» Articles » PMID: 35988716

Peroxisomal Regulation of Energy Homeostasis: Effect on Obesity and Related Metabolic Disorders

Overview
Journal Mol Metab
Specialty Cell Biology
Date 2022 Aug 21
PMID 35988716
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Peroxisomes are single membrane-bound organelles named for their role in hydrogen peroxide production and catabolism. However, their cellular functions extend well beyond reactive oxygen species (ROS) metabolism and include fatty acid oxidation of unique substrates that cannot be catabolized in mitochondria, and synthesis of ether lipids and bile acids. Metabolic functions of peroxisomes involve crosstalk with other organelles, including mitochondria, endoplasmic reticulum, lipid droplets and lysosomes. Emerging studies suggest that peroxisomes are important regulators of energy homeostasis and that disruption of peroxisomal functions influences the risk for obesity and the associated metabolic disorders, including type 2 diabetes and hepatic steatosis.

Scope Of Review: Here, we focus on the role of peroxisomes in ether lipid synthesis, β-oxidation and ROS metabolism, given that these functions have been most widely studied and have physiologically relevant implications in systemic metabolism and obesity. Efforts are made to mechanistically link these cellular and systemic processes.

Major Conclusions: Circulating plasmalogens, a form of ether lipids, have been identified as inversely correlated biomarkers of obesity. Ether lipids influence metabolic homeostasis through multiple mechanisms, including regulation of mitochondrial morphology and respiration affecting brown fat-mediated thermogenesis, and through regulation of adipose tissue development. Peroxisomal β-oxidation also affects metabolic homeostasis through generation of signaling molecules, such as acetyl-CoA and ROS that inhibit hydrolysis of stored lipids, contributing to development of hepatic steatosis. Oxidative stress resulting from increased peroxisomal β-oxidation-generated ROS in the context of obesity mediates β-cell lipotoxicity. A better understanding of the roles peroxisomes play in regulating and responding to obesity and its complications will provide new opportunities for their treatment.

Citing Articles

Do Lifestyle Interventions Mitigate the Oxidative Damage and Inflammation Induced by Obesity in the Testis?.

Moreira R, Oliveira P, Spadella M, Ferreira R, Alves M Antioxidants (Basel). 2025; 14(2).

PMID: 40002337 PMC: 11851673. DOI: 10.3390/antiox14020150.


Silybin A from reprograms lipid metabolism to induce a cell fate-dependent class switch from triglycerides to phospholipids.

Koeberle S, Thurmer M, Su F, Werner M, Grander J, Hofer L Theranostics. 2025; 15(5):2006-2034.

PMID: 39897559 PMC: 11780512. DOI: 10.7150/thno.99562.


Oxidised Apolipoprotein Peptidome Characterises Metabolic Dysfunction-Associated Steatotic Liver Disease.

Mocciaro G, George A, Allison M, Frontini M, Huang-Doran I, Reiman F Liver Int. 2025; 45(2):e16200.

PMID: 39822152 PMC: 11740006. DOI: 10.1111/liv.16200.


Recent advances in reactive oxygen species (ROS)-responsive drug delivery systems for photodynamic therapy of cancer.

Hu D, Li Y, Li R, Wang M, Zhou K, He C Acta Pharm Sin B. 2025; 14(12):5106-5131.

PMID: 39807318 PMC: 11725102. DOI: 10.1016/j.apsb.2024.10.015.


Regulation of Mitochondrial and Peroxisomal Metabolism in Female Obesity and Type 2 Diabetes.

Antelo-Cea D, Martinez-Rojas L, Cabrerizo-Ibanez I, Roudi Rashtabady A, Hernandez-Alvarez M Int J Mol Sci. 2024; 25(20).

PMID: 39457018 PMC: 11508381. DOI: 10.3390/ijms252011237.


References
1.
Stevens V, Carter B, McCullough M, Campbell P, Wang Y . Metabolomic Profiles Associated with BMI, Waist Circumference, and Diabetes and Inflammation Biomarkers in Women. Obesity (Silver Spring). 2019; 28(1):187-196. DOI: 10.1002/oby.22670. View

2.
Mikkelsen T, Xu Z, Zhang X, Wang L, Gimble J, Lander E . Comparative epigenomic analysis of murine and human adipogenesis. Cell. 2010; 143(1):156-69. PMC: 2950833. DOI: 10.1016/j.cell.2010.09.006. View

3.
Jansen G, Mihalik S, Watkins P, Moser H, Jakobs C, Denis S . Phytanoyl-CoA hydroxylase is present in human liver, located in peroxisomes, and deficient in Zellweger syndrome: direct, unequivocal evidence for the new, revised pathway of phytanic acid alpha-oxidation in humans. Biochem Biophys Res Commun. 1996; 229(1):205-10. DOI: 10.1006/bbrc.1996.1781. View

4.
Zhang C, Baker D, Yasuda S, Makarova N, Balazs L, Johnson L . Lysophosphatidic acid induces neointima formation through PPARgamma activation. J Exp Med. 2004; 199(6):763-74. PMC: 2212723. DOI: 10.1084/jem.20031619. View

5.
Chiang J . Bile acid metabolism and signaling. Compr Physiol. 2013; 3(3):1191-212. PMC: 4422175. DOI: 10.1002/cphy.c120023. View