Hepatic GPR75 exacerbates MASH through GNAI2-dependent signaling

This study demonstrates that GPR75 serves as a novel regulator of MASLD/MASH by modulating hepatic fatty acid metabolism. These findings suggest that GPR75 suppression may represent a potential therapeutic strategy for MASLD/MASH treatment.

Authors

Institutions

Publication Details

Journal
Hepatology
Published
2026-02-03
DOI
https://doi.org/10.1097/hep.0000000000001706
Primary Topic
Liver Disease Diagnosis and Treatment
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Hepatic GPR75 exacerbates MASH through GNAI2-dependent signaling

R Zhang, Na Yang, Hongye Fan, Yuan Xie et al.
Hepatology
Liver Disease Diagnosis and Treatment
article

Hepatic GPR75 exacerbates MASH through GNAI2-dependent signaling

R Zhang, Na Yang, Hongye Fan, Yuan Xie, Xule Yang, Jiye Aa
article en

Abstract

This study demonstrates that GPR75 serves as a novel regulator of MASLD/MASH by modulating hepatic fatty acid metabolism. These findings suggest that GPR75 suppression may represent a potential therapeutic strategy for MASLD/MASH treatment.

Hepatology
China Pharmaceutical University (CN), Chinese Academy of Medical Sciences & Peking Union Medical College (CN), Nanjing Drum Tower Hospital (CN), University of Chinese Academy of Sciences (CN), State Key Laboratory of Natural Medicine
Openalex Percentile: Top 68%
Liver Disease Diagnosis and Treatment
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.