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Cited by 227Neurological Disease Mechanisms and TreatmentsGut microbiota and healthProbiotics and Fermented Foods

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Neuroprotective Effects of Clostridium butyricum against Vascular Dementia in Mice via Metabolic Butyrate

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Liu, Jiaming, Sun, Jing, Wang, Fangyan, Yu, Xichong, Ling, Zongxin, Li, Haixiao, Zhang, Huiqing, Jin, Jiangtao, Chen, Wenqian, Pang, Mengqi, Yu, Junjie, He, Yiwen, Xu, Jiru·2015·BioMed Research International
DOI 10.1155/2015/412946PMC PMC4615854
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Abstract

Probiotics actively participate in neuropsychiatric disorders. However, the role of gut microbiota in brain disorders and vascular dementia (VaD) remains unclear. We used a mouse model of VaD induced by a permanent right unilateral common carotid arteries occlusion (rUCCAO) to investigate the neuroprotective effects and possible underlying mechanisms of Clostridium butyricum. Following rUCCAO, C. butyricum was intragastrically administered for 6 successive weeks. Cognitive function was estimated. Morphological examination was performed by electron microscopy and hematoxylin-eosin (H&E) staining. The BDNF-PI3K/Akt pathway-related proteins were assessed by western blot and immunohistochemistry. The diversity of gut microbiota and the levels of butyrate in the feces and the brains were determined. The results showed that C. butyricum significantly attenuated the cognitive dysfunction and histopathological changes in VaD mice. C. butyricum not only increased the levels of BDNF and Bcl-2 and decreased level of Bax but also induced Akt phosphorylation (p-Akt) and ultimately reduced neuronal apoptosis. Moreover, C. butyricum could regulate the gut microbiota and restore the butyrate content in the feces and the brains. These results suggest that C. butyricum might be effective in the treatment of VaD by regulating the gut-brain axis and that it can be considered a new therapeutic strategy against VaD.

