Brittni N. Moore, Alexandra D. Medcalf, Rachel Q. Muir, Chudan Xu, Francine Z. Marques, Jennifer L. Pluznick
{"title":"Commensal Microbiota Regulate Aldosterone","authors":"Brittni N. Moore, Alexandra D. Medcalf, Rachel Q. Muir, Chudan Xu, Francine Z. Marques, Jennifer L. Pluznick","doi":"10.1152/ajprenal.00051.2024","DOIUrl":null,"url":null,"abstract":"The gut microbiome regulates many important host physiological processes associated with cardiovascular health and disease; however, the impact of the gut microbiome on aldosterone is unclear. Investigating whether gut microbiota regulate aldosterone can offer novel insights into how the microbiome affects blood pressure. In this study, we aimed to determine whether gut microbiota regulate host aldosterone. We employed enzyme-linked immunosorbent assays (ELISAs) to assess plasma aldosterone and plasma renin activity (PRA) in female and male mice in which gut microbiota are intact, suppressed, or absent. In addition, we examined urinary aldosterone. Our findings demonstrated that when the gut microbiota is suppressed following antibiotic treatment, there is an increase in plasma and urinary aldosterone in both female and male mice. In contrast, an increase in PRA is seen only in males. We also found that when gut microbiota are absent (germ-free mice), plasma aldosterone is significantly increased compared to conventional animals (in both females and males), but PRA is not. Understanding how gut microbiota influence aldosterone levels could provide valuable insights into the development and treatment of hypertension and/or primary aldosteronism. This knowledge may open new avenues for therapeutic interventions, such as probiotics or dietary modifications to help regulate blood pressure via microbiota-based changes to aldosterone.","PeriodicalId":7583,"journal":{"name":"American Journal of Physiology - Renal Physiology","volume":"98 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-04-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"American Journal of Physiology - Renal Physiology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1152/ajprenal.00051.2024","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
The gut microbiome regulates many important host physiological processes associated with cardiovascular health and disease; however, the impact of the gut microbiome on aldosterone is unclear. Investigating whether gut microbiota regulate aldosterone can offer novel insights into how the microbiome affects blood pressure. In this study, we aimed to determine whether gut microbiota regulate host aldosterone. We employed enzyme-linked immunosorbent assays (ELISAs) to assess plasma aldosterone and plasma renin activity (PRA) in female and male mice in which gut microbiota are intact, suppressed, or absent. In addition, we examined urinary aldosterone. Our findings demonstrated that when the gut microbiota is suppressed following antibiotic treatment, there is an increase in plasma and urinary aldosterone in both female and male mice. In contrast, an increase in PRA is seen only in males. We also found that when gut microbiota are absent (germ-free mice), plasma aldosterone is significantly increased compared to conventional animals (in both females and males), but PRA is not. Understanding how gut microbiota influence aldosterone levels could provide valuable insights into the development and treatment of hypertension and/or primary aldosteronism. This knowledge may open new avenues for therapeutic interventions, such as probiotics or dietary modifications to help regulate blood pressure via microbiota-based changes to aldosterone.
肠道微生物群调节许多与心血管健康和疾病相关的重要宿主生理过程;然而,肠道微生物群对醛固酮的影响尚不清楚。研究肠道微生物群是否能调节醛固酮可以为了解微生物群如何影响血压提供新的视角。在这项研究中,我们旨在确定肠道微生物群是否能调节宿主的醛固酮。我们采用酶联免疫吸附试验(ELISAs)来评估肠道微生物群完整、受抑制或缺失的雌性和雄性小鼠的血浆醛固酮和血浆肾素活性(PRA)。此外,我们还检测了尿醛固酮。我们的研究结果表明,当抗生素治疗后肠道微生物群受到抑制时,雌性和雄性小鼠血浆和尿液中的醛固酮都会增加。相反,只有雄性小鼠的 PRA 增加。我们还发现,当肠道微生物群缺失时(无菌小鼠),血浆醛固酮会比常规动物显著增加(雌性和雄性),但 PRA 不会增加。了解肠道微生物群如何影响醛固酮水平可为高血压和/或原发性醛固酮增多症的发病和治疗提供有价值的见解。这些知识可能会为治疗干预开辟新的途径,如益生菌或饮食调整,以帮助通过基于微生物群的醛固酮变化来调节血压。