Regulation of lipid and glucose metabolism in hepatocytes by phytochemicals from coffee by-products and prevention of non-alcoholic fatty liver disease in vitro

M. Rebollo-Hernanz, E. Mejia, Y. Aguilera, M. Martín-Cabrejas
{"title":"Regulation of lipid and glucose metabolism in hepatocytes by phytochemicals from coffee by-products and prevention of non-alcoholic fatty liver disease in vitro","authors":"M. Rebollo-Hernanz, E. Mejia, Y. Aguilera, M. Martín-Cabrejas","doi":"10.3390/iecn2020-06996","DOIUrl":null,"url":null,"abstract":"This study aimed to assess the effect of the primary phytochemicals from coffee by-products and two aqueous extracts from the coffee husk and silverskin on lipid and glucose metabolism regulation in hepatocytes using an in vitro model of non-alcoholic fatty liver disease. Coffee husk and silverskin were used to prepare two aqueous extracts (CHE and CSE, respectively) using water. The phytochemical composition was determined using UPLC-MS/MS analysis. HepG2 cells were co-treated with 10–50 µmol L‒1 of either pure caffeine, chlorogenic acid, caffeic acid, protocatechuic acid, or gallic acid, and kaempferol, CHE, or CSE (20–100 µg mL‒1) in the presence or absence of palmitic acid (PA, 500 µmol L‒1). Different biomarkers of cell metabolism were assessed 24 h after the co-treatment in cell supernatants and lysates using chemical, biochemical, and immunochemical techniques. Phytochemicals from coffee by-products decreased PA-triggered lipid accumulation (16–94%, p < 0.05) by reducing fatty acid synthase activity and stimulating lipolysis (8–83%, p < 0.05). CHE, CSE, and therein-bioactive compounds promoted glucose uptake (13–45%) via the increase in the phosphorylation of the insulin receptor (1.9- to 2.7-fold), protein kinase B (AKT) (1.4- to 3.1-fold), AMPKα (1.6- to 2.4-fold), and PTEN (2.0- to 4.2-fold). In conclusion, our results proved that phytochemicals from coffee by-products, mainly caffeine and chlorogenic acid, could regulate hepatic lipid and glucose metabolism. Overall, our results generate new insights into the use of coffee by-products as a sustainable food ingredient to encounter non-alcoholic fatty liver disease.","PeriodicalId":320592,"journal":{"name":"Proceedings of The 1st International Electronic Conference on Nutrients - Nutritional and Microbiota Effects on Chronic Disease","volume":"11 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2020-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"5","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Proceedings of The 1st International Electronic Conference on Nutrients - Nutritional and Microbiota Effects on Chronic Disease","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3390/iecn2020-06996","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 5

Abstract

This study aimed to assess the effect of the primary phytochemicals from coffee by-products and two aqueous extracts from the coffee husk and silverskin on lipid and glucose metabolism regulation in hepatocytes using an in vitro model of non-alcoholic fatty liver disease. Coffee husk and silverskin were used to prepare two aqueous extracts (CHE and CSE, respectively) using water. The phytochemical composition was determined using UPLC-MS/MS analysis. HepG2 cells were co-treated with 10–50 µmol L‒1 of either pure caffeine, chlorogenic acid, caffeic acid, protocatechuic acid, or gallic acid, and kaempferol, CHE, or CSE (20–100 µg mL‒1) in the presence or absence of palmitic acid (PA, 500 µmol L‒1). Different biomarkers of cell metabolism were assessed 24 h after the co-treatment in cell supernatants and lysates using chemical, biochemical, and immunochemical techniques. Phytochemicals from coffee by-products decreased PA-triggered lipid accumulation (16–94%, p < 0.05) by reducing fatty acid synthase activity and stimulating lipolysis (8–83%, p < 0.05). CHE, CSE, and therein-bioactive compounds promoted glucose uptake (13–45%) via the increase in the phosphorylation of the insulin receptor (1.9- to 2.7-fold), protein kinase B (AKT) (1.4- to 3.1-fold), AMPKα (1.6- to 2.4-fold), and PTEN (2.0- to 4.2-fold). In conclusion, our results proved that phytochemicals from coffee by-products, mainly caffeine and chlorogenic acid, could regulate hepatic lipid and glucose metabolism. Overall, our results generate new insights into the use of coffee by-products as a sustainable food ingredient to encounter non-alcoholic fatty liver disease.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
咖啡副产品植物化学物质对肝细胞脂质和糖代谢的调节及体外预防非酒精性脂肪性肝病的研究
本研究旨在通过非酒精性脂肪性肝病的体外模型,评估咖啡副产品中的主要植物化学物质以及咖啡壳和银皮的两种水提取物对肝细胞脂质和葡萄糖代谢调节的影响。以咖啡壳和银皮为原料,用水制备两种水提取物(CHE和CSE)。采用UPLC-MS/MS法测定植物化学成分。HepG2细胞分别用10-50µmol L-1纯咖啡因、绿原酸、咖啡酸、原儿茶酸或没食子酸和山啡酚、CHE或CSE(20-100µg mL-1)在棕榈酸(PA, 500µmol L-1)存在或不存在的情况下共处理。在细胞上清液和裂解物共处理24小时后,使用化学、生化和免疫化学技术评估细胞代谢的不同生物标志物。咖啡副产品中的植物化学物质通过降低脂肪酸合成酶活性和刺激脂肪分解(8-83%,p < 0.05),降低了pa引发的脂质积累(16-94%,p < 0.05)。CHE、CSE及其生物活性化合物通过增加胰岛素受体(1.9- 2.7倍)、蛋白激酶B (AKT)(1.4- 3.1倍)、AMPKα(1.6- 2.4倍)和PTEN(2.0- 4.2倍)的磷酸化来促进葡萄糖摄取(13-45%)。综上所述,我们的研究结果证明,咖啡副产品中的植物化学物质,主要是咖啡因和绿原酸,可以调节肝脏脂质和葡萄糖代谢。总的来说,我们的研究结果对使用咖啡副产品作为一种可持续的食品成分来治疗非酒精性脂肪肝产生了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
EVALUATION AND DETERMINATIONS OF SECONDARY METABOLITES AND ITS ANTIOXIDANT ACTIVITIES OF VARIOUS FRACTIONS OF ALBIZIA MYRIOPHYLLA BARK Vitamin D supplementation is association with disease activity in systemic lupus erythematosus patients Cocoa and cocoa fibre intake modulate reactive oxygen species and immunoglobulin production in rats submitted to acute running exercise Dynamic Multi-Stage Gastrointestinal Digestion Model Assessment of Microbial Fermentation Products of Collagen Hydrolysates Elacteriospermum tapos ameliorates maternal obesity effect on serum leptin changes in male offspring
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1