Cited by 183Neurological Disorders and TreatmentsProbiotics and Fermented FoodsNeurological Disease Mechanisms and Treatments

Clostridium butyricum pretreatment attenuates cerebral ischemia/reperfusion injury in mice via anti-oxidation and anti-apoptosis

Sun, Jing, Ling, Zongxin, Wang, Fangyan, Chen, Wenqian, Li, Haixiao, Jin, Jiangtao, Zhang, Huiqing, Pang, Mengqi +2 more·2016·Neuroscience Letters

Abstract

Probiotics participate actively in the neuropsychiatric disorders. However, their roles on ischemic stroke remain unclear. This study aims to determine whether Clostridium butyricum (C. butyricum) could attenuate cerebral ischemia/reperfusion (I/R) injury and its possible mechanisms. Male ICR mice were intragastrically pretreated with C. butyricum for 2 successive weeks, and then subjected to cerebral I/R injury induced by the bilateral common carotid artery occlusion (BCCAO) for 20min. After 24h of the reperfusion, neurological deficit scores were evaluated. Histopathological changes of the hippocampus neurons were observed using Hematoxylin and eosin (H&E) and TUNEL staining. Malondialdehyde (MDA) contents and superoxide dismutase (SOD) activities in the brain were detected. The expression of Caspase-3, Bax and Bcl-2 were investigated by Western blot and immunohistochemistry analysis. The butyrate contents in the brain were determined. Our results showed that cerebral I/R injury led to neurological deficit, increased levels of Caspase-3 and Bax and decreased Bcl-2/Bax ratio. C. butyricum significantly improved neurological deficit, relieved histopathologic change, decreased MDA contents and increased SOD activities in the I/R injury mice. After C. butyricum pretreatment, the expression of Caspase-3 and Bax were significantly decreased, the Bcl-2/Bax ratio was significantly increased, and butyrate contents in the brain were significantly increased. These findings suggested t…

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Crossref · 10.1016/j.neulet.2015.12.047

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  • Levels of butyrate in the brain of mice supplemented with live Clostridium butyricum reached 0.4 to 0.7 μmol/g, about an order of magnitude higher than concentrations reported in peripheral blood.

    “the levels of butyrate in the brain of mice supplemented with live Clostridium butyricum reached a range from 0.4 to 0.7 μmol/g, which was about an order of magnitude higher than concentrations reported in peripheral blood (96, 97).”

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Authors
Sun, J., Ling, Z., Wang, F., Chen, W., Li, H., Jin, J., Zhang, H., Pang, M., Yu, J., & Liu, J.
Affiliations
  • Wenzhou Medical University (CN)
  • First Affiliated Hospital Zhejiang University (CN)
Corresponding author
  • Sun, Jing
  • Ling, Zongxin
  • Liu, Jiaming
Venue
Neuroscience Letters
Publisher
Elsevier BV
Published
2016-02
Volume
613
Pages
30-35
ISSN
0304-3940 (ISSN-L)
OpenAlex
W2228779853
Cited by
183
References
3
Citations by year
2026: 7 · 2025: 23 · 2024: 14 · 2023: 23 · 2022: 32 · 2021: 29 · 2020: 15 · 2019: 16 · 2018: 6 · 2017: 6 · 2016: 12
FWCI
4.27
Type
journal article
Language
en
Open access
closed
Locations
  • Neuroscience Letters (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • Zhejiang Medical Science and Technology (2016136369)
  • Zhejiang Science and Technology Development (2015C37010)
Topics
  • Life Sciences › Neuroscience › Neurology › Neurological Disorders and Treatments
  • Life Sciences › Agricultural and Biological Sciences › Food Science › Probiotics and Fermented Foods
  • Life Sciences › Neuroscience › Neurology › Neurological Disease Mechanisms and Treatments
Keywords
Clostridium butyricum, cerebral ischemia-reperfusion injury, ischemic stroke, probiotics, neuroprotection, oxidative stress, apoptosis, butyrate, caspase-3, Bax, Bcl-2, malondialdehyde, superoxide dismutase, hippocampus, bilateral common carotid artery occlusion, neurological deficit
MeSH terms
Animals, Brain, Brain Ischemia, Male, Mice, Inbred ICR, Neurons, Reperfusion Injury, Carotid Stenosis, Apoptosis, Carotid Artery, Common, Oxidative Stress, Proto-Oncogene Proteins c-bcl-2, Probiotics, Clostridium butyricum, bcl-2-Associated X Protein, Caspase 3

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