肠道菌群
封堵器
锡尔图因
生物
肠粘膜
紧密连接
平衡
胃肠道
免疫学
医学
炎症
SIRT2
病理
癌症研究
下调和上调
肠道疾病
病态的
肠-脑轴
细胞生物学
调节器
肠上皮
干细胞
祖细胞
潘尼斯电池
免疫荧光
祖细胞
内科学
肠绒毛
作者
Siyuan Wang,Minjie Wang,Xinyu Zhou,Ke Yan,Yufei Chen,Yihang Chen,Yaxuan Yao,Ying Dong,Jiuchang Zhong,J D Li
标识
DOI:10.1007/s00018-026-06229-7
摘要
)-dependent deacetylase, has been identified as a crucial regulator in the progression of cardiovascular diseases through multiple mechanistic pathways. However, the roles and underlying mechanisms of SIRT7 in the development of hypertensive intestinal injury remains unclear, and further investigation is required to determine whether SIRT7 can alleviate intestinal damage through modulation of the gut microbiota. In this study, SIRT7 expression and intestinal pathology were assessed in spontaneously hypertensive rats (SHRs). An intestinal SIRT7 overexpression model was subsequently established in SHRs to evaluate its effects on intestinal dysfunction and microbial composition. Histological and immunofluorescence staining were performed to examine the small intestine, and 16S rRNA amplicon sequencing was conducted to analyze the gut microbiota. There was a marked deficiency of SIRT7 in the intestinal tract of hypertensive animals, which was closely associated with reduced expression of tight junction proteins, including Occludin and zonula occludens-1, as well as intestinal pathological damage in SHRs. SIRT7 overexpression strikingly alleviated intestinal fibrosis, structural damage, and increased intestinal permeability. More importantly, restoration of SIRT7 partially reversed hypertension-associated gut microbiota dysbiosis. In summary, our findings provide novel mechanistic insights into the role of SIRT7 as a critical protector of intestinal barrier integrity and microenvironmental homeostasis under hypertensive stress, and highlight the intricate interplay between SIRT7 and the gut microbiota during hypertension.
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