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Mangosteen pericarp components alleviate progression of prostatic hyperplasia and mitochondrial dysfunction in rats

Prostatic hyperplasia, characterized by progressive hyperplasia of glandular and stromal tissues, is the most common proliferative abnormality of the prostate in aging men. A high-fat diet (HFD) usually is a major factor inducing oxidative stress, inflammation, and an abnormal state of the prostate....

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Autores principales: Tsai, Hui-Hsuan, Chen, Chia-Wen, Yu, Pei-Ling, Lin, Yu-Ling, Hsieh, Rong-Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6962454/
https://www.ncbi.nlm.nih.gov/pubmed/31941927
http://dx.doi.org/10.1038/s41598-019-56970-2
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author Tsai, Hui-Hsuan
Chen, Chia-Wen
Yu, Pei-Ling
Lin, Yu-Ling
Hsieh, Rong-Hong
author_facet Tsai, Hui-Hsuan
Chen, Chia-Wen
Yu, Pei-Ling
Lin, Yu-Ling
Hsieh, Rong-Hong
author_sort Tsai, Hui-Hsuan
collection PubMed
description Prostatic hyperplasia, characterized by progressive hyperplasia of glandular and stromal tissues, is the most common proliferative abnormality of the prostate in aging men. A high-fat diet (HFD) usually is a major factor inducing oxidative stress, inflammation, and an abnormal state of the prostate. Mangosteen pericarp powder (MPP) has abundant xanthones which can be antioxidant, anti-inflammatory, and antiproliferative agents. Therefore, the purpose of this study was to research whether MPP supplementation can affect the progression of prostatic hyperplasia. Twenty-four male F344 rats were randomly divided into four groups, including a control group (C), prostatic hyperplasia-induced group (P), prostatic hyperplasia-induced with low-dose MPP group (PL), and induced with high-dose MPP group (PH). The P, PL, and PH groups were given weekly intraperitoneal injections of 3,2′-dimethyl-4-aminobiphenyl (DMAB) at 25 mg/kg body weight for 10 weeks, and simultaneously fed an HFD for 24 weeks. Our findings first demonstrated that MPP consumption significantly decreased the prostate weight, serum testosterone and dihydrotestosterone concentrations, protein expression of proliferating cell nuclear antigen, and malondialdehyde levels and ameliorated mitochondrial function in prostatic tissues. These results suggest that MPP supplementation could be used to attenuate the progression of prostatic hyperplasia.
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spelling pubmed-69624542020-01-23 Mangosteen pericarp components alleviate progression of prostatic hyperplasia and mitochondrial dysfunction in rats Tsai, Hui-Hsuan Chen, Chia-Wen Yu, Pei-Ling Lin, Yu-Ling Hsieh, Rong-Hong Sci Rep Article Prostatic hyperplasia, characterized by progressive hyperplasia of glandular and stromal tissues, is the most common proliferative abnormality of the prostate in aging men. A high-fat diet (HFD) usually is a major factor inducing oxidative stress, inflammation, and an abnormal state of the prostate. Mangosteen pericarp powder (MPP) has abundant xanthones which can be antioxidant, anti-inflammatory, and antiproliferative agents. Therefore, the purpose of this study was to research whether MPP supplementation can affect the progression of prostatic hyperplasia. Twenty-four male F344 rats were randomly divided into four groups, including a control group (C), prostatic hyperplasia-induced group (P), prostatic hyperplasia-induced with low-dose MPP group (PL), and induced with high-dose MPP group (PH). The P, PL, and PH groups were given weekly intraperitoneal injections of 3,2′-dimethyl-4-aminobiphenyl (DMAB) at 25 mg/kg body weight for 10 weeks, and simultaneously fed an HFD for 24 weeks. Our findings first demonstrated that MPP consumption significantly decreased the prostate weight, serum testosterone and dihydrotestosterone concentrations, protein expression of proliferating cell nuclear antigen, and malondialdehyde levels and ameliorated mitochondrial function in prostatic tissues. These results suggest that MPP supplementation could be used to attenuate the progression of prostatic hyperplasia. Nature Publishing Group UK 2020-01-15 /pmc/articles/PMC6962454/ /pubmed/31941927 http://dx.doi.org/10.1038/s41598-019-56970-2 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Tsai, Hui-Hsuan
Chen, Chia-Wen
Yu, Pei-Ling
Lin, Yu-Ling
Hsieh, Rong-Hong
Mangosteen pericarp components alleviate progression of prostatic hyperplasia and mitochondrial dysfunction in rats
title Mangosteen pericarp components alleviate progression of prostatic hyperplasia and mitochondrial dysfunction in rats
title_full Mangosteen pericarp components alleviate progression of prostatic hyperplasia and mitochondrial dysfunction in rats
title_fullStr Mangosteen pericarp components alleviate progression of prostatic hyperplasia and mitochondrial dysfunction in rats
title_full_unstemmed Mangosteen pericarp components alleviate progression of prostatic hyperplasia and mitochondrial dysfunction in rats
title_short Mangosteen pericarp components alleviate progression of prostatic hyperplasia and mitochondrial dysfunction in rats
title_sort mangosteen pericarp components alleviate progression of prostatic hyperplasia and mitochondrial dysfunction in rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6962454/
https://www.ncbi.nlm.nih.gov/pubmed/31941927
http://dx.doi.org/10.1038/s41598-019-56970-2
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