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1.
Clin Neurol Neurosurg ; 246: 108542, 2024 Sep 11.
Artículo en Inglés | MEDLINE | ID: mdl-39303664

RESUMEN

OBJECTIVES: Based on the literature, tensor-based morphometry (TBM) parameters were related to neurocognitive functions such as memory, learning, language ability, and executive functions. The present study aims to evaluate the associations between TBM indices with executive functions, memory, language, and visuospatial abilities and the value of TBM in the clinical diagnosis of Alzheimer's disease (AD) among individuals with Alzheimer's disease continuum and mild cognitive impairment (MCI) from Alzheimer's Disease Neuroimaging Initiative (ADNI). METHODS: The authors used ADNI-memory (ADNI-MEM), ADNI-executive functions (ADNI-EF), ADNI-language (ADNI-LAN), and ADNI-visuospatial (ADNI-VS) composite scores. TBM parameters, including measure 1, which represents average within a statistically defined region-of-interest inside the temporal lobes and measure 2 which indicates average within an anatomically defined region-of-interest including bilateral temporal lobes were utilized in the current study. Statistical analysis was performed using IBM SPSS Statistics version 26, and Pearson's correlation, Bonferroni's correction, and multiple linear regression were utilized for data analysis. P <0.05 was considered statistically significant. RESULTS: After screening 800 participants, 270 (151 men, 119 women) were selected for a study with TBM scores and cognition-related assessments at 6, 12, and 24 months. Groups included healthy controls (n=53), MCI (n=158), and Alzheimer's Disease (AD) (n=59). TBM indices correlated with cognitive scores in MCI and AD groups but not healthy controls. Changes in TBM indices and cognitive scores were significantly correlated in MCI and AD groups over 24 months. TBM indices were weak predictors of cognitive decline at all time points. CONCLUSIONS: TBM can help physicians diagnose MCI and AD early. However, TBM could not strongly predict cognitive functions decline at all time points.

2.
Mol Biol Rep ; 51(1): 516, 2024 Apr 15.
Artículo en Inglés | MEDLINE | ID: mdl-38622329

RESUMEN

BACKGROUND: Resveratrol has received much attention due to its beneficial effects including antioxidant activity. The purpose of this study was to investigate the therapeutic effects of resveratrol treatment on oxidative stress and insulin resistance in the skeletal muscle of high-fat diet (HFD)-fed animals. METHODS AND RESULTS: A total of 30 six-week-old C57BL/6J mice were randomly allocated to three groups (10 animals in each group): The control group in which mice were fed a normal chow diet (NCD); the HFD group in which mice were fed an HFD for 26 weeks; and the HFD-resveratrol group in which HFD was replaced by a resveratrol supplemented-HFD (400 mg/kg diet) after 10 weeks of HFD feeding. At the end of this period, gastrocnemius muscle samples were examined to determine insulin resistance and the oxidative status in the presence of HFD and resveratrol. Resveratrol supplementation in HFD-fed mice reduced body and adipose tissue weight, improved insulin sensitivity, and decreased oxidative stress as indicated by lower malonaldehyde (MDA) levels and higher total antioxidant capacity. The supplement also increased the expression and activity of antioxidative enzymes in gastrocnemius muscle and modulated Nrf2 and Keap1 expression levels. CONCLUSIONS: These results suggest that resveratrol is effective in improving the antioxidant defense system of the skeletal muscle in HFD-fed mice, indicating its therapeutic potential to combat diseases associated with insulin resistance and oxidative stress.


Asunto(s)
Antioxidantes , Resistencia a la Insulina , Ratones , Animales , Antioxidantes/metabolismo , Resveratrol/farmacología , Resveratrol/metabolismo , Resistencia a la Insulina/fisiología , Dieta Alta en Grasa/efectos adversos , Factor 2 Relacionado con NF-E2/metabolismo , Proteína 1 Asociada A ECH Tipo Kelch/metabolismo , Ratones Endogámicos C57BL , Músculo Esquelético/metabolismo , Transducción de Señal , Insulina/metabolismo
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