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Hypotensive action of bromocriptine in the DOCA‐salt hypertensive rat: Contribution of spinal dopamine receptors
Author(s) -
Lahlou S,
Duarte G Pinto
Publication year - 1998
Publication title -
fundamental and clinical pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.655
H-Index - 73
eISSN - 1472-8206
pISSN - 0767-3981
DOI - 10.1111/j.1472-8206.1998.tb00992.x
Subject(s) - bromocriptine , domperidone , endocrinology , medicine , dopamine , agonist , dopamine receptor , dopamine agonist , dopaminergic , dopamine receptor d2 , dopamine antagonist , antagonist , stimulation , metoclopramide , chemistry , receptor , pharmacology , prolactin , hormone , vomiting
Summary— To assess the role of spinal dopamine receptors in mediation of hypotension induced by systemic administration of the dopamine D 2 receptor agonist, bromocriptine, conscious deoxycorticosterone acetate (DOCA)‐salt hypertensive rats were pretreated with either intravenous (iv; 500 μg/kg) or intrathecal (it; 40 μg/rat at T 9 ‐T 10 ) domperidone, a selective dopamine D 2 receptor antagonist that does not cross the blood‐brain barrier. In DOCA‐salt hypertensive rats, iv administration of a sub‐maximal dose of bromocriptine (150 μg/kg) induced a significant decrease in mean aortic pressure (MAP) which was greater and longer lasting than that in uninephrectomized control rats. Intravenous or it pretreatment with domperidone reduced partially, but significantly, the hypotensive effect of bromocriptine (reduction of about 57% and 45% of the maximal effect, respectively). The remaining responses observed during the 60 min postinjection period were still statistically significant as compared with vehicle injection. In contrast, the bromocriptine‐induced hypotension was fully abolished by iv pretreatment with metoclopramide (300 μg/kg), a dopamine D 2 receptor antagonist that crosses the blood‐brain barrier, or by combined pretreatment with iv and it domperidone. These results suggest that, in DOCA‐salt hypertensive rats, the hypotension induced by iv bromocriptine is mediated partly through a peripheral D 2 dopaminergic mechanism and partly through stimulation of spinal dopamine D 2 receptors, as has been demonstrated in conscious normotensive rats.