TY - JOUR
T1 - Protection by picolinamide, a novel inhibitor of poly (ADP-ribose) synthetase, against both streptozotocin-induced depression of proinsulin synthesis and reduction of NAD content in pancreatic islets
AU - Yamamoto, Hiroshi
AU - Okamoto, Hiroshi
N1 - Funding Information:
* This work has been supported in part by Grants-in-Aid for Cancer Research and for Scientific Research from the Ministry of Education, Science and Culture, Japan.
PY - 1980
Y1 - 1980
N2 - Picolinamide, 2-pyridinecarboxylic acid amide, was found to be a strong inhibitor of poly (ADP-ribose) synthetase of nuclei from rat pancreatic islet cells. Another experiment using isolated pancreatic islets of rats showed that picolinamide protects against streptozotocin-induced depression of proinsulin synthesis as well as against streptozotocin-induced reduction of NAD content. The protection by picolinamide against the NAD depression was considered to be due to the blockage of an increased degradation of NAD mediated by a streptozotocin-induced increase in poly (ADP-ribose) synthetase activity. A possible mechanism of streptozotocin diabetes and its prevention is discussed.
AB - Picolinamide, 2-pyridinecarboxylic acid amide, was found to be a strong inhibitor of poly (ADP-ribose) synthetase of nuclei from rat pancreatic islet cells. Another experiment using isolated pancreatic islets of rats showed that picolinamide protects against streptozotocin-induced depression of proinsulin synthesis as well as against streptozotocin-induced reduction of NAD content. The protection by picolinamide against the NAD depression was considered to be due to the blockage of an increased degradation of NAD mediated by a streptozotocin-induced increase in poly (ADP-ribose) synthetase activity. A possible mechanism of streptozotocin diabetes and its prevention is discussed.
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U2 - 10.1016/0006-291X(80)90762-7
DO - 10.1016/0006-291X(80)90762-7
M3 - Article
C2 - 6251809
AN - SCOPUS:0019310901
VL - 95
SP - 474
EP - 481
JO - Topics in Catalysis
JF - Topics in Catalysis
IS - 1
ER -