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The Effects of Korea Red Ginseng on Inflammatory Cytokines and Apoptosis in Rat Model with Chronic Nonbacterial Prostatitis

Chronic prostatitis typically occurs in aging men, and its symptoms include frequent and painful urination. In recent study, several studies have shown that Korean red ginseng (KRG) can be used in the prevention and treatment of various diseases. The objective of this study is to investigate whether...

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Autores principales: Kang, Sang Wook, Park, Je-Hoon, Seok, Hosik, Park, Hae Jeong, Chung, Joo-Ho, Kim, Chang-Ju, Kim, Young Ock, Han, Young Rok, Hong, DongWhan, Kim, Young Sik, Kim, Su Kang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6348920/
https://www.ncbi.nlm.nih.gov/pubmed/30756082
http://dx.doi.org/10.1155/2019/2462561
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author Kang, Sang Wook
Park, Je-Hoon
Seok, Hosik
Park, Hae Jeong
Chung, Joo-Ho
Kim, Chang-Ju
Kim, Young Ock
Han, Young Rok
Hong, DongWhan
Kim, Young Sik
Kim, Su Kang
author_facet Kang, Sang Wook
Park, Je-Hoon
Seok, Hosik
Park, Hae Jeong
Chung, Joo-Ho
Kim, Chang-Ju
Kim, Young Ock
Han, Young Rok
Hong, DongWhan
Kim, Young Sik
Kim, Su Kang
author_sort Kang, Sang Wook
collection PubMed
description Chronic prostatitis typically occurs in aging men, and its symptoms include frequent and painful urination. In recent study, several studies have shown that Korean red ginseng (KRG) can be used in the prevention and treatment of various diseases. The objective of this study is to investigate whether KRG can play a role in repressing the development of chronic nonbacterial prostatitis (CNP) in male Wistar rats. To induce CNP, rats were castrated and beta-estradiol (0.25 mg/kg) was subcutaneously (s.c.) injected daily. 7-week-old male Wistar rats were divided into 5 groups (the normal group, CNP group, positive group, and KRG group (0.25g/kg) and another KRG (0.50g/kg) group. After 4 weeks, all rats were sacrificed and their prostate and serum were analyzed. Compared to the positive group, the KRG groups (0.25g/kg and 0.50g/kg) showed similar protective properties on CNP based on the histopathologic morphology of the prostate and the inflammation cytokines in the prostate tissue. Also, results of the immunohistochemistry staining showed that expression levels of vascular endothelial growth factor A (VEGFA), interleukin 6 (IL6), interleukin 1 beta (IL-1ß), tumor necrosis factor (TNF-alpha), and cytochrome c oxidase subunit II (COX2) were also decreased in KRG group (0.25g/kg) and KRG group (0.50g/kg). These results suggested that KRG inhibited the development of CNP and might a useful herbal treatment or functional food for CNP.
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spelling pubmed-63489202019-02-12 The Effects of Korea Red Ginseng on Inflammatory Cytokines and Apoptosis in Rat Model with Chronic Nonbacterial Prostatitis Kang, Sang Wook Park, Je-Hoon Seok, Hosik Park, Hae Jeong Chung, Joo-Ho Kim, Chang-Ju Kim, Young Ock Han, Young Rok Hong, DongWhan Kim, Young Sik Kim, Su Kang Biomed Res Int Research Article Chronic prostatitis typically occurs in aging men, and its symptoms include frequent and painful urination. In recent study, several studies have shown that Korean red ginseng (KRG) can be used in the prevention and treatment of various diseases. The objective of this study is to investigate whether KRG can play a role in repressing the development of chronic nonbacterial prostatitis (CNP) in male Wistar rats. To induce CNP, rats were castrated and beta-estradiol (0.25 mg/kg) was subcutaneously (s.c.) injected daily. 7-week-old male Wistar rats were divided into 5 groups (the normal group, CNP group, positive group, and KRG group (0.25g/kg) and another KRG (0.50g/kg) group. After 4 weeks, all rats were sacrificed and their prostate and serum were analyzed. Compared to the positive group, the KRG groups (0.25g/kg and 0.50g/kg) showed similar protective properties on CNP based on the histopathologic morphology of the prostate and the inflammation cytokines in the prostate tissue. Also, results of the immunohistochemistry staining showed that expression levels of vascular endothelial growth factor A (VEGFA), interleukin 6 (IL6), interleukin 1 beta (IL-1ß), tumor necrosis factor (TNF-alpha), and cytochrome c oxidase subunit II (COX2) were also decreased in KRG group (0.25g/kg) and KRG group (0.50g/kg). These results suggested that KRG inhibited the development of CNP and might a useful herbal treatment or functional food for CNP. Hindawi 2019-01-14 /pmc/articles/PMC6348920/ /pubmed/30756082 http://dx.doi.org/10.1155/2019/2462561 Text en Copyright © 2019 Sang Wook Kang et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Kang, Sang Wook
Park, Je-Hoon
Seok, Hosik
Park, Hae Jeong
Chung, Joo-Ho
Kim, Chang-Ju
Kim, Young Ock
Han, Young Rok
Hong, DongWhan
Kim, Young Sik
Kim, Su Kang
The Effects of Korea Red Ginseng on Inflammatory Cytokines and Apoptosis in Rat Model with Chronic Nonbacterial Prostatitis
title The Effects of Korea Red Ginseng on Inflammatory Cytokines and Apoptosis in Rat Model with Chronic Nonbacterial Prostatitis
title_full The Effects of Korea Red Ginseng on Inflammatory Cytokines and Apoptosis in Rat Model with Chronic Nonbacterial Prostatitis
title_fullStr The Effects of Korea Red Ginseng on Inflammatory Cytokines and Apoptosis in Rat Model with Chronic Nonbacterial Prostatitis
title_full_unstemmed The Effects of Korea Red Ginseng on Inflammatory Cytokines and Apoptosis in Rat Model with Chronic Nonbacterial Prostatitis
title_short The Effects of Korea Red Ginseng on Inflammatory Cytokines and Apoptosis in Rat Model with Chronic Nonbacterial Prostatitis
title_sort effects of korea red ginseng on inflammatory cytokines and apoptosis in rat model with chronic nonbacterial prostatitis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6348920/
https://www.ncbi.nlm.nih.gov/pubmed/30756082
http://dx.doi.org/10.1155/2019/2462561
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