Alteration of Gut Microbes in Benign Prostatic Hyperplasia Model and Finasteride Treatment Model

Gut microbes are closely associated with disease onset and improvement. However, the effects of gut microbes on the occurrence, prevention, and treatment of benign prostatic hyperplasia (BPH) are still unclear. We investigated the alteration of gut microbiota with implications for the diagnosis, pre...

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Main Authors: Jinho An, Youngcheon Song, Sangbum Kim, Hyunseok Kong, Kyungjae Kim
Format: Article
Language:English
Published: MDPI AG 2023-03-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/24/6/5904
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author Jinho An
Youngcheon Song
Sangbum Kim
Hyunseok Kong
Kyungjae Kim
author_facet Jinho An
Youngcheon Song
Sangbum Kim
Hyunseok Kong
Kyungjae Kim
author_sort Jinho An
collection DOAJ
description Gut microbes are closely associated with disease onset and improvement. However, the effects of gut microbes on the occurrence, prevention, and treatment of benign prostatic hyperplasia (BPH) are still unclear. We investigated the alteration of gut microbiota with implications for the diagnosis, prevention, and treatment of BPH and identified correlations among various indicators, including hormone indicators, apoptosis markers in BPH, and finasteride treatment models. BPH induction altered the abundance of <i>Lactobacillus</i>, <i>Flavonifractor</i>, <i>Acetatifactor</i>, <i>Oscillibacter</i>, <i>Pseudoflavonifractor</i>, <i>Intestinimonas</i>, and <i>Butyricimonas</i> genera, which are related to BPH indicators. Among these, the altered abundance of <i>Lactobacillus</i> and <i>Acetatifactor</i> was associated with the promotion and inhibition of prostate apoptosis, respectively. Finasteride treatment altered the abundance of <i>Barnesiella</i>, <i>Acetatifactor</i>, <i>Butyricimonas</i>, <i>Desulfovibrio</i>, <i>Anaerobacterium</i>, and <i>Robinsoniella</i> genera, which are related to BPH indicators. Among these, altered abundances of <i>Desulfovibrio</i> and <i>Acetatifactor</i> were associated with the promotion and inhibition of prostate apoptosis, respectively. In addition, the abundances of <i>Lactobacillus</i> and <i>Acetatifactor</i> were normalized after finasteride treatment. In conclusion, the association between apoptosis and altered abundances of <i>Lactobacillus</i> and <i>Acetatifactor</i>, among other gut microbes, suggests their potential utility in the diagnosis, prevention, and treatment of BPH.
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spelling doaj.art-e66a0431ce574914b7bf785e0f5831f02023-11-17T11:40:45ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672023-03-01246590410.3390/ijms24065904Alteration of Gut Microbes in Benign Prostatic Hyperplasia Model and Finasteride Treatment ModelJinho An0Youngcheon Song1Sangbum Kim2Hyunseok Kong3Kyungjae Kim4College of Pharmacy, Sahmyook University, Seoul 01795, Republic of KoreaCollege of Pharmacy, Sahmyook University, Seoul 01795, Republic of KoreaCollege of Pharmacy, Sahmyook University, Seoul 01795, Republic of KoreaPADAM Natural Material Research Institute, Sahmyook University, Seoul 01795, Republic of KoreaCollege of Pharmacy, Sahmyook University, Seoul 01795, Republic of KoreaGut microbes are closely associated with disease onset and improvement. However, the effects of gut microbes on the occurrence, prevention, and treatment of benign prostatic hyperplasia (BPH) are still unclear. We investigated the alteration of gut microbiota with implications for the diagnosis, prevention, and treatment of BPH and identified correlations among various indicators, including hormone indicators, apoptosis markers in BPH, and finasteride treatment models. BPH induction altered the abundance of <i>Lactobacillus</i>, <i>Flavonifractor</i>, <i>Acetatifactor</i>, <i>Oscillibacter</i>, <i>Pseudoflavonifractor</i>, <i>Intestinimonas</i>, and <i>Butyricimonas</i> genera, which are related to BPH indicators. Among these, the altered abundance of <i>Lactobacillus</i> and <i>Acetatifactor</i> was associated with the promotion and inhibition of prostate apoptosis, respectively. Finasteride treatment altered the abundance of <i>Barnesiella</i>, <i>Acetatifactor</i>, <i>Butyricimonas</i>, <i>Desulfovibrio</i>, <i>Anaerobacterium</i>, and <i>Robinsoniella</i> genera, which are related to BPH indicators. Among these, altered abundances of <i>Desulfovibrio</i> and <i>Acetatifactor</i> were associated with the promotion and inhibition of prostate apoptosis, respectively. In addition, the abundances of <i>Lactobacillus</i> and <i>Acetatifactor</i> were normalized after finasteride treatment. In conclusion, the association between apoptosis and altered abundances of <i>Lactobacillus</i> and <i>Acetatifactor</i>, among other gut microbes, suggests their potential utility in the diagnosis, prevention, and treatment of BPH.https://www.mdpi.com/1422-0067/24/6/5904gut microbesbenign prostatic hyperplasiaapoptosisfinasteride<i>Lactobacillus</i><i>Acetatifactor</i>
spellingShingle Jinho An
Youngcheon Song
Sangbum Kim
Hyunseok Kong
Kyungjae Kim
Alteration of Gut Microbes in Benign Prostatic Hyperplasia Model and Finasteride Treatment Model
International Journal of Molecular Sciences
gut microbes
benign prostatic hyperplasia
apoptosis
finasteride
<i>Lactobacillus</i>
<i>Acetatifactor</i>
title Alteration of Gut Microbes in Benign Prostatic Hyperplasia Model and Finasteride Treatment Model
title_full Alteration of Gut Microbes in Benign Prostatic Hyperplasia Model and Finasteride Treatment Model
title_fullStr Alteration of Gut Microbes in Benign Prostatic Hyperplasia Model and Finasteride Treatment Model
title_full_unstemmed Alteration of Gut Microbes in Benign Prostatic Hyperplasia Model and Finasteride Treatment Model
title_short Alteration of Gut Microbes in Benign Prostatic Hyperplasia Model and Finasteride Treatment Model
title_sort alteration of gut microbes in benign prostatic hyperplasia model and finasteride treatment model
topic gut microbes
benign prostatic hyperplasia
apoptosis
finasteride
<i>Lactobacillus</i>
<i>Acetatifactor</i>
url https://www.mdpi.com/1422-0067/24/6/5904
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AT sangbumkim alterationofgutmicrobesinbenignprostatichyperplasiamodelandfinasteridetreatmentmodel
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