Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 6 de 6
Filtrar
Adicionar filtros








Intervalo de ano
1.
Journal of Peking University(Health Sciences) ; (6): 865-870, 2021.
Artigo em Chinês | WPRIM | ID: wpr-942266

RESUMO

OBJECTIVE@#To explore the stress distribution characteristics of the graft after anterior cruciate ligament (ACL) reconstruction, so as to provide theoretical reference for the surgical plan of ACL reconstruction.@*METHODS@#Based on 3D MRI and CT images, finite element models of the uninjured knee joint and knee joint after ACL reconstruction were established in this study. The uninjured knee model included femur, tibia, fibula, medial collateral ligament, lateral collateral ligament, ACL and posterior cruciate ligament. The ACL reconstruction knee model included femur, tibia, fibula, medial collateral ligament, lateral collateral ligament, ACL graft and posterior cruciate ligament. Linear elastic material properties were used for both the uninjured and ACL reconstruction models. The elastic modulus of bone tissue was set as 17 GPa and Poisson' s ratio was 0.36. The material properties of ligament tissue and graft were set as elastic modulus 390 MPa and Poisson's ratio 0.4. The femur was fixed as the boundary condition, and the tibia anterior tension of 134 N was applied as the loading condition. The stress states of the ACL of the intact joint and the ACL graft after reconstruction were solved and analyzed, including tension, pressure, shear force and von Mises stress.@*RESULTS@#The maximum compressive stress (6.34 MPa), von Mises stress (5.9 MPa) and shear stress (1.83 MPa) of the reconstructed ACL graft were all at the anterior femoral end. It was consistent with the position of maximum compressive stress (8.77 MPa), von Mises stress (8.88 MPa) and shear stress (3.44 MPa) in the ACL of the intact knee joint. The maximum tensile stress of the graft also appeared at the femoral end, but at the posterior side, which was consistent with the position of the maximum tensile stress of ACL of the uninjured knee joint. More-over, the maximum tensile stress of the graft was only 0.88 MPa, which was less than 2.56 MPa of ACL of the uninjured knee joint.@*CONCLUSION@#The maximum compressive stress, von Mises stress and shear stress of the ACL graft are located in the anterior femoral end, and the maximum tensile stress is located in the posterior femoral end, which is consistent with the position of the maximum tensile stress of the ACL of the uninjured knee joint. The anterior part of ACL and the graft bore higher stresses than the posterior part, which is consistent with the biomechanical characteristics of ACL.


Assuntos
Humanos , Lesões do Ligamento Cruzado Anterior/cirurgia , Reconstrução do Ligamento Cruzado Anterior , Fenômenos Biomecânicos , Fêmur/cirurgia , Análise de Elementos Finitos , Articulação do Joelho/cirurgia , Tíbia/cirurgia
2.
Acta Pharmaceutica Sinica ; (12): 1159-1163, 2012.
Artigo em Chinês | WPRIM | ID: wpr-274683

RESUMO

Influenza virus RNA-dependent RNA polymerase (RdRP) is essential for replication and expression of influenza virus genome. Viral genomic sequences encoding RdRP are highly conservative, thus making it a potential anti-influenza drug target. A cell-based influenza RdRP inhibitor screening assay was established by a luciferase reporter system to analyze the activity of RdRP. Specificity study and statistic analysis showed that the screening assay is sensitive and reproducible.


Assuntos
Humanos , Amantadina , Farmacologia , Antivirais , Farmacologia , Avaliação Pré-Clínica de Medicamentos , Métodos , Genes Reporter , Células HEK293 , Alphainfluenzavirus , Luciferases , Genética , Metabolismo , Oseltamivir , Farmacologia , Plasmídeos , RNA Polimerase Dependente de RNA , Metabolismo , Reprodutibilidade dos Testes , Ribavirina , Farmacologia , Sensibilidade e Especificidade , Transfecção , Zanamivir , Farmacologia
3.
Acta Pharmaceutica Sinica ; (12): 377-382, 2011.
Artigo em Chinês | WPRIM | ID: wpr-348945

RESUMO

With the emergence of drug resistant tuberculosis, it is very urgent to find novel anti-tuberculosis drugs, especially novel anti-drug-resistant tuberculosis drugs. Because of the slow growth and the need to work in a biosafty environment of Mycobacterium tuberculosis, the development of evaluation of drug effect is severely impeded. In order to solve these issues, non-pathogenic fast-growing Mycobacterium smegmatis is introduced as test organism. The inhA is one of a target of isoniazid (INH) overexpression or mutation of this gene in Mycobacterium tuberculosis conferring resistant to INH. A recombinant plasmid bearing inhA was constructed and electroporated into Mycobacterium smegmatis, using shuttle expression vector pMV261. Transformants were induced to express a protein of inhA, identified by SDS-PAGE. Results show that Mycobacterium smegmatis containing inhA plasmids exhibited 100-fold or greater increased resistance to INH, but it conferred no increased resistance to others first-line anti-tuberculosis drugs. Resazurin microtiter assay plate testing of Mycobacterium smegmatis susceptibility to drugs is a rapid, simple, and inexpensive method and could decrease color background of drugs by detecting fluorescence. It will be benefit for high-throughout screening of drugs of anti-isoniazid-resistant Mycobacteria.