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Figures

Figure 1 Open field test. (a) The total distance travelled over 1 h, (b) the time spent in the central area, and (c) the total rest time are presented for each group. Sham, sham-operated group; VaD, VaD model group; Cb H, C. butyricum- (1 × 108 CFU-) treated group; Cb M, C. butyricum- (1 × 107 CFU-) treated group; and Cb L, C. butyricum- (1 × 106 CFU-) treated group. Error bars indicate SEM; ∗ P < 0.05 versus sham group; # P < 0.05 and ## P < 0.01 versus VaD group.
Figure 1 Open field test. (a) The total distance travelled over 1 h, (b) the time spent in the central area, and (c) the total rest time are presented for each group. Sham, sham-operated group; VaD, VaD model group; Cb H, C. butyricum- (1 × 108 CFU-) treated group; Cb M, C. butyricum- (1 × 107 CFU-) treated group; and Cb L, C. butyricum- (1 × 106 CFU-) treated group. Error bars indicate SEM; ∗ P < 0.05 versus sham group; # P < 0.05 and ## P < 0.01 versus VaD group.CC BY · PubMed Central
Figure 2 Morris water maze. (a) Escape latency (s). (b) The time spent in the target quadrant (s). Sham, sham-operated group; VaD, VaD model group; Cb H, C. butyricum- (1 × 108 CFU-) treated group; Cb M, C. butyricum- (1 × 107 CFU-) treated group; and Cb L, C. butyricum- (1 × 106 CFU-) treated group. Error bars indicate SEM; ∗ P < 0.05 and ∗∗ P < 0.01 versus sham group; # P < 0.05 and ## P < 0.01 versus VaD group.
Figure 2 Morris water maze. (a) Escape latency (s). (b) The time spent in the target quadrant (s). Sham, sham-operated group; VaD, VaD model group; Cb H, C. butyricum- (1 × 108 CFU-) treated group; Cb M, C. butyricum- (1 × 107 CFU-) treated group; and Cb L, C. butyricum- (1 × 106 CFU-) treated group. Error bars indicate SEM; ∗ P < 0.05 and ∗∗ P < 0.01 versus sham group; # P < 0.05 and ## P < 0.01 versus VaD group.CC BY · PubMed Central
Figure 3 Representative photomicrographs of the ultrastructural changes observed in brain tissue. (a) A representative nucleolus in a hippocampal neuron of the sham-operated group. (b) A representative nucleolus of cerebral ischemia in the VaD group. (c) A representative nucleolus in the Cb L group, Cb M group (d), and Cb H group (e). Sham, sham-operated group; VaD, VaD model group; Cb H, C. butyricum- (1 × 108 CFU-) treated group; Cb M, C. butyricum- (1 × 107 CFU-) treated group; and Cb L, C. butyricum- (1 × 106 CFU-) treated group.
Figure 3 Representative photomicrographs of the ultrastructural changes observed in brain tissue. (a) A representative nucleolus in a hippocampal neuron of the sham-operated group. (b) A representative nucleolus of cerebral ischemia in the VaD group. (c) A representative nucleolus in the Cb L group, Cb M group (d), and Cb H group (e). Sham, sham-operated group; VaD, VaD model group; Cb H, C. butyricum- (1 × 108 CFU-) treated group; Cb M, C. butyricum- (1 × 107 CFU-) treated group; and Cb L, C. butyricum- (1 × 106 CFU-) treated group.CC BY · PubMed Central
Figure 4 Representative photomicrographs of the histopathological changes in area CA1 of the hippocampus in mice. (a) HE staining. (b) TUNEL staining. Cells with a brown-stained cytoplasm are considered positive. Sham, sham-operated group; VaD, VaD model group; Cb H, C. butyricum- (1 × 108 CFU-) treated group; Cb M, C. butyricum- (1 × 107 CFU-) treated group; and Cb L, C. butyricum- (1 × 106 CFU-) treated group. Magnification: 400x. Scale bar = 20 μm.
Figure 4 Representative photomicrographs of the histopathological changes in area CA1 of the hippocampus in mice. (a) HE staining. (b) TUNEL staining. Cells with a brown-stained cytoplasm are considered positive. Sham, sham-operated group; VaD, VaD model group; Cb H, C. butyricum- (1 × 108 CFU-) treated group; Cb M, C. butyricum- (1 × 107 CFU-) treated group; and Cb L, C. butyricum- (1 × 106 CFU-) treated group. Magnification: 400x. Scale bar = 20 μm.CC BY · PubMed Central
Figure 5 Western blot analysis. (a) Western blot of the expression levels of BDNF, p-Akt, Akt, Bcl-2, and Bax in mouse hippocampus. (b) A quantitative analysis of the protein levels of BDNF from each group normalized to the loading control β-actin (c). (d) Bar graphs showing the protein level ratios of p-Akt/Akt and Bcl-2/Bax from each group; Sham, sham-operated group; VaD, VaD model group; Cb H, C. butyricum- (1 × 108 CFU-) treated group; Cb M, C. butyricum- (1 × 107 CFU-) treated group; and Cb L, C. butyricum- (1 × 106 CFU-) treated group. Error bars indicate SD; n = 8 for each group. ∗ P < 0.01 and ∗∗ P < 0.01 versus sham group; # P < 0.05 and ## P < 0.01 versus VaD group.
