医学
胆汁酸
溶血磷脂酸
胆红素
内科学
胆汁淤积
胃肠病学
受体
生物信息学
药理学
生物
作者
Huasheng Yu,Kirk J. Wangensteen,Tong Deng,Yulong Li,Wenqin Luo
出处
期刊:Seminars in Liver Disease
[Georg Thieme Verlag KG]
日期:2021-06-23
卷期号:41 (03): 358-367
被引量:7
标识
DOI:10.1055/s-0041-1730923
摘要
Abstract Pruritus (itch) is a debilitating symptom in liver diseases with cholestasis, which severely affects patients' quality of life. Limited treatment options are available for cholestatic itch, largely due to the incomplete understanding of the underlying molecular mechanisms. Several factors have been proposed as pruritogens for cholestatic itch, such as bile acids, bilirubin, lysophosphatidic acid, and endogenous opioids. Recently, two research groups independently identified Mas-related G protein-coupled receptor X4 (MRGPRX4) as a receptor for bile acids and bilirubin and demonstrated its likely role in cholestatic itch. This discovery not only opens new avenues for understanding the molecular mechanisms in cholestatic itch but provides a promising target for developing novel anti-itch treatments. In this review, we summarize the current theories and knowledge of cholestatic itch, emphasizing MRGPRX4 as a bile acid and bilirubin receptor mediating cholestatic itch in humans. We also discuss some future perspectives in cholestatic itch research.
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