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Regulatory/modulatory effect of prune essence concentrate on intestinal function and blood lipids

Context:Prunus domestica Linn (Rosaceae) has been considered a functional food, owing to its various pharmacological activities, including antioxidant, anti-inflammatory, antidiabetic and anticancer. Objective: This placebo-controlled, randomized study was framed to check the beneficial activity of...

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Autores principales: Chiu, Hui-Fang, Huang, Yun-Chien, Lu, Yan-Ying, Han, Yi-Chun, Shen, You-Cheng, Golovinskaia, Oksana, Venkatakrishnan, Kamesh, Wang, Chin-Kun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6130511/
https://www.ncbi.nlm.nih.gov/pubmed/28164731
http://dx.doi.org/10.1080/13880209.2017.1285323
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author Chiu, Hui-Fang
Huang, Yun-Chien
Lu, Yan-Ying
Han, Yi-Chun
Shen, You-Cheng
Golovinskaia, Oksana
Venkatakrishnan, Kamesh
Wang, Chin-Kun
author_facet Chiu, Hui-Fang
Huang, Yun-Chien
Lu, Yan-Ying
Han, Yi-Chun
Shen, You-Cheng
Golovinskaia, Oksana
Venkatakrishnan, Kamesh
Wang, Chin-Kun
author_sort Chiu, Hui-Fang
collection PubMed
description Context:Prunus domestica Linn (Rosaceae) has been considered a functional food, owing to its various pharmacological activities, including antioxidant, anti-inflammatory, antidiabetic and anticancer. Objective: This placebo-controlled, randomized study was framed to check the beneficial activity of prune essence concentrates (PEC) in corroboration with intestinal function and lipid profile in mildly hypercholesterolemic subjects. Materials and methods: Sixty healthy mild hypercholesterolemic subjects were randomly chosen and segregated into three groups as placebo (consume 50 mL of simulated prune drink), PEC I (consume 50 mL of PEC/day) and PEC II (consume 100 mL of PEC/day) for 4 weeks with 2 weeks of follow-up without PEC consumption. Results: Intake of PEC (I and II) for 4 weeks substantially ameliorated (p < 0.05) the colony number of Bifidobacterium spp. (1.18- and 1.19-fold) and Lactobacillus spp. (1.07- and 1.16-fold), but markedly lowered (p < 0.05) the colony number of Clostridium perfringens (5.97 and 8.35%) and Escherichia coli (6.25 and 9.38%). Meanwhile, the total cholesterol (TC; 5.90 and 6.99%) levels and LDL-c (6.68 and 6.53%) were significantly reduced (p < 0.05), but no change in other lipid parameters. Whereas, the antioxidant capacity was also concomitantly elevated (p < 0.05) upon administration with PEC. Discussion and conclusion: Overall, the results suggest that the use of PEC may positively regulate the intestinal microflora and thereby effectively lower the TC levels and thus act as a hypocholesterolemic agent.
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spelling pubmed-61305112018-09-27 Regulatory/modulatory effect of prune essence concentrate on intestinal function and blood lipids Chiu, Hui-Fang Huang, Yun-Chien Lu, Yan-Ying Han, Yi-Chun Shen, You-Cheng Golovinskaia, Oksana Venkatakrishnan, Kamesh Wang, Chin-Kun Pharm Biol Research Article Context:Prunus domestica Linn (Rosaceae) has been considered a functional food, owing to its various pharmacological activities, including antioxidant, anti-inflammatory, antidiabetic and anticancer. Objective: This placebo-controlled, randomized study was framed to check the beneficial activity of prune essence concentrates (PEC) in corroboration with intestinal function and lipid profile in mildly hypercholesterolemic subjects. Materials and methods: Sixty healthy mild hypercholesterolemic subjects were randomly chosen and segregated into three groups as placebo (consume 50 mL of simulated prune drink), PEC I (consume 50 mL of PEC/day) and PEC II (consume 100 mL of PEC/day) for 4 weeks with 2 weeks of follow-up without PEC consumption. Results: Intake of PEC (I and II) for 4 weeks substantially ameliorated (p < 0.05) the colony number of Bifidobacterium spp. (1.18- and 1.19-fold) and Lactobacillus spp. (1.07- and 1.16-fold), but markedly lowered (p < 0.05) the colony number of Clostridium perfringens (5.97 and 8.35%) and Escherichia coli (6.25 and 9.38%). Meanwhile, the total cholesterol (TC; 5.90 and 6.99%) levels and LDL-c (6.68 and 6.53%) were significantly reduced (p < 0.05), but no change in other lipid parameters. Whereas, the antioxidant capacity was also concomitantly elevated (p < 0.05) upon administration with PEC. Discussion and conclusion: Overall, the results suggest that the use of PEC may positively regulate the intestinal microflora and thereby effectively lower the TC levels and thus act as a hypocholesterolemic agent. Taylor & Francis 2017-02-05 /pmc/articles/PMC6130511/ /pubmed/28164731 http://dx.doi.org/10.1080/13880209.2017.1285323 Text en © 2017 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Chiu, Hui-Fang
Huang, Yun-Chien
Lu, Yan-Ying
Han, Yi-Chun
Shen, You-Cheng
Golovinskaia, Oksana
Venkatakrishnan, Kamesh
Wang, Chin-Kun
Regulatory/modulatory effect of prune essence concentrate on intestinal function and blood lipids
title Regulatory/modulatory effect of prune essence concentrate on intestinal function and blood lipids
title_full Regulatory/modulatory effect of prune essence concentrate on intestinal function and blood lipids
title_fullStr Regulatory/modulatory effect of prune essence concentrate on intestinal function and blood lipids
title_full_unstemmed Regulatory/modulatory effect of prune essence concentrate on intestinal function and blood lipids
title_short Regulatory/modulatory effect of prune essence concentrate on intestinal function and blood lipids
title_sort regulatory/modulatory effect of prune essence concentrate on intestinal function and blood lipids
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6130511/
https://www.ncbi.nlm.nih.gov/pubmed/28164731
http://dx.doi.org/10.1080/13880209.2017.1285323
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