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1.
Sci Rep ; 14(1): 16318, 2024 Jul 15.
Artigo em Inglês | MEDLINE | ID: mdl-39009771

RESUMO

Considering the superior luminous intensity characteristics of lasers, a thermal simulation platform employing laser-induced heating in an aerobic environment was developed. Achieving a uniformly distributed flat-topped square laser beam output was facilitated through optical fibre bundling techniques, while precise control over laser power output was attained through current modulation. Utilising the aforementioned system, thermal shock simulation experiments were conducted in an aerobic environment, subjecting two types of high-temperature-resistant composites, namely C/C and C/SiC, to temperatures up to 1800 °C. These composites were lightweight, heat-resistant materials designed for hypersonic vehicle applications. The results show that the system and method can be used to simulate high temperatures, rapid temperature increases, and thermal shocks on C/C composite materials, with minimal variation in the coupling coefficient under aerobic conditions. The system and method can also provide key technology support for thermal-force-oxygen coupling testing of high temperature resistant materials.

2.
Materials (Basel) ; 15(4)2022 Feb 18.
Artigo em Inglês | MEDLINE | ID: mdl-35208097

RESUMO

In recent years, photonic crystal fibers (PCFs) have attracted increasing attention. Compared with traditional optical fibers, PCFs exhibit many unique optical properties and superior performance due to their high degree of structural design freedom. Using large-mode area (LMA) fibers with single-mode operation is essential to overcoming emerging problems as the power of fiber lasers scales up, which can effectively reduce the power density and mitigate the influence of nonlinear effects. With a brief introduction of the concept, classification, light transmission mechanism, basic properties, and theoretical analysis methods of PCFs, this paper mainly compiles the worldwide development of large-mode area and polarization-maintaining (PM) PCFs, and finally proposes possible technical routes to realize the single-mode operation of LMA-PCFs and PM-LMA-PCFs. Finally, the future development prospects of the PCFs are discussed.

3.
Exp Ther Med ; 18(6): 4591-4602, 2019 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-31777557

RESUMO

The present study aimed to investigate differentially expressed genes (DEGs) in whole blood (WB) obtained from patients with lumbar disc prolapse (LDP) and healthy volunteers. A total of 8 patients with LDP and 8 healthy volunteers were recruited. An Agilent SurePrint G3 human gene expression microarray 8×60 K was used to perform the microarray analyses. R was employed to identify DEGs, which were then subjected to bioinformatics analysis, including a Gene Ontology (GO) analysis, Kyoto Encyclopaedia of Genes and Genomes (KEGG) pathway analysis and protein-protein interaction (PPI) network analysis. DEGs in the degenerative annulus fibrosis (AF) and nucleus pulposus (NP) compared with non-degenerative tissues were also identified based on microarray data and the intersections of the three were assessed. Furthermore, reverse transcription-quantitative (RT-q)PCR was performed to confirm the aberrant expression levels of selected DEGs in the WB of all subjects. A total of 161 DEGs between LDP patients and the healthy controls were identified (128 upregulated and 33 downregulated). These DEGs were enriched in 293 biological process, 36 cellular component and 21 molecular function GO terms, as well as in 24 KEGG pathways. The PPI network contained 4 submodules, and Toll-like receptor 4 had the highest degree centrality. A total of 22 DEGs were common to the three groups of DEGs. The RT-qPCR assay confirmed that the expression levels of cytochrome P450 family 27 subfamily A member 1, superoxide dismutase 2, protein disulfide isomerase family A member 4, FKBP prolyl isomerase 11 and ectonucleotide pyrophosphatase/phosphodiesterase 4 were significantly different between the patient group and the volunteer group. In conclusion, several genes were identified as potential biomarkers in WB that should be further explored in future studies to determine their potential application in the clinical treatment and diagnosis of LDP, and the present bioinformatics analysis revealed several GO terms, KEGG pathways and submodules of the PPI network that may be involved in LDP, although the exact mechanisms remain elusive.

