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<t>Muribaculaceae</t> abundance regulates spermatogenesis in mice (A) Schematic diagram of the FMT experiment. Abx, a cocktail of broad-spectrum antibiotics. n = 5 for each group. (B) Statistical analysis of changes in body weight after FMT. Control-FMT, the group of mice transplanted with feces from control mice; BBR-FMT, the group of mice transplanted with feces from BBR-treated mice. n = 5 for each group. (C) Sperm concentrations from the cauda epididymides of the mice were analyzed with a hemocytometer under a light microscope. n = 5 for each group. (D) The correlation between Muribaculaceae abundance and sperm concentration was analyzed in the control, low-dose, medium-dose and high-dose groups. n = 4 for each group. (E) Schematic diagram of the PEG treatment experiment. n = 6 for each group. (F) PCA plot generated on the basis of the similarity of fecal samples in the control and PEG-treated groups. (G) The relative taxonomic abundances of the gut microbiota at the family level are shown in the histogram. (H) Sperm from the cauda epididymides of the mice were counted with a hemocytometer under a light microscope. n = 6 for each group. (I) The serum testosterone concentration in untreated and PEG-treated mice was measured via ELISA. n = 5 for each group. (J) The mRNA expression levels of genes related to testosterone synthesis were measured by RT-qPCR. n = 4 for each group. (K) The sperm concentrations of untreated, BBR-treated, and BBR+M. intestinale-treated mice were evaluated with a hemocytometer under a light microscope. n = 5 for each group. (L) The testosterone levels in mouse serum were measured by ELISA. n = 5 for each group. Data are expressed as the mean ± SEM. Differences without statistical significance are not labelled; *P < 0.05, **P < 0.01, ***P < 0.001.
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Muribaculaceae abundance regulates spermatogenesis in mice (A) Schematic diagram of the FMT experiment. Abx, a cocktail of broad-spectrum antibiotics. n = 5 for each group. (B) Statistical analysis of changes in body weight after FMT. Control-FMT, the group of mice transplanted with feces from control mice; BBR-FMT, the group of mice transplanted with feces from BBR-treated mice. n = 5 for each group. (C) Sperm concentrations from the cauda epididymides of the mice were analyzed with a hemocytometer under a light microscope. n = 5 for each group. (D) The correlation between Muribaculaceae abundance and sperm concentration was analyzed in the control, low-dose, medium-dose and high-dose groups. n = 4 for each group. (E) Schematic diagram of the PEG treatment experiment. n = 6 for each group. (F) PCA plot generated on the basis of the similarity of fecal samples in the control and PEG-treated groups. (G) The relative taxonomic abundances of the gut microbiota at the family level are shown in the histogram. (H) Sperm from the cauda epididymides of the mice were counted with a hemocytometer under a light microscope. n = 6 for each group. (I) The serum testosterone concentration in untreated and PEG-treated mice was measured via ELISA. n = 5 for each group. (J) The mRNA expression levels of genes related to testosterone synthesis were measured by RT-qPCR. n = 4 for each group. (K) The sperm concentrations of untreated, BBR-treated, and BBR+M. intestinale-treated mice were evaluated with a hemocytometer under a light microscope. n = 5 for each group. (L) The testosterone levels in mouse serum were measured by ELISA. n = 5 for each group. Data are expressed as the mean ± SEM. Differences without statistical significance are not labelled; *P < 0.05, **P < 0.01, ***P < 0.001.

Journal: Acta Biochimica et Biophysica Sinica

Article Title: Berberine alters the gut microbiota metabolism and impairs spermatogenesis

doi: 10.3724/abbs.2024174

Figure Lengend Snippet: Muribaculaceae abundance regulates spermatogenesis in mice (A) Schematic diagram of the FMT experiment. Abx, a cocktail of broad-spectrum antibiotics. n = 5 for each group. (B) Statistical analysis of changes in body weight after FMT. Control-FMT, the group of mice transplanted with feces from control mice; BBR-FMT, the group of mice transplanted with feces from BBR-treated mice. n = 5 for each group. (C) Sperm concentrations from the cauda epididymides of the mice were analyzed with a hemocytometer under a light microscope. n = 5 for each group. (D) The correlation between Muribaculaceae abundance and sperm concentration was analyzed in the control, low-dose, medium-dose and high-dose groups. n = 4 for each group. (E) Schematic diagram of the PEG treatment experiment. n = 6 for each group. (F) PCA plot generated on the basis of the similarity of fecal samples in the control and PEG-treated groups. (G) The relative taxonomic abundances of the gut microbiota at the family level are shown in the histogram. (H) Sperm from the cauda epididymides of the mice were counted with a hemocytometer under a light microscope. n = 6 for each group. (I) The serum testosterone concentration in untreated and PEG-treated mice was measured via ELISA. n = 5 for each group. (J) The mRNA expression levels of genes related to testosterone synthesis were measured by RT-qPCR. n = 4 for each group. (K) The sperm concentrations of untreated, BBR-treated, and BBR+M. intestinale-treated mice were evaluated with a hemocytometer under a light microscope. n = 5 for each group. (L) The testosterone levels in mouse serum were measured by ELISA. n = 5 for each group. Data are expressed as the mean ± SEM. Differences without statistical significance are not labelled; *P < 0.05, **P < 0.01, ***P < 0.001.

Article Snippet: A representative member of Muribaculaceae (M . intestinale , DSMZ 28989) was grown on chopped meat at 37°C anaerobically.

Techniques: Control, Light Microscopy, Concentration Assay, Generated, Enzyme-linked Immunosorbent Assay, Expressing, Quantitative RT-PCR