Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 7 de 7
Filtrar
1.
Chinese Journal of Integrated Traditional and Western Medicine ; (12): 847-853, 2015.
Artigo em Chinês | WPRIM | ID: wpr-237928

RESUMO

<p><b>OBJECTIVE</b>To study the molecular mechanism of Yangjing Zhongyu Decoction (YZD) n-butanol extracts (ZDC) and ethyl acetate extracts (YSYZ) in reducing androgen in porcine granulose cells by mitogen-activated protein kinase (MAPK) pathway.</p><p><b>METHODS</b>Porcine granulose cells were isolated and cultured. They were inoculated by MAPK inhibitor PD98059 at different concentrations, and then they were divided into the blank control group (0), 1, 3, 10, and 25 micromol/L groups. After 24-h culture the cytochrome P450c17a (CYP17) mRNA expression level was detected using Real-time fluorescent quantitative PCR. Contents of androgen (testosterone) in the supernate were detected using RIA and optimal PD98059 concentration screened. After intervened by 10 micromol/L PD98059 for 24 h, the culture solution was intervened by effective ingredients of with or without YZD or YSYZ at various concentrations (0, 1 , 5, 25, 50 mg/mL) at various time points (3, 6, 18, 24 h). Expression levels of p-ERK1/2, c-Fos and CYP17 were detected by Western blot. Testosterone content in the supernate was determined by radioimmunoassay (RIA).</p><p><b>RESULTS</b>Ten pLmol/L PD98059 could obviously decrease p-ERK1/2 protein expression and increase CYP17 mRMA expression, and elevate testosterone content in the supernate (P < 0.05). ZDC and YSYZ at 25 ng/mL could increase p-ERK1/2 protein expression and c-Fos levels, and reduce CYP17 protein expression, and lower testosterone content in the supernate after 6-h intervention (P < 0.01).</p><p><b>CONCLUSION</b>Effective ingredients of YZD could reduce androgen production in porcine granulose cells through increasing activities of MAPK.</p>


Assuntos
Animais , Feminino , Androgênios , Medicamentos de Ervas Chinesas , Farmacologia , Flavonoides , Células da Granulosa , Metabolismo , Proteína Quinase 3 Ativada por Mitógeno , Metabolismo , Proteínas Quinases Ativadas por Mitógeno , Metabolismo , RNA Mensageiro , Suínos
2.
Chinese Journal of Integrated Traditional and Western Medicine ; (12): 312-316, 2014.
Artigo em Chinês | WPRIM | ID: wpr-312824

RESUMO

<p><b>OBJECTIVE</b>To observe the effect of Yangjing Zhongyu Decoction (YZD) on mRNA and protein expression of PCNA, StAR, and FSHR in ovarian granulose cells (GCs) cultured by excess androgen.</p><p><b>METHODS</b>Ovarian GCs from porcine follicles were isolated and cultured in vitro. Follicular stimulating hormone (FSH) or YZD was added in the GCs treated by excess testosterone propionate. Totally 48 h later mRNA and protein expression of PCNA, StAR, and FSHR were detected by RT-PCR and Western blot.</p><p><b>RESULTS</b>Excess androgen inhibited mRNA and protein expression of PCNA, StAR, and FSHR of GCs. FSH and YZD could antagonize inhibition of excess androgens, and promote mRNA and protein expression of PCNA, StAR, and FSHR in GCs.</p><p><b>CONCLUSION</b>YZD could antagonize the inhibition of excess androgen on mRNA and protein expression of PCNA, StAR and FSHR in GCs. Thus, we inferred that YZD could improve the follicle dysplasia by promoting mRNA and protein expression of PCNA, StAR and FSHR in GCs.</p>


Assuntos
Animais , Feminino , Androgênios , Farmacologia , Células Cultivadas , Medicamentos de Ervas Chinesas , Farmacologia , Hormônio Foliculoestimulante , Farmacologia , Células da Granulosa , Biologia Celular , Metabolismo , Proteínas de Membrana Transportadoras , Genética , Metabolismo , Folículo Ovariano , Biologia Celular , Antígeno Nuclear de Célula em Proliferação , Genética , Metabolismo , RNA Mensageiro , Genética , Receptores do FSH , Genética , Metabolismo , Suínos
3.
Chinese Acupuncture & Moxibustion ; (12): 192-194, 2010.
Artigo em Chinês | WPRIM | ID: wpr-285179

RESUMO

<p><b>OBJECTIVE</b>To observe the therapeutic effect of acupoint sticking of Wuzhuyu (Evodia Rutaecarpa) for treatment of bradycardia.</p><p><b>METHODS</b>Sixty cases were randomly divided into an observation group and a control group, 30 cases in each group. The observation group was treated with acupoint sticking of Wuzhugu (Evodia Rutaecarpa) at Neiguan (PC 6) and Xinshu (BL 15) once each day. The control group was treated with oral administration of Xinbao pills, 3 pills each time, thrice each day. The therapeutic effects and changes of 24 hours' holter were observed after 4 weeks.</p><p><b>RESULTS</b>After treatment, 24 hours' average heart rate was significantly improved in the two groups, with significant differences as compared with those before treatment (both P<0.01) and with no significant difference between the two groups (P>0.05). The total effective rate was 86.7% (26/30) in the observation group and 83.3% (25/30) in the control group, their therapeutic effect being similar.</p><p><b>CONCLUSION</b>Acupoint sticking of Wuzhugu (Evodia Rutaecarpa) can significantly raise the levels of 24 hours' average heart rate in the patients of bradycardia. This therapy and Xinbao pills have similar therapeutic effect on the improvement of clinical symptom and heart rate levels.</p>


