Pharmacological and molecular characterization of 5-hydroxytryptamine7 receptors in the rat adrenal gland

被引:39
作者
Contesse, V [1 ]
Lenglet, S [1 ]
Grumolato, L [1 ]
Anouar, Y [1 ]
Lihrmann, I [1 ]
Lefebvre, H [1 ]
Delarue, C [1 ]
Vaudry, H [1 ]
机构
[1] Univ Rouen, Unite Associee Ctr Natl Rech Sci, INSERM,European Inst Peptide Res,IFRMP 23, U413,Lab Cellular & Mol Neuroendocrinol, F-76821 Mont St Aignan, France
关键词
D O I
10.1124/mol.56.3.552
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Serotonin (5-hydroxytryptamine; 5-HT) is a potent stimulator of aldosterone secretion in the rat adrenal gland but the type of receptor involved in the mechanism of action of 5-HT remains unknown. The aim of the present study was to determine the pharmacological profile and to clone the receptor responsible for the corticotropic effect of 5-HT in rat glomerulosa cells. A series of 10 serotonergic receptor agonists and 12 receptor antagonists was used to characterize the receptor mediating the effect of 5-HT on aldosterone secretion from perifused rat adrenocortical slices. Correlation analysis between the potencies of the different compounds in our model and those previously reported for various recombinant 5-HT receptors showed that the rat adrenal 5-HT receptor exhibits the same pharmacological profile as the 5-HT, receptor transiently expressed in COS-7 cells (r = 0.82 for agonists, p < .05; r = 0.83 for antagonists, p < .01). Polymerase chain reaction with specific primers revealed the expression of 5-HT7 receptor mRNA in the rat adrenal gland. Cloning of the polymerase chain reaction product confirmed that the amplified DNA corresponded to the 5-HT7 receptor cDNA sequence. Western blot analysis showed the presence of a protein with an apparent molecular mass of 66 kDa in the adrenal cortex but not in the medulla. Taken together, these data demonstrate that the rat adrenal glomerulosa expresses functional 5-HT7 receptors. Rat glomerulosa cells will thus provide a robust and sensitive bioassay for future studies on native 5-HT7 receptors.
引用
收藏
页码:552 / 561
页数:10
相关论文
共 47 条
[1]   CLONING OF ANOTHER HUMAN SEROTONIN RECEPTOR (5-HT1F) - A 5TH 5-HT1 RECEPTOR SUBTYPE COUPLED TO THE INHIBITION OF ADENYLATE-CYCLASE [J].
ADHAM, N ;
KAO, HT ;
SCHECHTER, LE ;
BARD, J ;
OLSEN, M ;
URQUHART, D ;
DURKIN, M ;
HARTIG, PR ;
WEINSHANK, RL ;
BRANCHEK, TA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (02) :408-412
[2]  
BARD JA, 1993, J BIOL CHEM, V268, P23422
[3]   MOLECULAR-BIOLOGY OF 5-HT RECEPTORS [J].
BOESS, FG ;
MARTIN, IL .
NEUROPHARMACOLOGY, 1994, 33 (3-4) :275-317
[4]  
BRANCHEK TA, 1997, SEROTONINERGIC NEURO, P475
[5]  
Carson MJ, 1996, GLIA, V17, P317, DOI 10.1002/(SICI)1098-1136(199608)17:4<317::AID-GLIA6>3.0.CO
[6]  
2-W
[7]  
Castro E, 1997, J NEUROCHEM, V69, P2123
[8]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[9]   A UNIQUE SEROTONIN RECEPTOR IN CHOROID-PLEXUS IS LINKED TO PHOSPHATIDYLINOSITOL TURNOVER [J].
CONN, PJ ;
SANDERSBUSH, E ;
HOFFMAN, BJ ;
HARTIG, PR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (11) :4086-4088
[10]   EFFECT OF A SERIES OF 5-HT4 RECEPTOR AGONISTS AND ANTAGONISTS ON STEROID-SECRETION BY THE ADRENAL-GLAND IN-VITRO [J].
CONTESSE, V ;
HAMEL, C ;
DELARUE, C ;
LEFEBVRE, H ;
VAUDRY, H .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1994, 265 (1-2) :27-33