| Literature DB >> 33584734 |
Jiaming Liu1,2, Yangjie Jin2, Yanglie Ye2, Yahui Tang2, Shanshan Dai2, Mengfang Li2, Guangju Zhao2, Guangliang Hong2, Zhong-Qiu Lu2.
Abstract
Short chain fatty acids (SCFAs) are known to be actively involved in multiple brain disorders, but their roles in sepsis-associated encephalopathy (SAE) remain unclear. Here, we investigated the neuroprotective effects of SCFAs on SAE in mice. Male C57BL/6 mice were intragastrically pretreated with SCFAs for seven successive days, and then subjected to SAE induced by cecal ligation and puncture. The behavioral impairment, neuronal degeneration, and levels of inflammatory cytokines were assessed. The expressions of tight junction (TJ) proteins, including occludin and zoula occludens-1 (ZO-1), cyclooxygenase-2 (COX-2), cluster of differentiation 11b (CD11b), and phosphorylation of JNK and NF-κB p65 in the brain, were measured by western blot and Immunofluorescence analysis. Our results showed that SCFAs significantly attenuated behavioral impairment and neuronal degeneration, and decreased the levels of IL-1β and IL-6 in the brain of SAE mice. Additionally, SCFAs upregulated the expressions of occludin and ZO-1 and downregulated the expressions of COX-2, CD11b, and phosphorylation of JNK and NF-κB p65 in the brain of SAE mice. These findings suggested that SCFAs could exert neuroprotective effects against SAE in mice.Entities:
Keywords: behavioral impairment; neuroinflammation; neuroprotection; sepsis-associated encephalopathy; short chain fatty acids
Year: 2021 PMID: 33584734 PMCID: PMC7876449 DOI: 10.3389/fimmu.2021.626894
Source DB: PubMed Journal: Front Immunol ISSN: 1664-3224 Impact factor: 7.561