دورية أكاديمية

Transcriptome and proteomics conjoint analysis reveal anti‐alcoholic liver injury effect of Dianhong Black Tea volatile substances

التفاصيل البيبلوغرافية
العنوان: Transcriptome and proteomics conjoint analysis reveal anti‐alcoholic liver injury effect of Dianhong Black Tea volatile substances
المؤلفون: Tinghui Gao, JiaoJiao Fu, Lin Liu, Jing Bai, Yangjun Lv, Yuejin Zhu, Yu Lan, Xiaonian Cao, Huafang Feng, Caihong Shen, Sijing Liu, Shikang Zhang, Jinlin Guo
المصدر: Food Science & Nutrition, Vol 12, Iss 1, Pp 313-327 (2024)
بيانات النشر: Wiley, 2024.
سنة النشر: 2024
المجموعة: LCC:Nutrition. Foods and food supply
مصطلحات موضوعية: alcoholic liver injury, black tea, proteomics, transcriptome, volatile substances, Nutrition. Foods and food supply, TX341-641
الوصف: Abstract Dianhong Black Tea, a fermented tea containing various bioactive ingredients, has been found to have a significant role in alleviating alcoholic liver injury (ALI). One of its main unique components, Dianhong Black Tea volatile substances (DBTVS), may have potential anti‐ALI effects. However, its effects and underlying molecular mechanisms are still unknown. In this study, we aimed to investigate the potential of DBTVS as an anti‐ALI agent using alcohol‐fed rats. We assessed the effect of DBTVS on ALI by analyzing serum transaminase and lipid levels, as well as conducting hematoxylin–eosin and oil red O staining. Additionally, GC‐MS was used to detect the components of DBTVS, while transcriptome, proteomics analysis, Western blot, and molecular docking were employed to uncover the underlying mechanisms. Our results demonstrated that DBTVS significantly reduced serum ALT and AST levels and improved lipid metabolism disorders. Moreover, we identified 14 components in DBTVS, with five of them exhibiting strong binding affinity with key proteins. These findings suggested that DBTVS could be a promising agent for the prevention and treatment of ALI. Its potential therapeutic effects may be attributed to its ability to regulate lipid metabolism through the PPAR signaling pathway.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2048-7177
Relation: https://doaj.org/toc/2048-7177
DOI: 10.1002/fsn3.3763
URL الوصول: https://doaj.org/article/6f441b6fc82f443c86ab70a151766c83
رقم الأكسشن: edsdoj.6f441b6fc82f443c86ab70a151766c83
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:20487177
DOI:10.1002/fsn3.3763