Figure 5 Western blot analysis. (a) Western blot of the expression levels of BDNF, p-Akt, Akt, Bcl-2, and Bax in mouse hippocampus. (b) A quantitative analysis of the protein levels of BDNF from each group normalized to the loading control β-actin (c). (d) Bar graphs showing the protein level ratios of p-Akt/Akt and Bcl-2/Bax from each group; Sham, sham-operated group; VaD, VaD model group; Cb H, C. butyricum- (1 × 108 CFU-) treated group; Cb M, C. butyricum- (1 × 107 CFU-) treated group; and Cb L, C. butyricum- (1 × 106 CFU-) treated group. Error bars indicate SD; n = 8 for each group. ∗ P < 0.01 and ∗∗ P < 0.01 versus sham group; # P < 0.05 and ## P < 0.01 versus VaD group.CC BY · PubMed Central
Figure 6 Immunohistochemical staining. Representative images of the immunohistochemical staining of BDNF, p-Akt, Bcl-2, and Bax in area CA1 of the hippocampus. Cells with a brown-stained cytoplasm are considered positive. Sham, sham-operated group; VaD, VaD model group; Cb H, C. butyricum- (1 × 108 CFU-) treated group; Cb M, C. butyricum- (1 × 107 CFU-) treated group; and Cb L, C. butyricum- (1 × 106 CFU-) treated group. Magnification: 400x. Scale bar = 20 μm.
Figure 6 Immunohistochemical staining. Representative images of the immunohistochemical staining of BDNF, p-Akt, Bcl-2, and Bax in area CA1 of the hippocampus. Cells with a brown-stained cytoplasm are considered positive. Sham, sham-operated group; VaD, VaD model group; Cb H, C. butyricum- (1 × 108 CFU-) treated group; Cb M, C. butyricum- (1 × 107 CFU-) treated group; and Cb L, C. butyricum- (1 × 106 CFU-) treated group. Magnification: 400x. Scale bar = 20 μm.CC BY · PubMed Central
Figure 7 PCR-DGGE analysis of the predominant fecal microbiota in mice. (a) PCR-DGGE fingerprints used to analyze the fecal microbiota of the samples from the VaD model group (A), sham-operated group (H), and C. butyricum- (B, 1 × 106 CFU-; C, 1 × 107 CFU-; and D, 1 × 108 CFU-) treated groups. Each lane represents one subject that was randomly selected from each group. The bands marked in the DGGE gel were identified by cloning and sequencing to facilitate the interpretation of the figure. Bands: 1: Bacteroides sp.; 2: Hespellia sp.; 3: Clostridium XVIII sp.; 4: TM7 genera incertae sedis; 5: TM7 genera incertae sedis; 6: Anaerostipes sp.; 7: Barnesiella sp.; 8: Barnesiella sp.; 9: Roseburia sp.; 10: Acinetobacter sp.; 11: unclassified Helicobacteraceae sp.; 12: Streptobacillus sp.; 13: Barnesiella sp.; 14: Clostridium XIVa sp.; 15: Alistipes sp.; 16: unclassified Lachnospiraceae sp.; 17: Lachnospiraceae incertae sedis Alistipes sp.; 18: Anaerostipes sp.; 19: unclassified Porphyromonadaceae sp.; and 20: Butyricimonas sp. (b) Dendrogram of the DGGE profiles shown in (a).
Figure 7 PCR-DGGE analysis of the predominant fecal microbiota in mice. (a) PCR-DGGE fingerprints used to analyze the fecal microbiota of the samples from the VaD model group (A), sham-operated group (H), and C. butyricum- (B, 1 × 106 CFU-; C, 1 × 107 CFU-; and D, 1 × 108 CFU-) treated groups. Each lane represents one subject that was randomly selected from each group. The bands marked in the DGGE gel were identified by cloning and sequencing to facilitate the interpretation of the figure. Bands: 1: Bacteroides sp.; 2: Hespellia sp.; 3: Clostridium XVIII sp.; 4: TM7 genera incertae sedis; 5: TM7 genera incertae sedis; 6: Anaerostipes sp.; 7: Barnesiella sp.; 8: Barnesiella sp.; 9: Roseburia sp.; 10: Acinetobacter sp.; 11: unclassified Helicobacteraceae sp.; 12: Streptobacillus sp.; 13: Barnesiella sp.; 14: Clostridium XIVa sp.; 15: Alistipes sp.; 16: unclassified Lachnospiraceae sp.; 17: Lachnospiraceae incertae sedis Alistipes sp.; 18: Anaerostipes sp.; 19: unclassified Porphyromonadaceae sp.; and 20: Butyricimonas sp. (b) Dendrogram of the DGGE profiles shown in (a).CC BY · PubMed Central
Figure 8 Absolute concentration of butyrate (μmol g−1 wet weight). Sham, sham-operated group; VaD, VaD model group; Cb H, C. butyricum- (1 × 108 CFU-) treated group; Cb M, C. butyricum- (1 × 107 CFU-) treated group; and Cb L, C. butyricum- (1 × 106 CFU-) treated group. Error bars indicate SD; n = 8 for each group. ∗ P < 0.05 versus sham group, ∗∗ P < 0.01 versus sham group, and # P < 0.05 and ## P < 0.01 versus VaD group.
Figure 8 Absolute concentration of butyrate (μmol g−1 wet weight). Sham, sham-operated group; VaD, VaD model group; Cb H, C. butyricum- (1 × 108 CFU-) treated group; Cb M, C. butyricum- (1 × 107 CFU-) treated group; and Cb L, C. butyricum- (1 × 106 CFU-) treated group. Error bars indicate SD; n = 8 for each group. ∗ P < 0.05 versus sham group, ∗∗ P < 0.01 versus sham group, and # P < 0.05 and ## P < 0.01 versus VaD group.CC BY · PubMed Central

