Arginine vasopressin (AVP) or its VI receptor antagonist d(CH2)(5)Tyr(
Me)AVP was administered directly into the septal brain area of adult m
ale rats by means of inverse microdialysis. Immediately after a 30-min
dialysis period, during which either approximately 0.25 ng AVP or 5 n
g of the V1 antagonist were delivered into the brain tissue, anxiety-r
elated behaviour of the animals was measured on an elevated plus-maze
apparatus. While synthetic AVP failed to alter plus-maze behaviour com
pared to vehicle-treated controls, animals treated with the V1 recepto
r antagonist made more entries into (P < 0.01) and spent more time on
the open arms (P < 0.05), indicating reduced anxiety. Since administra
tion of neither AVP nor the VI antagonist significantly influenced gen
eral locomotor activity of the rats on the plus-maze and in an open he
ld, these data point towards a critical involvement of intraseptally r
eleased AVP in the emotional evaluation of novel situations.