In Vitro Anti-Inflammatory Effects of Three Fatty Acids from Royal Jelly

Trans-10-hydroxy-2-decenoic acid (10-H2DA), 10-hydroxydecanoic acid (10-HDAA), and sebacic acid (SEA) are the three major fatty acids in royal jelly (RJ). Previous studies have revealed several pharmacological activities of 10-H2DA and 10-HDAA, although the anti-inflammatory effects and underlying m...

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Main Authors: Yi-Fan Chen, Kai Wang, Yan-Zheng Zhang, Yu-Fei Zheng, Fu-Liang Hu
Format: Article
Language:English
Published: Hindawi Limited 2016-01-01
Series:Mediators of Inflammation
Online Access:http://dx.doi.org/10.1155/2016/3583684
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spelling doaj-4a57950d4dfe43b996c940c5a10f95f32020-11-24T22:59:18ZengHindawi LimitedMediators of Inflammation0962-93511466-18612016-01-01201610.1155/2016/35836843583684In Vitro Anti-Inflammatory Effects of Three Fatty Acids from Royal JellyYi-Fan Chen0Kai Wang1Yan-Zheng Zhang2Yu-Fei Zheng3Fu-Liang Hu4College of Animal Sciences, Zhejiang University, Hangzhou 310058, ChinaInstitute of Apicultural Research, Chinese Academy of Agricultural Sciences, Beijing 100093, ChinaCollege of Animal Sciences, Zhejiang University, Hangzhou 310058, ChinaCollege of Animal Sciences, Zhejiang University, Hangzhou 310058, ChinaCollege of Animal Sciences, Zhejiang University, Hangzhou 310058, ChinaTrans-10-hydroxy-2-decenoic acid (10-H2DA), 10-hydroxydecanoic acid (10-HDAA), and sebacic acid (SEA) are the three major fatty acids in royal jelly (RJ). Previous studies have revealed several pharmacological activities of 10-H2DA and 10-HDAA, although the anti-inflammatory effects and underlying mechanisms by which SEA acts are poorly understood. In the present study, we evaluated and compared the in vitro anti-inflammatory effects of these RJ fatty acids in lipopolysaccharide-stimulated RAW 264.7 macrophages. The results showed that 10-H2DA, 10-HDAA, and SEA had potent, dose-dependent inhibitory effects on the release of the major inflammatory-mediators, nitric oxide, and interleukin-10, and only SEA decreased TNF-α production. Several key inflammatory genes have also been modulated by these RJ fatty acids, with 10-H2DA showing distinct modulating effects as compared to the other two FAs. Furthermore, we found that these three FAs regulated several proteins involved in MAPK and NF-κB signaling pathways. Taken together, these findings provide additional references for using RJ against inflammatory diseases.http://dx.doi.org/10.1155/2016/3583684
collection DOAJ
language English
format Article
sources DOAJ
author Yi-Fan Chen
Kai Wang
Yan-Zheng Zhang
Yu-Fei Zheng
Fu-Liang Hu
spellingShingle Yi-Fan Chen
Kai Wang
Yan-Zheng Zhang
Yu-Fei Zheng
Fu-Liang Hu
In Vitro Anti-Inflammatory Effects of Three Fatty Acids from Royal Jelly
Mediators of Inflammation
author_facet Yi-Fan Chen
Kai Wang
Yan-Zheng Zhang
Yu-Fei Zheng
Fu-Liang Hu
author_sort Yi-Fan Chen
title In Vitro Anti-Inflammatory Effects of Three Fatty Acids from Royal Jelly
title_short In Vitro Anti-Inflammatory Effects of Three Fatty Acids from Royal Jelly
title_full In Vitro Anti-Inflammatory Effects of Three Fatty Acids from Royal Jelly
title_fullStr In Vitro Anti-Inflammatory Effects of Three Fatty Acids from Royal Jelly
title_full_unstemmed In Vitro Anti-Inflammatory Effects of Three Fatty Acids from Royal Jelly
title_sort in vitro anti-inflammatory effects of three fatty acids from royal jelly
publisher Hindawi Limited
series Mediators of Inflammation
issn 0962-9351
1466-1861
publishDate 2016-01-01
description Trans-10-hydroxy-2-decenoic acid (10-H2DA), 10-hydroxydecanoic acid (10-HDAA), and sebacic acid (SEA) are the three major fatty acids in royal jelly (RJ). Previous studies have revealed several pharmacological activities of 10-H2DA and 10-HDAA, although the anti-inflammatory effects and underlying mechanisms by which SEA acts are poorly understood. In the present study, we evaluated and compared the in vitro anti-inflammatory effects of these RJ fatty acids in lipopolysaccharide-stimulated RAW 264.7 macrophages. The results showed that 10-H2DA, 10-HDAA, and SEA had potent, dose-dependent inhibitory effects on the release of the major inflammatory-mediators, nitric oxide, and interleukin-10, and only SEA decreased TNF-α production. Several key inflammatory genes have also been modulated by these RJ fatty acids, with 10-H2DA showing distinct modulating effects as compared to the other two FAs. Furthermore, we found that these three FAs regulated several proteins involved in MAPK and NF-κB signaling pathways. Taken together, these findings provide additional references for using RJ against inflammatory diseases.
url http://dx.doi.org/10.1155/2016/3583684
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