P. Barili et al., DOPAMINE D-2-LIKE RECEPTORS IN THE KIDNEY OF SPONTANEOUSLY HYPERTENSIVE RATS - A RADIOLIGAND BINDING ASSAY AND LIGHT-MICROSCOPE AUTORADIOGRAPHY STUDY, Journal of autonomic pharmacology, 18(2), 1998, pp. 89-97
1 Dopamine D-2-like receptors were investigated in sections of kidney
from male spontaneously hypertensive rats (SHRs) at 6 and 14 weeks of
age using radioligand binding assay and autoradiographic techniques wi
th [H-3]-spiperone as a ligand. 2 Systolic blood pressure values were
slightly higher in 6-week-old SHRs in comparison with age-matched norm
otensive Wistar-Kyoto (WKY) rats and considerably higher in 14-week-ol
d SHRs in comparison with the other groups investigated. Renal dopamin
e levels were higher in SHRs aged 6 and 14 weeks in comparison with ag
e-matched WKY rats. Noradrenaline concentrations were similar in 6-wee
k-old SHRs and normotensive WKY rats, and increased slightly in SHRs a
ged 14 weeks. 3 The density of [H-3]-spiperone binding sites was simil
ar in SHRs and WKY rats at 6 weeks of age, and decreased in SHRs at 14
weeks in comparison with age-matched normotensive animals. Light micr
oscope autoradiography revealed the accumulation of silver grains in t
he tunica adventitia, in the adventitia-media border of intrarenal art
eries and within cortical tubules. A few specific silver grains were a
lso developed in the glomerular tuft. No changes in the density and pa
ttern of silver grains were noticeable between SHRs and WKY rats at 6
weeks of age, whereas a reduction in silver grains largely affecting v
ascular binding sites was observed at 14 weeks of age. 4 Renal denerva
tion considerably decreased the density of [H-3]-spiperone binding sit
es in sections of rat kidney, with an almost complete loss of vascular
binding sites. 5 The above findings indicate the occurrence of a decr
ease of dopamine D-2-like receptors in the kidney of SHRs with the pro
gress of hypertension. Dopamine D-2-like receptors which are mainly pr
ejunctional are involved in the modulation of sympathetic neurotransmi
ssion in the kidney, The loss of these receptors in SHRs may contribut
e to the pathophysiology of hypertension.