
Research Square (Research Square), Journal Year: 2024, Volume and Issue: unknown
Published: May 3, 2024
Language: Английский
Research Square (Research Square), Journal Year: 2024, Volume and Issue: unknown
Published: May 3, 2024
Language: Английский
Frontiers in Psychiatry, Journal Year: 2024, Volume and Issue: 15
Published: May 17, 2024
Background Evidence has suggested that microRNAs (miRNAs) may play an important role in the pathogenesis of psychiatric disorders (PDs), but results remain inconclusive. We aimed to identify specific differentially expressed miRNAs and their overlapping miRNA expression profiles schizophrenia (SZ), major depression disorder (MDD), bipolar (BD), three PDs. Methods The literatures up September 30, 2023 related peripheral blood PDs were searched screened from multiple databases. differences levels between groups illustrated by standardized mean difference (SMD) 95% confidence interval (95% CI). Results In total, 30 included meta-analysis, including 16 for SZ, 12 MDD, 2 BD, each was reported more than 3 independent studies. Compared with control group, miR-181b-5p, miR-34a-5p, miR-195-5p, miR-30e-5p, miR-7-5p, miR-132-3p, miR-212-3p, miR-206, miR-92a-3p miR-137-3p upregulated while miR-134-5p, miR-107 miR-99b-5p downregulated. miR-124-3p, miR-139-5p, miR-182-5p, miR-221-3p, miR-34a-5p miR-93-5p upregulated, miR-144-5p miR-135a-5p However, we failed statistically BD. Interestingly, miR-132-3p both SZ MDD. Conclusions Our study identified 13 9 among which MDD systematically analyzing qualified These be used as potential biomarkers diagnosis future. Systematic Review Registration http://www.crd.york.ac.uk/PROSPERO , identifier CRD42023486982.
Language: Английский
Citations
5European Journal of Pharmacology, Journal Year: 2025, Volume and Issue: 997, P. 177469 - 177469
Published: March 5, 2025
Language: Английский
Citations
0Journal of Advanced Research, Journal Year: 2025, Volume and Issue: unknown
Published: April 1, 2025
Severe acute pancreatitis (SAP) is a critical inflammatory disease with high morbidity and mortality. Current treatments focused on symptomatic relief but failed to prevent inflammation progression in cellular level. In order develop an SAP-targeting drug delivery system alleviate SAP level illustrate its mechanism, we explored the use of proanthocyanidin (PYD) pentoxifylline (PTX) loaded into macrophage membrane-coated self-assembly nanoparticles (FePTX@CM NPs) for targeted treatment. The combination application these two drugs was innovative aid. We developed NPs by strategy cell membrane coating. Its particle size zeta potential were measured dynamic light scatter (DLS). morphology observed transmission electron microscopy (TEM). And encapsulation efficiency evaluated nano-flow cytometry. total protein profile determined via Coomassie brilliant blue. explore mechanism our against animal levels. Bioinformatics approaches, TEM, immunofluorescent assay co-immunoprecipitation performed comprehensively explain specific anti-SAP FePTX@CM NPs. After inflammation-driven targeting, PYD inhibited pancreatic amylase lipase release suppressing mitochondrial reactive oxygen species (mtROS)/Golgi stress, while PTX prevented SAP-associated PANoptosis inhibiting Zbp1 signal pathway. protection effect biomimetic worked from different aspects symptoms relative cells. demonstrated effective pancreas reduced systemic especially pro-inflammatory recruitment activation, minimized tissue damage mouse models, offering promising therapeutic clinical management.
Language: Английский
Citations
0Translational Psychiatry, Journal Year: 2025, Volume and Issue: 15(1)
Published: April 11, 2025
Abstract Frontotemporal dementia is a debilitating neurodegenerative disorder characterized by frontal and temporal lobe degeneration, resulting in behavioral changes, language difficulties, cognitive decline. In this study, smallRNA sequencing was conducted on postmortem brain tissues obtained from the of FTD patients with GRN , MAPT or C9ORF72 mutations. Our analysis identified miR-129-5p as consistently deregulated across all analyzed mutation conditions regions. Functional investigations in-vitro models revealed novel role astrocytes, where its loss led to neuroinflammation impaired neuronal support functions, including reduced glutamate uptake. Depletion astrocytes also resulted spines altered network activity cell culture system. These findings highlight potential therapeutic target diseases sheds light pathogenesis.
Language: Английский
Citations
0Molecular Psychiatry, Journal Year: 2025, Volume and Issue: unknown
Published: April 23, 2025
Language: Английский
Citations
0bioRxiv (Cold Spring Harbor Laboratory), Journal Year: 2024, Volume and Issue: unknown
Published: April 19, 2024
Abstract Frontotemporal dementia is a debilitating neurodegenerative disorder characterized by frontal and temporal lobe degeneration, resulting in behavioral changes, language difficulties, cognitive decline. In this study, smallRNA sequencing was conducted on postmortem brain tissues obtained from FTD patients with GRN , MAPT or C9ORF72 mutations, focusing the lobes. Our analysis identified miR-129-5p as consistently deregulated across all mutation conditions regions. Functional investigations revealed novel role of astrocytes, where its loss led to neuroinflammation impaired neuronal support functions, including reduced glutamate uptake. Depletion astrocytes resulted spines altered network activity. These findings highlight potential therapeutic target diseases also sheds light pathogenesis.
Language: Английский
Citations
2Research Square (Research Square), Journal Year: 2024, Volume and Issue: unknown
Published: May 3, 2024
Language: Английский
Citations
0