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Biol. Res ; 47: 1-11, 2014. graf, tab
Artículo en Inglés | LILACS | ID: biblio-950746

RESUMEN

BACKGROUND: Accumulating evidence indicates that reactive oxygen species (ROS) are an important etiological factor for the induction of dermal papilla cell senescence and hair loss, which is also known alopecia. Arctiin is an active lignin isolated from Arctium lappa and has anti-inflammation, anti-microbial, and anti-carcinogenic effects. In the present study, we found that arctiin exerts anti-oxidative effects on human hair dermal papilla cells (HHDPCs). RESULTS: To better understand the mechanism, we analyzed the level of hydrogen peroxide (H2O2)-induced cytotoxicity, cell death, ROS production and senescence after arctiin pretreatment of HHDPCs. The results showed that arctiin pretreatment significantly inhibited the H2O2-induced reduction in cell viability. Moreover, H2O2-induced sub-G1 phase accumulation and G2 cell cycle arrest were also downregulated by arctiin pretreatment. Interestingly, the increase in intracellular ROS mediated by H2O2 was drastically decreased in HHDPCs cultured in the presence of arctiin. This effect was confirmed by senescence associated-beta galactosidase (SA-ß-gal) assay results; we found that arctiin pretreatment impaired H2O2-induced senescence in HHDPCs. Using microRNA (miRNA) microarray and bioinformatic analysis, we showed that this anti-oxidative effect of arctiin in HHDPCs was related with mitogen-activated protein kinase (MAPK) and Wnt signaling pathways. CONCLUSIONS: Taken together, our data suggest that arctiin has a protective effect on ROS-induced cell dysfunction in HHDPCs and may therefore be useful for alopecia prevention and treatment strategies.


Asunto(s)
Humanos , Envejecimiento/metabolismo , Especies Reactivas de Oxígeno/antagonistas & inhibidores , Folículo Piloso/efectos de los fármacos , MicroARNs/metabolismo , Furanos/farmacología , Glucósidos/farmacología , Envejecimiento/efectos de los fármacos , Regulación hacia Abajo/efectos de los fármacos , Regulación hacia Arriba/efectos de los fármacos , Línea Celular , Supervivencia Celular/efectos de los fármacos , Muerte Celular/efectos de los fármacos , beta-Galactosidasa/análisis , Folículo Piloso/citología , Folículo Piloso/metabolismo , Dermis/citología , Dermis/efectos de los fármacos , Dermis/metabolismo , Análisis de Secuencia por Matrices de Oligonucleótidos , MicroARNs/efectos de los fármacos , Puntos de Control del Ciclo Celular/efectos de los fármacos , Peróxido de Hidrógeno/farmacología
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