Suppr超能文献

-灵之 8 对改善高脂饮食兔动脉粥样硬化和非酒精性脂肪肝的抗炎作用。

The Anti-Inflammatory Effect of -Ling-Zhi 8 on Ameliorating Atherosclerosis and Nonalcoholic Fatty Liver in High-Fat Diet Rabbits.

机构信息

Department of Medical Research, Taichung Veterans General Hospital, Taichung 407219, Taiwan.

Department of Biology, National Changhua University of Education, Changhua 50007, Taiwan.

出版信息

Int J Mol Sci. 2024 Oct 20;25(20):11278. doi: 10.3390/ijms252011278.

Abstract

Inflammation plays a crucial role in atherosclerosis and nonalcoholic fatty liver disease (NAFLD). We previously engineered a recombinant strain expressing the Ling-Zhi immunomodulatory protein (-LZ8). This study investigated the anti-atherosclerotic effects of -LZ8 in rabbits fed a high-fat diet (HFD). Changes in body weight, serum lipid profiles, and liver function were monitored. The aorta and liver tissues were analyzed for gross pathology and histopathology. Eight-week administration of -LZ8 with HFD ameliorated atherosclerosis by downregulating protein and gene expression associated with lipid metabolism and inflammation in the aortas. The rabbits receiving -LZ8 exhibited a significant dose-dependent reduction in hepatic fat accumulation. RNA sequencing of the livers revealed that inflammatory genes in the -LZ8 groups were downregulated compared to the HFD group. Disease ontology enrichment analysis indicated that these genes were involved in atherosclerosis. Gene set enrichment analysis plots revealed significant enrichment in the gene sets related to cholesterol homeostasis. CIBERSORT immune cell fraction analysis indicated significant infiltration by regulatory T cells, CD8+ T cells, activated dendritic cells, and natural killer cells in the -LZ8 group. Our studies underscore LZ8's role in precision nutrition, providing a potential solution to the current challenges in modifying atherosclerosis and NAFLD.

摘要

炎症在动脉粥样硬化和非酒精性脂肪性肝病(NAFLD)中起着至关重要的作用。我们之前构建了一株表达灵芝免疫调节蛋白(-LZ8)的重组菌株。本研究旨在探讨-LZ8 在高脂饮食(HFD)喂养的兔子中抗动脉粥样硬化的作用。监测体重、血清脂质谱和肝功能的变化。分析主动脉和肝脏组织的大体病理和组织病理。8 周的-LZ8 联合 HFD 治疗可通过下调与主动脉脂质代谢和炎症相关的蛋白和基因表达来改善动脉粥样硬化。给予-LZ8 的兔子肝脏脂肪堆积显著减少,且呈剂量依赖性。肝脏的 RNA 测序显示,与 HFD 组相比,LZ8 组的炎症基因表达下调。疾病本体富集分析表明,这些基因参与了动脉粥样硬化。基因集富集分析图显示与胆固醇稳态相关的基因集显著富集。CIBERSORT 免疫细胞分数分析表明,-LZ8 组中调节性 T 细胞、CD8+T 细胞、活化树突状细胞和自然杀伤细胞显著浸润。我们的研究强调了 LZ8 在精准营养中的作用,为当前改变动脉粥样硬化和非酒精性脂肪性肝病的挑战提供了一种潜在的解决方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a83b/11508337/cb08a5f0f669/ijms-25-11278-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验