1.Center for Evidence-Based and Translational Medicine, Zhongnan Hospital of Wuhan University, Wuhan 430071 , China
2.Department of Gastrointestinal Surgery, Huaihe Hospital of Henan University, Kaifeng 475000 , Henan, China
3.Department of Gastroenterology, Zhongnan Hospital of Wuhan University, Wuhan 430071 , China
4.Department of Stomatology, Zhongnan Hospital of Wuhan University, Wuhan 430071 , China
5.Department of Urology, Zhongnan Hospital of Wuhan University, Wuhan 430071 , China
* hhyyqcj@vip.henu.edu.cn;
119140546@qq.com;
zengxiantao1128 @163.com; zengxiantao1128@whu.edu.cn
纸质出版:2023-02
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Alterations of gut microbiota diversity, composition and metabonomics in testosterone-induced benign prostatic hyperplasia rats[J]. 解放军医学杂志(英文版), 2023,10(1):1-16.
Li LY, Han J, Wu L, Fang C, Li WG, Gu JM, et al. Alterations of gut microbiota diversity, composition and metabonomics in testosterone-induced benign prostatic hyperplasia rats. Mil Med Res. 2022;9(1):12.
Alterations of gut microbiota diversity, composition and metabonomics in testosterone-induced benign prostatic hyperplasia rats[J]. 解放军医学杂志(英文版), 2023,10(1):1-16. DOI: 10.1186/s40779-022-00373-4.
Li LY, Han J, Wu L, Fang C, Li WG, Gu JM, et al. Alterations of gut microbiota diversity, composition and metabonomics in testosterone-induced benign prostatic hyperplasia rats. Mil Med Res. 2022;9(1):12. DOI: 10.1186/s40779-022-00373-4.
Background:
2
Studies had shown many diseases affect the stability of human microbiota
but how this relates to benign prostatic hyperplasia (BPH) has not been well understood. Hence
this study aimed to investigate the regulation of BPH on gut microbiota composition and metabonomics.
Methods:
2
We analyzed gut samples from rats with BPH and healthy control rats
the gut microbiota composition and metabonomics were detected by 16S rDNA sequencing and liquid chromatography tandem mass spectrometry (LC–MS/MS).
Results:
2
High-throughput sequencing results showed that gut microbiota beta-diversity increased (
P
<
0.01) in the BPH group
vs
. control group.
Muribaculaceae
(
P
<
0.01)
Turicibacteraceae
(
P
<
0.05)
Turicibacter
(
P
<
0.01) and
Coprococcus
(
P
<
0.01) were significantly decreased in the BPH group
whereas that of
Mollicutes
(
P
<
0.05) and
Prevotella
(
P
<
0.05) were significantly increased compared with the control group. Despite profound interindividual variability
the levels of several predominant genera were different. In addition
there were no statistically significant differences in several bacteria. BPH group
vs
. control group:
Firmicutes
(52.30%
vs
. 57.29%
P
>
0.05)
Bacteroidetes
(46.54%
vs
. 41.64%
P
>
0.05)
Clostridia
(50.89%
vs
. 54.66%
P
>
0.05)
Ruminococcaceae
(25.67%
vs
. 20.56%
P
>
0.05). LC–MS/MS of intestinal contents revealed that differential metabolites were mainly involved in cellular processes
environmental information processing
metabolism and organismal systems. The most important pathways were global and overview maps
lipid metabolism
amino acid metabolism
digestive system and endocrine system. Through enrichment analysis
we found that the differential metabolites were significantly enriched in metabolic pathways
steroid hormone biosynthesis
ovarian steroidogenesis
biosynthesis of unsaturated fatty acids and bile secretion. Pearson correlation analysis (
R
=0.94) showed that there was a strong correlation between
Prevotellaceae
Corynebacteriaceae
Turicibacteraceae
Bifidobacteriaceae
and differential metabolites.
Conclusions:
2
Our findings suggested an association between the gut microbiota and BPH
but the causal relationship between the two groups is unclear. Thus
further studies are warranted to elucidate the potential mechanisms and causal relationships between BPH and gut microbiota.
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