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Absorption of Arginine-Vasopressin and Arginine-Vasotocin in Small Intestine of the Frog Rana temporaria

机译:蛙林蛙小肠中精氨酸加压素和精氨酸加压素的吸收

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摘要

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-vasotocine (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.
机译:体外实验表明,青蛙小肠中的精氨酸加压素(AVP)有部分吸收。使用水渗透法记录青蛙膀胱上皮的渗透渗透率并进行免疫酶分析,研究了九肽吸收的动力学和效率。在吸收过程中,保留了完整的激素循环结构及其生理活性,就像在精氨酸-血管毒素(AVT)吸收的情况下一样。与蛋白酶抑制剂一起进入肠道后,AVP吸收增加。通过使用抗AVP的多克隆抗体的免疫电子和免疫荧光显微术的方法,在肠细胞的细胞质中显示了激素标记的位置。因此,获得了青蛙小肠中AVP吸收和上皮转移的形态学证据。这些数据扩大了关于完整多肽分子吸收方面脊椎动物肠道吸收上皮的研究不足的概念。

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