Se. File et al., Bimodal modulation by nicotine of anxiety in the social interaction test: Role of the dorsal hippocampus, BEHAV NEURO, 112(6), 1998, pp. 1423-1429
In conditions generating moderate levels of anxiety in the social interacti
on test (low Light, unfamiliar arena or high light, familiar arena), parent
eral administration of nicotine had bimodal actions, low doses (0.01 and 0.
1 mg/kg ip) had anxiolytic effects and high doses (0.5 and 1.0 mg/kg ip) ha
d anxiogenic effects. In test conditions where anxiety was lowest (low ligh
t, familiar arena) and highest (high light, unfamiliar arena), nicotine was
without effect after intraperitoneal or hippocampal administration. Thus,
nicotine plays a modulatory role in which the activity of other neurotransm
itters is crucial to its expression. After bilateral administration to the
dorsal hippocampus, nicotine (0.1-8.0 mu g) had anxiogenic effects in condi
tions of moderate anxiety; mecamylamine (30 ng) was silent in these conditi
ons, indicating no intrinsic tone. Our results show that the dorsal hippoca
mpus is one area that can mediate anxiogenic effects in the social interact
ion test, but the brain region mediating anxiolytic effects remains to be i
dentified.