Neurological Sciences, Год журнала: 2025, Номер unknown
Опубликована: Апрель 8, 2025
Язык: Английский
Neurological Sciences, Год журнала: 2025, Номер unknown
Опубликована: Апрель 8, 2025
Язык: Английский
Pharmaceutics, Год журнала: 2025, Номер 17(3), С. 281 - 281
Опубликована: Фев. 20, 2025
The blood–brain barrier (BBB) is a critical structure that maintains brain homeostasis by selectively regulating nutrient influx and waste efflux. Not surprisingly, it often compromised in neurodegenerative diseases. In addition to its involvement these pathologies, the BBB also represents significant challenge for drug delivery into central nervous system. Nanoparticles (NPs) have been widely explored as carriers capable of overcoming this effectively transporting therapies brain. However, their potential directly address ameliorate dysfunction has received limited attention. review, we examine how NPs enhance across treat diseases explore emerging strategies restore integrity vital structure.
Язык: Английский
Процитировано
1Journal of Clinical Medicine, Год журнала: 2025, Номер 14(2), С. 545 - 545
Опубликована: Янв. 16, 2025
Introduction: Amyotrophic lateral sclerosis (ALS) is a complex, progressive neurodegenerative disorder characterized by the degeneration of motor neurons in brain, brainstem, and spinal cord. Several neuroimaging techniques can help reveal pathophysiology ALS. One these electroencephalogram (EEG), noninvasive relatively inexpensive tool for examining electrical activity brain with excellent temporal precision. Methods: This mechanistic review examines pattern resting-state EEG activity. With focus on publications published between January 1995 October 2024, we carried out comprehensive search 2024 across number databases, including PubMed/Medline, Research Gate, Google Scholar, Cochrane. Results: The literature yielded 17 studies included this review. varied significantly their methodology patient characteristics. Despite this, common biomarker typical ALS was found-reduced alpha power. Regarding other oscillations, findings are less consistent sometimes contradictory. As review, three possible explanations provided. main most important one increased cortical excitability. In addition, due to limitations studies, recommendations future research topic outlined enable further better understanding patterns Conclusions: Most showed power deficits patients, reflecting pathological hyperexcitability cerebral cortex. Future should address methodological identified small sample sizes, inconsistent frequency-band definitions, insufficient functional outcome measures, solidify extend current findings.
Язык: Английский
Процитировано
0The International Journal of Biochemistry & Cell Biology, Год журнала: 2025, Номер unknown, С. 106735 - 106735
Опубликована: Янв. 1, 2025
Язык: Английский
Процитировано
0Advanced Exercise and Health Science, Год журнала: 2025, Номер unknown
Опубликована: Фев. 1, 2025
Язык: Английский
Процитировано
0Frontiers in Bioscience-Landmark, Год журнала: 2025, Номер 30(3)
Опубликована: Март 18, 2025
Background: Amyotrophic lateral sclerosis (ALS) is a progressive multisystem disease characterized by limb and trunk muscle weakness that attributed, in part, to abnormalities mitochondrial ultrastructure impaired functions. This study investigated the time course of structural functional rearrangements skeletal mitochondria combination with motor impairments Tg (copper-zinc superoxide dismutase enzyme (SOD1) G93A) dl1/GurJ (referred as SOD1-G93A/low) male mice, familial ALS model, compared non-transgenic littermates. Methods: The neurological status functions were assessed weekly using paw grip endurance method grid suspension test two-limb four-limb tasks. Transmission electron microscopy followed quantitative analysis was performed ultrastructural alterations quadriceps femoris. Functional high-resolution Oxygraph-2k (O2K) respirometry methods for assessing calcium retention capacity index content lipid peroxidation products freshly isolated preparations. Results: Based on behavioral phenotyping data, specific age groups identified: postnatal day 56 (P56) (n = 10–11), 84 (P84) 156 (P154) 10–12), representing pre-symptomatic, early-symptomatic late-symptomatic stages progression SOD1-G93A/low respectively. Electron showed mosaic destructive changes subsarcolemmal fibers femoris from 84-day-old mice. Morphometric revealed an elevation mean size SOD1-G93A mice at P84 P154. In addition, P154 transgenic group demonstrated decrease sarcomere width number per unit area. At symptomatic stage, exhibited decreased respiratory control ratio, ADP-stimulated, uncoupled respiration rates muscle, measured respirometry. parallel, lower increased levels control. Conclusions: Taken together, these results indicate stage-dependent associated defective oxidative phosphorylation, homeostasis, damage mouse which appears be promising direction development therapies ALS.
Язык: Английский
Процитировано
0Journal of Clinical Neuroscience, Год журнала: 2025, Номер 135, С. 111203 - 111203
Опубликована: Март 28, 2025
Язык: Английский
Процитировано
0Neurological Sciences, Год журнала: 2025, Номер unknown
Опубликована: Апрель 8, 2025
Язык: Английский
Процитировано
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