Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 12 de 12
Filtrar
Mais filtros










Base de dados
Intervalo de ano de publicação
1.
J Food Sci ; 83(6): 1476-1483, 2018 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-29802735

RESUMO

As potential and valuable antiseptics in the food industry, clove oil and its main effective composition eugenol show beneficial advantages on antibacterial and antifungal activity, aromaticity, and safety. Researches find that both clove oil and eugenol express significantly inhibitory effects on numerous kinds of food source microorganisms, and the mechanisms are associated with reducing the migratory and adhesion and inhibiting the synthesis of biofilm and various virulence factors of these microorganisms. Clove oil and eugenol are generally regarded as safe in vivo experiments. However, they may express certain cytotoxicity on fibroblasts and other cells in vitro. Studies on the quality and additive standard of clove oil and eugenol should be strengthened to promote the antiseptic effects of them in the food antiseptic field.


Assuntos
Antibacterianos/farmacologia , Antifúngicos/farmacologia , Óleo de Cravo/farmacologia , Eugenol/farmacologia , Conservação de Alimentos , Óleos Voláteis/farmacologia , Syzygium/química , Antissepsia , Óleo de Cravo/química , Humanos , Extratos Vegetais/farmacologia
2.
Biosci Trends ; 11(6): 612-618, 2018 Jan 09.
Artigo em Inglês | MEDLINE | ID: mdl-29238002

RESUMO

Great achievements have been made in human cancer research, but most of this research is focused on conditions at the microscopic rather than the systemic level. Recent studies have increasingly cited the ancient Chinese theory of yin-yang in an effort to expand beyond the microscopic level. Various cancer-associated genes and proteins such as mitogen-activated protein kinase (MAPK), p38, p53, c-Myc, tumor necrosis factor (TNF)-α, NF-κB, Cyclin D1, and cyclin-dependent kinase (CDK) and cells such as T cells, B cells, macrophages, neutrophils, and fibroblasts have been reported to regulate various types of cancers in a yin-yang manner. These studies have brought the theory of yin-yang into vogue in cancer research worldwide.


Assuntos
Genes Neoplásicos , Proteínas de Neoplasias/genética , Neoplasias , Yin-Yang , Imunidade Adaptativa/genética , Apoptose/genética , Apoptose/imunologia , Proliferação de Células/genética , Humanos , Neoplasias/genética , Neoplasias/metabolismo , Neoplasias/patologia , Microambiente Tumoral/genética , Microambiente Tumoral/imunologia
3.
J Mol Neurosci ; 61(1): 115-122, 2017 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-27601172

RESUMO

This present paper focus on transcriptome changes of astrocytes before and after oxygen glucose deprivation (OGD) injury. Cortical astrocytes of Sprague-Dawley (SD) rats were cultured in OGD condition for 6 h, and the damage of cells was analyzed by cell's activity detection, lactate dehydrogenase leakage rate detection, annexin V-FITC (fluorescein isothiocyanate)/PI (propidium iodide) apoptosis detection, and transcriptome change detection through Affymetrix GeneChip Rat Genome 230 2.0 Array; some regulated genes were detected by quantitative real-time polymerase chain reaction (qPCR). After OGD injury, activity of astrocytes was decreased, and apoptosis of injured cells was increased. mRNA expressions of 404 genes were upregulated and 454 genes were downregulated, including upregulation of MAPK signal pathway and downregulation of PI3k/Akt pathway. Otherwise, pathways of the focal adhesion (percentage of all regulated genes, 11.4 %), HIF-1 (10.2 %), and one carbon pool by folate (3.4 %), etc. were upregulated, and steroid biosynthesis (7 %), basal cell carcinoma (9.9 %), and terpenoid backbone (5.6 %), etc. were down-regulated. These results indicate that apoptosis of astrocytes induced by OGD injury is associated with the MAPK and PI3k/Akt pathways.


Assuntos
Astrócitos/metabolismo , Glucose/deficiência , Oxigênio/metabolismo , Transcriptoma , Animais , Apoptose , Hipóxia Celular , Células Cultivadas , Subunidade alfa do Fator 1 Induzível por Hipóxia/genética , Subunidade alfa do Fator 1 Induzível por Hipóxia/metabolismo , Sistema de Sinalização das MAP Quinases , Fosfatidilinositol 3-Quinases/metabolismo , Proteínas Proto-Oncogênicas c-akt/genética , Proteínas Proto-Oncogênicas c-akt/metabolismo , Ratos , Ratos Sprague-Dawley
4.
Mol Cell Biochem ; 425(1-2): 113-123, 2017 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-27844252

