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The aim of this study was to investigate whether the pentobarbitone anesthetized cat is a suitable preparation in which to characterize renal tubular dopamine receptors. Intravenous infusion of dopamine (10–100 μg/kg/min) resulted in a dose-related increase in mean blood pressure (MBP). urine output, sodium excretion (UNaV), and fractional sodium excretion (FENa). This diuretic effect occurred despite little change in glomerular filtration rate, suggesting that it is a consequence of decreased tubular reabsorption. Dopamine (10–100 μg/kg/min, i.v.) also induced marked dose-renal blood flow was not significantly reduced. The increases in MBP, urine output, UNaV, and FENainduced by dopamine (10–100 μg/kg/min, i.v.), were unaffected by pretreatment of cats with either the selective dopamine DA1or DA2receptor antagonists, SCH 23390 (30 μg/kg, i.v.), or domperidone (100 μg/kg, i.v.), respectively. In contrast, pretreatment of cats with the nonselective α-adrenoceptor antagonist, phentolamine (1 mg/kg, i.v.) prevented dopamine-induced increases in urine output and MBP. Infusion of the selective dopamine DA1receptor agonist fenoldopam (0.01–10 μg/kg/min) into the left renal artery failed to increase left renal vascular conductance, or left kidney urine output, UNaV, or FENa. In conclusion, this study provides no evidence for the involvement of renal tubular dopamine receptors in dopamine-induced diuresis in anesthetized cats. Rather, the diuretic effect appears to be linked to stimulation of α-andrenoceptors.

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