Assuntos
Idoso , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Pontos de Acupuntura , Terapia por Acupuntura , Bradicardia , Terapêutica , Resultado do Tratamento
4.
Acta Academiae Medicinae Sinicae ; (6): 13-16, 2009.
Artigo em Chinês | WPRIM | ID: wpr-259086

RESUMO

<p><b>OBJECTIVE</b>To screen serum biomarkers in patients with mycosis fungoides (MF) using surface-enhanced laser desorption and ionization with time-of-flight detection mass spectrometry (SELDI-TOF-MS) technique.</p><p><b>METHODS</b>Serum was analyzed from 14 patients with MF and 17 controls using CM10 Protein-chip to capture serum proteins, followed by Biomarker Wizard software analysis.</p><p><b>RESULTS</b>In all specimens, about 131 protein peaks could be detected when the relative molecular weight ranged from 0 to 50 000. When comparing the protein fingerprint between these two groups, 14 differentially expressed protein peaks were found. By searching SWISS-PRO database, we found 7 670Da peaks accord with C-C motif chemokine 22.</p><p><b>CONCLUSION</b>SELDI-TOF-MS technique can be used for screening serum protein biomarkers in patients with MF.</p>


Assuntos
Humanos , Biomarcadores Tumorais , Sangue , Proteínas Sanguíneas , Micose Fungoide , Sangue , Espectrometria de Massas por Ionização e Dessorção a Laser Assistida por Matriz , Métodos
5.
Journal of Zhejiang University. Science. B ; (12): 286-290, 2008.
Artigo em Inglês | WPRIM | ID: wpr-277272

RESUMO

Serum samples from endometrial cancer (EC) patients and healthy females were analyzed using surface-enhanced laser desorption-ionization time-of-flight mass spectrometry (SELDI-TOF-MS) to discover the potential diagnostic biomarker for detection of EC. A preliminary training set of spectra derived from 40 EC patients and 30 healthy women were used to develop a proteomic model that effectively discriminated cancer patients from healthy women. The training set had a specificity of 100% and sensitivity of 92.5% in the EC detection. A blind test set, including 20 new cancer cases and 10 healthy women, was used to validate the sensitivity and specificity of this multivariate model, which had a corresponding results of 60% in specificity and 75% in sensitivity, respectively. The combination of SELDI-TOF-MS with bioinformatics tools could help find new biomarkers and establish the detection of EC with high sensitivity and specificity.


Assuntos
Feminino , Humanos , Biomarcadores Tumorais , Metabolismo , Estudos de Casos e Controles , Neoplasias do Endométrio , Diagnóstico , Metabolismo , Regulação Neoplásica da Expressão Gênica , Oncologia , Métodos , Modelos Biológicos , Proteínas de Neoplasias , Estadiamento de Neoplasias , Análise Serial de Proteínas , Proteômica , Métodos , Sensibilidade e Especificidade , Espectrometria de Massas por Ionização e Dessorção a Laser Assistida por Matriz , Métodos
6.
Chinese Journal of Oncology ; (12): 652-656, 2004.
Artigo em Chinês | WPRIM | ID: wpr-331239

RESUMO

<p><b>OBJECTIVE</b>Human selenoprotein P (HSelP) is unique protein that contains 10 selenocysteines encoded by 10 inframe UGA, which typically function as stop codon. The function of HSelP remains unclear, in part due to the inability to express it by gene recombinant technique. This study is to investigate expression and purification of recombinant HSelP in prokaryotic expression system, and its activity to induce apoptosis in vitro.</p><p><b>METHODS</b>The shorter HSelP isoform was cloned. After the selenocysteine (SeCys) at 40th position from N terminus of the HSelP shorter isoform was mutated into cysteine by PCR, it was expressed in E. coli. The expressed product was purified with DEAE column and identified by Western blot. Subsequently, its function on induction of mitochondrial apoptotic activity was studied.</p><p><b>RESULTS</b>The mutant HSelP shorter isoform expressed in prokaryotic system was purified by DEAE column to 90% homogeneity. The purified product, HSelP280m, induced the opening of mitochondrial permeability transition pore (PTP) and decreased the transmembrane potential in a dose-dependent manner. These events could be abolished by PTP specific inhibitors.</p><p><b>CONCLUSION</b>HSelP280m can induce the opening of mitochondrial PTP, which provides a basis for investigating the structure and function of recombinant HSelP.</p>


Assuntos
Animais , Humanos , Masculino , Camundongos , Apoptose , Clonagem Molecular , Cisteína , Genética , Escherichia coli , Metabolismo , Canais Iônicos , Potenciais da Membrana , Camundongos Endogâmicos BALB C , Mitocôndrias Hepáticas , Fisiologia , Proteínas de Transporte da Membrana Mitocondrial , Mutação , Isoformas de Proteínas , Proteínas , Genética , Metabolismo , Farmacologia , Selênio , Selenocisteína , Genética , Selenoproteína P , Selenoproteínas
7.
Chinese Journal of Obstetrics and Gynecology ; (12)2000.
Artigo em Chinês | WPRIM | ID: wpr-683526

RESUMO

Objective To analyze the alterations of serum protein fingerprint in patients with hypertensive disorder complicating pregnancy(HDCP),screen serum biomarker and establish a diagnostic model of HDCP.Methods Surface-enhanced laser desorption lionization-time of flight-mass spectrometry (SELDI-TOF-MS)technology was used to analyze serum including 25 cases of HDCP patients and 30 cases of age-,gravity-and parity-matched healthy term pregnant women on IMAC3-Cu proteinchip before delivery. Biomarker Wizard and Biomarker Pattern software was used to detect protein peaks significantly different between HDCP and controls,and establish a primary diagnostic model of HDCP.This model was further evaluated by blind test using other 16 parts of serum protein fingerprint.Results Ten protein peaks were significantly different at the molecular range of 2000-50 000(P

SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA