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1.
Aging Dis ; 14(3): 858-878, 2023 Jun 01.
Artículo en Inglés | MEDLINE | ID: mdl-37191427

RESUMEN

The metabolism of L-tryptophan (TRP) regulates homeostasis, immunity, and neuronal function. Altered TRP metabolism has been implicated in the pathophysiology of various diseases of the central nervous system. TRP is metabolized through two main pathways, the kynurenine pathway and the methoxyindole pathway. First, TRP is metabolized to kynurenine, then kynurenic acid, quinolinic acid, anthranilic acid, 3-hydroxykynurenine, and finally 3-hydroxyanthranilic acid along the kynurenine pathway. Second, TRP is metabolized to serotonin and melatonin along the methoxyindole pathway. In this review, we summarize the biological properties of key metabolites and their pathogenic functions in 12 disorders of the central nervous system: schizophrenia, bipolar disorder, major depressive disorder, spinal cord injury, traumatic brain injury, ischemic stroke, intracerebral hemorrhage, multiple sclerosis, Alzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis, and Huntington's disease. Furthermore, we summarize preclinical and clinical studies, mainly since 2015, that investigated the metabolic pathway of TRP, focusing on changes in biomarkers of these neurologic disorders, their pathogenic implications, and potential therapeutic strategies targeting this metabolic pathway. This critical, comprehensive, and up-to-date review helps identify promising directions for future preclinical, clinical, and translational research on neuropsychiatric disorders.

2.
Neurol Res ; 44(1): 65-89, 2022 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-34308784

RESUMEN

Traumatic brain injury (TBI) is a medical emergency with high morbidity and mortality. Motor, memory, and emotion-related deficits are common symptoms following TBI, yet treatment is very limited. To develop new drugs and find new therapeutic avenues, a wide variety of TBI models have been established to mimic the heterogeneity of TBI. In this regard, along with histologic measures, behavioral functional outcomes provide valuable insight into the underlying neuropathology and guide neurorehabilitation efforts for neuropsychiatric impairment after TBI. Development, characterization, and application of behavioral tests that can assess functional neurologic deficits are essential to the development of translational therapies. This comprehensive review aims to summarize 19 common behavioral tests from three aspects (motor, memory, and emotion-related) that are associated with TBI pathology. Discussion covers the apparatus, the test steps, the evaluation indexes, data collection and analysis, animal performance and applications, advantages and disadvantages as well as precautions to eliminate bias wherever possible. We discussed recent studies on TBI-related preconditioning, biomarkers, and optimized behavioral protocols. The neuropsychologic tests employed in clinics were correlated with those used in mouse TBI models. In summary, this review provides a comprehensive, up-to-date reference for TBI researchers to choose the right neurobehavioral protocol according to the research objectives of their translational investigation.


Asunto(s)
Escala de Evaluación de la Conducta , Lesiones Traumáticas del Encéfalo , Animales , Lesiones Traumáticas del Encéfalo/patología , Modelos Animales de Enfermedad , Emociones , Ratones
3.
Biomed Res Int ; 2022: 9940566, 2022.
Artículo en Inglés | MEDLINE | ID: mdl-35127947

RESUMEN

Mesothelioma (MESO) is a mesothelial originate neoplasm with high morbidity and mortality. Despite advancement in technology, early diagnosis still lacks effectivity and is full of pitfalls. Approaches of cancer diagnosis and therapy utilizing immune biomarkers and transcription factors (TFs) have attracted more and more attention. But the molecular mechanism of these features in MESO bone metastasis has not been thoroughly studied. Utilizing high-throughput genome sequencing data and lists of specific gene subsets, we performed several data mining algorithm. Single-sample Gene Set Enrichment Analysis (ssGSEA) was applied to identify downstream immune cells. Potential pathways involved in MESO bone metastasis were identified using Gene Oncology (GO) analysis, Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis, Gene Set Variation Analysis (GSVA), Gene Set Enrichment Analysis (GSEA), and Cox regression analysis. Ultimately, a model to help early diagnosis and to predict prognosis was constructed based on differentially expressed immune-related genes between bone metastatic and nonmetastatic MESO groups. In conclusion, immune-related gene SDC2, regulated by TFs TCF7L1 and POLR3D, had an important role on immune cell function and infiltration, providing novel biomarkers and therapeutic targets for metastatic MESO.


Asunto(s)
Neoplasias Óseas , Mesotelioma , Neoplasias Óseas/diagnóstico , Neoplasias Óseas/genética , Humanos , Mesotelioma/diagnóstico , Mesotelioma/genética , Pronóstico , Factores de Transcripción/genética
4.
J Colloid Interface Sci ; 428: 128-32, 2014 Aug 15.
Artículo en Inglés | MEDLINE | ID: mdl-24910044

RESUMEN

Dye-sensitized solar cells (DSSCs) are fabricated with gallium nitride-titanium dioxide (GaN-TiO2) composite photoelectrodes to enhance the power conversion efficiency. The value of power conversion efficiency increases with the incorporation of GaN in TiO2 matrix and reaches a maximum at 0.05 wt% GaN. Internal resistance in the DSSC is characterized by electrochemical impedance spectroscopy (EIS). From the EIS of electrolyte/dye/GaN-TiO2 interface resistances under illumination and in the dark, a decrease in the charge transfer resistance and an increase in the charge recombination resistance of the DSSCs are obtained after the inclusion of GaN (0.01-0.05 wt%) in the TiO2 matrix. The power conversion efficiency of the DSSC based on the GaN (0.05 wt%)-TiO2 composite photoelectrode is enhanced by ∼61% in comparison with a pristine TiO2 photoelectrode.

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