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pubmed-article:9408008pubmed:abstractTextThe pharmacological profile and the microanatomical localisation of a putative dopamine D3 receptor in the rat renal cortex were investigated using radioligand binding assay and light microscope autoradiography techniques. [3H]7-hydroxy-N,N-di-n-propyl-2-aminotetraline ([3H]7-OH-DPAT) was used as a ligand. [3H]7-OH-DPAT was bound specifically to sections of renal cortex. The binding was time-, temperature- and concentration-dependent, of high affinity and guanine nucleotide-insensitive. The dissociation constant (Kd) value was 0.57 +/- 0.02 nM and the maximum density of binding sites (Bmax) was 62.4 +/- 3.5 fmol/mg tissue. The pharmacological profile of [3H]7-OH-DPAT binding to sections of rat renal cortex suggests the labelling of a dopamine D3 receptor. Light microscope autoradiography revealed the accumulation of the radioligand primarily within cortical tubules and to a lesser extent in the glomerular tuft. In glomeruli, binding sites were found mainly in mesangium and mesangial cells. The demonstration of a putative dopamine D3 receptor in slide-mounted sections of rat renal cortex suggests that appropriate radioligand binding assay techniques combined with autoradiography, may contribute to characterise peripheral dopamine receptor subtypes.lld:pubmed
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pubmed-article:9408008pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:9408008pubmed:articleTitlePharmacological characterisation and autoradiographic localisation of a putative dopamine D3 receptor in the rat kidney.lld:pubmed
pubmed-article:9408008pubmed:affiliationDipartimento di Scienze Farmacologiche e Medicina Sperimentale, Università di Camerino, Italy.lld:pubmed
pubmed-article:9408008pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:9408008pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed