The effects of the
dopamine agonists TL-99,
M-7 (N, N-dimethyl analogues of aminotetralins) and N, N-dinpropyldopamine (NNPD) on stimulation-evoked pressor responses and
tachycardia in pithed Sprague-Dawley rats were investigated when pressor responses to the compounds per se had subsided. Various antagonists were used to characterise the effects of the
dopamine agonists. 2
M-7 (3 micrograms/kg i.v.), and NNPD (1 mg/kg i.v.), but not
TL-99 (1-30 micrograms/kg i.v.), inhibited pressor responses evoked by low frequency electrical stimulation of the spinal cord in the pithed rat. 3
M-7 (3 micrograms/kg i.v.), but neither NNPD (1 mg/kg i.v.) nor
TL-99 (1-30 micrograms/kg), inhibited
tachycardia evoked by low frequency electrical stimulation of the spinal cord in the pithed rat. 4 The inhibition of stimulation-evoked pressor responses by
M-7 and NNPD was prevented by
pimozide,
metoclopramide and
sulpiride but not by yohimibine,
atropine,
cimetidine or
propranolol. 5 The inhibition of stimulation-evoked
tachycardia by
M-7 was prevented by
yohimbine (and to a certain extent by
sulpiride) but not
pimozide,
metoclopramide,
atropine or
cimetidine. 6 Pressor responses elicited by
TL-99,
M-7 and NNPD were selective antagonised by
yohimbine, but not by
prazosin, indicating that these responses were mediated by stimulation of vascular postsynaptic alpha 2-adrenoreceptors. 7 This study demonstrates that, in the rat, presynaptic
dopamine receptors exist on sympathetic pre- or postganglionic nerve endings to blood vessels, but not on sympathetic pre- or postganglionic nerve endings to the heart, where inhibition by
M-7 of stimulation-evoked
tachycardia is mediated by stimulation of presynaptic alpha 2-adrenoreceptors.