Cargando…

Preventive Effect of 3‐Aminobenzamide on the Reduction of NAD Levels in Rat Liver Following Administration of Diethylnitrosamine

Nicotinamide adenine dinucleotide is utilized as the substrate of a chromatin‐bound enzyme, poly(ADP‐ribose) polymerase. The effects of diethylnitrosamine and/or 3‐aminobenzamide, a potent inhibitor of poly(ADP‐ribose) polymerase, on the cellular NAD levels in rat liver were investigated. 3‐Aminoben...

Descripción completa

Detalles Bibliográficos
Autores principales: Uchida, Kazuhiko, Takahashi, Seiichi, Fujiwara, Kunio, Ueda, Kunihiro, Nakae, Dai, Emi, Yohko, Tsutsumi, Masahiro, Shiraiwa, Kazumi, Ohnishi, Takeo, Konishi, Yoichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1988
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5917636/
https://www.ncbi.nlm.nih.gov/pubmed/3143698
http://dx.doi.org/10.1111/j.1349-7006.1988.tb01532.x
Descripción
Sumario:Nicotinamide adenine dinucleotide is utilized as the substrate of a chromatin‐bound enzyme, poly(ADP‐ribose) polymerase. The effects of diethylnitrosamine and/or 3‐aminobenzamide, a potent inhibitor of poly(ADP‐ribose) polymerase, on the cellular NAD levels in rat liver were investigated. 3‐Aminobenzamide (600 mg/kg) administered intraperitoneally was not detectable in the liver within 12 hr after administration; the inhibitor had a calculated half life of 90 min. Diethylnitrosamine reduced the NAD levels in rat liver in a dose‐dependent way. The NAD content reached a minimum level at 8 hr, returning to 78% of the control value after 48 hr. The reduction of the NAD levels caused by diethylnitrosamine was completely prevented when 3‐aminobenzamide was administered either simultaneously with diethylnitrosamine or 4 hr after diethylnitrosamine treatment. Furthermore, an immunohistochemical study showed that nuclear poly(ADP‐ribose) decreased 1 hr after the administration of 3‐aminobenzamide. These results suggest that inhibition of poly(ADF‐ribosyl)ation is involved in the initiation of liver carcinogenesis by diethylnitrosamine and 3‐aminobenzamide.