
Biochemical and Biophysical Research Communications, Год журнала: 2024, Номер 734, С. 150735 - 150735
Опубликована: Сен. 24, 2024
Язык: Английский
Biochemical and Biophysical Research Communications, Год журнала: 2024, Номер 734, С. 150735 - 150735
Опубликована: Сен. 24, 2024
Язык: Английский
Antioxidants, Год журнала: 2025, Номер 14(3), С. 302 - 302
Опубликована: Фев. 28, 2025
Excessive alcohol consumption significantly impacts human health, particularly the brain, due to its susceptibility oxidative stress, which contributes neurodegenerative conditions. Alcohol metabolism in brain occurs primarily via catalase, followed by CYP2E1 pathways. Excess metabolized generates reactive oxygen/nitrogen species (ROS/RNS), leading cell injury altering many different Elevated stress impairs autophagic processes, increasing post-translational modifications and further exacerbating mitochondrial dysfunction ER death. The literature highlights that alcohol-induced disrupts autophagy mitophagy, contributing neuronal damage. Key mechanisms include dysfunction, epigenetics, accumulation of oxidatively modified proteins, lead neuroinflammation impaired cellular quality control. These processes are exacerbated chronic exposure, resulting suppression protective pathways like NRF2-mediated antioxidant responses increased changes brain. Alcohol-mediated neurotoxicity involves complex interactions between metabolism, regulation, influenced various factors such as drinking patterns, nutritional status, genetic/environmental factors, highlighting need for molecular studies unravel these develop targeted interventions.
Язык: Английский
Процитировано
0Frontiers in Immunology, Год журнала: 2025, Номер 16
Опубликована: Март 4, 2025
Background Acute kidney injury (AKI) after transplantation is one of the main causes graft loss and poor patient prognosis, it important to explore new targets for treating AKI in transplantation. Methods Based on AKI-related dataset GSE30718, most relevant modular genes among them were firstly screened using WGCNA intersected with DEGs, used as candidate AKI. Second, machine learning algorithms utilized identify key them, HPA database was expression landscape. Next, we constructed a rat renal IRI model explored role IRI. Finally, combined ssGSEA enrichment analysis animal experiments further validate potential mechanism action genes. Results In total, identified 98 417 which yield total 24 by three types learning, namely, Random Forest, LASSO regression SVM, obtained 1 gene ALDH2, Using database, found that ALDH2 has high level tissues mainly located tubular epithelial cells. increasing alleviated impairment function decreased NGAL, marker injury, BAX, an apoptotic protein, well reducing inflammatory factors IL1β IL6. experiments, able inhibit activation MAPK signaling pathway. Conclusion may serve novel target treatment AKI, protective effect IRI, this be achieved inhibiting
Язык: Английский
Процитировано
0LWT, Год журнала: 2025, Номер unknown, С. 117768 - 117768
Опубликована: Апрель 1, 2025
Язык: Английский
Процитировано
0Biochemical and Biophysical Research Communications, Год журнала: 2024, Номер 734, С. 150735 - 150735
Опубликована: Сен. 24, 2024
Язык: Английский
Процитировано
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