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NLRP3 炎性小体激活的阻断可改善坏死性小肠结肠炎诱导的小鼠急性炎症损伤和长期认知障碍。

Blockage of NLRP3 inflammasome activation ameliorates acute inflammatory injury and long-term cognitive impairment induced by necrotizing enterocolitis in mice.

机构信息

Department of Pediatric Surgery, Xinhua hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, China.

Shanghai Institute for Pediatric Research, School of Medicine, Shanghai Jiaotong University, Shanghai, China.

出版信息

J Neuroinflammation. 2021 Mar 6;18(1):66. doi: 10.1186/s12974-021-02111-4.

DOI:10.1186/s12974-021-02111-4
PMID:33676524
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7937302/
Abstract

BACKGROUND

Necrotizing enterocolitis (NEC) is an inflammatory gastrointestinal disease in premature neonates with high mortality and morbidity, while the underlining mechanism of intestinal injury and profound neurological dysfunction remains unclear. Here, we aimed to investigate the involvement of NLPR3 inflammasome activation in NEC-related enterocolitis and neuroinflammation, especially long-term cognitive impairment, meanwhile, explore the protective effect of NLRP3 inhibitor MCC950 on NEC in mice.

METHODS

NLRP3 inflammasome activation in the intestine and brain was assessed in the NEC mouse model, and NLRP3 inhibitor MCC950 was administrated during the development of NEC. Survival rate, histopathological injury of the intestine and brain, and expression of mature IL-1β and other pro-inflammatory cytokines were analyzed. Long-term cognitive impairment was evaluated by behavioral test.

RESULTS

The expression of NLRP3 and mature IL-1β in the intestine and brain was greatly upregulated in NEC mice compared to the controls. MCC950 treatment efficiently improved NEC survival rate, reduced intestinal and brain inflammation, and ameliorated the severity of pathological damage in both organs. Additionally, in vivo blockage of NLRP3 inflammasome with MCC950 in early life of NEC pups potently protected against NEC-associated long-term cognitive impairment.

CONCLUSIONS

Our findings suggest that NLRP3 inflammasome activation participates in NEC-induced intestinal and brain injury, and early intervention with NLRP3 inhibitor may provide beneficial therapeutic effect on NEC infants.

摘要

背景

坏死性小肠结肠炎(NEC)是一种早产儿炎症性胃肠道疾病,死亡率和发病率都很高,而肠道损伤和严重神经功能障碍的潜在机制仍不清楚。在这里,我们旨在研究 NLPR3 炎性体激活在 NEC 相关肠炎和神经炎症中的作用,特别是长期认知障碍,同时,探讨 NLRP3 抑制剂 MCC950 对 NEC 小鼠的保护作用。

方法

在 NEC 小鼠模型中评估肠道和大脑中的 NLRP3 炎性体激活,并用 NLRP3 抑制剂 MCC950 进行干预。分析存活率、肠道和大脑的组织病理学损伤、成熟的 IL-1β 和其他促炎细胞因子的表达。通过行为测试评估长期认知障碍。

结果

与对照组相比,NEC 小鼠的肠道和大脑中 NLRP3 和成熟的 IL-1β 的表达大大上调。MCC950 治疗可有效提高 NEC 的存活率,减轻肠道和大脑的炎症,并改善两个器官的病理损伤程度。此外,在 NEC 幼仔的生命早期用 MCC950 阻断 NLRP3 炎性体可有效预防 NEC 相关的长期认知障碍。

结论

我们的研究结果表明,NLRP3 炎性体激活参与了 NEC 诱导的肠道和大脑损伤,早期干预 NLRP3 抑制剂可能对 NEC 婴儿有有益的治疗作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bddd/7937302/96c128be528a/12974_2021_2111_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bddd/7937302/39d7fc59548c/12974_2021_2111_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bddd/7937302/420e9879158b/12974_2021_2111_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bddd/7937302/e2e0c449b3b9/12974_2021_2111_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bddd/7937302/2542f150eedf/12974_2021_2111_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bddd/7937302/96c128be528a/12974_2021_2111_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bddd/7937302/39d7fc59548c/12974_2021_2111_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bddd/7937302/420e9879158b/12974_2021_2111_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bddd/7937302/e2e0c449b3b9/12974_2021_2111_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bddd/7937302/2542f150eedf/12974_2021_2111_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bddd/7937302/96c128be528a/12974_2021_2111_Fig5_HTML.jpg

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