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Gintonin absorption in intestinal model systems

Recently, we identified a novel ginseng-derived lysophosphatidic acid receptor ligand, called gintonin. We showed that gintonin induces [Ca2+]i transient-mediated morphological changes, proliferation, and migration in cells expressing lysophosphatidic acid receptors and that oral administration of g...

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Published in:Journal of ginseng research 2018, 42(1), , pp.35-41
Main Authors: Lee, Byung-Hwan, Choi, Sun-Hye, Kim, Hyeon-Joong, Park, Sang-Deuk, Rhim, Hyewhon, Kim, Hyoung-Chun, Hwang, Sung-Hee, Nah, Seung-Yeol
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cited_by cdi_FETCH-LOGICAL-c581t-e6caf5ec1512f9399d6a996b3ce8ac90fc45695d56ea4d7087145e01e30bdd833
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container_title Journal of ginseng research
container_volume 42
creator Lee, Byung-Hwan
Choi, Sun-Hye
Kim, Hyeon-Joong
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Kim, Hyoung-Chun
Hwang, Sung-Hee
Nah, Seung-Yeol
description Recently, we identified a novel ginseng-derived lysophosphatidic acid receptor ligand, called gintonin. We showed that gintonin induces [Ca2+]i transient-mediated morphological changes, proliferation, and migration in cells expressing lysophosphatidic acid receptors and that oral administration of gintonin exhibits anti-Alzheimer disease effects in model mice. However, little is known about the intestinal absorption of gintonin. The aim of this study was to investigate gintonin absorption using two model systems. Gintonin membrane permeation was examined using a parallel artificial membrane permeation assay, and gintonin absorption was evaluated in a mouse everted intestinal sac model. The parallel artificial membrane permeation assay showed that gintonin could permeate an artificial membrane in a dose-dependent manner. In the everted sac model, gintonin absorption increased with incubation time (from 0 min to 60 min), followed by a decrease in absorption. Gintonin absorption into everted sacs was also dose dependent, with a nonlinear correlation between gintonin absorption and concentration at 0.1–3 mg/mL and saturation at 3–5 mg/mL. Gintonin absorption was inhibited by the Rho kinase inhibitor Y-27632 and the sodium–glucose transporter inhibitor phloridzin. Moreover, lipid extraction with methanol also attenuated gintonin absorption, suggesting the importance of the lipid portion of gintonin in absorption. This result shows that gintonin might be absorbed through passive diffusion, paracellular, and active transport pathways. The present study shows that gintonin could be absorbed in the intestine through transcellular and paracellular diffusion, and active transport. In addition, the lipid component of gintonin might play a key role in its intestinal absorption.
doi_str_mv 10.1016/j.jgr.2016.12.007
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Gintonin absorption into everted sacs was also dose dependent, with a nonlinear correlation between gintonin absorption and concentration at 0.1–3 mg/mL and saturation at 3–5 mg/mL. Gintonin absorption was inhibited by the Rho kinase inhibitor Y-27632 and the sodium–glucose transporter inhibitor phloridzin. Moreover, lipid extraction with methanol also attenuated gintonin absorption, suggesting the importance of the lipid portion of gintonin in absorption. This result shows that gintonin might be absorbed through passive diffusion, paracellular, and active transport pathways. The present study shows that gintonin could be absorbed in the intestine through transcellular and paracellular diffusion, and active transport. 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Gintonin absorption into everted sacs was also dose dependent, with a nonlinear correlation between gintonin absorption and concentration at 0.1–3 mg/mL and saturation at 3–5 mg/mL. Gintonin absorption was inhibited by the Rho kinase inhibitor Y-27632 and the sodium–glucose transporter inhibitor phloridzin. Moreover, lipid extraction with methanol also attenuated gintonin absorption, suggesting the importance of the lipid portion of gintonin in absorption. This result shows that gintonin might be absorbed through passive diffusion, paracellular, and active transport pathways. The present study shows that gintonin could be absorbed in the intestine through transcellular and paracellular diffusion, and active transport. 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source Open Access: PubMed Central; Elsevier ScienceDirect Journals; IngentaConnect Journals
subjects everted intestinal sac
gintonin
gintonin absorption
Panax ginseng
기타의약학
title Gintonin absorption in intestinal model systems
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