Steyaert H, Tonon M C, Tong Y, Smihrouet F, Testart J, Pelletier G, Vaudry H
European Institute for Peptide Research, Laboratory of Molecular Endocrinology, CNRS URA 650, University of Rouen, Mont-Saint-Aignan, France.
Endocrinology. 1991 Oct;129(4):2101-9. doi: 10.1210/endo-129-4-2101.
Endozepine is the generic name for a family of peptides that are capable of displacing benzodiazepines and the 3-carboxylate ester of beta-carboline from their specific binding sites on synaptosomal membranes. The 104-amino acid polypeptide diazepam-binding inhibitor (DBI) and the octadecaneuropeptide (ODN) generated by tryptic digestion of DBI are two members of the endozepine family. In the present study we have used RIA, HPLC, in situ hybridization, and immunohistochemical techniques to identify and localize endozepine-like molecules in the rat gastrointestinal tract. Significant amounts of endozepine-like immunoreactivity (LI) were detected throughout the gut; the highest concentrations were found in the duodenum and antrum. HPLC analysis revealed that the immunoreactive material eluted as a major peak with a higher retention time than that of synthetic ODN. The distribution of the immunoreactive peptide(s) was studied using the peroxidase-antiperoxidase technique at the light microscope level. Endozepine-LI was localized only in the epithelial cell layer of the intestine in both goblet cells and enterocytes. In the stomach, endozepine-LI appeared to be restricted to deep layer of the epithelial cells. The diffuse neuroendocrine cells (amine precursor uptake and decarboxylation system) as well as myenteric and neuronal cells were devoid of immunoreactivity. A good correlation was observed between RIA and immunocytochemical data, in that the esophagus, which contained very low concentrations of endozepine-LI, also exhibited weak immunostaining of secretory cells. In situ hybridization using a 35S-labeled cRNA probe showed that endozepine mRNA was located in the mucosa. Taken together, these results show that in the rat, epithelial cells synthesize endozepine-LI material. Since epithelial cells also contain a high density of peripheral-type benzodiazepine-binding sites, our data indicate that endozepines may play a role in water, electrolyte, and/or mucus regulation in the rat gastrointestinal tract. The occurrence of high levels of endozepine-LI in the rat stomach also suggests that endozepines can be involved in the regulation of gastric acid secretion through modulation of local gamma-aminobutyric acid-ergic neurotransmission.
内源性苯二氮䓬类物质是一族肽的通用名称,这类肽能够从突触体膜上的特定结合位点取代苯二氮䓬类药物和β-咔啉的3-羧酸酯。104个氨基酸的多肽地西泮结合抑制剂(DBI)以及由DBI经胰蛋白酶消化产生的十八肽(ODN)是内源性苯二氮䓬类物质家族的两个成员。在本研究中,我们使用放射免疫分析(RIA)、高效液相色谱(HPLC)、原位杂交和免疫组织化学技术来鉴定和定位大鼠胃肠道中的内源性苯二氮䓬类样分子。在整个肠道中均检测到大量的内源性苯二氮䓬类样免疫反应性(LI);十二指肠和胃窦中的浓度最高。HPLC分析显示,免疫反应性物质以一个主峰形式洗脱,其保留时间比合成ODN的保留时间长。使用过氧化物酶-抗过氧化物酶技术在光学显微镜水平研究了免疫反应性肽的分布。内源性苯二氮䓬类LI仅定位于肠上皮细胞层中的杯状细胞和肠细胞。在胃中,内源性苯二氮䓬类LI似乎局限于上皮细胞的深层。弥漫性神经内分泌细胞(胺前体摄取和脱羧系统)以及肌间神经丛和神经元细胞均无免疫反应性。在RIA和免疫细胞化学数据之间观察到良好的相关性,即含有极低浓度内源性苯二氮䓬类LI的食管,其分泌细胞的免疫染色也较弱。使用35S标记的cRNA探针进行的原位杂交显示,内源性苯二氮䓬类mRNA位于黏膜中。综上所述,这些结果表明在大鼠中,上皮细胞合成内源性苯二氮䓬类LI物质。由于上皮细胞还含有高密度的外周型苯二氮䓬类结合位点,我们的数据表明内源性苯二氮䓬类物质可能在大鼠胃肠道的水、电解质和/或黏液调节中发挥作用。大鼠胃中高水平内源性苯二氮䓬类LI的存在也表明,内源性苯二氮䓬类物质可通过调节局部γ-氨基丁酸能神经传递参与胃酸分泌的调节。