RESUMO

Stroke is a serious disease with complex pathomechanism and limited therapeutic effect in clinic. Our previous research has found obvious therapeutic effect of Puerarin (Pur) on stroke injury of rat. The aim of this study is to investigate the transcriptome changes of oxygen-glucose deprivation/reoxygenation (OGD/R)-injured astrocytes before and after the intervention of Pur. Cells activity and apoptosis detection indicated that the activity of OGD/R-injured astrocytes was improved, and the apoptosis was ameliorated by Pur. Affymetrix GeneChip Rat Genome 230 2.0 Array assays indicated that after intervention of Pur, mRNA expressions of 31 genes were up-regulated and 40 genes were down-regulated in OGD group, whereas mRNA expression of 36 genes were up-regulated, and 88 genes were down-regulated in OGD/R group. Pathway analysis indicated that the olfactory transduction pathway and the JAK (janus kinase) 2/STAT (signal transducer and activator of transcription) three pathways were down-regulated by Pur during OGD/R injury of astrocytes. These data indicated that Pur regulates transcriptome and expresses protective effect on astrocytes during OGD/R injury, and may be a potential therapeutic agent for the treatment of stroke.


Assuntos
Astrócitos/metabolismo , Glucose/metabolismo , Isoflavonas/farmacologia , Traumatismo por Reperfusão/metabolismo , Transcriptoma/efeitos dos fármacos , Animais , Astrócitos/patologia , Hipóxia Celular/efeitos dos fármacos , Ratos , Ratos Sprague-Dawley , Traumatismo por Reperfusão/patologia
5.
Fundam Clin Pharmacol ; 30(6): 490-501, 2016 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-27414248

RESUMO

Alzheimer's disease (AD) is a neurodegenerative disorder in which the death of brain cells leads to memory loss and cognitive decline. To reduce the death rate and improve the biological activity of neurocytes, neurotrophic factors (NTFs) exhibit therapeutic effect on AD. However, therapeutic application of exogenous NTFs in treatment of AD is largely limited due to short half-life, poor stability, etc. Various extracts of traditional Chinese medicine (TCM) have been shown to exhibit therapeutic effects on AD, and some of these effects are associated with regulation on the expression of nerve growth factor, brain-derived neurotrophic factor (BDNF), and glial cell line-derived neurotrophic factor (GDNF) and their associated receptors. This article reviews the progress on promotion of Panax ginseng, Rehmannia glutinosa Libosch., Epimedium, Polygala tenuifolia Willd, and seven other TCMs on secretion of NTFs during AD, with a view to preparation development and clinical application of these TCMs on AD.


Assuntos
Doença de Alzheimer/tratamento farmacológico , Produtos Biológicos/farmacologia , Produtos Biológicos/uso terapêutico , Fatores de Crescimento Neural/metabolismo , Doença de Alzheimer/metabolismo , Animais , Modelos Animais de Doenças , Meia-Vida , Humanos , Medicina Tradicional Chinesa/métodos
6.
J Hematol Oncol ; 9(1): 44, 2016 05 04.
Artigo em Inglês | MEDLINE | ID: mdl-27146823

RESUMO

BACKGROUND: Long noncoding RNA HOX antisense intergenic RNA myeloid 1 (HOTAIRM1) has been characterized as a critical factor in all-trans retinoic acid (ATRA)-induced differentiation of acute promyelocytic leukemia (APL) cells. However, the essential transcription factor for gene expression of HOTAIRM1 is still unknown. FINDINGS: Chromatin immunoprecipitation (ChIP) assays revealed that PU.1 constitutively bound to the regulatory region of HOTAIRM1. Co-expression of PU.1 led to the transactivation of the regulatory region of HOTAIRM1 in a reporter assay. Detailed analysis showed that two PU.1 motifs, which were located around +1100 bp downstream of the transcriptional start site of the HOTAIRM1 promoter, were responsible for the PU.1-dependent transactivation. The induction of HOTAIRM1 by ATRA was dependent on PU.1, and ectopic expression of PU.1 significantly up-regulated HOTAIRM1. Furthermore, low HOTAIRM1 expression was observed in APL cells, which was attributed to the reduced PU.1 expression rather than the repression by PML-RARα via the direct binding. CONCLUSION: PU.1 directly activates the expression of HOTAIRM1 through binding to the regulatory region of HOTAIRM1 during granulocytic differentiation. The reduced PU.1 expression, rather than PML-RARα itself, results in the low expression of HOTAIRM1 in APL cells. Our findings enrich the knowledge on the regulation of lncRNAs and the underlying mechanisms of the abnormal expression of lncRNAs involved in APL.


