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1.
Planta Med ; 81(10): 804-12, 2015 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-26039262

RESUMEN

Understanding the molecular mechanism of action of traditional medicines is an important step towards developing marketable drugs from them. Piperine, an active constituent present in the Piper species, is used extensively in Ayurvedic medicines (practiced on the Indian subcontinent). Among others, piperine is known to possess a male contraceptive effect; however, the molecular mechanism of action for this effect is not very clear. In this regard, detailed docking and molecular dynamics simulation studies of piperine with the androgen-binding protein and androgen receptors were carried out. Androgen receptors control male sexual behavior and fertility, while the androgen-binding protein binds testosterone and maintains its concentration at optimal levels to stimulate spermatogenesis in the testis. It was found that piperine docks to the androgen-binding protein, similar to dihydrotestosterone, and to androgen receptors, similar to cyproterone acetate (antagonist). Also, the piperine-androgen-binding protein and piperine-androgen receptors interactions were found to be stable throughout 30 ns of molecular dynamics simulation. Further, two independent simulations for 10 ns each also confirmed the stability of these interactions. Detailed analysis of the piperine-androgen-binding protein interactions shows that piperine interacts with Ser42 of the androgen-binding protein and could block the binding with its natural ligands dihydrotestosterone/testosterone. Moreover, piperine interacts with Thr577 of the androgen receptors in a manner similar to the antagonist cyproterone acetate. Based on the in silico results, piperine was tested in the MDA-kb2 cell line using the luciferase reporter gene assay and was found to antagonize the effect of dihydrotestosterone at nanomolar concentrations. Further detailed biochemical experiments could help to develop piperine as an effective male contraceptive agent in the future.


Asunto(s)
Alcaloides/química , Alcaloides/farmacología , Proteína de Unión a Andrógenos/metabolismo , Benzodioxoles/química , Benzodioxoles/farmacología , Anticonceptivos Masculinos/farmacología , Piperidinas/química , Piperidinas/farmacología , Alcamidas Poliinsaturadas/química , Alcamidas Poliinsaturadas/farmacología , Receptores Androgénicos/metabolismo , Alcaloides/metabolismo , Proteína de Unión a Andrógenos/química , Benzodioxoles/metabolismo , Dominio Catalítico , Línea Celular/efectos de los fármacos , Simulación por Computador , Anticonceptivos Masculinos/química , Dihidrotestosterona/farmacología , Humanos , Enlace de Hidrógeno , Masculino , Metribolona/química , Metribolona/metabolismo , Metribolona/farmacología , Simulación del Acoplamiento Molecular , Simulación de Dinámica Molecular , Piperidinas/metabolismo , Alcamidas Poliinsaturadas/metabolismo , Conformación Proteica , Receptores Androgénicos/química , Serina/metabolismo
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