The aim was to evaluate the effects of calphostin C (CC), a protein ki
nase C inhibitor, on lytic herpes simplex virus-type 1 infection of cu
ltured rat astrocytes. At 24 h postinjection, the cell culture receivi
ng CC treatment at 50 nM concentration showed decreased cell. detachme
nt and retraction versus untreated infected controls; likewise, the in
fective virus yield was significantly lower in a dose-dependent manner
. In contrast, image analysis failed to disclose differences in viral
antigen immunolabeling at low drug concentrations, thus suggesting tha
t CC-induced inhibition of cytopathic effects and infectivity takes pl
ace through mechanisms not involving viral protein synthesis. Given th
e low dose required and the apparent lack of cytotoxic effects, presen
t findings encourage additional studies on CC antiviral potential in t
he whole organism.