8-Hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT)-induced temperature reduction, lower lip retraction and tail flick responses are widely used models of 5-HT1A receptor function. To obtain information about the sites of receptors mediating these effects we measured these responses, parallel over wide dose ranges after intracerebroventricular (i.c.v., 0.6-67 mu g/kg) and intravenous (i.v., 3-500 mu g/kg) administration. Analysis of the dose-response curves provided evidence for a 9.8-fold ratio of the potency of 8-OH-DPAT following i.c.v. compared to i.v. administration on body temperature reduction (ED(50) values are 5.1 and 50 mu g/kg, after i.c.v. and i.v. administration, respectively) and a 2.9-fold ratio in potency for lower lip retraction (ED(50) values are 29 and 86 mu g/kg, after i.c.v. and i.v. administration, respectively). 8-OH-DPAT was less potent in the induction of tail flicks than of the other responses and had a lower potency after i.c.v. than after i.v. administration (ED(50) values, the first one extrapolated, are 526 and 246 mu g/kg, after i.c.v. and i.v. administration, respectively). In addition, the i.c.v. ED(50) for temperature reduction was significantly lower than those for lower lip retraction or tail flick responses. The relative potency, that is, the ratio of i.v. and i.c.v. ED(50) was significantly higher for temperature reduction than for lower lip retraction or tail flick responses (ED(50) i.v./ED(50) i.c.v. values are 9.8, 2.9, and 0.47, respectively). These data provide evidence that distinct sites of action are involved in these models. Temperature reduction is mediated mainly by postsynaptic receptors in the close vicinity of the lateral ventricle. Receptors that mediate lower lip retraction are located more distantly in the brain, supporting previous evidence that they are somatodendritic autoreceptors, and receptors in the spinal cord are probably responsible for tail flick responses. (C) 1997 Elsevier Science B.V.