Inositol, a precursor for membrane phosphoinositides involved in signal tra
nsduction, has been found to be clinically effective in a number of psychia
tric disorders and to reverse behavioural effects of lithium. To gain insig
ht into the mechanism of action of inositol, it is critical to establish it
s efficacy in animal models. Following the initial report by Cohen et al. (
1997b) that inositol was anxiolytic in the elevated plus maze model of anxi
ety, the effect of chronic intraperitoneal and chronic dietary inositol adm
inistration in rats was tested in four experiments. There was a significant
increase in closed arm and total arm entries following chronic injection o
f inositol, but no effect of inositol when it was given chronically in rat
chow.
Because the first 2 experiments suggested that the mode of drug administrat
ion affected the control levels of anxiety (open arm entries and time in op
en arms) in control groups, the effect of chronic dietary inositol was test
ed in rats that were exposed to a mild and a more severe form of stress. Ch
ronic saline injections elevated anxiety in the plus maze, which was only m
arginally affected by chronic dietary inositol. Following 3 weeks administr
ation of 5% dietary inositol rats were pre-exposed to a cat. There was a cl
ear increase in number of entries into open arms, suggesting an anxiolytic
effect of inositol.