RESUMEN
PURPOSE: The first 3 weeks of life is the peak time of oligodendrocytes development and also the critical period of cholesterol increasing dramatically in central nervous system in rats. Neonatal hypoxia-ischemia (HI) brain damage happening in this period may disturb the brain cholesterol balance as well as white matter development. MATERIALS AND METHODS: To test this hypothesis, postnatal day 7 (P7) Sprague-Dawley rats were subjected to HI insult. Cholesterol concentrations from brain and plasma were measured. White matter integrity was evaluated by densitometric analysis of myelin basic protein (MBP) immunostaining and electron microscopy. Brain TNF-alpha and IL-6 levels were also measured. RESULTS: HI-induced brain cholesterol, but not the plasma cholesterol, levels decreased significantly during the first three days after HI compared with naïve and sham operated rats (p<0.05). Obvious hypomyelination was indicated by marked reductions in MBP immunostaining on both P10 and P14 (p<0.01) and less and thinner myelinated axons were detected on P21 by electron microscopy observation. High expressions of brain TNF-alpha and IL-6 12 h after HI (p<0.05) were also observed. DISCUSSION: The present work provides evidence that HI insult destroyed brain cholesterol homeostasis, which might be important in the molecular pathology of hypoxic-ischemic white matter injury. Proinflammatory cytokines insulting oligodendrocytes, may cause cholesterol unbalance. Furthermore, specific therapeutic interventions to maintain brain cholesterol balance may be effective for the recovery of white matter function.
Asunto(s)
Encéfalo/metabolismo , Colesterol/metabolismo , Hipoxia-Isquemia Encefálica/metabolismo , Hipoxia-Isquemia Encefálica/patología , Factores de Edad , Análisis de Varianza , Animales , Animales Recién Nacidos , Encéfalo/crecimiento & desarrollo , Encéfalo/ultraestructura , Ensayo de Inmunoadsorción Enzimática/métodos , Interleucina-6/metabolismo , Microscopía Electrónica de Transmisión , Proteína Básica de Mielina/metabolismo , Ratas , Ratas Sprague-Dawley , Factor de Necrosis Tumoral alfa/metabolismoRESUMEN
Different pathways act synergistically to participate in many biological processes. Thus, the purpose of our study was to extract dysregulated pathways to investigate the pathogenesis of colorectal cancer (CRC) based on the functional dependency among pathways. Protein-protein interaction (PPI) information and pathway data were retrieved from STRING and Reactome databases, respectively. After genes were aligned to the pathways, each pathway activity was calculated using the principal component analysis (PCA) method, and the seed pathway was discovered. Subsequently, we constructed the pathway interaction network (PIN), where each node represented a biological pathway based on gene expression profile, PPI data, as well as pathways. Dysregulated pathways were then selected from the PIN according to classification performance and seed pathway. A PIN including 11,960 interactions was constructed to identify dysregulated pathways. Interestingly, the interaction of mRNA splicing and mRNA splicing-major pathway had the highest score of 719.8167. Maximum change of the activity score between CRC and normal samples appeared in the pathway of DNA replication, which was selected as the seed pathway. Starting with this seed pathway, a pathway set containing 30 dysregulated pathways was obtained with an area under the curve score of 0.8598. The pathway of mRNA splicing, mRNA splicing-major pathway, and RNA polymerase I had the maximum genes of 107. Moreover, we found that these 30 pathways had crosstalks with each other. The results suggest that these dysregulated pathways might be used as biomarkers to diagnose CRC.
