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1.
Mol Neurobiol ; 60(4): 2209-2222, 2023 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-36637746

RESUMEN

The glymphatic system contributes to the clearance of amyloid-ß from the brain and is disrupted in Alzheimer's disease. However, whether the system is involved in the removal of α-synuclein (α-syn) and whether it is suppressed in Parkinson's disease (PD) remain largely unknown. In mice receiving the intranigral injection of recombinant human α-syn, we found that the glymphatic suppression via aquaporin-4 (AQP4) gene deletion or acetazolamide treatment reduced the clearance of injected α-syn from the brain. In mice overexpressing the human A53T-α-syn, we revealed that AQP4 deficiency accelerated the accumulation of α-syn, facilitated the loss of dopaminergic neurons, and accelerated PD-like symptoms. We also found that the overexpression of A53T-α-syn reduced the expression/polarization of AQP4 and suppressed the glymphatic activity of mice. The study demonstrates a close interaction between the AQP4-mediated glymphatic system and parenchymal α-syn, indicating that restoring the glymphatic activity is a potential therapeutic target to delay PD progression.


Asunto(s)
Enfermedad de Alzheimer , Sistema Glinfático , Enfermedad de Parkinson , Ratones , Humanos , Animales , Enfermedad de Parkinson/genética , alfa-Sinucleína/metabolismo , Sistema Glinfático/metabolismo , Encéfalo/metabolismo
2.
J Cereb Blood Flow Metab ; 42(11): 2017-2031, 2022 11.
Artículo en Inglés | MEDLINE | ID: mdl-35786032

RESUMEN

Accumulating evidence indicates that the glymphatic system has a critical role in maintaining brain homeostasis. However, the detailed anatomy of the glymphatic pathway is not well understood, mostly due to a lack of high spatial resolution 3D visualization. In this study, a fluorescence micro-optical sectioning tomography (fMOST) was used to characterize the glymphatic architecture in the mouse brain. At 30 and 120 min after intracisternal infusion with fluorescent dextran (Dex-3), lectin was injected to stain the cerebral vasculature. Using fMOST, a high-resolution 3D dataset of the brain-wide distribution of Dex-3 was acquired. Combined with fluorescence microscopy and microplate array, the heterogeneous glymphatic flow and the preferential irrigated regions were identified. These cerebral regions containing large-caliber penetrating arteries and/or adjacent to the subarachnoid space had more robust CSF flow compared to other regions. Moreover, the major glymphatic vessels for CSF influx and fluid efflux in the entire brain were shown in 3D. This study demonstrates the regional heterogeneity in the glymphatic system and provides an anatomical resource for further investigation of the glymphatic function.


Asunto(s)
Sistema Glinfático , Animales , Encéfalo/irrigación sanguínea , Líquido Cefalorraquídeo/fisiología , Dextranos , Sistema Glinfático/metabolismo , Lectinas , Ratones , Espacio Subaracnoideo
3.
Neurosci Bull ; 36(12): 1524-1537, 2020 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-32710307

RESUMEN

Following intrathecal injection of fluorescent tracers, ex vivo imaging of brain vibratome slices has been widely used to study the glymphatic system in the rodent brain. Tracer penetration into the brain is usually quantified by image-processing, even though this approach requires much time and manual operation. Here, we illustrate a simple protocol for the quantitative determination of glymphatic activity using spectrophotofluorometry. At specific time-points following intracisternal or intrastriatal injection of fluorescent tracers, certain brain regions and the spinal cord were harvested and tracers were extracted from the tissue. The intensity of tracers was analyzed spectrophotometrically and their concentrations were quantified from standard curves. Using this approach, the regional and dynamic delivery of subarachnoid CSF tracers into the brain parenchyma was assessed, and the clearance of tracers from the brain was also determined. Furthermore, the impairment of glymphatic influx in the brains of old mice was confirmed using our approach. Our method is more accurate and efficient than the imaging approach in terms of the quantitative determination of glymphatic activity, and this will be useful in preclinical studies.


Asunto(s)
Encéfalo/diagnóstico por imagen , Sistema Glinfático , Espectrometría de Fluorescencia , Espectrofotometría , Animales , Líquido Cefalorraquídeo , Sistema Glinfático/diagnóstico por imagen , Procesamiento de Imagen Asistido por Computador , Ratones
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