oridonin: A Review of Its Pharmacology, Pharmacokinetics and Toxicity
title_full_unstemmed Oridonin: A Review of Its Pharmacology, Pharmacokinetics and Toxicity
title_short Oridonin: A Review of Its Pharmacology, Pharmacokinetics and Toxicity
title_sort oridonin: a review of its pharmacology, pharmacokinetics and toxicity
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8289702/
https://www.ncbi.nlm.nih.gov/pubmed/34295243
http://dx.doi.org/10.3389/fphar.2021.645824
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