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Lagotis brachystachya maxim attenuates chronic alcoholic liver injury combined with gouty arthritis in rats via its anti-inflammatory activity

Lagotis brachystachya Maxim, a common herb in Tibetan medicine, is mainly used to treat pneumonia, hepatitis, yellow water disease (gouty arthritis). Since long-term heavy drinking is also a risk factor for gouty arthritis, the present study aimed to evaluate the underlying protective role and mecha...

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Autores principales: Guo, Min-Xia, Zhang, Man-Man, Yang, Hai-Yan, Zhang, Chu-Ling, Cheng, Hong-Yu, Li, Na-Zhi, Yi, Li-Tao, Zhu, Ji-Xiao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9513826/
https://www.ncbi.nlm.nih.gov/pubmed/36176434
http://dx.doi.org/10.3389/fphar.2022.995777
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author Guo, Min-Xia
Zhang, Man-Man
Yang, Hai-Yan
Zhang, Chu-Ling
Cheng, Hong-Yu
Li, Na-Zhi
Yi, Li-Tao
Zhu, Ji-Xiao
author_facet Guo, Min-Xia
Zhang, Man-Man
Yang, Hai-Yan
Zhang, Chu-Ling
Cheng, Hong-Yu
Li, Na-Zhi
Yi, Li-Tao
Zhu, Ji-Xiao
author_sort Guo, Min-Xia
collection PubMed
description Lagotis brachystachya Maxim, a common herb in Tibetan medicine, is mainly used to treat pneumonia, hepatitis, yellow water disease (gouty arthritis). Since long-term heavy drinking is also a risk factor for gouty arthritis, the present study aimed to evaluate the underlying protective role and mechanism of extracts of Lagotis brachystachya (ELB) in chronic alcoholic liver injury combined with gouty arthritis. The rat chronic alcoholic liver injury combined with gouty arthritis model was established by long-term alcohol consumption and monosodium urate (MSU) injection. The therapeutical action of ELB was then evaluated by biochemical measurement, histopathological examination, ankle swelling assessment, and protein detection. According to biochemical measurements and histopathological evaluation, ELB could alleviate the symptoms of alcoholic liver injury combined with gouty arthritis. In addition, chronic alcohol consumption and MSU activated inflammatory-related signaling such as TLR4/MyD88/NF-κB, NLRP3, and JAK2/STAT3 pathways in the liver and synovial tissues, while ELB significantly inhibited the activation of the inflammatory signaling pathway. In conclusion, ELB is protective in rats with chronic alcoholic liver injury and gouty arthritis, possibly mediated by the inhibition of TLR4/MyD88/NF-κB, NLRP3, and JAK2-STAT3 signaling pathways in both the hepatic and synovial tissues.
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spelling pubmed-95138262022-09-28 Lagotis brachystachya maxim attenuates chronic alcoholic liver injury combined with gouty arthritis in rats via its anti-inflammatory activity Guo, Min-Xia Zhang, Man-Man Yang, Hai-Yan Zhang, Chu-Ling Cheng, Hong-Yu Li, Na-Zhi Yi, Li-Tao Zhu, Ji-Xiao Front Pharmacol Pharmacology Lagotis brachystachya Maxim, a common herb in Tibetan medicine, is mainly used to treat pneumonia, hepatitis, yellow water disease (gouty arthritis). Since long-term heavy drinking is also a risk factor for gouty arthritis, the present study aimed to evaluate the underlying protective role and mechanism of extracts of Lagotis brachystachya (ELB) in chronic alcoholic liver injury combined with gouty arthritis. The rat chronic alcoholic liver injury combined with gouty arthritis model was established by long-term alcohol consumption and monosodium urate (MSU) injection. The therapeutical action of ELB was then evaluated by biochemical measurement, histopathological examination, ankle swelling assessment, and protein detection. According to biochemical measurements and histopathological evaluation, ELB could alleviate the symptoms of alcoholic liver injury combined with gouty arthritis. In addition, chronic alcohol consumption and MSU activated inflammatory-related signaling such as TLR4/MyD88/NF-κB, NLRP3, and JAK2/STAT3 pathways in the liver and synovial tissues, while ELB significantly inhibited the activation of the inflammatory signaling pathway. In conclusion, ELB is protective in rats with chronic alcoholic liver injury and gouty arthritis, possibly mediated by the inhibition of TLR4/MyD88/NF-κB, NLRP3, and JAK2-STAT3 signaling pathways in both the hepatic and synovial tissues. Frontiers Media S.A. 2022-09-13 /pmc/articles/PMC9513826/ /pubmed/36176434 http://dx.doi.org/10.3389/fphar.2022.995777 Text en Copyright © 2022 Guo, Zhang, Yang, Zhang, Cheng, Li, Yi and Zhu. 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
Guo, Min-Xia
Zhang, Man-Man
Yang, Hai-Yan
Zhang, Chu-Ling
Cheng, Hong-Yu
Li, Na-Zhi
Yi, Li-Tao
Zhu, Ji-Xiao
Lagotis brachystachya maxim attenuates chronic alcoholic liver injury combined with gouty arthritis in rats via its anti-inflammatory activity
title Lagotis brachystachya maxim attenuates chronic alcoholic liver injury combined with gouty arthritis in rats via its anti-inflammatory activity
title_full Lagotis brachystachya maxim attenuates chronic alcoholic liver injury combined with gouty arthritis in rats via its anti-inflammatory activity
title_fullStr Lagotis brachystachya maxim attenuates chronic alcoholic liver injury combined with gouty arthritis in rats via its anti-inflammatory activity
title_full_unstemmed Lagotis brachystachya maxim attenuates chronic alcoholic liver injury combined with gouty arthritis in rats via its anti-inflammatory activity
title_short Lagotis brachystachya maxim attenuates chronic alcoholic liver injury combined with gouty arthritis in rats via its anti-inflammatory activity
title_sort lagotis brachystachya maxim attenuates chronic alcoholic liver injury combined with gouty arthritis in rats via its anti-inflammatory activity
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9513826/
https://www.ncbi.nlm.nih.gov/pubmed/36176434
http://dx.doi.org/10.3389/fphar.2022.995777
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