4.
Genet Test Mol Biomarkers ; 23(9): 610-617, 2019 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-31368816

RESUMO

Aims: This study was designed to investigate differentially expressed genes (DEGs) in the annulus fibrosus (AF), nucleus pulposus (NP), and whole blood (WB) of intervertebral disk degeneration (IDD) patients. Materials and Methods: We retrieved microarray data set GSE70362, which contains the gene expression profiles of 24 AF and 24 NP samples from the Gene Expression Omnibus and identified DEGs in degenerative AF (AF-DEGs) and NP (NP-DEGs) samples compared with nondegenerative samples. We also examined gene expression profiles in WB from patients with IDD and healthy volunteers to identify DEGs in WB (WB-DEGs). We performed functional analyses on the DEGs common to AF-DEGs, NP-DEGs, and WB-DEGs. Expression of the common DEGs was partially validated by quantitative real-time-polymerase chain reaction (QRT-PCR). Results: In total, 846 AF-DEGs, 902 NP-DEGs, and 862 WB-DEGs were identified, and 22 DEGs were common among the three groups. Functional analyses showed that the common DEGs were enriched in 33 biological processes, 16 cellular components, 4 molecular functions, and 9 Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways; 13 of the common DEGs were included in the protein-protein interaction (PPI) network and superoxide dismutase 2 (SOD2) was identified as a hub gene in the PPI network. The QRT-PCR results for the expression of the genes protein disulfide isomerase family A member 4, FKBP prolyl isomerase 11, ectonucleotide pyrophosphatase/phosphodiesterase 4, SOD2, and actin binding LIM protein 1, were consistent with the gene chip hybridization results. Conclusions: This study identified key genes for future investigations of the underlying molecular mechanisms of IDD. These genes may provide future targets for the clinical treatment and diagnosis of IDD.


Assuntos
Degeneração do Disco Intervertebral/genética , Transcriptoma , Adulto , Anel Fibroso/metabolismo , Biologia Computacional , Feminino , Perfilação da Expressão Gênica , Humanos , Degeneração do Disco Intervertebral/metabolismo , Proteínas com Domínio LIM/sangue , Proteínas com Domínio LIM/genética , Proteínas com Domínio LIM/metabolismo , Masculino , Análise em Microsséries , Proteínas dos Microfilamentos/sangue , Proteínas dos Microfilamentos/genética , Proteínas dos Microfilamentos/metabolismo , Pessoa de Meia-Idade , Núcleo Pulposo/metabolismo , Diester Fosfórico Hidrolases/sangue , Isomerases de Dissulfetos de Proteínas/sangue , Isomerases de Dissulfetos de Proteínas/genética , Isomerases de Dissulfetos de Proteínas/metabolismo , Mapas de Interação de Proteínas , Superóxido Dismutase/sangue , Superóxido Dismutase/genética , Superóxido Dismutase/metabolismo
5.
Exp Ther Med ; 16(6): 5031-5040, 2018 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-30542457

