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Functional Characterisation of Eel Dopamine D2 Receptors and Involvement in the Direct Inhibition of Pituitary Gonadotrophins.
Jolly, C; Rousseau, K; Prézeau, L; Vol, C; Tomkiewicz, J; Dufour, S; Pasqualini, C.
Affiliation
  • Jolly C; Muséum National d'Histoire Naturelle, Sorbonne Universités, Research Unit BOREA, Biologie des Organismes et Ecosystèmes Aquatiques, CNRS 7208, IRD207, UPMC, UCN, UA, Paris, France.
  • Rousseau K; Muséum National d'Histoire Naturelle, Sorbonne Universités, Research Unit BOREA, Biologie des Organismes et Ecosystèmes Aquatiques, CNRS 7208, IRD207, UPMC, UCN, UA, Paris, France.
  • Prézeau L; CNRS UMR5203, Institut de Génomique Fonctionnelle, Montpellier, France.
  • Vol C; INSERM U661, Montpellier, France.
  • Tomkiewicz J; Université de Montpellier 1 & 2, Montpellier, France.
  • Dufour S; CNRS UMR5203, Institut de Génomique Fonctionnelle, Montpellier, France.
  • Pasqualini C; INSERM U661, Montpellier, France.
J Neuroendocrinol ; 28(9)2016 09.
Article in En | MEDLINE | ID: mdl-27453551
ABSTRACT
In various vertebrate species, dopamine (DA) exerts an inhibitory action on reproduction. In the European eel, DA plays a pivotal role in the inhibitory control of gonadotroph function and the blockade of puberty. In vivo studies have suggested that this effect is mediated by receptors pharmacologically related to the D2 family. In the European eel, two distinct D2 receptor (D2-R) paralogous genes have been identified (D2A-R and D2B-R) and both were shown to be expressed in the pituitary. We investigated the potential role of each paralogue in the control of gonadotroph function in this species. Eel recombinant D2A-R or D2B-R were expressed in HEK 293 cells, with a universal Gα subunit, and receptor activation was followed by inositol phosphate production. Recombinant D2-Rs exhibited a comparable affinity for DA, although they had differential affinities for mammalian D2-R agonists and antagonists, supporting subtle structure/activity differences. Furthermore, using eel pituitary cell primary cultures, the expression by gonadotroph cells of both native eel D2-R paralogues was examined by in situ hybridisation of D2A-R or D2B-R transcripts, coupled with immunofluorescence of luteinising hormone (LH)ß or follicle-stimulating (FSH)ß. LH and to a lesser extent, FSH cells expressed both D2-R transcripts but with a clear predominance of D2B-R. Notably, D2B-R transcripts were detected for the majority of LH cells. Accordingly, using these cultures, we showed that DA potently inhibited basal and testosterone-stimulated LHß expression and less potently basal and activin-stimulated FSHß expression. We also tested some D2-R antagonists, aiming to select the most adequate one to be used in innovative protocols for induction of eel sexual maturation. We identified eticlopride as the most potent inhibitor of DA action on basal and stimulated LH expression in vitro. Our data suggest a differential functionalisation of the duplicated receptor genes and demonstrate that mainly D2B-R is involved in the dopaminergic inhibitory control of eel gonadotroph function.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Receptors, Dopamine D2 / Fish Proteins / Follicle Stimulating Hormone, beta Subunit / Luteinizing Hormone, beta Subunit / Eels / Gonadotropins, Pituitary Limits: Animals / Female / Humans Language: En Journal: J Neuroendocrinol Journal subject: ENDOCRINOLOGIA / NEUROLOGIA Year: 2016 Type: Article Affiliation country: France

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Receptors, Dopamine D2 / Fish Proteins / Follicle Stimulating Hormone, beta Subunit / Luteinizing Hormone, beta Subunit / Eels / Gonadotropins, Pituitary Limits: Animals / Female / Humans Language: En Journal: J Neuroendocrinol Journal subject: ENDOCRINOLOGIA / NEUROLOGIA Year: 2016 Type: Article Affiliation country: France