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

Ross Fiziol Zh Im I M Sechenova · 2016

Last updated 2026-05-28

In experiments with rats, hormone-like drugs given by mouth still worked but required doses 50 to 200 times higher than when injected to produce the same effects on water reabsorption and sodium and potassium loss in urine. Blocking gut enzymes slightly boosted how much of the drug was absorbed, but only about 0.5 % of the oral dose entered the bloodstream. The GLP-1 drug exenatide did not show any effects when given by mouth, but it did increase sodium and potassium excretion after an injection.

AI summary of the abstract below.

JournalRoss Fiziol Zh Im I M Sechenova, 2016
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Molecules
Conditions studied Chronic Kidney Disease

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.

Verbatim abstract via PubMed 30193436 ↗