Influence of osmolality on gastrointestinal fluid volume and drug absorption: potential impact on oral salt supplementation

Abstract Background The syndrome of inappropriate secretion of antidiuretic hormone (SIADH) is the most frequent cause of hyponatremia in patients with cerebrovascular disease, and is often treated with oral salt tablets. However, we have shown that osmolality-dependent variations in gastrointestina...

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Main Authors: Miyuki Takemura, Yuki Tanaka, Katsuhisa Inoue, Ikumi Tamai, Yoshiyuki Shirasaka
Format: Article
Language:English
Published: BMC 2021-09-01
Series:Journal of Pharmaceutical Health Care and Sciences
Subjects:
Online Access:https://doi.org/10.1186/s40780-021-00212-z
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spelling doaj-3460494e5b48410e96aded2d5a4e082d2021-09-05T11:13:14ZengBMCJournal of Pharmaceutical Health Care and Sciences2055-02942021-09-01711810.1186/s40780-021-00212-zInfluence of osmolality on gastrointestinal fluid volume and drug absorption: potential impact on oral salt supplementationMiyuki Takemura0Yuki Tanaka1Katsuhisa Inoue2Ikumi Tamai3Yoshiyuki Shirasaka4Faculty of Pharmacy, Institute of Medical, Pharmaceutical and Health Sciences, Kanazawa UniversitySchool of Pharmacy, Tokyo University of Pharmacy and Life SciencesSchool of Pharmacy, Tokyo University of Pharmacy and Life SciencesFaculty of Pharmacy, Institute of Medical, Pharmaceutical and Health Sciences, Kanazawa UniversityFaculty of Pharmacy, Institute of Medical, Pharmaceutical and Health Sciences, Kanazawa UniversityAbstract Background The syndrome of inappropriate secretion of antidiuretic hormone (SIADH) is the most frequent cause of hyponatremia in patients with cerebrovascular disease, and is often treated with oral salt tablets. However, we have shown that osmolality-dependent variations in gastrointestinal (GI) fluid volume can alter the concentration of a poorly permeable drug in the GI tract, potentially affecting its absorption. Here, we examined the effect of ingestion of hyperosmotic solution (10% NaCl) on drug concentration and absorption in the GI tract. Methods The effects of osmolality on luminal fluid volume and drug absorption in rat intestine (jejunum, ileum and colon) were examined by means of an in situ closed loop method using fluorescein isothiocyanate-dextran 4000 (FD-4) and atenolol. In vivo absorption in rats was determined by measuring the plasma concentration after oral administration of the test compounds dissolved in purified water or hyperosmotic solution (10% NaCl). Results Administration of hyperosmotic solution directly into the GI tract significantly increased the GI fluid volume, owing to secretion of water into the lumen. After administration in hyperosmotic solution, the luminal concentration of non-permeable FD-4 was significantly lower than the initial dosing concentration, whereas after administration in purified water, the luminal concentration exceeded the initial concentration. The fraction absorbed of atenolol was markedly lower after administration in hyperosmotic solution than after administration in purified water. An in vivo pharmacokinetic study in rats was consistent with these findings. Conclusions Administration of hyperosmotic NaCl solution increased GI fluid volume and reduced the plasma level of orally administered atenolol. This may imply that oral salt tablets used to treat hyponatremia in SIADH patients could decrease the intestinal absorption of concomitantly administered drugs, resulting in lower plasma exposure.https://doi.org/10.1186/s40780-021-00212-zDrug absorptionGastrointestinal tractPharmacokineticsOsmolalityMembrane permeability
collection DOAJ
language English
format Article
sources DOAJ
author Miyuki Takemura
Yuki Tanaka
Katsuhisa Inoue
Ikumi Tamai
Yoshiyuki Shirasaka
spellingShingle Miyuki Takemura
Yuki Tanaka
Katsuhisa Inoue
Ikumi Tamai
Yoshiyuki Shirasaka
Influence of osmolality on gastrointestinal fluid volume and drug absorption: potential impact on oral salt supplementation
Journal of Pharmaceutical Health Care and Sciences
Drug absorption
Gastrointestinal tract
Pharmacokinetics
Osmolality
Membrane permeability
author_facet Miyuki Takemura
Yuki Tanaka
Katsuhisa Inoue
Ikumi Tamai
Yoshiyuki Shirasaka
author_sort Miyuki Takemura
title Influence of osmolality on gastrointestinal fluid volume and drug absorption: potential impact on oral salt supplementation
title_short Influence of osmolality on gastrointestinal fluid volume and drug absorption: potential impact on oral salt supplementation
title_full Influence of osmolality on gastrointestinal fluid volume and drug absorption: potential impact on oral salt supplementation
title_fullStr Influence of osmolality on gastrointestinal fluid volume and drug absorption: potential impact on oral salt supplementation
title_full_unstemmed Influence of osmolality on gastrointestinal fluid volume and drug absorption: potential impact on oral salt supplementation
title_sort influence of osmolality on gastrointestinal fluid volume and drug absorption: potential impact on oral salt supplementation
publisher BMC
series Journal of Pharmaceutical Health Care and Sciences
issn 2055-0294
publishDate 2021-09-01
description Abstract Background The syndrome of inappropriate secretion of antidiuretic hormone (SIADH) is the most frequent cause of hyponatremia in patients with cerebrovascular disease, and is often treated with oral salt tablets. However, we have shown that osmolality-dependent variations in gastrointestinal (GI) fluid volume can alter the concentration of a poorly permeable drug in the GI tract, potentially affecting its absorption. Here, we examined the effect of ingestion of hyperosmotic solution (10% NaCl) on drug concentration and absorption in the GI tract. Methods The effects of osmolality on luminal fluid volume and drug absorption in rat intestine (jejunum, ileum and colon) were examined by means of an in situ closed loop method using fluorescein isothiocyanate-dextran 4000 (FD-4) and atenolol. In vivo absorption in rats was determined by measuring the plasma concentration after oral administration of the test compounds dissolved in purified water or hyperosmotic solution (10% NaCl). Results Administration of hyperosmotic solution directly into the GI tract significantly increased the GI fluid volume, owing to secretion of water into the lumen. After administration in hyperosmotic solution, the luminal concentration of non-permeable FD-4 was significantly lower than the initial dosing concentration, whereas after administration in purified water, the luminal concentration exceeded the initial concentration. The fraction absorbed of atenolol was markedly lower after administration in hyperosmotic solution than after administration in purified water. An in vivo pharmacokinetic study in rats was consistent with these findings. Conclusions Administration of hyperosmotic NaCl solution increased GI fluid volume and reduced the plasma level of orally administered atenolol. This may imply that oral salt tablets used to treat hyponatremia in SIADH patients could decrease the intestinal absorption of concomitantly administered drugs, resulting in lower plasma exposure.
topic Drug absorption
Gastrointestinal tract
Pharmacokinetics
Osmolality
Membrane permeability
url https://doi.org/10.1186/s40780-021-00212-z
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