RESUMO

Degeneration of the intervertebral disc (IVD), which consists of the annulus fibrosus (AF) and nucleus pulposus (NP), is a multifactorial physiological process associated with lower back pain. Despite decades of research, the knowledge of the underlying molecular mechanisms of IVD degeneration (IDD) has remained limited. The present study aimed to reveal the differential gene expression patterns in AF and NP during the process of IDD and to identify key biomarkers contributing to these differences. The microarray dataset GSE70362 containing 24 AF and 24 NP samples was retrieved from the Gene Expression Omnibus database. Of these, 8 healthy samples were discarded. GeneSpring11.5 software was employed to identify differentially expressed genes (DEGs). Metascape online tools were used to perform enrichment analyses. Finally, the DEGs were mapped with the Search Tool for the Retrieval of Interacting Genes, and a protein-protein interaction (PPI) network was constructed in Cytoscape software. A total of 87 DEGs were identified. Gene ontology enrichment revealed that these DEGs were mainly involved in the inflammatory response, the extracellular matrix and RNA polymerase II transcription factor activity. Pathway enrichment revealed that the DEGs were mainly involved in the transforming growth factor (TGF-ß) and estrogen signaling pathways. Matrix metalloproteinase (MMP)1 and interleukin (IL)6 were included in the genes enriched in rheumatoid arthritis, whereas bone morphogenetic protein (BMP)2 and thrombospondin 1 (THBS1) were among the genes enriched in the TGF-ß signaling pathway. In the PPI network, IL6 was identified as the central gene. In conclusion, as MMP1 has been demonstrated degrade collagen III at higher rates compared with other types of collagen (which is at a higher quantity in AF than NP), collagen types may be in different distribution patterns, which may contribute to the upregulation of MMP1 in AF. Differences in the expression of BMP2, ESR1 and THBS1 may explain for the pathological differences between AF and NP. IL6 may have a key role in different degeneration processes in AF and NP.

6.
Sheng Wu Yi Xue Gong Cheng Xue Za Zhi ; 29(5): 991-4, 2012 Oct.
Artigo em Chinês | MEDLINE | ID: mdl-23198447

RESUMO

Like functions of other organisms, most of the physiological and behavioral functions of human are characterized by day-night rhythms. The rhythms which exhibit approximately 24-hour periodicity are called as circadian rhythms. This review is to summarize the progress of studies on relation of circadian rhythum disruption and cancer. The research results from animal experiments and population-based epidemiological studies have showed that cancer is closly related to circadian rhythm. Although numrous studies have demonstrated the close relation between circadian rhythm disruption and cancer, the mechanism is not yet clear. The current studies attributed decreased level of melatonin secretion and disruption of clock genes expression to the mechanism of carcinogenesis of circadian rhythm disruption.


Assuntos
Transtornos Cronobiológicos/fisiopatologia , Neoplasias/fisiopatologia , Animais , Humanos , Neoplasias/epidemiologia , Fatores de Risco , Estados Unidos/epidemiologia
7.
Zhongguo Zhen Jiu ; 31(2): 125-8, 2011 Feb.
Artigo em Chinês | MEDLINE | ID: mdl-21442813

RESUMO

OBJECTIVE: To compare the curative effects of simple obesity of spleen deficiency and dampness excess treated by hour-prescription of points and routine acupuncture therapy. METHODS: Sixty cases were randomly divided into an observation group and a control group; Taibai (SP 3), Gongsun (SP 4), Sanyinjiao (SP 6), Yinlingquan (SP 9), Fujie (SP 14) and Daheng (SP 15) were applied in both groups. Hour-prescription of points (the acupoints of Spleen Meridian were selected at the period of the day from 10:04 a.m. to 12:04 a.m. when the Spleen Meridian is most energetic at Chengdu) was applied in observation group, and routine acupuncture was applied in control group (acupoints weren't selected at 10:04 a.m. to 12:04 a.m.). Once a day, and 10 days of treatment made one session, totally 3 sessions were required. RESULTS: The total effective rate was 86.2% (25/29) in observation group, and 75.9% (22/29) in control group. The total effect in observation group was superior to that in control group (P < 0.05). The observation group was better than the control group in reduction of weight, body mass index, obesity degree, awaist circumference and the ratio between waist and hip with significant differences between two groups (P < 0.01, P < 0.05). CONCLUSION: The therapeutic effect of obesity of spleen deficiency and dampness excess treated by hour-prescription of points therapy is superior to that by routine acupuncture therapy.


Assuntos
Pontos de Acupuntura , Terapia por Acupuntura/métodos , Medicina Tradicional Chinesa , Obesidade/terapia , Baço/fisiopatologia , Adulto , Feminino , Humanos , Masculino
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