P. Barili et al., PHARMACOLOGICAL CHARACTERIZATION AND AUTORADIOGRAPHIC LOCALIZATION OFDOPAMINE-RECEPTORS IN THE RAT ADRENAL-MEDULLA, European journal of pharmacology, 310(2-3), 1996, pp. 129-135
The pharmacological profile and the anatomical localization of dopamin
e D-1-like and D-2-like receptors were studied in sections of rat adre
nal medulla, with radioligand binding and autoradiographic techniques,
respectively. [H-3]([R]-(+)-chloro-2,3,4,5-tetrahydro-5-phenyl-l H-3b
enzazepin-al hemimaleate) (SCH 23390) was used as a ligand for dopamin
e D-1-like receptors and [H-3]spiperone was used as a ligand for dopam
ine D-2-like receptors. Radioligand binding and light microscope autor
adiography did not show specific [3H]SCH 23390 binding in sections of
rat adrenal medulla. This suggests that rat adrenal medulla does not e
xpress dopamine D-1-like receptors, [3H]Spiperone was specifically bou
nd to sections of rat adrenal medulla. The binding was time-, temperat
ure- and concentration-dependent, with a dissociation constant (K-d) o
f 1.05 nM and a maximum density of binding sites (B-max) of 100.2 +/-
3.8 fmol/mg tissue. The pharmacological profile of [H-3]spiperone bind
ing to rat adrenal medulla was similar to that displayed by neostriatu
m, which is known to express dopamine D-2 receptors. Light microscope
autoradiography showed the accumulation of specifically bound [3H]spip
erone as silver grains within sections of adrenal medulla. Silver grai
ns were found primarily over the cellular membrane of chromaffin cells
. The above data indicate that chromaffin cells of the rat adrenal med
ulla express dopamine receptors belonging to the dopamine D-2 receptor
subtype. These receptors are probably involved in the modulation of c
atecholamine release from chromaffin cells, as documented by functiona
l studies.