Ginkgolic acid conjugates (GAC) (6-alkylsalicylates, namely n-tridecyl
-, n-pentadecyl-, n-heptadecyl-, n-pentadecenyl- and n-heptadecenylsal
icylates) isolated from the leaves of Indian Ginkgo biloba Linn., (IGb
) were tested for their putative role in anxiety in rats. Elevated plu
s maze, open-field behaviour, novelty-induced feeding latency and soci
al interaction were the rodent behavioural models used in this study.
GAC (0.3 and 0.6 mg/kg, each, PO) on single acute administration, show
ed dose-related changes in the behaviour. GAC (0.6 mg/kg) and DZ augme
nted open arm entries, the open arm/closed arm entries ratio and incre
ased time spent in the open arm on the elevated plus maze. In the open
field, GAC (0.6 mg/kg) and DZ significantly increased ambulation and
reduced the immobility time. EGb 761 showed a similar profile. GAC (0.
6 mg/kg) and DZ significantly attenuated the increased latency to feed
in novel environment. By contrast, EGb 761 and Ginkocer further augme
nted feeding latency. None of the drugs tested showed any significant
effect in the social interaction test. GAC showed consistent and signi
ficant anxiolytic activity in all the variables investigated. By contr
ast, EGb 761 and Ginkocer, which are devoid of GAC, did not evoke sign
ificant activity. However, increased rearing and decreased immobility
time only in open field behaviour shown by EGb 761 may be due to some
antianxiety activity of a lesser degree. Our observations suggest that
GAC may be the active constituents of Ginkgo biloba responsible for t
he anxiolytic activity.