粘膜炎
下调和上调
封堵器
前列腺素E
前列腺素E2
药理学
肠道菌群
势垒函数
回肠
生物
前列腺素
生物化学
紧密连接
内科学
免疫学
内分泌学
医学
细胞生物学
毒性
基因
作者
Dong Liu,Fei Tang,Zhang Li,Jingnan Zhang,Xiaolan Zhao,Liyue Xu,Cheng Peng,Hui Ao
标识
DOI:10.1021/acs.jafc.3c05051
摘要
in the gut and suppressed KEGG pathways such as cortisol synthesis and secretion and arachidonic acid metabolism. Further validation studies indicated that AKHO downregulated the expressions of prostaglandin E2 (PGE2), microsomal prostaglandin E synthase-1 (mPGES-1), and PGE2 receptor EP4, as well as upregulated the expression of glucocorticoid (GC) receptor (GR), leading to improved intestinal epithelial barrier function. Taken together, AKHO elicited protective effects against 5-FU-induced mucositis by regulating the expressions of tight junction proteins via modulation of GC/GR and mPGES-1/PGE2/EP4 pathway, providing novel insights into the utilization and development of this pharmaceutical/food resource.
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