Intracerebroventricular administration of the angiotensin AT-2 recepto
r antagonist, PD 123319, inhibited drinking induced in rats by hyperto
nic NaCl, carbachol, isoproterenol, hypovolemia, and water deprivation
, but had no effect on food intake. In contrast. the AT-1 antagonist,
losartan potassium. had no effect on these intakes. A model of thirst
is presented that incorporates an AT-2 receptor in a final common path
way for drinking.