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The IFNγ-PDL1 Pathway Enhances CD8T-DCT Interaction to Promote Hypertension.IFNγ-PDL1 通路增强 CD8T-DCT 相互作用,促进高血压。
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2
Heart Disease and Stroke Statistics-2022 Update: A Report From the American Heart Association.《心脏病与卒中统计-2022 更新:美国心脏协会报告》。
Circulation. 2022 Feb 22;145(8):e153-e639. doi: 10.1161/CIR.0000000000001052. Epub 2022 Jan 26.
3
Effects of fecal microbiota transplant on DNA methylation in subjects with metabolic syndrome.肠道微生物群移植对代谢综合征患者 DNA 甲基化的影响。
Gut Microbes. 2021 Jan-Dec;13(1):1993513. doi: 10.1080/19490976.2021.1993513.
4
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5
Low protein diets for non-diabetic adults with chronic kidney disease.非糖尿病成年慢性肾病患者的低蛋白饮食
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Renal Perfusion Pressure Determines Infiltration of Leukocytes in the Kidney of Rats With Angiotensin II-Induced Hypertension.肾灌注压决定血管紧张素Ⅱ诱导高血压大鼠肾脏白细胞浸润。
Hypertension. 2020 Sep;76(3):849-858. doi: 10.1161/HYPERTENSIONAHA.120.15295. Epub 2020 Aug 3.
7
Amplification of Salt-Sensitive Hypertension and Kidney Damage by Immune Mechanisms.免疫机制增强盐敏感型高血压及肾脏损害。
Am J Hypertens. 2021 Feb 18;34(1):3-14. doi: 10.1093/ajh/hpaa124.
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Deletion of the myeloid endothelin-B receptor confers long-term protection from angiotensin II-mediated kidney, eye and vessel injury.髓样内皮素 B 受体缺失可提供长期保护,防止血管紧张素 II 介导的肾脏、眼睛和血管损伤。
Kidney Int. 2020 Nov;98(5):1193-1209. doi: 10.1016/j.kint.2020.05.042. Epub 2020 Jun 20.
9
Multi-omic profiling reveals associations between the gut mucosal microbiome, the metabolome, and host DNA methylation associated gene expression in patients with colorectal cancer.多组学分析揭示了结直肠癌患者肠道黏膜微生物组、代谢组与宿主 DNA 甲基化相关基因表达之间的关联。
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肠-免疫-肾轴:膳食蛋白质对盐敏感性高血压的影响。

Gut-Immune-Kidney Axis: Influence of Dietary Protein in Salt-Sensitive Hypertension.

机构信息

Department of Physiology, Medical College of Georgia, Augusta University, Augusta, GA.

出版信息

Hypertension. 2022 Nov;79(11):2397-2408. doi: 10.1161/HYPERTENSIONAHA.122.18556. Epub 2022 Aug 19.

DOI:10.1161/HYPERTENSIONAHA.122.18556
PMID:35983758
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9790111/
Abstract

Humans with salt-sensitive hypertension demonstrate increased morbidity, increased mortality, and renal end-organ damage when compared with normotensive subjects or those with salt-resistant hypertension. Substantial evidence from humans and animals has also demonstrated the role of dietary components other than salt to modulate hypertension. Evidence presented in this review provides support for the view that immunity and inflammation serve to amplify the development of salt-sensitive hypertension and leads to malignant disease accompanied by end-organ damage. Interestingly, salt-sensitive disease is modulated by changes in dietary protein intake, which also influences immune mechanisms. Together, the evidence presented in this review from animal and human studies indicates that changes in dietary protein source have profound effects on the gut microbiota, microbiota-derived metabolites, DNA methylation, gene expression, immune cell activation, the production of cytokines and other factors, and the development of salt-sensitive hypertension and related disease phenotypes.

摘要

与血压正常的受试者或盐抵抗性高血压患者相比,盐敏感型高血压患者的发病率、死亡率更高,且肾脏终末器官受损的风险也更高。大量来自人类和动物的证据也表明,除了盐以外,饮食成分在调节高血压方面也发挥了作用。本综述中提出的证据支持这样一种观点,即免疫和炎症有助于放大盐敏感型高血压的发展,并导致伴有终末器官损伤的恶性疾病。有趣的是,盐敏感疾病可通过饮食蛋白质摄入的变化来调节,而饮食蛋白质摄入也会影响免疫机制。综上所述,本综述中来自动物和人类研究的证据表明,饮食蛋白质来源的变化对肠道微生物群、微生物衍生代谢物、DNA 甲基化、基因表达、免疫细胞激活、细胞因子等因子的产生以及盐敏感型高血压和相关疾病表型的发展有深远影响。