Prutskova N P, Seliverstova E V
Zh Evol Biokhim Fiziol. 2012 Jan-Feb;48(1):54-62.
Experiments in vitro demonstrated a partial absorption of arginine-vasopressin (AVP) in the frog small intestine. Dynamics and efficiency of the nonapeptide absorption are studied with use of hydroosmotic method of recording of the osmotic permeability of the frog urinary bladder epithelium and immunoenzyme analysis. In the process of absorption there were preserved intactness of the hormone cyclic structure and its physiological activity, like in the case of the arginine-vasotocin (AVT) absorption. The AVP absorption increased at its administration into the gut with inhibitor of proteases. By methods of immunoelectron and immunofluorescent microscopy with use of polyclonal antibody to AVP, location of the label to the hormone was shown in the enterocyte cytoplasm. Thus, there was obtained a morphological evidence for the AVP absorption and transepithelial transfer in the frog small intestine. These data enlarge the concept of the poorly studied properties of the absorbing epithelium of the vertebrate intestine with respect to absorption of intact molecules of polypeptides.
体外实验表明,精氨酸加压素(AVP)在蛙小肠中有部分吸收。采用记录蛙膀胱上皮渗透通透性的水渗透法和免疫酶分析法,研究了这种九肽吸收的动力学和效率。在吸收过程中,激素的环状结构及其生理活性保持完整,这与精氨酸催产素(AVT)的吸收情况类似。当在肠道中同时给予蛋白酶抑制剂时,AVP的吸收增加。利用针对AVP的多克隆抗体,通过免疫电子显微镜和免疫荧光显微镜方法,在肠细胞胞质中显示了标记物与该激素的结合。因此,获得了AVP在蛙小肠中吸收和跨上皮转运的形态学证据。这些数据扩展了关于脊椎动物肠道吸收上皮在完整多肽分子吸收方面研究较少的特性的概念。