Assuntos
Diferenciação Celular , Granulócitos/citologia , Proteínas Proto-Oncogênicas/fisiologia , RNA Longo não Codificante/genética , Transativadores/fisiologia , Linhagem Celular , Linhagem Celular Tumoral , Regulação da Expressão Gênica , Humanos , Leucemia Promielocítica Aguda/genética , Leucemia Promielocítica Aguda/patologia , Ligação Proteica , Proteínas Proto-Oncogênicas/metabolismo , RNA Longo não Codificante/metabolismo , Sequências Reguladoras de Ácido Ribonucleico , Transativadores/metabolismo , Tretinoína/farmacologia
7.
Zhongguo Zhong Yao Za Zhi ; 40(12): 2278-84, 2015 Jun.
Artigo em Chinês | MEDLINE | ID: mdl-26591509

RESUMO

Puerarin is one of the most important effective components of Pueraria lobata which exhibited classic estrogen-like biological activities and had remarkable cardiovascular protections in vivo and in vitro experiments. These protections of puerarin are mainly exhibited on improving the myocardial cells membrane potential and arrhythmia based on effecting the Na+, K+ , and Ca2+ channels,resisting myocardial fibrosis damage, diastolic effect on blood vessels, promoting angiogenesis, resisting calcification and atherosclerosis, improving blood flow, antiplatelet aggregation, reducing lipid and resisting diabetes. The main mechanisms are to improve the membrane potential and reduce cardiovascular damage caused by inflammation, oxidative stress and apoptosis, and the main regulated signal pathways are the PI3K/Akt, the NF-kappa B and the caspases.


Assuntos
Doenças Cardiovasculares/prevenção & controle , Medicamentos de Ervas Chinesas/farmacologia , Isoflavonas/farmacologia , Substâncias Protetoras/farmacologia , Pueraria/química , Animais , Doenças Cardiovasculares/genética , Doenças Cardiovasculares/metabolismo , Humanos , Estresse Oxidativo/efeitos dos fármacos , Transdução de Sinais/efeitos dos fármacos
8.
Neural Regen Res ; 10(4): 605-9, 2015 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-26170822

RESUMO

The phytoestrogen puerarin has been shown to protect neurons and astrocytes in the brain, and is therefore an attractive drug in the treatment of Alzheimer's disease, Parkinson's disease and cerebral ischemia. Whether puerarin exhibits the same biological processes in neurons and astrocytes in vitro has rarely been reported. In this study, cortical neurons and astrocytes of newborn Sprague-Dawley rats were separated, identified and co-cultured in a system based on Transwell membranes. The retention time and distribution of puerarin in each cell type was detected by fluorescence spectrophotometry and fluorescence microscope. The concentration of puerarin in both co-cultured and separately cultured neurons was greater than that of astrocytes. Puerarin concentration reached a maximum 20 minutes after it was added. At 60 minutes after its addition, a scant amount of drug was detected in astrocytes; however in both separately cultured and co-cultured neurons, the concentration of puerarin achieved a stable level of about 12.8 ng/mL. The results indicate that puerarin had a higher concentration and longer retention time in neurons than that observed in astrocytes.

9.
Exp Hematol Oncol ; 5: 30, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-27999732

RESUMO

Long noncoding RNAs (lncRNAs) have emerged as a class of pivotal regulators of gene expression. Recent studies have shown that lncRNAs contribute to the initiation, maintenance, and development of acute myeloid leukemia (AML). In this review, we summarize the current knowledge of the lncRNAs that play critical roles in AML. We first briefly describe the characteristics of lncRNAs, and then focus on their regulatory roles in AML, including the modulation of differentiation, proliferation, cell cycle, and apoptosis. We further emphasize the action of lncRNAs during leukemogenesis by describing how they interact with RNA, protein and chromatin DNA to exert their functions. We also highlight an urgent need to investigate the mechanisms by which lncRNAs contribute to the pathogenesis of AML. Finally, we discuss the prognostic value of lncRNAs in AML patients.

10.
Chin J Nat Med ; 12(6): 407-14, 2014 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-24969520

RESUMO

Contemporary pharmacological research has demonstrated that puerarin, the most important phytoestrogen extracted from Pueraria lobata(Willd.) Ohwi, has protecting functions on the cardiovascular system, nervous system, osteoporosis, liver injury, and inflammation in vivo and in vitro. Most of these research studies focused on inhibiting oxidative stress and apoptosis through regulating various bioactivators and signal pathways. Among these, superoxide dismutase (SOD), endothelial nitric oxide synthase (eNOS) and malondialdehyde (MDA), and PI3K/Akt, MAPK, and NF-κB are of great importance. The data cited in this review were mainly obtained from articles listed in PubMed and Elsevier SDOL published from 1959 to 2013, and the search term used was "puerarin".


