Somatostatin receptor subtype 1 modulates basal inhibition of growth hormone release in somatotrophs

被引:74
作者
Kreienkamp, HJ
Akgün, E
Baumeister, H
Meyerhof, W
Richter, D
机构
[1] Univ Hamburg, Inst Zellbiochem & Klin Neurobiol, D-20246 Hamburg, Germany
[2] Deutsch Inst Ernahrungsforsch Potsdam Rehbrucke, D-14558 Bergholz Rehbrucke, Germany
关键词
SSTR1 null mutation; growth hormone release;
D O I
10.1016/S0014-5793(99)01582-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Somatostatin (SST) inhibits the secretion of many peptide hormones including growth hormone (GH). The various functions of SST are mediated through at least five different receptor subtypes (SSTR1-5), their precise physiological roles have not been solved yet. Here we report on studies concerning the functional role of SSTR1 in the modulation of GH release from somatotrophs. Primary cell cultures from pituitaries of wild-type SSTR1 mice exposed to the SSTR1 selective somatostatin analog CH-275 show reduction of basal levels of GH secretion whereas somatotrophs isolated from SSTR1 null mutant mice did not respond to the agonist-mediated effect, This suggests that SSTR1 is involved in modulating basal GH levels in primary pituitary cell cultures and, together with SSTR2, may control the secretion of GH in the body. (C) 1999 Federation of European Biochemical Societies.
引用
收藏
页码:464 / 466
页数:3
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