TY - JOUR
T1 - Peroxisome proliferator-activated receptor agonists
T2 - A new hope towards the management of alcoholic liver disease
AU - Durairajan, Siva Sundara Kumar
AU - Singh, Abhay Kumar
AU - Iyaswamy, Ashok
N1 - Publisher Copyright:
©The Author(s) 2024. Published by Baishideng Publishing Group Inc. All rights reserved.
PY - 2024/9/21
Y1 - 2024/9/21
N2 - In this editorial, we examine a paper by Koizumi et al, on the role of peroxisome proliferator-activated receptor (PPAR) agonists in alcoholic liver disease (ALD). The study determined whether elafibranor protected the intestinal barrier and reduced liver fibrosis in a mouse model of ALD. The study also underlines the role of PPARs in intestinal barrier function and lipid homeostasis, which are both affected by ALD. Effective therapies are necessary for ALD because it is a critical health issue that affects people worldwide. This editorial analyzes the possibility of PPAR agonists as treatments for ALD. As key factors of inflammation and metabolism, PPARs offer multiple methods for managing the complex etiology of ALD. We assess the abilities of PPARα, PPARγ, and PPARβ/δ agonists to prevent steatosis, inflammation, and fibrosis due to liver diseases. Recent research carried out in preclinical and clinical settings has shown that PPAR agonists can reduce the severity of liver disease. This editorial discusses the data analyzed and the obstacles, advantages, and mechanisms of action of PPAR agonists for ALD. Further research is needed to understand the efficacy, safety, and mechanisms of PPAR agonists for treating ALD.
AB - In this editorial, we examine a paper by Koizumi et al, on the role of peroxisome proliferator-activated receptor (PPAR) agonists in alcoholic liver disease (ALD). The study determined whether elafibranor protected the intestinal barrier and reduced liver fibrosis in a mouse model of ALD. The study also underlines the role of PPARs in intestinal barrier function and lipid homeostasis, which are both affected by ALD. Effective therapies are necessary for ALD because it is a critical health issue that affects people worldwide. This editorial analyzes the possibility of PPAR agonists as treatments for ALD. As key factors of inflammation and metabolism, PPARs offer multiple methods for managing the complex etiology of ALD. We assess the abilities of PPARα, PPARγ, and PPARβ/δ agonists to prevent steatosis, inflammation, and fibrosis due to liver diseases. Recent research carried out in preclinical and clinical settings has shown that PPAR agonists can reduce the severity of liver disease. This editorial discusses the data analyzed and the obstacles, advantages, and mechanisms of action of PPAR agonists for ALD. Further research is needed to understand the efficacy, safety, and mechanisms of PPAR agonists for treating ALD.
KW - Alcoholic liver disease
KW - Hepatoprotection
KW - Inflammation
KW - Liver fibrosis
KW - Metabolic regulation
KW - Peroxisome proliferator-activated receptors
KW - Peroxisome proliferator-activated receptors agonists
UR - http://www.scopus.com/inward/record.url?scp=85204067085&partnerID=8YFLogxK
UR - https://www.wjgnet.com/1007-9327/full/v30/i35/3965.htm
U2 - 10.3748/wjg.v30.i35.3965
DO - 10.3748/wjg.v30.i35.3965
M3 - Editorial
AN - SCOPUS:85204067085
SN - 1007-9327
VL - 30
SP - 3965
EP - 3971
JO - World Journal of Gastroenterology
JF - World Journal of Gastroenterology
IS - 35
ER -