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Chinese Journal of Natural Medicines (English Ed.) ; (6): 186-193, 2014.
Artigo em Inglês | WPRIM | ID: wpr-812288

RESUMO

AIM@#To evaluate the anti-HIV activity and mechanism of action of wikstroelide M, a daphnane diterpene from Daphne acutiloba Rehder (Thymelaeaceae).@*METHODS@#The anti-HIV activities of wikstroelide M against different HIV strains were evaluated by cytopathic effect assay and p24 quantification assay with ELISA. The inhibitory effect of wikstroelide M on HIV reverse transcription was analyzed by real-time PCR and ELISA. The effect of wikstroelide M on HIV-1 integrase nuclear translocation was observed with a cell-based imaging assay. The effect of wikstroelide M on LEDGF/p75-IN interaction was assayed by molecular docking.@*RESULTS@#Wikstroelide M potently inhibited different HIV-1 strains, including HIV-1IIIB, HIV-1A17, and HIV-19495, induced a cytopathic effect, with EC50 values ranging from 3.81 to 15.65 ng·mL⁻¹. Wikstroelide M also had high inhibitory activities against HIV-2ROD and HIV-2CBL-20-induced cytopathic effects with EC50 values of 18.88 and 31.90 ng·mL⁻¹. The inhibitory activities of wikstroelide M on the three HIV-1 strains were further confirmed by p24 quantification assay, with EC50 values ranging from 15.16 to 35.57 ng·mL⁻¹. Wikstroelide M also potently inhibited HIV-1IIIB induced cytolysis in MT-4 cells, with an EC50 value of 9.60 ng·mL⁻¹. The mechanistic assay showed that wikstroelide M targeted HIV-1 reverse transcriptase and nuclear translocation of integrase through disrupting the interaction between integrase and LEDGF/p75.@*CONCLUSION@#Wikstroelide M may be a potent HIV-1 and HIV-2 inhibitor, the mechanisms of action may include inhibition of reverse trascriptase activity and inhibition of integrase nuclear translocation through disrupting the interaction between integrase and LEDGF/p75.


Assuntos
Humanos , Fármacos Anti-HIV , Farmacologia , Usos Terapêuticos , Linhagem Celular , Daphne , Química , Diterpenos , Farmacologia , Infecções por HIV , Tratamento Farmacológico , Virologia , Integrase de HIV , Metabolismo , Inibidores de Integrase de HIV , Farmacologia , Usos Terapêuticos , Transcriptase Reversa do HIV , HIV-1 , HIV-2 , Peptídeos e Proteínas de Sinalização Intercelular , Metabolismo , Fitoterapia , Extratos Vegetais , Farmacologia , Usos Terapêuticos , Integração Viral , Replicação Viral
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