Assuntos
Anti-Inflamatórios/farmacologia , Antioxidantes/farmacologia , Isoflavonas/farmacologia , Fitoestrógenos/farmacologia , Fitoterapia , Extratos Vegetais/farmacologia , Pueraria/química , Anti-Inflamatórios/uso terapêutico , Antioxidantes/uso terapêutico , Apoptose/efeitos dos fármacos , Doenças Cardiovasculares/prevenção & controle , Humanos , Isoflavonas/uso terapêutico , Hepatopatias/prevenção & controle , Fármacos Neuroprotetores/farmacologia , Fármacos Neuroprotetores/uso terapêutico , Estresse Oxidativo/efeitos dos fármacos , Fitoestrógenos/uso terapêutico , Extratos Vegetais/uso terapêutico
11.
Analyst ; 137(17): 3989-94, 2012 Sep 07.
Artigo em Inglês | MEDLINE | ID: mdl-22822478

RESUMO

The DNA polymerase assay is fundamental for related molecular biology investigations and drug screenings, however, the commonly used radioactive method is laborious and restricted. Herein, we report a novel, simple and cost-effective fluorometric DNA polymerase detection method by utilizing graphene oxide (GO) as a signal switch. In this strategy, in the absence of DNA polymerase, the fluorophore-labeled template ssDNA could be strongly adsorbed and almost entirely quenched by GO. However, as DNA polymerase exists, the polymerized dsDNA product might lead to a much lower quenching efficiency after addition of GO due to the much weaker interaction of dsDNA with GO than ssDNA, thus resulting in a much higher fluorescence signal detected. As proof of concept, the quantitative DNA polymerase activity assay was performed using the Klenow fragment exo(-) (KF(-)) as a model. It was confirmed that, after optimization of detection conditions, KF(-) activity could be sensitively detected through facile fluorescence measurements, with a detection limit of 0.05 U mL(-1) and a good linear correlation between 0.05-2.5 U mL(-1) (R(2) = 0.9928). In addition, this GO-based method was further inspected to evaluate the inhibitive behaviors of several drugs toward KF(-) activity, the result of which firmly demonstrated its potential application in polymerization-targeted drug screening.


Assuntos
DNA Polimerase Dirigida por DNA/análise , Fluorometria , Grafite/química , Óxidos/química , DNA de Cadeia Simples/química , Corantes Fluorescentes/química
12.
Int J Antimicrob Agents ; 29(5): 576-81, 2007 May.
Artigo em Inglês | MEDLINE | ID: mdl-17314033

RESUMO

The objective of this study was to characterise the beta-lactamase genes of cephalosporin-resistant Escherichia coli isolated from farm animals in Guangdong Province of China. Of 592 E. coli isolates recovered from farm animals from 2003-2005, 50 (8.4%) showed cephalosporin resistance. Polymerase chain reaction and sequencing analysis showed that 14 isolates (2.4%) from chickens, ducks, pigs and partridges were positive for the bla(CTX-M) gene (10 for bla(CTX-M-14) and 4 for bla(CTX-M-27)). CMY-2 was detected for the first time in mainland China in six E. coli isolates (1.0%) from chickens and goose. Except for one isolate, bla(CTX-M)- and bla(CMY-2)-containing isolates also harboured the bla(TEM-1b) gene. Conjugation experiments demonstrated that the bla(CTX-M) and bla(TEM) genes could be transferred to E. coli DH5alpha. Pulsed-field gel electrophoresis (PFGE) showed that the 14 CTX-M-producing isolates belonged to 12 different types. Two isolates (one from a chicken, the other from a pig) containing CTX-M-14 showed indistinguishable PFGE patterns, indicating clonal dissemination of this strain among animals from different farms. This study describes for the first time the emergence of CTX-M- and CMY-2-producing E. coli among farm animals in China, with the CTX-M-9 group being the predominant extended-spectrum beta-lactamase detected.


Assuntos
Animais Domésticos/microbiologia , Escherichia coli/enzimologia , beta-Lactamases/química , Animais , Antibacterianos/farmacologia , Resistência às Cefalosporinas , Galinhas , China , Clonagem Molecular , Farmacorresistência Bacteriana , Patos , Eletroforese em Gel de Campo Pulsado , Escherichia coli/efeitos dos fármacos , Fezes/microbiologia , Testes de Sensibilidade Microbiana , Suínos , beta-Lactamases/genética , beta-Lactamases/isolamento & purificação
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...