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Long-chain bases from sea cucumber mitigate endoplasmic reticulum stress and inflammation in obesity mice

Endoplasmic reticulum (ER) stress and inflammation can induce hyperglycemia. Long-chain bases (LCBs) from sea cucumber exhibit antihyperglycemic activities. However, their effects on ER stress and inflammation are unknown. We investigated the effects of LCBs on ER stress and inflammatory response in...

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Autores principales: Hu, Shiwei, Wang, Jinhui, Wang, Jingfeng, Xue, Changhu, Wang, Yuming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taiwan Food and Drug Administration 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9328807/
https://www.ncbi.nlm.nih.gov/pubmed/28911649
http://dx.doi.org/10.1016/j.jfda.2016.10.011
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author Hu, Shiwei
Wang, Jinhui
Wang, Jingfeng
Xue, Changhu
Wang, Yuming
author_facet Hu, Shiwei
Wang, Jinhui
Wang, Jingfeng
Xue, Changhu
Wang, Yuming
author_sort Hu, Shiwei
collection PubMed
description Endoplasmic reticulum (ER) stress and inflammation can induce hyperglycemia. Long-chain bases (LCBs) from sea cucumber exhibit antihyperglycemic activities. However, their effects on ER stress and inflammation are unknown. We investigated the effects of LCBs on ER stress and inflammatory response in high-fat, fructose diet-induced obesity mice. Reactive oxygen species and free fatty acids were measured. Inflammatory cytokines in serum and their mRNA expressions in epididymal adipose tissues were investigated. Hepatic ER stress-related key genes were detected. c-Jun NH(2)-terminal kinase and nuclear factor κB inflammatory pathways were also evaluated in the liver. Results showed that LCBs reduced serum and hepatic reactive oxygen species and free fatty acids concentrations. LCBs decreased serum proinflammatory cytokines levels, namely interleukin (IL)-1β, tumor necrosis factor-α, IL-6, macrophage inflammatory protein 1, and c-reactive protein, and increased anti-inflammatory cytokine IL-10 concentration. The mRNA and protein expressions of these cytokines in epididymal adipose tissues were regulated by LCBs as similar to their circulatory contents. LCBs inhibited phosphorylated c-Jun NH(2)-terminal kinase and inhibitor κ kinase β, and nuclear factor κB nuclear translocation. LCBs also inhibited mRNA expression of ER stress markers glucose regulated protein, activating transcription factor 6, double-stranded RNA-activated protein kinase-like endoplasmic reticulum kinase, and X-box binding protein 1, and phosphorylation of eukaryotic initiation factor-α and inositol requiring enzyme 1α. These results indicate that LCBs can alleviate ER stress and inflammatory response. Nutritional supplementation with LCBs may offer an adjunctive therapy for RE stress-associated inflammation.
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spelling pubmed-93288072022-08-09 Long-chain bases from sea cucumber mitigate endoplasmic reticulum stress and inflammation in obesity mice Hu, Shiwei Wang, Jinhui Wang, Jingfeng Xue, Changhu Wang, Yuming J Food Drug Anal Original Article Endoplasmic reticulum (ER) stress and inflammation can induce hyperglycemia. Long-chain bases (LCBs) from sea cucumber exhibit antihyperglycemic activities. However, their effects on ER stress and inflammation are unknown. We investigated the effects of LCBs on ER stress and inflammatory response in high-fat, fructose diet-induced obesity mice. Reactive oxygen species and free fatty acids were measured. Inflammatory cytokines in serum and their mRNA expressions in epididymal adipose tissues were investigated. Hepatic ER stress-related key genes were detected. c-Jun NH(2)-terminal kinase and nuclear factor κB inflammatory pathways were also evaluated in the liver. Results showed that LCBs reduced serum and hepatic reactive oxygen species and free fatty acids concentrations. LCBs decreased serum proinflammatory cytokines levels, namely interleukin (IL)-1β, tumor necrosis factor-α, IL-6, macrophage inflammatory protein 1, and c-reactive protein, and increased anti-inflammatory cytokine IL-10 concentration. The mRNA and protein expressions of these cytokines in epididymal adipose tissues were regulated by LCBs as similar to their circulatory contents. LCBs inhibited phosphorylated c-Jun NH(2)-terminal kinase and inhibitor κ kinase β, and nuclear factor κB nuclear translocation. LCBs also inhibited mRNA expression of ER stress markers glucose regulated protein, activating transcription factor 6, double-stranded RNA-activated protein kinase-like endoplasmic reticulum kinase, and X-box binding protein 1, and phosphorylation of eukaryotic initiation factor-α and inositol requiring enzyme 1α. These results indicate that LCBs can alleviate ER stress and inflammatory response. Nutritional supplementation with LCBs may offer an adjunctive therapy for RE stress-associated inflammation. Taiwan Food and Drug Administration 2016-11-29 /pmc/articles/PMC9328807/ /pubmed/28911649 http://dx.doi.org/10.1016/j.jfda.2016.10.011 Text en © 2017 Taiwan Food and Drug Administration https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC-BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ).
spellingShingle Original Article
Hu, Shiwei
Wang, Jinhui
Wang, Jingfeng
Xue, Changhu
Wang, Yuming
Long-chain bases from sea cucumber mitigate endoplasmic reticulum stress and inflammation in obesity mice
title Long-chain bases from sea cucumber mitigate endoplasmic reticulum stress and inflammation in obesity mice
title_full Long-chain bases from sea cucumber mitigate endoplasmic reticulum stress and inflammation in obesity mice
title_fullStr Long-chain bases from sea cucumber mitigate endoplasmic reticulum stress and inflammation in obesity mice
title_full_unstemmed Long-chain bases from sea cucumber mitigate endoplasmic reticulum stress and inflammation in obesity mice
title_short Long-chain bases from sea cucumber mitigate endoplasmic reticulum stress and inflammation in obesity mice
title_sort long-chain bases from sea cucumber mitigate endoplasmic reticulum stress and inflammation in obesity mice
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9328807/
https://www.ncbi.nlm.nih.gov/pubmed/28911649
http://dx.doi.org/10.1016/j.jfda.2016.10.011
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