当前位置:
X-MOL 学术
›
Hepatology
›
论文详情
Our official English website, www.x-mol.net, welcomes your feedback! (Note: you will need to create a separate account there.)
Suppressed farnesoid X receptor by iron overload in mice and humans potentiates iron-induced hepatotoxicity
Hepatology ( IF 13.5 ) Pub Date : 2021-12-06 , DOI: 10.1002/hep.32270 Hui Xiong 1 , Chunze Zhang 2 , Lifeng Han 3 , Tong Xu 1 , Khawar Saeed 1 , Jing Han 1 , Jing Liu 1 , Curtis D Klaassen 4 , Frank J Gonzalez 5 , Yuanfu Lu 6 , Youcai Zhang 1
Hepatology ( IF 13.5 ) Pub Date : 2021-12-06 , DOI: 10.1002/hep.32270 Hui Xiong 1 , Chunze Zhang 2 , Lifeng Han 3 , Tong Xu 1 , Khawar Saeed 1 , Jing Han 1 , Jing Liu 1 , Curtis D Klaassen 4 , Frank J Gonzalez 5 , Yuanfu Lu 6 , Youcai Zhang 1
Affiliation
Iron overload (IO) is a frequent finding in the general population. As the major iron storage site, the liver is subject to iron toxicity. Farnesoid X receptor (FXR) regulates bile acid metabolism and is implicated in various liver diseases. We aimed to determine whether FXR plays a role in regulating iron hepatotoxicity.
中文翻译:
小鼠和人类铁过载抑制法尼醇 X 受体增强铁诱导的肝毒性
铁超负荷 (IO) 在普通人群中很常见。作为主要的铁储存场所,肝脏受到铁毒性的影响。法尼醇 X 受体 (FXR) 调节胆汁酸代谢并与各种肝病有关。我们旨在确定 FXR 是否在调节铁肝毒性中发挥作用。
更新日期:2021-12-06
中文翻译:
小鼠和人类铁过载抑制法尼醇 X 受体增强铁诱导的肝毒性
铁超负荷 (IO) 在普通人群中很常见。作为主要的铁储存场所,肝脏受到铁毒性的影响。法尼醇 X 受体 (FXR) 调节胆汁酸代谢并与各种肝病有关。我们旨在确定 FXR 是否在调节铁肝毒性中发挥作用。