Lipidomic Profiling Reveals HSD17B13 Deficiency-Associated Dysregulated Hepatic Phospholipid Metabolism in Aged Mice DOI Creative Commons
Cong Zhang, Yong Feng, Xiaoyan Zhang

и другие.

Metabolites, Год журнала: 2025, Номер 15(6), С. 353 - 353

Опубликована: Май 27, 2025

Objectives: HSD17B13 (17β-hydroxysteroid dehydrogenase 13), a lipid droplet-associated enzyme, has emerged as key regulator of hepatic metabolism and potential therapeutic target for metabolic-associated fatty liver disease (MAFLD). While its role in homeostasis inflammation been partially revealed, the impact deficiency on aged mice remains poorly understood. In this study, we performed comprehensive lipidomic profiling tissues from Hsd17b13 gene knockout (Hsd17b13 KO) to investigate effects deletion composition metabolic pathways. Methods: Changes profiles were assessed through liquid chromatography-tandem mass spectrometry (LC-MS/MS)-based analysis. Results: The profiles, including triglycerides (TGs), diglycerides (DGs), phosphatidylcholines (PCs), phosphatidylethanolamines (PEs), phosphatidylglycerols (PGs), ceramides (Cers), exhibited notable alterations KO mice. Conclusions: plays pivotal during aging, it is involved regulation phospholipid metabolism. Our study highlights importance maintaining age-related diseases.

Язык: Английский

Multi‐Omics Analysis Reveals Disturbances of Purine Metabolism and Glutamate Metabolism in the Hippocampus of Lipopolysaccharide‐Induced Mouse Model of Depression DOI Creative Commons
Wenwen Li, Rui Xiao, Xueyi Chen

и другие.

Brain and Behavior, Год журнала: 2025, Номер 15(5)

Опубликована: Май 1, 2025

ABSTRACT Background Depression is a global health concern characterized by high incidence, disability, and disease burden. Neuroimmunity, through the secretion of inflammatory mediators mediation neuroinflammation, plays significant role in depression's pathogenesis. However, underlying molecular mechanisms remain poorly understood. Methods In this pioneering study, we employed comprehensive multi‐omics approach, integrating 2‐DE proteomics, liquid chromatography mass spectrometry‐based metabolomics, real‐time polymerase chain reaction (PCR) array, to investigate hippocampal profiles lipopolysaccharide (LPS)‐induced immune inflammation‐related depression. This innovative approach aimed explore potential pathogenesis depression systematically data across multiple layers. Results Compared control group, identified 81 differential proteins, 44 metabolites, 4 mRNAs LPS‐treated mice. Integrated analysis these multidimensional revealed that purine metabolism glutamate are most significantly altered pathways LPS‐induced Additionally, constructed corresponding compound‐reaction‐enzyme‐gene regulatory network. Conclusion study suggests may be which neuroinflammation regulates depression‐like behaviors. Our findings confirm important inflammation provide new clue for diagnosis treatment disorder. Notably, represents effort field, providing unprecedented insights into

Язык: Английский

Процитировано

0

Nicotinamide mononucleotide supplementation in aging male animals affects lipoxygenase related arachidonic acid metabolism pathway by regulating intracellular calcium overload DOI

Xuecun Liu,

Yuanyuan Jiang, Jinhui Wang

и другие.

Journal of Functional Foods, Год журнала: 2025, Номер 129, С. 106854 - 106854

Опубликована: Май 12, 2025

Язык: Английский

Процитировано

0

Lipidomic Profiling Reveals HSD17B13 Deficiency-Associated Dysregulated Hepatic Phospholipid Metabolism in Aged Mice DOI Creative Commons
Cong Zhang, Yong Feng, Xiaoyan Zhang

и другие.

Metabolites, Год журнала: 2025, Номер 15(6), С. 353 - 353

Опубликована: Май 27, 2025

Objectives: HSD17B13 (17β-hydroxysteroid dehydrogenase 13), a lipid droplet-associated enzyme, has emerged as key regulator of hepatic metabolism and potential therapeutic target for metabolic-associated fatty liver disease (MAFLD). While its role in homeostasis inflammation been partially revealed, the impact deficiency on aged mice remains poorly understood. In this study, we performed comprehensive lipidomic profiling tissues from Hsd17b13 gene knockout (Hsd17b13 KO) to investigate effects deletion composition metabolic pathways. Methods: Changes profiles were assessed through liquid chromatography-tandem mass spectrometry (LC-MS/MS)-based analysis. Results: The profiles, including triglycerides (TGs), diglycerides (DGs), phosphatidylcholines (PCs), phosphatidylethanolamines (PEs), phosphatidylglycerols (PGs), ceramides (Cers), exhibited notable alterations KO mice. Conclusions: plays pivotal during aging, it is involved regulation phospholipid metabolism. Our study highlights importance maintaining age-related diseases.

Язык: Английский

Процитировано

0