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鼠李糖乳杆菌或罗伊氏乳杆菌 GG 干预有助于改善肠道屏障功能,降低皮质酮水平,并改善 LPS 暴露后代的社交行为。

Lactobacillus reuteri or Lactobacillus rhamnosus GG intervention facilitates gut barrier function, decreases corticosterone and ameliorates social behavior in LPS-exposed offspring.

机构信息

Chongqing Key Laboratory of Child Neurodevelopment and Cognitive Disorders, Children's Hospital of Chongqing Medical University, Ministry of Education Key Laboratory of Child Development and Disorders, National Clinical Research Center for Child Health and Disorders, Chongqing, China.

School of Medicine, Jianghan University, Wuhan, China.

出版信息

Food Res Int. 2024 Dec;197(Pt 1):115212. doi: 10.1016/j.foodres.2024.115212. Epub 2024 Oct 20.

Abstract

Probiotic therapy with Lactobacillus reuteri and Lactobacillus rhamnosus (LGG) demonstrates potential as an adjunctive treatment for autism spectrum disorder (ASD). In a rat model of ASD induced by lipopolysaccharide (LPS) injection during pregnancy, we evaluated the effects of these probiotics on offspring. Administration of L. reuteri or LGG for three weeks post-birth improved social deficits and reduced anxiety in LPS-exposed rats. Additionally, probiotics significantly modified short-chain fatty acid profiles, increasing butyric acid levels and decreasing propionic acid levels. They also enhanced colonic barrier integrity by upregulating tight junction proteins, including ZO-1, Occludin, and Claudin4. RNA sequencing identified differential gene expression in pathways related to inflammation, the HPA axis, and reactive oxygen species metabolism, with NADPH oxidase 1 (NOX1) emerging as a crucial gene. Validation studies confirmed that Lactobacillus strains reduced inflammatory cytokines, inhibited corticosterone secretion, increased antioxidant levels, and suppressed the NF-κB/NOX1 pathway. In an HO-induced oxidative stress model using Caco-2 cells, pre-treatment with L. reuteri, LGG, or NF-κB inhibitors enhanced cellular antioxidants, inhibited NF-κB/NOX1 activation, and improved barrier function. Overall, L. reuteri and LGG administration improved social behavior, bolstered colonic barrier function, and mitigated HPA axis overactivation in LPS-exposed rats, while also alleviating oxidative stress in the colon and Caco-2 cells. These findings suggest that L. reuteri and LGG have substantial clinical potential for ASD treatment by targeting multiple pathophysiological mechanisms, including inflammation, HPA axis dysregulation, and oxidative stress, thereby presenting a promising adjunctive therapeutic strategy for enhancing social behavior and gut health in ASD.

摘要

鼠李糖乳杆菌和罗伊氏乳杆菌(LGG)的益生菌疗法显示出作为自闭症谱系障碍(ASD)辅助治疗的潜力。在怀孕期间注射脂多糖(LPS)诱导的 ASD 大鼠模型中,我们评估了这些益生菌对后代的影响。出生后三周内给予鼠李糖乳杆菌或 LGG 治疗可改善 LPS 暴露大鼠的社交缺陷和焦虑。此外,益生菌还显著改变了短链脂肪酸谱,增加了丁酸水平,降低了丙酸水平。它们还通过上调紧密连接蛋白,包括 ZO-1、Occludin 和 Claudin4,增强了结肠屏障的完整性。RNA 测序确定了与炎症、HPA 轴和活性氧代谢相关的途径中的差异基因表达,其中 NADPH 氧化酶 1(NOX1)是一个关键基因。验证研究证实,乳酸菌株减少了炎症细胞因子,抑制了皮质酮的分泌,增加了抗氧化剂水平,并抑制了 NF-κB/NOX1 途径。在使用 Caco-2 细胞的 HO 诱导氧化应激模型中,预先用鼠李糖乳杆菌、LGG 或 NF-κB 抑制剂预处理可增强细胞抗氧化剂,抑制 NF-κB/NOX1 激活,并改善屏障功能。总之,L. reuteri 和 LGG 的给药改善了 LPS 暴露大鼠的社交行为,增强了结肠屏障功能,并减轻了 HPA 轴的过度激活,同时还减轻了结肠和 Caco-2 细胞的氧化应激。这些发现表明,L. reuteri 和 LGG 通过靶向多个病理生理机制,包括炎症、HPA 轴失调和氧化应激,具有治疗 ASD 的巨大临床潜力,因此为增强 ASD 患者的社交行为和肠道健康提供了一种有前途的辅助治疗策略。

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