Sex Hormone Androgen Elevates Blood Pressure Through Gut Microbiota-TMAO Pathway.

IF 8.2 1区 医学 Q1 PERIPHERAL VASCULAR DISEASE
Ying Li, Hong-Li Jiang, Lei Chen, Jia-Yue Yu, Sachin Aryal, Ya-Nan Gao, Ying-Bao Zhu, Wen-Fang Lu, Zhi-Ming Dai, Li-Li Huang, Qi Liu, Hua Liu, Li-Min Wei, Xue Zhao, Xiao-Min Liu, Juan Bai, Xiao-Lian Shi, Qing Su, Meng-Lu Xu, Ishan Manandhar, Pritam Bardhan, Ya-Nan Wang, Ting Yao, Bina Joe, Tao Yang, Hong-Bao Li
{"title":"Sex Hormone Androgen Elevates Blood Pressure Through Gut Microbiota-TMAO Pathway.","authors":"Ying Li, Hong-Li Jiang, Lei Chen, Jia-Yue Yu, Sachin Aryal, Ya-Nan Gao, Ying-Bao Zhu, Wen-Fang Lu, Zhi-Ming Dai, Li-Li Huang, Qi Liu, Hua Liu, Li-Min Wei, Xue Zhao, Xiao-Min Liu, Juan Bai, Xiao-Lian Shi, Qing Su, Meng-Lu Xu, Ishan Manandhar, Pritam Bardhan, Ya-Nan Wang, Ting Yao, Bina Joe, Tao Yang, Hong-Bao Li","doi":"10.1161/HYPERTENSIONAHA.125.25052","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Hypertension is a leading risk factor for all-cause mortality worldwide, affecting ≈1.3 billion people. Imbalanced gut microbiota contributes to blood pressure elevation. We recently reported sex differences in the responses of gut microbiota to environmental stimuli, such as salt, with male gut microbiota being more vulnerable to induce high blood pressure than female microbiota. In this study, we investigated the mechanisms by which gut microbiota regulate blood pressure in a sex-dependent manner.</p><p><strong>Methods: </strong>Antibiotic treatment, gonadectomy, sex hormone replenishment, and treatment with trimethylamine N-oxide or its blocker were performed in male and female spontaneously hypertensive rats.</p><p><strong>Results: </strong>We observed sex differences in gut microbiota composition and sex-specific blood pressure responses to antibiotic treatment in pubertal spontaneously hypertensive rats. In gonadectomized rats treated with sex hormones, we found that the male sex hormone dihydrotestosterone elevated blood pressure, reshaped gut microbiota, and increased levels of microbiota-derived metabolites, trimethylamine and treatment with trimethylamine N-oxide. The accumulation of treatment with trimethylamine N-oxide in plasma and the paraventricular nucleus of the hypothalamus was associated with inflammation and sympathetic activation.</p><p><strong>Conclusions: </strong>These findings underscore the mechanistic role of dihydrotestosterone in gut microbiota-mediated sex-specific blood pressure regulation and suggest that targeting the gut microbiota-treatment with trimethylamine N-oxide pathway may provide new therapeutic strategies for male hypertension.</p>","PeriodicalId":13042,"journal":{"name":"Hypertension","volume":" ","pages":""},"PeriodicalIF":8.2000,"publicationDate":"2025-08-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Hypertension","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1161/HYPERTENSIONAHA.125.25052","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PERIPHERAL VASCULAR DISEASE","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Hypertension is a leading risk factor for all-cause mortality worldwide, affecting ≈1.3 billion people. Imbalanced gut microbiota contributes to blood pressure elevation. We recently reported sex differences in the responses of gut microbiota to environmental stimuli, such as salt, with male gut microbiota being more vulnerable to induce high blood pressure than female microbiota. In this study, we investigated the mechanisms by which gut microbiota regulate blood pressure in a sex-dependent manner.

Methods: Antibiotic treatment, gonadectomy, sex hormone replenishment, and treatment with trimethylamine N-oxide or its blocker were performed in male and female spontaneously hypertensive rats.

Results: We observed sex differences in gut microbiota composition and sex-specific blood pressure responses to antibiotic treatment in pubertal spontaneously hypertensive rats. In gonadectomized rats treated with sex hormones, we found that the male sex hormone dihydrotestosterone elevated blood pressure, reshaped gut microbiota, and increased levels of microbiota-derived metabolites, trimethylamine and treatment with trimethylamine N-oxide. The accumulation of treatment with trimethylamine N-oxide in plasma and the paraventricular nucleus of the hypothalamus was associated with inflammation and sympathetic activation.

Conclusions: These findings underscore the mechanistic role of dihydrotestosterone in gut microbiota-mediated sex-specific blood pressure regulation and suggest that targeting the gut microbiota-treatment with trimethylamine N-oxide pathway may provide new therapeutic strategies for male hypertension.

性激素雄激素通过肠道微生物-氧化三甲胺途径升高血压。
背景:高血压是全球全因死亡的主要危险因素,影响约13亿人。肠道菌群失衡会导致血压升高。我们最近报道了肠道微生物群对环境刺激(如盐)反应的性别差异,男性肠道微生物群比女性肠道微生物群更容易引起高血压。在这项研究中,我们研究了肠道微生物群以性别依赖的方式调节血压的机制。方法:对雄性和雌性自发性高血压大鼠进行抗生素治疗、性腺切除术、性激素补充、三甲胺n -氧化物或其阻滞剂治疗。结果:我们观察到了青春期自发性高血压大鼠肠道菌群组成和性别特异性血压对抗生素治疗的反应的性别差异。在接受性激素治疗的去性腺的大鼠中,我们发现雄性性激素双氢睾酮升高了血压,重塑了肠道微生物群,并增加了微生物衍生代谢物三甲胺和三甲胺n -氧化物治疗的水平。三甲胺n -氧化物在血浆和下丘脑室旁核中的积累与炎症和交感神经激活有关。结论:这些发现强调了双氢睾酮在肠道微生物介导的性别特异性血压调节中的机制作用,并提示三甲胺n -氧化物途径靶向肠道微生物治疗可能为男性高血压提供新的治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Hypertension
Hypertension 医学-外周血管病
CiteScore
15.90
自引率
4.80%
发文量
1006
审稿时长
1 months
期刊介绍: Hypertension presents top-tier articles on high blood pressure in each monthly release. These articles delve into basic science, clinical treatment, and prevention of hypertension and associated cardiovascular, metabolic, and renal conditions. Renowned for their lasting significance, these papers contribute to advancing our understanding and management of hypertension-related issues.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信