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Role of dopamine 2 ‐receptors in mediating renal vascular response to low dose dopamine infusion in the rat. Acta Physiol Scand 130 , 563–569. Received 6 November 1986, accepted 15 March 1987. ISSN 0001–6772. Department of Developmental Physiology, Karolinska Institute, St Göran's Children's Hospital, Stockholm, Sweden. The effects of the interaction of dopamine (DA) and the DA 2 ‐receptors on regional blood flows and cardiac output have been studied in the rat. By means of the microsphere technique the blood flow (BF) and vascular resistance (VR) were determined in the kidney, duodenum, spleen, liver, and lung during infusion of DA in the absence and presence of selective DA 2 ‐receptor blockade with S‐Sulpiride (S‐SP), and during infusion of a selective DA 2 ‐receptor agonist (LY‐171555, LY). In order to evaluate the role of the presynaptic DA 2 ‐receptor, the experiments were performed without α‐ and β‐adrenergic blockade. Dopamine was given in such low doses that stimulation of the adrenergic receptors should be negligible. Dopamine, LY and DA + S‐SP did not significantly influence BF and VR in the spleen, liver and lung. Dopamine significantly increased BF and decreased VR in the kidney and the duodenum; LY significantly increased BF in the the kidney but not in the duodenum and decreased VR in both the kidney and the duodenum. In the presence of selective DA,‐receptor blockade, DA did not significantly influence BF or VR in the kidney but in the duodenum BF increased and VR decreased to the same extent as in the absence of blockade. In conclusion; the kidney and the intestine are more abundantly supplied with vascular DA‐receptors than other organs. In the kidney the interaction between DA and the DA 2 ‐receptors significantly contributes the the DA‐induced vasodilation. The interaction between DA and the DA 2 ‐receptors is of less importance for the DA‐induced vasodilatation in the intestine.
Seri et al. (Sat,) studied this question.