Assuntos
Antibacterianos , Farmacologia , Antibióticos Antituberculose , Farmacologia , Antituberculosos , Farmacologia , Proteínas de Bactérias , Genética , Metabolismo , Farmacorresistência Bacteriana , Eletroporação , Etambutol , Farmacologia , Isoniazida , Farmacologia , Testes de Sensibilidade Microbiana , Mycobacterium smegmatis , Genética , Metabolismo , Oxirredutases , Genética , Metabolismo , Plasmídeos , Rifampina , Farmacologia , Estreptomicina , Farmacologia
4.
Acta Pharmaceutica Sinica ; (12): 247-252, 2010.
Artigo em Chinês | WPRIM | ID: wpr-250635

RESUMO

Strict regulation of HIV-1 PR function is critical for efficient production of mature viral particles. During viral protein expression and viral assembly, HIV-1 PR located within Gag-Pol precursor must be inactive to prevent premature cytoplasmic processing of the viral Gag and Gag-Pol precursors. Premature activation of HIV-1 precursors leads to major defects in viral assembly and production of viral particles. A cell-level premature activation of HIV-1 precursors assay using bioluminescence resonance energy transfer (BRET) was established. Three thousand compounds were screened to evaluate this assay. The results showed that the assay is sensitive, specific and stable (Z' factor is 0.905).


Assuntos
Humanos , Fármacos Anti-HIV , Farmacologia , Benzoxazinas , Farmacologia , Técnicas de Transferência de Energia por Ressonância de Bioluminescência , Métodos , Proteínas de Fusão gag-pol , Genética , Metabolismo , Células HEK293 , Protease de HIV , Metabolismo , Fisiologia , HIV-1 , Ensaios de Triagem em Larga Escala , Métodos , Plasmídeos , Genética , Precursores de Proteínas , Metabolismo , Fisiologia , Piridazinas , Farmacologia , Transfecção , Vírion , Montagem de Vírus , Produtos do Gene gag do Vírus da Imunodeficiência Humana , Genética , Metabolismo
5.
Acta Pharmaceutica Sinica ; (12): 257-262, 2010.
Artigo em Chinês | WPRIM | ID: wpr-250633

RESUMO

The HIV-1 Rev protein facilitates nuclear export of unspliced and singly spliced viral transcripts containing RRE RNA through the CRM1 export pathway. Inhibition of Rev-mediated RNA nuclear export can arrest HIV-1 transcriptional process, which clearly, reveals a target for anti-HIV drug development. In this work, a cell-based assay has been established for screening anti-HIV compounds targeting the Rev-mediated RNA nuclear export. This assay utilized a codon-optimized green fluorescent protein (GFP) as reporter gene, which expression is in a Rev-dependent manner. Any compound that inhibits the Rev-mediated RNA nuclear export is identified by reducing emission of GFP. The Z' score of this model is 0.8220. Three thousands compounds were screened and the positive rate was 9.3% with a cutoff at 50% inhibition. IMB7C7, one of the positive compounds, efficiently inhibits viral production from HIV-1 infected cells.


Assuntos
Humanos , Transporte Ativo do Núcleo Celular , Fármacos Anti-HIV , Farmacologia , Núcleo Celular , Metabolismo , Códon , Ácidos Graxos Insaturados , Farmacologia , Genes Reporter , Proteínas de Fluorescência Verde , Genética , Metabolismo , Células HEK293 , HIV-1 , Genética , Ensaios de Triagem em Larga Escala , Carioferinas , Genética , Metabolismo , RNA Viral , Receptores Citoplasmáticos e Nucleares , Genética , Metabolismo , Transfecção , Replicação Viral , Produtos do Gene rev do Vírus da Imunodeficiência Humana , Genética , Metabolismo
6.
China Biotechnology ; (12)2006.
Artigo em Chinês | WPRIM | ID: wpr-686253

RESUMO

Objective:Osteoprotegerin (OPG) is a key molecule negatively regulating osteoclast differentiation and activation; and the conserved mycobacterial heat shock 70 (HSP70) peptide p111-125 has also been found to inhibit inflammation reactions in chronic arthritis. BaculoDirectTM baculovirus expression system was selected to express recombinant OPG-HSP70 in insect cells.Methods:The human functional fragment (p22-194) of OPG and functional fragment (p111-125) of mycobacterial HSP70 gene were cloned into the transfer vector pENTRTM/SD/D-TOPO. The recombinant plasmid was performed an LR reaction with the BaculoDirectTM Linear DNA to generate recombinant baculovirus DNA. The cultured Sf9 insect cells were directly transferred with the recombinant baculovirus DNA,and the pure recombinant baculovirus was obtained. Then recombinant baculovirus was infected Sf9 insect cells again to express the OPG-HSP70 gene.Results:The target protein was detected at the time of 48h post infection,reached at highest yield at the time of 72h post-infection. A 28kDa protein immunostaining band was detected by Western blotting from lysate of those cells.And the purified protein was obtained by using Ni-NTA system. Functional stuies on the fusion protein showed it significantly reduce osteoclast cell number[(3.10?0.640) cells under each microscope field in treatment group by comparing to (10.70?0.817)cells in the control group] in the osteoclast inhibition test,and reduce the inflammation reaction in a delayed type hypersensitivity (DTH) mice model (P

SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA