4.7 Article

Cattle Bile Arisaema Aqueous Extracts Protect Against Febrile Seizures in Rats Through Regulating Neurotransmitters and Suppressing Neuroinflammation

期刊

FRONTIERS IN PHARMACOLOGY
卷 13, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fphar.2022.889055

关键词

cattle bile Arisaema; febrile seizures; neuronal damage; neurotransmitter; neuroinflammation; anti-convulsant

资金

  1. National Key Research and Development Program of China [2018YFC1707100]
  2. Chief Scientist of Qi-Huang Project of National Traditional Chinese Medicine Inheritance and Innovation One Hundred Million Talent Project (2021)
  3. Heilongjiang Touyan Innovation Team Program (2019)
  4. Qi-Huang Scholar of National Traditional Chinese Medicine Leading Talents Support Program (2018)

向作者/读者索取更多资源

This study investigates the anti-convulsant effect and potential mechanism of cattle bile Arisaema (CBA) on febrile seizures. Results show that CBA can effectively lower the incidence rate and generation times of seizures, ameliorate neuronal damage, and regulate neurotransmitter disorder induced by febrile seizures.
Cattle bile Arisaema (CBA) is a traditional medicine used for the treatment of febrile seizures (FS) for thousands of years in China. However, its application is greatly limited due to cost reasons, and pig bile Arisaema (PBA) is the main commercial product instead. Additionally, the underlying mechanism of CBA for the treatment of FS still remains unknown. In this study, we investigated the anti-convulsant effect and potential mechanism of the CBA aqueous extract for the first time through a hot-water bath-induced FS rat model. Our results showed that pre-treatment with CBA dramatically lowered the incidence rate and generation times and prolonged the latency of FS. In addition, CBA effectively ameliorated neuronal damage and regulated neurotransmitter disorder induced by FS in the rat hippocampus. The enzyme-linked immunosorbent assay, western blotting, immunohistochemical, and qRT-PCR results exhibited that CBA suppressed the expression of GFAP, TLR4, NF-kappa B, HMGB1, NLRP3, TNF-alpha, IL-1 beta, and IL-6 and consequently inhibited the neuroinflammation induced by FS. Interestingly, although the CBA and PBA aqueous extracts possessed the same trend on the changes caused by FS, the improvement of FS by CBA is markedly better than that by PBA. These findings indicate that CBA exerts a protective effect on febrile seizures through regulating neurotransmitter disorder and suppressing neuroinflammation.

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