Ginsenosides for therapeutically targeting inflammation through modulation of oxidative stress.


Journal

International immunopharmacology
ISSN: 1878-1705
Titre abrégé: Int Immunopharmacol
Pays: Netherlands
ID NLM: 100965259

Informations de publication

Date de publication:
Aug 2023
Historique:
received: 05 03 2023
revised: 20 05 2023
accepted: 04 06 2023
medline: 26 7 2023
pubmed: 19 6 2023
entrez: 18 6 2023
Statut: ppublish

Résumé

Ginsenosides are steroid glycosides derived from ginseng plants such as Panax ginseng, Panax quinquefolium, and Panax notoginseng. Advances in recent studies have identified numerous physiological functions of each type of ginsenoside, i.e., immunomodulatory, antioxidative, and anti-inflammatory functions, in the context of inflammatory diseases. Accumulating evidence has revealed the molecular mechanisms by which the single or combined ginsenoside(s) exhibit anti-inflammatory effects, although it remains largely unclear. It is well known that excessive production of reactive oxygen species (ROS) is associated with pathological inflammation and cell death in a variety of cells, and that inhibition of ROS generation ameliorates the local and systemic inflammatory responses. The mechanisms by which ginsenosides attenuate inflammation are largely unknown; however, targeting ROS is suggested as one of the crucial mechanisms for the ginsenosides to control the pathological inflammation in the immune and non-immune cells. This review will summarize the latest progress in ginsenoside studies, particularly in the context of antioxidant mechanisms for its anti-inflammatory effects. A better understanding of the distinct types and the combined action of ginsenosides will pave the way for developing potential preventive and therapeutic modalities in treating various inflammation-related diseases.

Identifiants

pubmed: 37331298
pii: S1567-5769(23)00784-1
doi: 10.1016/j.intimp.2023.110461
pii:
doi:

Substances chimiques

Ginsenosides 0
Reactive Oxygen Species 0
Antioxidants 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

110461

Informations de copyright

Copyright © 2023 The Author(s). Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Seungwha Paik (S)

Department of Microbiology, Chungnam National University School of Medicine, Daejeon, 35015, South Korea; Department of Medical Science, Chungnam National University School of Medicine, Daejeon, 35015, South Korea. Electronic address: swpaik11@cnu.ac.kr.

Gyu Yong Song (GY)

Infection Control Convergence Research Center, Chungnam National University School of Medicine, Daejeon, 35015, South Korea; College of Pharmacy, Chungnam National University, Daejeon, 34134, South Korea.

Eun-Kyeong Jo (EK)

Department of Microbiology, Chungnam National University School of Medicine, Daejeon, 35015, South Korea; Department of Medical Science, Chungnam National University School of Medicine, Daejeon, 35015, South Korea; Infection Control Convergence Research Center, Chungnam National University School of Medicine, Daejeon, 35015, South Korea. Electronic address: hayoungj@cnu.ac.kr.

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Classifications MeSH