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益生菌通过调节肠脑轴与布瓦西坦一起减轻戊四氮点燃小鼠的癫痫进展、行为异常,并防止神经退行性变。

Probiotics by Modulating Gut-Brain Axis Together With Brivaracetam Mitigate Seizure Progression, Behavioral Incongruities, and Prevented Neurodegeneration in Pentylenetetrazole-Kindled Mice.

机构信息

Department of Pharmacology, Faculty of Pharmacy, Bahauddin Zakariya University, Multan, Pakistan.

The Institute of Pharmaceutical Sciences, University of Veterinary & Animal Sciences, Lahore, Pakistan.

出版信息

CNS Neurosci Ther. 2024 Nov;30(11):e70078. doi: 10.1111/cns.70078.

DOI:10.1111/cns.70078
PMID:39470120
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11520030/
Abstract

BACKGROUND

The microbiota-gut-brain axis (MGBA) is a central nexus that integrates higher cognitive and emotional centers of the central nervous system (CNS) within the intricate functioning of the intestine. Accumulating evidence suggests that dysbiosis in the taxonomic diversity of gut flora plays a salient role in the progression of epilepsy and comorbid secondary complications.

METHODS

In the current study, we investigated the impact of long-term oral bacteriotherapy (probiotics; 10 mL/kg; 10 colony-forming unit/ml) as an adjunctive treatment intervention with brivaracetam (BRV; 10 mg/kg) over 21 days on pentylenetetrazole (PTZ) induced augmented epileptic response and associated electrographical and behavioral perturbations in mice. Moreover, we also unveiled antioxidant capacity and histopathologic changes in treated versus non-treated animals.

RESULTS

Results revealed combination increases seizure threshold and prevented high ictal spiking. Additionally, it alleviated PTZ-induced neuropsychiatric disturbances such as anxiety and depressive-like phenotype along with cognitive deficits. Furthermore, dual therapy prompted physiological oxidant/antioxidant balance as evidenced by increased activity of antioxidant enzymes (SOD and catalase) and reduced levels of oxidative stressor (MDA). This therapeutic intervention with commensal species suppressed network-driven neuroinflammation and preserved normal cytoarchitecture with intact morphology in the pyramidal layers of cornu ammonis (CA1 and CA3).

CONCLUSION

Our study provides supporting evidence for the use of probiotics as adjunctive therapy with anti-seizure medications to modulate epileptogenic processes and related multimorbidities, particularly in individuals with drug-resistant seizures.

摘要

背景

微生物群-肠道-大脑轴(MGBA)是一个中枢枢纽,它将中枢神经系统(CNS)的高级认知和情绪中枢与肠道的复杂功能整合在一起。越来越多的证据表明,肠道菌群的分类多样性失调在癫痫的进展和合并的继发性并发症中起着重要作用。

方法

在目前的研究中,我们研究了长期口服细菌治疗(益生菌;10ml/kg;10 个菌落形成单位/ml)作为辅助治疗干预与溴维瑞坦(BRV;10mg/kg)联合治疗 21 天对戊四氮(PTZ)诱导的增强癫痫反应以及相关的电生理和行为改变的影响。此外,我们还揭示了治疗组与未治疗组动物的抗氧化能力和组织病理学变化。

结果

结果表明,联合治疗可提高癫痫发作阈值,防止高发作峰。此外,它还减轻了 PTZ 诱导的神经精神障碍,如焦虑和抑郁样表型以及认知缺陷。此外,双治疗促使生理氧化还原平衡,表现为抗氧化酶(SOD 和过氧化氢酶)活性增加和氧化应激物(MDA)水平降低。这种共生物种的治疗干预抑制了网络驱动的神经炎症,并保持了角回(CA1 和 CA3)锥体层的正常细胞结构和完整形态。

结论

我们的研究为益生菌作为抗癫痫药物的辅助治疗提供了支持,以调节致痫过程和相关的多种疾病,特别是在耐药性癫痫患者中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aea6/11520030/a272faadbcd7/CNS-30-e70078-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aea6/11520030/b58bd8c42c82/CNS-30-e70078-g002.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aea6/11520030/f0e36799ee6d/CNS-30-e70078-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aea6/11520030/45ce059b2d03/CNS-30-e70078-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aea6/11520030/a1f1f6ffb03e/CNS-30-e70078-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aea6/11520030/27bbd007be59/CNS-30-e70078-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aea6/11520030/a272faadbcd7/CNS-30-e70078-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aea6/11520030/b58bd8c42c82/CNS-30-e70078-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aea6/11520030/cfc22c7f315c/CNS-30-e70078-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aea6/11520030/904633a41228/CNS-30-e70078-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aea6/11520030/01c712f2c5dc/CNS-30-e70078-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aea6/11520030/f0e36799ee6d/CNS-30-e70078-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aea6/11520030/45ce059b2d03/CNS-30-e70078-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aea6/11520030/a1f1f6ffb03e/CNS-30-e70078-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aea6/11520030/27bbd007be59/CNS-30-e70078-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aea6/11520030/a272faadbcd7/CNS-30-e70078-g003.jpg

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