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Naproxen-Derived New Compound Inhibits the NF-κB, MAPK and PI3K/Akt Signaling Pathways Synergistically with Resveratrol in RAW264.7 Cells
Naproxen is widely used for anti-inflammatory treatment but it can lead to serious side effects. To improve the anti-inflammatory activity and safety, a novel naproxen derivative containing cinnamic acid (NDC) was synthesized and used in combination with resveratrol. The results showed that the comb...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10146875/ https://www.ncbi.nlm.nih.gov/pubmed/37110629 http://dx.doi.org/10.3390/molecules28083395 |
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author | Ou, Yi You, Zonglin Yao, Min Cao, Yingfan Xue, Xiu Chen, Min Wu, Rihui Gan, Lishe Li, Dongli Wu, Panpan Xu, Xuetao Wong, Wingleung Wong, Vincent Kam Wai Liu, Wenfeng Ye, Jiming Jin, Jingwei |
author_facet | Ou, Yi You, Zonglin Yao, Min Cao, Yingfan Xue, Xiu Chen, Min Wu, Rihui Gan, Lishe Li, Dongli Wu, Panpan Xu, Xuetao Wong, Wingleung Wong, Vincent Kam Wai Liu, Wenfeng Ye, Jiming Jin, Jingwei |
author_sort | Ou, Yi |
collection | PubMed |
description | Naproxen is widely used for anti-inflammatory treatment but it can lead to serious side effects. To improve the anti-inflammatory activity and safety, a novel naproxen derivative containing cinnamic acid (NDC) was synthesized and used in combination with resveratrol. The results showed that the combination of NDC and resveratrol at different ratios have a synergistic anti-inflammatory efficacy in RAW264.7 macrophage cells. It was indicated that the combination of NDC and resveratrol at a ratio of 2:1 significantly inhibited the expression of carbon monoxide (NO), tumor necrosis factor α (TNF-α), interleukin 6 (IL-6), induced nitric oxide synthase (iNOS), cyclooxygenase 2 (COX-2) and reactive oxygen species (ROS) without detectable side effects on cell viability. Further studies revealed that these anti-inflammatory effects were mediated by the activation of nuclear factor kappa-B (NF-κB), mitogen-activated protein kinase (MAPK) and phosphoinositide-3 kinase (PI3K)/protein kinase B (Akt) signaling pathways, respectively. Taken together, these results highlighted the synergistic NDC and resveratrol anti-inflammatory activity that could be further explored as a strategy for the treatment of inflammatory disease with an improved safety profile. |
format | Online Article Text |
id | pubmed-10146875 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-101468752023-04-29 Naproxen-Derived New Compound Inhibits the NF-κB, MAPK and PI3K/Akt Signaling Pathways Synergistically with Resveratrol in RAW264.7 Cells Ou, Yi You, Zonglin Yao, Min Cao, Yingfan Xue, Xiu Chen, Min Wu, Rihui Gan, Lishe Li, Dongli Wu, Panpan Xu, Xuetao Wong, Wingleung Wong, Vincent Kam Wai Liu, Wenfeng Ye, Jiming Jin, Jingwei Molecules Article Naproxen is widely used for anti-inflammatory treatment but it can lead to serious side effects. To improve the anti-inflammatory activity and safety, a novel naproxen derivative containing cinnamic acid (NDC) was synthesized and used in combination with resveratrol. The results showed that the combination of NDC and resveratrol at different ratios have a synergistic anti-inflammatory efficacy in RAW264.7 macrophage cells. It was indicated that the combination of NDC and resveratrol at a ratio of 2:1 significantly inhibited the expression of carbon monoxide (NO), tumor necrosis factor α (TNF-α), interleukin 6 (IL-6), induced nitric oxide synthase (iNOS), cyclooxygenase 2 (COX-2) and reactive oxygen species (ROS) without detectable side effects on cell viability. Further studies revealed that these anti-inflammatory effects were mediated by the activation of nuclear factor kappa-B (NF-κB), mitogen-activated protein kinase (MAPK) and phosphoinositide-3 kinase (PI3K)/protein kinase B (Akt) signaling pathways, respectively. Taken together, these results highlighted the synergistic NDC and resveratrol anti-inflammatory activity that could be further explored as a strategy for the treatment of inflammatory disease with an improved safety profile. MDPI 2023-04-12 /pmc/articles/PMC10146875/ /pubmed/37110629 http://dx.doi.org/10.3390/molecules28083395 Text en © 2023 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 Ou, Yi You, Zonglin Yao, Min Cao, Yingfan Xue, Xiu Chen, Min Wu, Rihui Gan, Lishe Li, Dongli Wu, Panpan Xu, Xuetao Wong, Wingleung Wong, Vincent Kam Wai Liu, Wenfeng Ye, Jiming Jin, Jingwei Naproxen-Derived New Compound Inhibits the NF-κB, MAPK and PI3K/Akt Signaling Pathways Synergistically with Resveratrol in RAW264.7 Cells |
title | Naproxen-Derived New Compound Inhibits the NF-κB, MAPK and PI3K/Akt Signaling Pathways Synergistically with Resveratrol in RAW264.7 Cells |
title_full | Naproxen-Derived New Compound Inhibits the NF-κB, MAPK and PI3K/Akt Signaling Pathways Synergistically with Resveratrol in RAW264.7 Cells |
title_fullStr | Naproxen-Derived New Compound Inhibits the NF-κB, MAPK and PI3K/Akt Signaling Pathways Synergistically with Resveratrol in RAW264.7 Cells |
title_full_unstemmed | Naproxen-Derived New Compound Inhibits the NF-κB, MAPK and PI3K/Akt Signaling Pathways Synergistically with Resveratrol in RAW264.7 Cells |
title_short | Naproxen-Derived New Compound Inhibits the NF-κB, MAPK and PI3K/Akt Signaling Pathways Synergistically with Resveratrol in RAW264.7 Cells |
title_sort | naproxen-derived new compound inhibits the nf-κb, mapk and pi3k/akt signaling pathways synergistically with resveratrol in raw264.7 cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10146875/ https://www.ncbi.nlm.nih.gov/pubmed/37110629 http://dx.doi.org/10.3390/molecules28083395 |
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