In the present study we identified the degeneration and apoptotic cell deat
h in rat brain after deltamethrin treatment. By hematoxylin-eosin (H&E) sta
ining, a large number of degenerative cells (pyknosis of nuclei, disruption
of eosinophilic cytoplasm) were seen in the hippocampus and cortex at 24 a
nd 48 h after deltamethrin treatment at a dose of 12.5 mg/kg (i.p.) in corn
oil. The similar morphological changes of degenerative cells were observed
by cresyl violet staining. Numerous apoptotic cells were detected by in si
tu end labeling (ISEL) and flow cytometric analysis in the hippocampus and
cortex at 24 and 48 h following deltamethrin treatment at the same dose, wh
ereas no ISEL-positive cells were seen in the same brain regions of control
rats. Moreover, using DNA gel electrophoresis, it was demonstrated that DN
A fragmentation was markedly induced in the hippocampus and cortex at 24, 4
8 and 72 h after treatment. In addition, the protein synthesis inhibitor cy
cloheximide inhibited the DNA fragmentation elicited by deltamethrin in rat
brain. These results indicate that deltamethrin induces degeneration and a
poptotic cell death in rat brain, suggesting an important role played by ap
optosis in neurotoxicity of deltamethrin. (C) 2000 Elsevier Science ireland
Ltd. All rights reserved.