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1.
NMR Biomed ; 35(9): e4751, 2022 09.
Artículo en Inglés | MEDLINE | ID: mdl-35478360

RESUMEN

Because retinitis pigmentosa (RP) has been shown to cause degenerative changes in the entire visual pathway, there is an urgent need to perform longitudinal assessments of RP-induced degeneration and identify imaging protocols to detect this degeneration as early as possible. In this study, we assessed a transgenic rat model of RP by using complementary noninvasive magnetic resonance imaging techniques, namely, proton magnetic resonance spectroscopy (1 H-MRS), to investigate the metabolic changes in RP. Our study demonstrated decreased concentrations and ratios to creatine (Cr) of N-acetylaspartate (NAA), glutamate (Glu), γ-aminobutyric acid (GABA), and taurine (Tau), whereas myo-inositol (Ins) and choline (Cho) were increased in the visual cortex of Royal College of Surgeons (RCS) rats compared with control rats (p < 0.05). Furthermore, with the progression of RP, the concentrations of NAA, Glu, GABA, and Tau, and the ratios of GABA/Cr and Tau/Cr significantly decreased over time, whereas the concentrations of Ins and Cho and the ratio of Ins/Cr significantly increased over time (p < 0.05). In addition, in RCS rats, NAA/Cr decreased significantly from 3 to 4 months postnatal (p < 0.001), and Cho/Cr increased significantly from 4 to 5 months postnatal (p = 0.005). Meanwhile, the 1 H-MRS indicators in 5-month postnatal RCS rats could be confirmed by immunohistochemical staining. In conclusion, with the progression of RP, the metabolic alterations in the visual cortex indicated progressive reprogramming with the decrease of neurons and axons, accompanied by the proliferation of gliocytes.


Asunto(s)
Retinitis Pigmentosa , Vías Visuales , Animales , Ácido Aspártico/metabolismo , Colina/metabolismo , Creatina/metabolismo , Ácido Glutámico/metabolismo , Humanos , Inositol/metabolismo , Imagen por Resonancia Magnética , Espectroscopía de Resonancia Magnética , Espectroscopía de Protones por Resonancia Magnética/métodos , Ratas , Retinitis Pigmentosa/diagnóstico por imagen , Vías Visuales/metabolismo , Ácido gamma-Aminobutírico
2.
Biochem Biophys Res Commun ; 485(4): 796-801, 2017 Apr 15.
Artículo en Inglés | MEDLINE | ID: mdl-28257839

RESUMEN

Cross-modal plasticity within the visual and auditory cortices of early binocularly blind macaques is not well studied. In this study, four healthy neonatal macaques were assigned to group A (control group) or group B (binocularly blind group). Sixteen months later, blood oxygenation level-dependent functional imaging (BOLD-fMRI) was conducted to examine the activation in the visual and auditory cortices of each macaque while being tested using pure tones as auditory stimuli. The changes in the BOLD response in the visual and auditory cortices of all macaques were compared with immunofluorescence staining findings. Compared with group A, greater BOLD activity was observed in the bilateral visual cortices of group B, and this effect was particularly obvious in the right visual cortex. In addition, more activated volumes were found in the bilateral auditory cortices of group B than of group A, especially in the right auditory cortex. These findings were consistent with the fact that there were more c-Fos-positive cells in the bilateral visual and auditory cortices of group B compared with group A (p < 0.05). In conclusion, the bilateral visual cortices of binocularly blind macaques can be reorganized to process auditory stimuli after visual deprivation, and this effect is more obvious in the right than the left visual cortex. These results indicate the establishment of cross-modal plasticity within the visual and auditory cortices.


Asunto(s)
Corteza Auditiva/fisiopatología , Ceguera/fisiopatología , Visión Binocular , Corteza Visual/fisiopatología , Estimulación Acústica , Animales , Animales Recién Nacidos , Corteza Auditiva/diagnóstico por imagen , Corteza Auditiva/metabolismo , Ceguera/diagnóstico por imagen , Técnica del Anticuerpo Fluorescente , Macaca , Imagen por Resonancia Magnética/métodos , Oxígeno/sangre , Proteínas Proto-Oncogénicas c-fos/metabolismo , Corteza Visual/diagnóstico por imagen , Corteza Visual/metabolismo
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