Fujimura M, Greeley G H, Hancock M B, Alwmark A, Santos A, Cooper C W, Reumont K J, Ishizuka J, Thompson J C
Department of Surgery, University of Texas Medical Branch, Galveston 77550.
Pancreas. 1988;3(1):49-52. doi: 10.1097/00006676-198802000-00009.
Calcitonin gene-related peptide (CGRP)- and somatostatin (SRIF)-containing cells were identified by immunocytochemical techniques in pancreatic islet cells of the rat. CGRP-containing cells were found primarily in the peripheral portion of the pancreatic islets. In addition, CGRP-containing cells also contained somatostatin, which identifies the islet CGRP-containing cells as D cells. In the present study, we also tested the effect of CGRP on gastrin-releasing peptide (GRP; 10(-9) M)- or cholecystokinin (CCK-8, 10(-9) M)-stimulated release of insulin from isolated rat islets in vitro. At concentrations of 10(-8)-10(-11) M, CGRP inhibited GRP- and CCK-8-stimulated release of insulin significantly when compared with GRP or CCK-8 alone. At the lowest concentration of CGRP (10(-11) M), the inhibitory effect of CGRP on CCK-8-stimulated release of insulin was statistically significant (p less than 0.05) and exceptionally potent (65-90% inhibition). We have also found that CGRP does not stimulate the release of SRIF from isolated islet cells. These findings suggest that CGRP may play a regulatory role in the release of insulin.
通过免疫细胞化学技术在大鼠胰岛细胞中鉴定出含降钙素基因相关肽(CGRP)和生长抑素(SRIF)的细胞。含CGRP的细胞主要位于胰岛的外周部分。此外,含CGRP的细胞还含有生长抑素,这表明含胰岛CGRP的细胞为D细胞。在本研究中,我们还测试了CGRP对体外分离的大鼠胰岛中胃泌素释放肽(GRP;10⁻⁹ M)或胆囊收缩素(CCK - 8,10⁻⁹ M)刺激的胰岛素释放的影响。与单独使用GRP或CCK - 8相比,浓度为10⁻⁸ - 10⁻¹¹ M的CGRP显著抑制GRP和CCK - 8刺激的胰岛素释放。在最低浓度的CGRP(10⁻¹¹ M)时,CGRP对CCK - 8刺激的胰岛素释放的抑制作用具有统计学意义(p < 0.05)且效力极强(65 - 90%抑制)。我们还发现CGRP不会刺激分离的胰岛细胞释放SRIF。这些发现表明CGRP可能在胰岛素释放中起调节作用。