MOLECULAR-PROPERTIES OF SOMATOSTATIN RECEPTORS

被引:160
作者
REISINE, T
BELL, GI
机构
[1] UNIV CHICAGO,HOWARD HUGHES MED INST,DEPT BIOCHEM & MOLEC BIOL,CHICAGO,IL 60637
[2] UNIV CHICAGO,HOWARD HUGHES MED INST,DEPT MED,CHICAGO,IL 60637
关键词
D O I
10.1016/0306-4522(95)00072-Q
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The neuropeptide somatostatin is widely distributed in the central nervous system and in peripheral tissues and may be involved in the regulation of a number of physiological functions including movement and cognition. Somatostatin may also have a role in the development of the central nervous system, in particular, the cerebellum and spinal cord. somatostatin induces its actions by interacting with a family of membrane associated receptors. Recently, five somatostatin receptors have been cloned and referred to as SSTR1-SSTR5. The distribution of the expression of the mRNAs for these receptors are distinct but overlapping. Preliminary pharmacological analysis of these receptors may lead to the development of selective ligands at these receptors. These compounds may ge useful in identifying the selective functions of these receptor subtypes. Some somatostatin analogues have antiproliferative actions and are used presently to treat carcinoids. Development of subtype selective somatostatin analogues could be helpful in further identifying somatostatin receptor-expressing tumors and in the treatment of cancer. The cloning of these receptors hs now opened up the possibility of more clearly investigating the functions of somatostatin in the brain and peripheral tissues and will facilitate the generation of new somatostatin drugs that may be employed for the treatment of a number of diseases.
引用
收藏
页码:777 / 790
页数:14
相关论文
共 150 条
[71]  
MAYOR F, 1987, J BIOL CHEM, V262, P6468
[72]   SOMATOSTATIN-INDUCED INHIBITION OF NEURONAL CA2+ CURRENT MODULATED BY CGMP-DEPENDENT PROTEIN-KINASE [J].
MERINEY, SD ;
GRAY, DB ;
PILAR, GR .
NATURE, 1994, 369 (6478) :336-339
[73]   CLONING OF A CDNA-ENCODING A NOVEL PUTATIVE G-PROTEIN-COUPLED RECEPTOR EXPRESSED IN SPECIFIC RAT-BRAIN REGIONS [J].
MEYERHOF, W ;
PAUST, HJ ;
SCHONROCK, C ;
RICHTER, D .
DNA AND CELL BIOLOGY, 1991, 10 (09) :689-694
[74]   MOLECULAR-CLONING OF A SOMATOSTATIN-28 RECEPTOR AND COMPARISON OF ITS EXPRESSION PATTERN WITH THAT OF A SOMATOSTATIN-14 RECEPTOR IN RAT-BRAIN [J].
MEYERHOF, W ;
WULFSEN, I ;
SCHONROCK, C ;
FEHR, S ;
RICHTER, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (21) :10267-10271
[75]   SOMATOSTATIN INCREASES AN INWARDLY RECTIFYING POTASSIUM CONDUCTANCE IN GUINEA-PIG SUBMUCOUS PLEXUS NEURONS [J].
MIHARA, S ;
NORTH, RA ;
SURPRENANT, A .
JOURNAL OF PHYSIOLOGY-LONDON, 1987, 390 :335-355
[76]   PRIMARY STRUCTURE OF THE GENE ENCODING RAT PREPROSOMATOSTATIN [J].
MONTMINY, MR ;
GOODMAN, RH ;
HOROVITCH, SJ ;
HABENER, JF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (11) :3337-3340
[77]   SOMATOSTATIN AUGMENTS THE M-CURRENT IN HIPPOCAMPAL-NEURONS [J].
MOORE, SD ;
MADAMBA, SG ;
JOELS, M ;
SIGGINS, GR .
SCIENCE, 1988, 239 (4837) :278-280
[78]  
MURRAYWHELAN R, 1992, J BIOL CHEM, V267, P2960
[79]  
OCARROLL AM, 1992, MOL PHARMACOL, V42, P939
[80]  
OCARROLL AM, 1994, MOL PHARMACOL, V48, P291