
Research Square (Research Square), Journal Year: 2024, Volume and Issue: unknown
Published: Nov. 6, 2024
Language: Английский
Research Square (Research Square), Journal Year: 2024, Volume and Issue: unknown
Published: Nov. 6, 2024
Language: Английский
Journal of Nanobiotechnology, Journal Year: 2025, Volume and Issue: 23(1)
Published: Jan. 16, 2025
Language: Английский
Citations
2Cell Communication and Signaling, Journal Year: 2025, Volume and Issue: 23(1)
Published: Feb. 8, 2025
Neutrophils are the first responders among peripheral immune cells to infiltrate central nervous system following a traumatic brain injury (TBI), triggering neuroinflammation that can exacerbate secondary tissue damage. The precise molecular controls dictate inflammatory behavior of neutrophils post-TBI, however, remain largely elusive. Our comprehensive analysis landscape surrounding trauma in TBI mice has revealed significant alteration abundance β2 integrin (ITGB2), predominantly expressed by and closely associated with responses. Using fluid percussion (FPI) mouse model, we investigated therapeutic efficacy Rovelizumab, an agent blocks ITGB2. treatment demonstrated improvements neurologic function mice, attenuating blood–brain barrier permeability, mitigating oxidative stress mediator release, enhancing cerebral perfusion. Moreover, ITGB2 blockade effectively limited adherence, migration, infiltration neutrophils, impeded formation neutrophil extracellular traps (NETs) upon their activation. Finally, it was mediates these effects mainly through its interaction intercellular adhesion molecule-1 (ICAM 1) endotheliocyte. These findings collectively illuminate as crucial switch governs adverse post-TBI could be targeted improve clinical outcome patients.
Language: Английский
Citations
1International Journal of Pharmaceutics, Journal Year: 2025, Volume and Issue: unknown, P. 125316 - 125316
Published: Feb. 1, 2025
Language: Английский
Citations
0Small, Journal Year: 2025, Volume and Issue: unknown
Published: April 22, 2025
Abstract Depression, a severe disorder affecting both physical and mental health, is commonly treated with first‐line antidepressants, which often exhibit limited efficacy due to poor penetration of the blood‐brain barrier (BBB) significant side effects, thus requiring exploitation biocompatible effective treatments. Recent studies suggest that depression closely linked an imbalance in oxidative stress subsequent inflammatory responses. Antioxidant therapies targeting are therefore emerging as promising strategies. In this study, exosome‐functionalized geniposide (GEN) self‐carried Prussian blue (PB) nanotherapeutic approach fabricated realize efficient BBB for synergistic therapy. The porous PB carrier possesses multi‐enzyme capabilities, can effectively scavenge accumulated ROS, protecting slightly acidic environment released GEN from oxidation, subsequently works simultaneously activate Nrf2‐ARE pathway, enhancing body's defense mechanisms synergistically. triple‐amplified anti‐oxidant strategy nanomaterial shown mitigate microglial activation reduction neuroplasticity, ultimately alleviating pathological markers depression. Overall, constructed nanomaterials underscore therapeutic potential anti‐oxidative removal ROS pathway treatment
Language: Английский
Citations
0Research Square (Research Square), Journal Year: 2024, Volume and Issue: unknown
Published: Nov. 6, 2024
Language: Английский
Citations
0