Therapeutic strategies for hypertension: exploring the role of microbiota-derived short-chain fatty acids in kidney physiology and development.

IF 2.6 3区 医学 Q1 PEDIATRICS
Giovane G Tortelote
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引用次数: 0

Abstract

Gut microbiota have emerged as a key regulator of systemic health, influencing various physiological processes, including kidney development, function, and blood pressure regulation. This review highlights the role of microbiota-derived short-chain fatty acids (SCFAs), primarily acetate, propionate, and butyrate, in the gut-kidney axis, focusing on their signaling mechanisms, vascular effects, and developmental implications. Evidence suggests that SCFAs modulate kidney development and function and exert anti-inflammatory, antioxidant, and vasoregulatory effects through specific G protein-coupled receptors (GPR41, GPR43, GPR109A, OLFR78, and OLFR558). Human studies and research using genetically modified animals have demonstrated that gut dysbiosis disrupts SCFA metabolism, potentially contributing to hypertension, endothelial dysfunction, and chronic kidney disease (CKD). Germ-free microbiota-transplantation studies revealed that the presence of gut microbiota directly influences vascular tone and systemic blood pressure via SCFA-mediated mechanisms. Furthermore, acetate, a SCFA, is shown to impact fetal kidney development and nephron progenitor cell dynamics. Sex-specific effects of gut microbiota on vascular remodeling and immune responses further highlight the complexity of microbiome-host interactions. In pediatric patients, altered SCFA profiles are associated with CKD progression and relapse in nephrotic syndrome. Clinical data suggest that plasma SCFA levels may serve as biomarkers for hypertension risk and cardiovascular outcomes in children with kidney disease. Therapeutically, interventions targeting SCFA pathways, such as probiotics, prebiotics, dietary fiber diet, and receptor agonists, may help restore gut-kidney axis balance and improve kidney and cardiovascular outcomes. This review illustrates the critical role of SCFAs as mediators linking the gut microbiota to kidney and vascular health. Continued investigation into SCFA signaling may uncover novel strategies for preventing and managing hypertension, CKD, and developmental nephropathies.

高血压的治疗策略:探索微生物来源的短链脂肪酸在肾脏生理和发育中的作用。
肠道微生物群已成为系统健康的关键调节器,影响各种生理过程,包括肾脏发育、功能和血压调节。这篇综述强调了微生物衍生的短链脂肪酸(SCFAs),主要是醋酸盐、丙酸盐和丁酸盐,在肠肾轴中的作用,重点是它们的信号机制、血管效应和发育意义。有证据表明,SCFAs通过特异性G蛋白偶联受体(GPR41、GPR43、GPR109A、OLFR78和OLFR558)调节肾脏发育和功能,并发挥抗炎、抗氧化和血管调节作用。人类研究和转基因动物研究表明,肠道生态失调会破坏SCFA代谢,可能导致高血压、内皮功能障碍和慢性肾脏疾病(CKD)。无菌菌群移植研究表明,肠道菌群的存在通过scfa介导的机制直接影响血管张力和全身血压。此外,醋酸酯,一种SCFA,被证明会影响胎儿肾脏发育和肾元祖细胞动力学。肠道微生物群对血管重塑和免疫反应的性别特异性影响进一步凸显了微生物群-宿主相互作用的复杂性。在儿科患者中,SCFA谱的改变与肾病综合征的CKD进展和复发有关。临床数据表明,血浆SCFA水平可作为肾脏病患儿高血压风险和心血管结局的生物标志物。在治疗上,针对SCFA通路的干预措施,如益生菌、益生元、膳食纤维饮食和受体激动剂,可能有助于恢复肠肾轴平衡,改善肾脏和心血管预后。这篇综述说明了SCFAs作为连接肠道微生物群与肾脏和血管健康的介质的关键作用。对SCFA信号的持续研究可能会发现预防和治疗高血压、慢性肾病和发展性肾病的新策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Pediatric Nephrology
Pediatric Nephrology 医学-泌尿学与肾脏学
CiteScore
4.70
自引率
20.00%
发文量
465
审稿时长
1 months
期刊介绍: International Pediatric Nephrology Association Pediatric Nephrology publishes original clinical research related to acute and chronic diseases that affect renal function, blood pressure, and fluid and electrolyte disorders in children. Studies may involve medical, surgical, nutritional, physiologic, biochemical, genetic, pathologic or immunologic aspects of disease, imaging techniques or consequences of acute or chronic kidney disease. There are 12 issues per year that contain Editorial Commentaries, Reviews, Educational Reviews, Original Articles, Brief Reports, Rapid Communications, Clinical Quizzes, and Letters to the Editors.
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