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  1. 2015, International Journal of Clinical and Experimental Pathology, 8, 4695
  2. 2010, Gastroenterology & Hepatology, 6, 39

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Metadata

Authors
Liu, J., Sun, J., Wang, F., Yu, X., Ling, Z., Li, H., Zhang, H., Jin, J., Chen, W., Pang, M., Yu, J., He, Y., & Xu, J.
Affiliations
  • Wenzhou Medical University (CN)
  • School of Environmental Science and Public Health, Wenzhou Medical University, Wenzhou, Zhejiang 325035, China
  • First Affiliated Hospital Zhejiang University (CN)
  • Xi'an Jiaotong University (CN)
Corresponding author
Xu, Jiru
ORCID
Venue
BioMed Research International
Publisher
Wiley
Published
2015
Volume
2015
Pages
1-12
ISSN
  • 1110-7243 (ISSN-L)
  • 2314-6133
  • 2314-6141
DOI
10.1155/2015/412946
PMC
PMC4615854
OpenAlex
W2114102190
Cited by
225
References
46
Citations by year
2026: 15 · 2025: 22 · 2024: 26 · 2023: 33 · 2022: 32 · 2021: 24 · 2020: 25 · 2019: 21 · 2018: 14 · 2017: 5 · 2016: 7 · 2015: 1
FWCI
4.81
Type
journal article
Language
en
Open access
Licence
Locations
  • BioMed Research International (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Funders
  • Zhejiang Science and Technology Development Funds (2015C37090, LY13B070012)
  • Natural Science Foundation of Zhejiang Province (2015C37090, LY13B070012)
Topics
  • Life Sciences › Neuroscience › Neurology › Neurological Disease Mechanisms and Treatments
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
  • Life Sciences › Agricultural and Biological Sciences › Food Science › Probiotics and Fermented Foods
Keywords
Clostridium butyricum, vascular dementia, butyrate, gut microbiota, gut-brain axis, neuroprotection, cognitive impairment, neuronal apoptosis, brain-derived neurotrophic factor, PI3K/Akt signaling, carotid artery occlusion, probiotics
MeSH terms
Animals, Brain, Butyrates, Carotid Arteries, Disease Models, Animal, Hippocampus, Immunohistochemistry, Male, Mice, Inbred ICR, Microscopy, Electron, Phosphorylation, Dementia, Vascular, Apoptosis, Neuroprotective Agents, Brain-Derived Neurotrophic Factor, Phosphatidylinositol 3-Kinases, Probiotics, Clostridium butyricum, Mice

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