[EFFECTS OF ORALLY AND PARENTERALLY ADMINISTERED ANALOGS OF PEPTIDE HORMONES ON RENAL WATER AND ION TRANSPORT].

A V Kutina, D V Golosova, A S Marina, T A Karavashkina, Yu V Natochin
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Abstract

In experiments with female Wistar rats it was shown that analogs of neurohypophysial hormones administered to gastrointestinal tract preserved their specific physiological activity - they increased solute-free water reabsorption and urinary sodium and potassium excretion. Doses of deamino-vasotocin exerted antidiuretic and natriuretic effects following its oral administration were 50 and 200 times higher compared to maximal effective ones after intramuscular injection. Inhibition of gastrointestinal proteases by aprotinine enhanced effects of nonapeptides; the amount of peptide absorbed from the intestine under these conditions was approximately 0.5 % of orally introduced substance. In contrast to analogs of neurohypophysial nonapeptides, glucagon-like peptide-1 mimetic (exenatide) did not exert its physiological effects after oral administration, whereas it increased urinary sodium and potassium excretion following intramuscular injection.

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[口服和静脉注射肽激素类似物对肾脏水和离子运输的影响]。
在雌性Wistar大鼠的实验中,研究人员发现,类似的神经垂体激素被施用于胃肠道,保留了它们特定的生理活性——它们增加了无溶质水的再吸收和尿钠和钾的排泄。口服脱氨基-血管催产素的抗利尿和利钠剂量分别是肌肉注射后最大有效剂量的50倍和200倍。抑肽酶对胃肠蛋白酶的抑制作用增强了非肽的作用在这些条件下,从肠道吸收的肽量约为口服引入物质的0.5%。与神经垂体非肽类似物相比,胰高血糖素样肽-1模拟物(艾塞那肽)在口服后没有发挥其生理作用,而在肌肉注射后增加尿钠和钾的排泄。
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