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The central carbon energy metabolism, which is crucial to the metabolic pathway in almost all living organisms and in the regulation of responses to various kinds of stress. Most of serious metabolic disorders in basic life activities of life are attributed to energy metabolism disorders. Metabolic dysfunction-associated fatty liver disease (MAFLD) and other metabolic disease are usually accompanied with the disturbance of energy metabolism. Maintaining energy homeostasis is crucial for overall health and even survival. To date, there is no systematic study on energy metabolites profile of MAFLD. In this study, we established a method for the simultaneous quantification of 31 endogenous metabolites involved three pathways in the tricarboxylic acid (TCA) cycle, glycolysis and oxidative phosphorylation metabolic pathway by using the UPLC-MS/MS system. This present method offers significant advantages including simple and fast preparation of a wide range of mice and human biological samples and was successfully validated with satisfactory linearity, sensitivity, accuracy, precision, matrix effects, recovery and stability. Target metabolomics analysis was performed in different tissues and organs of mice and the substantial metabolic disparity among mice and human was demonstrated, further verifying the applicability and reliability of our method. Multivariate statistical analysis approach was conducted on 31 variables in human and mice serum samples. Based on VIP> 1, P value< 0.05, seven differential metabolites were screened out for MAFLD in human and mice. ROC analysis indicated that the seven potential markers provided a good diagnostic efficiency for MAFLD. The method demonstrated a simple and promising strategy to rapidly determine the energy metabolism status in mice and human, which can provide valuable results for mechanistic studies. This work provides metabolomic information for the study of metabolic diseases and analytical methodologies for clinical target analysis and efficacy evaluation related to energy metabolism in medical institutions.
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http://dx.doi.org/10.1016/j.jpba.2025.116989 | DOI Listing |
Cell Mol Life Sci
September 2025
Department of Gastroenterology, The Second Hospital of Shandong University, Jinan, China.
Metabolic associated steatohepatitis (MASH) is a severe form of metabolic dysfunction-associated steatotic liver disease (MASLD) characterized by hepatocellular injury, inflammation, and fibrosis. Despite advances in understanding its pathophysiology, the molecular mechanisms driving MASH progression remain unclear. This study investigates the role of long non-coding RNA Linc01271 in MASLD/MASH pathogenesis, ant its involvement in the miR-149-3p/RAB35 axis and PI3K/AKT/mTOR signaling pathway.
View Article and Find Full Text PDFCancer Discov
September 2025
Moffitt Cancer Center, Tampa, FL, United States.
There is growing interest in understanding the mechanisms underlying differences in cancer incidence among species (comparative oncology). The naked mole-rat (NMR) is often referenced as "cancer-resistant" and prior studies focused on identifying mechanisms explaining this. However, efforts to assess this in vivo have been limited.
View Article and Find Full Text PDFJ Virol
September 2025
Division of Pediatric Infectious Disease, Department of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
Rift Valley fever virus (RVFV) causes mild to severe disease in livestock and humans. It was first identified in 1931 during an epizootic in Kenya and has spread across Africa and into the Middle East. Hematopoietic cells are one of the major targets of RVFV ; however, their contribution to RVFV pathogenesis remains poorly understood.
View Article and Find Full Text PDFmBio
September 2025
Department of Microbiology, Howard Taylor Ricketts Laboratory, The University of Chicago, Lemont, Illinois, USA.
infection is a frequent cause of sepsis in humans, a disease associated with high mortality and without specific intervention. Clumping factor A (ClfA) displayed on the bacterial surface plays a key role in promoting replication during invasive disease. Decades of research have pointed to a wide array of ligands engaged by ClfA.
View Article and Find Full Text PDFJ Virol
September 2025
National Key Laboratory of Veterinary Public Health and Safety, Key Laboratory for Prevention and Control of Avian Influenza and Other Major Poultry Diseases, Ministry of Agriculture and Rural Affairs, College of Veterinary Medicine, China Agricultural University, Beijing, China.
Swine influenza A virus (swIAV) is an important zoonotic pathogen with the potential to cause human influenza pandemics. Swine are considered "mixing vessels" for generating novel reassortant influenza A viruses. In 2009, a swine-origin reassortant virus (2009 pandemic H1N1, pdm/09 H1N1) spilled over to humans, causing a global influenza pandemic.
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