Asunto(s)
Adenoma/genética , Adenoma/metabolismo , Neoplasias Colorrectales/genética , Neoplasias Colorrectales/metabolismo , Mapas de Interacción de Proteínas/genética , Área Bajo la Curva , Biomarcadores de Tumor/genética , Estudios de Casos y Controles , Perfilación de la Expresión Génica/métodos , Regulación de la Expresión Génica , Humanos , Análisis de Componente Principal , Análisis por Matrices de Proteínas , Empalme del ARN , Valores de Referencia , Transducción de Señal , TranscriptomaRESUMEN
Grazing is the primary land use in the Hulunber meadow steppe. However, the quantitative effects of grazing on ecosystem carbon dioxide (CO2) fluxes in this zone remain unclear. A controlled experiment was conducted from 2010 to 2014 to study the effects of six stocking rates on CO2 flux, and the results showed that there were significant differences in CO2 fluxes by year, treatment, and month. The effects of light and intermediate grazing remained relatively constant with grazing year, whereas the effects of heavy grazing increased substantially with grazing duration. CO2 flux significantly decreased with increasing grazing intensity and duration, and it was significantly positively correlated with rainfall, soil moisture (SM), the carbon to nitrogen ratio (C/N ratio), soil available phosphorus (SAP), soil NH4+-N, soil NO3-N, aboveground biomass (AGB), coverage, height, and litter and negatively correlated with air temperature, total soil N (TN) and microbial biomass N (MBN). A correspondence analysis showed that the main factors influencing changes in CO2 emissions under grazing were AGB, height, coverage, SM, NH4+-N and NO3-N. Increased rainfall and reduced grazing resulted in greater CO2 emissions. Our study provides important information to improve our understanding of the role of livestock grazing in GHG emissions.
RESUMEN
Hyaluronidase (Hyal), which is related to mammalian diseases, is greatly significant for mammal. It is the major enzyme for degrading hyaluronan (HA), which is a linear high molecular polymer that is ubiquitous in mammalian extracellular matrix. Previous studies suggested that the levels of Hyals play significant roles in predicting, determining and curing many diseases. This review summarizes previous studies on the classification and biophysical and therapeutic applications of mammalian Hyals and focuses on the current medicinal and clinical applications of Hyals.
Asunto(s)
Ácido Hialurónico/metabolismo , Hialuronoglucosaminidasa/administración & dosificación , Hialuronoglucosaminidasa/metabolismo , Animales , Matriz Extracelular , Humanos , Hialuronoglucosaminidasa/química , Mamíferos , Neoplasias/tratamiento farmacológico , Neoplasias/enzimologíaRESUMEN
The crystal structure, electronic and magnetic properties of LaMn(7)O(12) ((LaMn(3)(3+))(A)Mn(4)(3+)O(12)) are investigated by GGA (LSDA) and GGA + U (LSDA + U) (0.0 ≤ U ≤ 5.0 eV) methods. Based on two experimentally refined structures (distinguished by the distortion parameter Δ, namely S(I) (Δ = 8.5 × 10(-5)) and S(II) (Δ = 25.0 × 10(-4))), GGA and GGA + U with U < 3.0 eV calculations indicate that S(I) with a small distortion is the lowest-energy crystal structure while GGA + U with 3.0 ≤ U ≤ 5.0 eV calculations show that S(II) with a larger distortion is the ground-state crystal structure. Within the LSDA method, S(II) is always the ground-state structure no matter if U is considered or not. There are two independent magnetic sublattices: Mn(3+) within the A site and Mn(3+) within the B site. First, it is predicted that A-site Mn(3+) ions are preferably AFM-coupled in G-type (antiferromagnetically coupled in three directions). Based on this result, four magnetic configurations (FM-[Formula: see text], AFM1-[Formula: see text], AFM2-[Formula: see text] and AFM3-[Formula: see text]) are designed, and their total energies are calculated. Our results demonstrate that AFM2 and AFM3 are the lowest magnetic state, respectively, for S(I) and S(II). Correspondingly, LaMn(7)O(12) is metallic with no orbital ordering at AFM2 for S(I) while it is an insulator with orbital ordering at AFM3 for S(II). Thus, modulation of the distortion parameter Δ, e.g. by chemical doping, could be employed as a new avenue to induce a magnetic phase transition and the corresponding metal-to-insulator transition in LaMn(7)O(12).