Suda K, Takahashi H, Fukase N, Manaka H, Tominaga M, Sasaki H
Third Department of Internal Medicine, Yamagata University School of Medicine, Japan.
Life Sci. 1989;45(19):1793-8. doi: 10.1016/0024-3205(89)90519-5.
Using glucagon-like peptide-1 N-terminus and C-terminus directed antisera, we investigated concentration and molecular forms of GLP-1 immunoreactivity (IR) in extracts of various tissues of the dog. GLP-1 IR measured with C-terminus-directed antiserum R2337 (GLP-1 IR-CT) was high in the ileum, appendix, jejunum, colon, and gastric fundus and body. GLP-1 IR measured with N-terminus-directed antiserum R1043 (GLP-1 IR-NT) was high only in the pancreas, and gastric fundus and body. Only GLP-1 IR-CT was found in the hypothalamus, thalamus and medulla oblongata. No immunoreactive materials were detected in the liver, spleen and kidney. Gel-filtration with Sephadex G-50 showed two peaks of both GLP-1 IR-CT and GLP-1 IR-NT, at 10kd and at the position of GLP-1 (1-36 amide) in the pancreatic extract, and one peak at 10kd in the stomach extract. Ileal extracts showed 3 peaks of GLP-1 IR-CT at 10kd, at the position of GLP-1(1-36 amide) and GLP-1(7-36 amide), respectively, but GLP-1 IR-NT was coeluted with GLP-1(1-36 amide). Hypothalamic extracts showed a single peak at the position of GLP-1(7-36 amide). These results suggest that processing of preproglucagon differs in different organs, and that the main GLP-1-related products are a large molecular form and GLP-1(1-36 amide) or GLP-1(1-37) in the pancreas, and GLP-1(7-36 amide) or GLP-1 (7-37) in the ileum and hypothalamus.
我们使用胰高血糖素样肽-1(GLP-1)N端和C端定向抗血清,研究了犬各种组织提取物中GLP-1免疫反应性(IR)的浓度和分子形式。用C端定向抗血清R2337测定的GLP-1 IR(GLP-1 IR-CT)在回肠、阑尾、空肠、结肠以及胃底和胃体中含量较高。用N端定向抗血清R1043测定的GLP-1 IR(GLP-1 IR-NT)仅在胰腺以及胃底和胃体中含量较高。在下丘脑、丘脑和延髓中仅发现了GLP-1 IR-CT。在肝脏、脾脏和肾脏中未检测到免疫反应性物质。用Sephadex G-50进行凝胶过滤显示,在胰腺提取物中,GLP-1 IR-CT和GLP-1 IR-NT均有两个峰,分别位于10kd以及GLP-1(1-36酰胺)的位置,而在胃提取物中GLP-1 IR-NT和GLP-1 IR-CT在10kd处有一个峰。回肠提取物显示GLP-1 IR-CT在10kd、GLP-1(1-36酰胺)和GLP-1(7-36酰胺)的位置分别有3个峰,但GLP-1 IR-NT与GLP-1(1-36酰胺)共洗脱。下丘脑提取物在GLP-1(7-36酰胺)的位置有一个单峰。这些结果表明,前胰高血糖素原在不同器官中的加工方式不同,并且在胰腺中主要的GLP-1相关产物是一种大分子形式以及GLP-1(1-36酰胺)或GLP-1(1-37),而在回肠和下丘脑中是GLP-1(7-36酰胺)或GLP-1(7-37)。