ID | 112025 |
Author |
Afroz, Sheuli
Tokushima University
Yagi, Ayano
Tokushima University
Fujikawa, Kouki
Tokushima University
Rahman, M. Motiur
Tokushima University
Morito, Katsuya
Tokushima University
Watanabe, Shiro
University of Toyama
Kiyokage, Emi
Kawasaki Medical School|Kawasaki University of Medical Welfare
Toida, Kazunori
Kawasaki Medical School|Osaka University
Ishida, Tatsuhiro
Tokushima University
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Kogure, Kentaro
Tokushima University
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Tokumura, Akira
Yasuda Women’s University
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|
Keywords | Lysophosphatidic acid
Medicinal herbs
Indomethacin
Prostaglandin E2
Cell death
Cell proliferation
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Content Type |
Journal Article
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Description | Lysophosphatidic acid (LPA) is a bioactive phospholipid that induces diverse biological responses. Recently, we found that LPA ameliorates NSAIDs-induced gastric ulcer in mice. Here, we quantified LPA in 21 medicinal herbs used for treatment of gastrointestinal (GI) disorders. We found that half of them contained LPA at relatively high levels (40–240 μg/g) compared to soybean seed powder (4.6 μg/g), which we previously identified as an LPA-rich food. The LPA in peony (Paeonia lactiflora) root powder is highly concentrated in the lipid fraction that ameliorates indomethacin-induced gastric ulcer in mice. Synthetic 18:1 LPA, peony root LPA and peony root lipid enhanced prostaglandin E2 production in a gastric cancer cell line, MKN74 cells that express LPA2 abundantly. These materials also prevented indomethacin-induced cell death and stimulated the proliferation of MKN74 cells. We found that LPA was present in stomach fluids at 2.4 μM, which is an effective LPA concentration for inducing a cellular response in vitro. These results indicated that LPA is one of the active components of medicinal herbs for the treatment of GI disorder and that orally administered LPA-rich herbs may augment the protective actions of endogenous LPA on gastric mucosa.
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Journal Title |
Prostaglandins & Other Lipid Mediators
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ISSN | 10988823
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NCID | AA11221062
AA11532903
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Publisher | Elsevier
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Volume | 135
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Start Page | 36
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End Page | 44
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Published Date | 2018-02-17
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Rights | © 2018. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/
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EDB ID | |
DOI (Published Version) | |
URL ( Publisher's Version ) | |
FullText File | |
language |
eng
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TextVersion |
Author
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departments |
Pharmaceutical Sciences
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