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Effects of Panax ginseng on the nerve growth factor expression in testosterone induced benign prostatic hyperplasia
The prostatic hyperplasia in benign prostatic hyperplasia (BPH) leads to obstructive micturition symptoms. Previous studies showed that pontine micturition center (PMC), ventrolateral periaqueductal gray (vlPAG), and medial preopticnucleus (MPA) regions in the brain have been known to regulate the u...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5775092/ https://www.ncbi.nlm.nih.gov/pubmed/29379359 http://dx.doi.org/10.1016/j.sjbs.2016.07.005 |
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author | Kim, Su Kang GyuKo, Il Park, Hae Jeong Chung, Joo-Ho Cho, Kyu Bong Kwon, Oh Young Park, Kyeong Hun Ahn, Young Sub Park, Chun Geon Kim, Young Ock |
author_facet | Kim, Su Kang GyuKo, Il Park, Hae Jeong Chung, Joo-Ho Cho, Kyu Bong Kwon, Oh Young Park, Kyeong Hun Ahn, Young Sub Park, Chun Geon Kim, Young Ock |
author_sort | Kim, Su Kang |
collection | PubMed |
description | The prostatic hyperplasia in benign prostatic hyperplasia (BPH) leads to obstructive micturition symptoms. Previous studies showed that pontine micturition center (PMC), ventrolateral periaqueductal gray (vlPAG), and medial preopticnucleus (MPA) regions in the brain have been known to regulate the urinary bladder function. The present study shows the influences of Panax ginseng on nerve growth factor (NGF) expressions in PMC, vlPAG, and MPA regions in the brain. Wistar rats were used for the present study. The rats split into four groups; 4 groups (n = 6) in control group, BPH-induced group, BPH-induced and P. ginseng-treated group, and BPH-induced and finasteride-treated group. BPH in rats was induced by testosterone and the animals were evaluated for NGF expression in PMC, vlPAG, and MPA regions in the brain. The NGF expression was identified using immunohistochemistry (IHC). The NGF expression by IHC showed spots with dark brown color. In our results, NGF expressions in PMC, vlPAG, and MPA regions in the brainstem of the BPH-induced group showed increase than the control animal. These increased NGF expressions in three regions were decreased using treatment with P. ginseng (200 mg/kg). These results suggest that P. ginseng has therapeutic effects on the symptoms of BPH and is associated with the regulation of NGF expression in the brain. In conclusion, the administration of P. ginseng helps nerve growth factor activation. |
format | Online Article Text |
id | pubmed-5775092 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-57750922018-01-29 Effects of Panax ginseng on the nerve growth factor expression in testosterone induced benign prostatic hyperplasia Kim, Su Kang GyuKo, Il Park, Hae Jeong Chung, Joo-Ho Cho, Kyu Bong Kwon, Oh Young Park, Kyeong Hun Ahn, Young Sub Park, Chun Geon Kim, Young Ock Saudi J Biol Sci Article The prostatic hyperplasia in benign prostatic hyperplasia (BPH) leads to obstructive micturition symptoms. Previous studies showed that pontine micturition center (PMC), ventrolateral periaqueductal gray (vlPAG), and medial preopticnucleus (MPA) regions in the brain have been known to regulate the urinary bladder function. The present study shows the influences of Panax ginseng on nerve growth factor (NGF) expressions in PMC, vlPAG, and MPA regions in the brain. Wistar rats were used for the present study. The rats split into four groups; 4 groups (n = 6) in control group, BPH-induced group, BPH-induced and P. ginseng-treated group, and BPH-induced and finasteride-treated group. BPH in rats was induced by testosterone and the animals were evaluated for NGF expression in PMC, vlPAG, and MPA regions in the brain. The NGF expression was identified using immunohistochemistry (IHC). The NGF expression by IHC showed spots with dark brown color. In our results, NGF expressions in PMC, vlPAG, and MPA regions in the brainstem of the BPH-induced group showed increase than the control animal. These increased NGF expressions in three regions were decreased using treatment with P. ginseng (200 mg/kg). These results suggest that P. ginseng has therapeutic effects on the symptoms of BPH and is associated with the regulation of NGF expression in the brain. In conclusion, the administration of P. ginseng helps nerve growth factor activation. Elsevier 2018-01 2016-08-13 /pmc/articles/PMC5775092/ /pubmed/29379359 http://dx.doi.org/10.1016/j.sjbs.2016.07.005 Text en © 2016 Production and hosting by Elsevier B.V. on behalf of King Saud University. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Kim, Su Kang GyuKo, Il Park, Hae Jeong Chung, Joo-Ho Cho, Kyu Bong Kwon, Oh Young Park, Kyeong Hun Ahn, Young Sub Park, Chun Geon Kim, Young Ock Effects of Panax ginseng on the nerve growth factor expression in testosterone induced benign prostatic hyperplasia |
title | Effects of Panax ginseng on the nerve growth factor expression in testosterone induced benign prostatic hyperplasia |
title_full | Effects of Panax ginseng on the nerve growth factor expression in testosterone induced benign prostatic hyperplasia |
title_fullStr | Effects of Panax ginseng on the nerve growth factor expression in testosterone induced benign prostatic hyperplasia |
title_full_unstemmed | Effects of Panax ginseng on the nerve growth factor expression in testosterone induced benign prostatic hyperplasia |
title_short | Effects of Panax ginseng on the nerve growth factor expression in testosterone induced benign prostatic hyperplasia |
title_sort | effects of panax ginseng on the nerve growth factor expression in testosterone induced benign prostatic hyperplasia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5775092/ https://www.ncbi.nlm.nih.gov/pubmed/29379359 http://dx.doi.org/10.1016/j.sjbs.2016.07.005 |
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