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The Effect of A Potent Calcium Channel Blocker, Nifedipine, on the Castration-induced Apoptosis of the Rat Ventral Prostate / 대한비뇨기과학회지
Korean Journal of Urology ; : 905-911, 1997.
Artigo em Coreano | WPRIM | ID: wpr-88275
ABSTRACT
The rapid involution of the rat ventral prostate after castration is an active process initiated by removal of the inhibitory effects of androgen on prostatic cell death. The degradation of genomic DNA into nucleosomal-sized fragments if an early event in this process and is catalyzed by Ca2+Mg2+-dependent endonuclease activity which is dependent upon calcium ions. The morphologic correlation of the involution process involves a series of structural changes which are collectively referred to as apoptosis. Since the castration-induced endonuclease is dependent upon calcium ions for maximal activity, a potential involvement of a intracellular calcium in the castration-induced prostatic cell death was investigated. Acute disturbance in intracellular calcium homeostasis within the ventral prostate by means of a potent calcium channel blocker, nifedipine, simultaneous with castration resulted in a significant decrease in prostatic apoptosis. This result points to a potential role intracellular calcium levels in the mechanism of activation of castration-induced death of the androgen-dependent epithelial cells in the ventral prostate.
Assuntos

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Próstata / DNA / Nifedipino / Canais de Cálcio / Castração / Cálcio / Morte Celular / Apoptose / Desoxirribonuclease I / Células Epiteliais Limite: Animais Idioma: Coreano Revista: Korean Journal of Urology Ano de publicação: 1997 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Próstata / DNA / Nifedipino / Canais de Cálcio / Castração / Cálcio / Morte Celular / Apoptose / Desoxirribonuclease I / Células Epiteliais Limite: Animais Idioma: Coreano Revista: Korean Journal of Urology Ano de publicação: 1997 Tipo de documento: Artigo