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Anti-Inflammatory Activity and Mechanism of Cryptochlorogenic Acid from Ageratina adenophora

Ageratina adenophora is an invasive plant known for its toxicity to livestock. Current research on this plant has shifted from toxicity prevention to the beneficial utilization of plant resources. This study was performed to investigate the effects and mechanisms of cryptochlorogenic acid (CCGA) iso...

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Autores principales: Ma, Xiaoping, Okyere, Samuel Kumi, Hu, Liwen, Wen, Juan, Ren, Zhihua, Deng, Junliang, Hu, Yanchun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8839916/
https://www.ncbi.nlm.nih.gov/pubmed/35276797
http://dx.doi.org/10.3390/nu14030439
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author Ma, Xiaoping
Okyere, Samuel Kumi
Hu, Liwen
Wen, Juan
Ren, Zhihua
Deng, Junliang
Hu, Yanchun
author_facet Ma, Xiaoping
Okyere, Samuel Kumi
Hu, Liwen
Wen, Juan
Ren, Zhihua
Deng, Junliang
Hu, Yanchun
author_sort Ma, Xiaoping
collection PubMed
description Ageratina adenophora is an invasive plant known for its toxicity to livestock. Current research on this plant has shifted from toxicity prevention to the beneficial utilization of plant resources. This study was performed to investigate the effects and mechanisms of cryptochlorogenic acid (CCGA) isolated from Ageratina adenophora on the inflammatory responses induced by lipopolysaccharide (LPS) in RAW264.7 cells. RAW264.7 cells were pretreated with CCGA (200, 100, and 50 μg/mL) and subsequently stimulated with LPS (1 μg/mL) for 16 h. The cytotoxicity of CCGA was tested using the Cell Counting Kit (CCK8). The mechanism of action of CCGA in attenuating inflammation was also identified using enzyme-linked immunosorbent assay (ELISA), quantitative reverse transcription-polymerase chain reaction, and Western blot. The results showed that CCGA had a maximal safe concentration of 200 mg/mL. Moreover, CCGA reduced the level of nitric oxide (NO) and iNOS in LPS-induced RAW264.7 cells (p < 0.01). In addition, CCGA reduced the levels of pro-inflammatory cytokines (TNF-α, IL-1β, IL-6, and IL-8) and cyclooxygenase-2 (COX-2) in LPS-induced RAW264.7 cells at both the mRNA and protein levels (p < 0.01). CCGA prevented the activation of nuclear factor-kappa B (NF-kB) in LPS-induced RAW264.7 cells via the inhibition of IKK and IκB phosphorylation and the degradation of IκB proteins (p < 0.01). This finding indicated that CCGA isolated from A. adenophora may be a potential candidate for the treatment of inflammation-related diseases.
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spelling pubmed-88399162022-02-13 Anti-Inflammatory Activity and Mechanism of Cryptochlorogenic Acid from Ageratina adenophora Ma, Xiaoping Okyere, Samuel Kumi Hu, Liwen Wen, Juan Ren, Zhihua Deng, Junliang Hu, Yanchun Nutrients Article Ageratina adenophora is an invasive plant known for its toxicity to livestock. Current research on this plant has shifted from toxicity prevention to the beneficial utilization of plant resources. This study was performed to investigate the effects and mechanisms of cryptochlorogenic acid (CCGA) isolated from Ageratina adenophora on the inflammatory responses induced by lipopolysaccharide (LPS) in RAW264.7 cells. RAW264.7 cells were pretreated with CCGA (200, 100, and 50 μg/mL) and subsequently stimulated with LPS (1 μg/mL) for 16 h. The cytotoxicity of CCGA was tested using the Cell Counting Kit (CCK8). The mechanism of action of CCGA in attenuating inflammation was also identified using enzyme-linked immunosorbent assay (ELISA), quantitative reverse transcription-polymerase chain reaction, and Western blot. The results showed that CCGA had a maximal safe concentration of 200 mg/mL. Moreover, CCGA reduced the level of nitric oxide (NO) and iNOS in LPS-induced RAW264.7 cells (p < 0.01). In addition, CCGA reduced the levels of pro-inflammatory cytokines (TNF-α, IL-1β, IL-6, and IL-8) and cyclooxygenase-2 (COX-2) in LPS-induced RAW264.7 cells at both the mRNA and protein levels (p < 0.01). CCGA prevented the activation of nuclear factor-kappa B (NF-kB) in LPS-induced RAW264.7 cells via the inhibition of IKK and IκB phosphorylation and the degradation of IκB proteins (p < 0.01). This finding indicated that CCGA isolated from A. adenophora may be a potential candidate for the treatment of inflammation-related diseases. MDPI 2022-01-19 /pmc/articles/PMC8839916/ /pubmed/35276797 http://dx.doi.org/10.3390/nu14030439 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 Article
Ma, Xiaoping
Okyere, Samuel Kumi
Hu, Liwen
Wen, Juan
Ren, Zhihua
Deng, Junliang
Hu, Yanchun
Anti-Inflammatory Activity and Mechanism of Cryptochlorogenic Acid from Ageratina adenophora
title Anti-Inflammatory Activity and Mechanism of Cryptochlorogenic Acid from Ageratina adenophora
title_full Anti-Inflammatory Activity and Mechanism of Cryptochlorogenic Acid from Ageratina adenophora
title_fullStr Anti-Inflammatory Activity and Mechanism of Cryptochlorogenic Acid from Ageratina adenophora
title_full_unstemmed Anti-Inflammatory Activity and Mechanism of Cryptochlorogenic Acid from Ageratina adenophora
title_short Anti-Inflammatory Activity and Mechanism of Cryptochlorogenic Acid from Ageratina adenophora
title_sort anti-inflammatory activity and mechanism of cryptochlorogenic acid from ageratina adenophora
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8839916/
https://www.ncbi.nlm.nih.gov/pubmed/35276797
http://dx.doi.org/10.3390/nu14030439
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