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Pharmacological effects of different ginger juices on the concurrent symptoms in animal models of functional dyspepsia: A comparative study

OBJECTIVE: Patients with gastrointestinal disorders commonly suffer from poor treatment outcomes and adverse effects of traditional pharmacological therapy. Herbal medicine is a favorable alternative due to the low risk of side effects. This study was performed to explore the antiemetic effects and...

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Autores principales: Zhong, Ling‐yun, Tong, Heng‐li, Zhu, Jing, Lv, Mu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6657707/
https://www.ncbi.nlm.nih.gov/pubmed/31367349
http://dx.doi.org/10.1002/fsn3.990
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author Zhong, Ling‐yun
Tong, Heng‐li
Zhu, Jing
Lv, Mu
author_facet Zhong, Ling‐yun
Tong, Heng‐li
Zhu, Jing
Lv, Mu
author_sort Zhong, Ling‐yun
collection PubMed
description OBJECTIVE: Patients with gastrointestinal disorders commonly suffer from poor treatment outcomes and adverse effects of traditional pharmacological therapy. Herbal medicine is a favorable alternative due to the low risk of side effects. This study was performed to explore the antiemetic effects and the improvement effect on gastrointestinal function of components of three ginger juice excipients. METHODS: The compositions were analyzed by liquid chromatograph mass spectrometer (LC‐MS), especially the gingerols of dried ginger juice (DGJ), fresh ginger juice (FGJ), and fresh ginger boiled juice (FGBJ). Furthermore, the respective gastrointestinal effects on rat models with functional dyspepsia (FD) were compared. RESULTS: The 6‐keto‐PGF(1α) levels in the serum of the treated groups were significantly reduced (p < 0.05), as compared with the control group. Compared with the cisplatin group, there was an apparent reduction in kaolin intake for DGJ, FGJ, and FGBJ (p < 0.01; p < 0.01; p < 0.05). The intestinal propulsive rate of the rats in the treated group was significantly higher than that in the control group (p < 0.05). Ginger juices significantly improved gastrointestinal function in rats. Eight common components were found in DGJ, FGJ, and FGBJ, among which 6‐paradol, 10‐gingerol, and 12‐shogaol led to inhibited gastric mucosal damage function effect according to the Pearson correlation analysis. Only 6‐shogaol was found to have a positive correlation with gastrointestinal function effect through Pearson correlation analysis. CONCLUSION: Ginger juice should be recommended for the medicinal materials used in the treatment of concurrent symptoms of FD.
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spelling pubmed-66577072019-07-31 Pharmacological effects of different ginger juices on the concurrent symptoms in animal models of functional dyspepsia: A comparative study Zhong, Ling‐yun Tong, Heng‐li Zhu, Jing Lv, Mu Food Sci Nutr Original Research OBJECTIVE: Patients with gastrointestinal disorders commonly suffer from poor treatment outcomes and adverse effects of traditional pharmacological therapy. Herbal medicine is a favorable alternative due to the low risk of side effects. This study was performed to explore the antiemetic effects and the improvement effect on gastrointestinal function of components of three ginger juice excipients. METHODS: The compositions were analyzed by liquid chromatograph mass spectrometer (LC‐MS), especially the gingerols of dried ginger juice (DGJ), fresh ginger juice (FGJ), and fresh ginger boiled juice (FGBJ). Furthermore, the respective gastrointestinal effects on rat models with functional dyspepsia (FD) were compared. RESULTS: The 6‐keto‐PGF(1α) levels in the serum of the treated groups were significantly reduced (p < 0.05), as compared with the control group. Compared with the cisplatin group, there was an apparent reduction in kaolin intake for DGJ, FGJ, and FGBJ (p < 0.01; p < 0.01; p < 0.05). The intestinal propulsive rate of the rats in the treated group was significantly higher than that in the control group (p < 0.05). Ginger juices significantly improved gastrointestinal function in rats. Eight common components were found in DGJ, FGJ, and FGBJ, among which 6‐paradol, 10‐gingerol, and 12‐shogaol led to inhibited gastric mucosal damage function effect according to the Pearson correlation analysis. Only 6‐shogaol was found to have a positive correlation with gastrointestinal function effect through Pearson correlation analysis. CONCLUSION: Ginger juice should be recommended for the medicinal materials used in the treatment of concurrent symptoms of FD. John Wiley and Sons Inc. 2019-06-17 /pmc/articles/PMC6657707/ /pubmed/31367349 http://dx.doi.org/10.1002/fsn3.990 Text en © 2019 The Authors. Food Science & Nutrition published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Zhong, Ling‐yun
Tong, Heng‐li
Zhu, Jing
Lv, Mu
Pharmacological effects of different ginger juices on the concurrent symptoms in animal models of functional dyspepsia: A comparative study
title Pharmacological effects of different ginger juices on the concurrent symptoms in animal models of functional dyspepsia: A comparative study
title_full Pharmacological effects of different ginger juices on the concurrent symptoms in animal models of functional dyspepsia: A comparative study
title_fullStr Pharmacological effects of different ginger juices on the concurrent symptoms in animal models of functional dyspepsia: A comparative study
title_full_unstemmed Pharmacological effects of different ginger juices on the concurrent symptoms in animal models of functional dyspepsia: A comparative study
title_short Pharmacological effects of different ginger juices on the concurrent symptoms in animal models of functional dyspepsia: A comparative study
title_sort pharmacological effects of different ginger juices on the concurrent symptoms in animal models of functional dyspepsia: a comparative study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6657707/
https://www.ncbi.nlm.nih.gov/pubmed/31367349
http://dx.doi.org/10.1002/fsn3.990
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