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Enhancing effect of Panax ginseng on Zip4-mediated zinc influx into the cytosol
BACKGROUND: Zinc homeostasis is essential for human health and is regulated by several zinc transporters including ZIP and ZnT. ZIP4 is expressed in the small intestine and is important for zinc absorption from the diet. We investigated in the present study the effects of Panax ginseng (P. ginseng)...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9058843/ https://www.ncbi.nlm.nih.gov/pubmed/35509828 http://dx.doi.org/10.1016/j.jgr.2021.06.006 |
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author | Ikeda, Yoshito Munekane, Masayuki Yamada, Yasuyuki Kawakami, Mizuki Amano, Ikuko Sano, Kohei Mukai, Takahiro Kambe, Taiho Shitan, Nobukazu |
author_facet | Ikeda, Yoshito Munekane, Masayuki Yamada, Yasuyuki Kawakami, Mizuki Amano, Ikuko Sano, Kohei Mukai, Takahiro Kambe, Taiho Shitan, Nobukazu |
author_sort | Ikeda, Yoshito |
collection | PubMed |
description | BACKGROUND: Zinc homeostasis is essential for human health and is regulated by several zinc transporters including ZIP and ZnT. ZIP4 is expressed in the small intestine and is important for zinc absorption from the diet. We investigated in the present study the effects of Panax ginseng (P. ginseng) extract on modulating Zip4 expression and cellular zinc levels in mouse Hepa cells. METHODS: Hepa cells were transfected with a luciferase reporter plasmid that contains metal-responsive elements, incubated with P. ginseng extract, and luciferase activity was measured. Using (65)ZnCl(2), zinc uptake in P. ginseng-treated cells was measured. The expression of Zip4 mRNA and protein in Hepa cells was also investigated. Finally, using a luciferase reporter assay system, the effects of several ginsenosides were monitored. RESULTS: The luciferase activity in cells incubated with P. ginseng extract was significantly higher than that of control cells cultured in normal medium. Hepa cells treated with P. ginseng extract exhibited higher zinc uptake. P. ginseng extract induced Zip4 mRNA expression, which resulted in an enhancement of Zip4 protein expression. Furthermore, some ginsenosides, such as ginsenoside Rc and Re, enhanced luciferase activity driven by intracellular zinc levels. CONCLUSION: P. ginseng extract induced Zip4 expression at the mRNA and protein level and resulted in higher zinc uptake in Hepa cells. Some ginsenosides facilitated zinc influx. On the basis of these results, we suggest a novel effect of P. ginseng on Zip4-mediated zinc influx, which may provide a new strategy for preventing zinc deficiency. |
format | Online Article Text |
id | pubmed-9058843 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-90588432022-05-03 Enhancing effect of Panax ginseng on Zip4-mediated zinc influx into the cytosol Ikeda, Yoshito Munekane, Masayuki Yamada, Yasuyuki Kawakami, Mizuki Amano, Ikuko Sano, Kohei Mukai, Takahiro Kambe, Taiho Shitan, Nobukazu J Ginseng Res Research Article BACKGROUND: Zinc homeostasis is essential for human health and is regulated by several zinc transporters including ZIP and ZnT. ZIP4 is expressed in the small intestine and is important for zinc absorption from the diet. We investigated in the present study the effects of Panax ginseng (P. ginseng) extract on modulating Zip4 expression and cellular zinc levels in mouse Hepa cells. METHODS: Hepa cells were transfected with a luciferase reporter plasmid that contains metal-responsive elements, incubated with P. ginseng extract, and luciferase activity was measured. Using (65)ZnCl(2), zinc uptake in P. ginseng-treated cells was measured. The expression of Zip4 mRNA and protein in Hepa cells was also investigated. Finally, using a luciferase reporter assay system, the effects of several ginsenosides were monitored. RESULTS: The luciferase activity in cells incubated with P. ginseng extract was significantly higher than that of control cells cultured in normal medium. Hepa cells treated with P. ginseng extract exhibited higher zinc uptake. P. ginseng extract induced Zip4 mRNA expression, which resulted in an enhancement of Zip4 protein expression. Furthermore, some ginsenosides, such as ginsenoside Rc and Re, enhanced luciferase activity driven by intracellular zinc levels. CONCLUSION: P. ginseng extract induced Zip4 expression at the mRNA and protein level and resulted in higher zinc uptake in Hepa cells. Some ginsenosides facilitated zinc influx. On the basis of these results, we suggest a novel effect of P. ginseng on Zip4-mediated zinc influx, which may provide a new strategy for preventing zinc deficiency. Elsevier 2022-03 2021-06-15 /pmc/articles/PMC9058843/ /pubmed/35509828 http://dx.doi.org/10.1016/j.jgr.2021.06.006 Text en © 2021 The Korean Society of Ginseng. Publishing services by Elsevier B.V. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Article Ikeda, Yoshito Munekane, Masayuki Yamada, Yasuyuki Kawakami, Mizuki Amano, Ikuko Sano, Kohei Mukai, Takahiro Kambe, Taiho Shitan, Nobukazu Enhancing effect of Panax ginseng on Zip4-mediated zinc influx into the cytosol |
title | Enhancing effect of Panax ginseng on Zip4-mediated zinc influx into the cytosol |
title_full | Enhancing effect of Panax ginseng on Zip4-mediated zinc influx into the cytosol |
title_fullStr | Enhancing effect of Panax ginseng on Zip4-mediated zinc influx into the cytosol |
title_full_unstemmed | Enhancing effect of Panax ginseng on Zip4-mediated zinc influx into the cytosol |
title_short | Enhancing effect of Panax ginseng on Zip4-mediated zinc influx into the cytosol |
title_sort | enhancing effect of panax ginseng on zip4-mediated zinc influx into the cytosol |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9058843/ https://www.ncbi.nlm.nih.gov/pubmed/35509828 http://dx.doi.org/10.1016/j.jgr.2021.06.006 |
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