1 Regional haemodynamic responses to the cannabinoid agonist, WIN 55212-2 (5 ± 250 mg kg 71 i.v.) were assessed in conscious, normotensive, Hannover, Sprague-Dawley (HSD) rats, and in hypertensive, transgenic ((mRen-2)27) (abbreviated to TG) rats. 2 In HSD rats, WIN 55212-2 caused pressor, and renal and mesenteric vasoconstrictor eects, with a hindquarters vasodilator eect occurring only at the highest dose. In TG rats, the eects of the cannabinoid agonist were qualitatively similar to those seen in HSD rats, except there was no hindquarters vasodilatation. 3 In both strains of rat, in the presence of losartan, pentolinium and a vasopressin (V 1 -receptor) antagonist, the pressor and vasoconstrictor eects of WIN 55212-2 were abolished, but the hindquarters vasodilator response was enhanced (HSD rats) or was seen only in that circumstance (TG rats). Under these conditions, both strains of rat showed a modest fall in blood pressure, together with mesenteric vasodilatation. 4 In additional experiments in normotensive SD rats from Charles River (CRSD), it was shown that, in the presence of the V 1 -receptor antagonist alone, or losartan alone, or the two antagonists together, the cardiovascular eects of WIN 55212-2 (50 or 150 mg kg 71 ) were not attenuated. Hence, the eects described above were likely due to pentolinium. 5 There were no consistent dierences between HSD and TG rats in their haemodynamic responses to methoxamine or noradrenaline, indicating the two strains were not likely to dier markedly in their responsiveness to any putative sympathetic activation induced by WIN 55212-2. 6 Collectively, the results indicate that the predominant cardiovascular eects of WIN 55212-2 in conscious HSD and TG rats (i.e., pressor and vasoconstrictor actions) can be attributed largely to indirect, pentolinium-sensitive mechanisms, which appear to dier little in the normotensive and hypertensive state, at least in conscious animals. Under the conditions of our experiments, signs of cannabinoid-induced vasodilatation were modest.