Na. Sharif et al., CHRONIC MANIPULATION OF DIETARY SALT MODULATES RENAL PHYSIOLOGY AND KIDNEY DOPAMINE-RECEPTOR SUBTYPES - FUNCTIONAL AND AUTORADIOGRAPHIC STUDIES, General pharmacology, 26(4), 1995, pp. 727-735
1. Compared to rats maintained on the normal NaCl (0.33%) diet, animal
s maintained on the low NaCl (0%) diet for 4 weeks exhibited increased
plasma aldosterone and chloride and decreased urinary sodium excretio
n. 2. Rats maintained on the high NaCl (8%) diet for 4 weeks showed in
creased systolic blood pressure, water intake, urine volume, sodium an
d dopamine excretion and decreased plasma aldosterone and glomerular f
iltration rate. 3. Administration of SCH 23390 (10 mg/kg, po), but not
domperidone to the high salt diet rats attenuated the diuretic effect
, indicating the involvement of DA(1) rather than DA(2) receptors. The
dopamine decarboxylase inhibitor, carbidopa (30 mg/kg, i.p.), also re
duced the high salt-induced diuresis. 4. Kidney sections from rats fed
the low NaCl diet showed a 63-100% decrease (P < 0.001-0.02) in corti
cal and medullary DA(1) and DA(2) binding sites, while rats fed the hi
gh NaCl diet demonstrated only a 70% decrease (P < 0.01-0.02) in corti
cal DA(1) binding, without affecting DA(2) binding. 5. These data indi
cate that chronic modification of dietary salt profoundly affects the
sodium, water and dopamine excretion and leads to selective modulation
of renal dopamine receptor subtypes.