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Journal ArticleDOI

Continuous intravenous infusion of LY171555, a potent selective D2 receptor agonist, lowers blood pressure in the conscious rat.

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TLDR
The data suggest that continuous intravenous administration of quinpirole produces a transient centrally mediated pressor effect which is followed by a more sustained, peripherally mediated depressor response.
Abstract
Cardiovascular responses to sustained infusion of quinpirole (LY171555), a dopamine (DA) D2 receptor agonist, and bolus injection of quinpirole following sustained infusion were examined in conscious, unrestrained Sprague-Dawley rats to investigate the contributions of central and peripheral D2 receptors to the regulation of cardiovascular function. Continuous intravenous administration of quinpirole induced a transient pressor response followed by normalization of mean arterial pressure (MAP) and, at higher doses, a decrease in MAP below control levels. Intravenous bolus injections of quinpirole administered 30 min after termination of the infusion produced dose-dependent depressor responses which were blocked by pretreatment with domperidone, a peripheral D2 antagonist. The data suggest that continuous intravenous administration of quinpirole produces a transient centrally mediated pressor effect which is followed by a more sustained, peripherally mediated depressor response.

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Journal ArticleDOI

Pressor responses to brain dopaminergic stimulation

TL;DR: Differential changes in sympathetic vasomotor tone may be involved in the apparent de‐sensitization induced by quinpirole and the antihypertensive effects of sympathoinhibitory drugs, such as clonidine and rilmenidine, is markedly inhibited.
Journal ArticleDOI

In vivo venodilator action of fenoldopam, a dopamine D1-receptor agonist

TL;DR: It is indicated that fenoldopam reduces MAP and MCFP, and markedly increases CO through reductions of arterial and venous resistances, and in contrast, R(−)‐propylnorapomorphine elevates MAP through an increase in arterial resistance but has minimal effects on CO, MCFP and ven Mous resistance.
Journal ArticleDOI

Pretreatment with quinpirole inhibits the central antihypertensive effects of rilmenidine and α-methyldopa in conscious rats

TL;DR: Treatment with quinpirole has marked effects on central sympathetic vasomotor mechanisms which are the target of antihypertensive drugs such as rilmenidine and α-methyldopa, and at least some of these effects may occur at the level of the sympathetic baroreflex.
Journal ArticleDOI

Role of the renin-angiotensin system in the compensation of quinpirole-induced blood pressure decrease

TL;DR: The data show that stimulation of dopamine D2-like receptors dose-dependently decreased blood pressure, which was potentiated by both interruption of the renal innervation and AT1 receptor blockade, while exogenous ANG II restored the enhancement of the blood pressure response to quinpirole.
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