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Coexpression of dopamine D 1 and D 3 receptors in islands of Calleja and shell of nucleus accumbens of the rat: opposite and synergistic functional interactions
Author(s) -
Ridray Sophie,
Griffon Nathalie,
Mig Virginie,
Souil Evelyne,
Carboni Suzanna,
Diaz Jorge,
Schwartz JeanCharles,
Sokoloff Pierre
Publication year - 1998
Publication title -
european journal of neuroscience
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.346
H-Index - 206
eISSN - 1460-9568
pISSN - 0953-816X
DOI - 10.1046/j.1460-9568.1998.00173.x
Subject(s) - quinpirole , nucleus accumbens , agonist , dopamine , medicine , sch 23390 , dopamine receptor d1 , receptor , dopamine receptor , dopamine receptor d2 , endocrinology , dopamine receptor d3 , biology , basal ganglia , chemistry , central nervous system
Using double in situ hybridization, we found extensive coexpression of dopamine D 1 and D 3 receptor (D 1 R and D 3 R) mRNAs in neurons of the island of Calleja major (ICjM) and ventromedial shell of nucleus accumbens (ShV), respectively. Thus, at least 79 and 63% of D 3 R mRNA‐expressing neurons in ICjM and ShV also expressed the D 1 R mRNA. Coexpression of D 1 R and D 3 R mRNAs was found to occur in substance P (SP) mRNA‐expressing neurons in both areas, suggesting SP mRNA as a marker of the activity of coexpressing neurons. Administration of SKF 38393, a D 1 R receptor agonist, increased c‐fos mRNA in ICjM, whereas administration of quinpirole, a D 2 R/D 3 R agonist, decreased it; SCH 23390, a D 1 R antagonist and nafadotride, a preferential D 3 R antagonist, given alone, had effects opposite to those of the corresponding agonists. These data indicate that basal c‐fos expression in ICjM is maintained by endogenous dopamine acting tonically upon two receptor subtypes subserving opposite effects on the same cell. However, in ShV, whereas SKF 38393 also increased c‐ fos mRNA, quinpirole had no effect, a difference presumably reflecting the lower fraction of neurons coexpressing D 1 R and D 3 R in this area. In contrast, in ShV from reserpine‐treated rats, SKF 38393 increased SP mRNA and quinpirole potentiated this effect. These contrasting interactions of D 1 R‐ and D 3 R‐mediated signalling events, i.e. in either opposite or synergistic directions, most likely occurring at the single cell level, may serve to increase the dopamine response threshold of the target cells in ICjM and to maintain a strong tonic activity of ShV neurons.