Masiello P, Cubeddu T L, Frosina G, Bergamini E
Diabetologia. 1985 Sep;28(9):683-6. doi: 10.1007/BF00291976.
The addition of 3-aminobenzamide (a potent inhibitor of poly(ADP-ribose)synthetase) into the incubation medium, prevents streptozotocin-induced inhibition of glucose-stimulated insulin release from isolated islets [control 142 +/- 14 microU X islet-1 X h-1; streptozotocin (0.5 mg/ml) 31 +/- 8; 3-aminobenzamide (1.0 mg/ml) 96 +/- 11; streptozotocin plus 3-aminobenzamide 122 +/- 19]. In vivo, intraperitoneal 3-aminobenzamide 300 mg/kg body weight prevents the appearance of overt diabetes in streptozotocin-treated rats. These protective effects of 3-aminobenzamide are dose-dependent and are similar to those exerted by nicotinamide. Taking into account that poly ADP-ribosylation is involved in the repair of damaged DNA, the protection exerted by 3-aminobenzamide against the diabetogenic effect of streptozotocin strongly supports the view that this acute effect may be a major consequence of the activation of DNA repair mechanisms in islet cells.
在孵育培养基中添加3-氨基苯甲酰胺(一种聚(ADP-核糖)合成酶的有效抑制剂),可防止链脲佐菌素诱导的离体胰岛中葡萄糖刺激的胰岛素释放受到抑制[对照组142±14微单位×胰岛⁻¹×小时⁻¹;链脲佐菌素(0.5毫克/毫升)31±8;3-氨基苯甲酰胺(1.0毫克/毫升)96±11;链脲佐菌素加3-氨基苯甲酰胺122±19]。在体内,腹腔注射3-氨基苯甲酰胺300毫克/千克体重可防止链脲佐菌素处理的大鼠出现明显的糖尿病。3-氨基苯甲酰胺的这些保护作用具有剂量依赖性,且与烟酰胺的作用相似。鉴于多聚ADP-核糖基化参与受损DNA的修复,3-氨基苯甲酰胺对链脲佐菌素致糖尿病作用的保护作用有力地支持了这样一种观点,即这种急性效应可能是胰岛细胞中DNA修复机制激活的主要后果。