Hara A, Niwa M, Nakashima M, Iwai T, Uematsu T, Yoshimi N, Mori H
Department of Pathology, Gifu University School of Medicine, Japan.
J Cereb Blood Flow Metab. 1998 Aug;18(8):819-23. doi: 10.1097/00004647-199808000-00001.
Delayed neuronal death in the gerbil hippocampal CA1 sector occurs 48 to 72 hours after severe forebrain ischemia. DNA fragmentation is observed in the hippocampal CA1 neurons at around that time. We show here that an inhibitor of proteolytic process of apoptosis, N-tosyl-L-phenylalanyl chloromethyl ketone (TPCK), protected hippocampal neuronal damage by inhibition of the DNA fragmentation in a dose-dependent manner and that TPCK induced an apoptosis-regulating molecule, Bcl-2 protein, in the surviving neurons. These results suggest the prevention of apoptosis-related DNA fragmentation by TPCK may be an attractive therapeutic strategy for preserving hippocampal neurons from ischemic insult.
