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肠道菌群通过调节盐诱导高血压时肠道源性皮质酮的合成来调节血压。

Intestinal Flora Modulates Blood Pressure by Regulating the Synthesis of Intestinal-Derived Corticosterone in High Salt-Induced Hypertension.

机构信息

From the Department of Cardiology, The Key Laboratory of Cardiovascular Remodeling and Function Research, Chinese Ministry of Education, Chinese National Health Commission and Chinese Academy of Medical Sciences, The State and Shandong Province Joint Key Laboratory of Translational Cardiovascular Medicine, Qilu Hospital of Shandong University, Jinan (X. Yan, J.J., X. Yin, J.G., X.W., S.Z., P.B., Y.Z., Q.Z.).

Division of Endocrinology and Metabolism (X.S., Z.W.), Shandong Provincial Hospital Affiliated to Shandong University, Jinan, China.

出版信息

Circ Res. 2020 Mar 27;126(7):839-853. doi: 10.1161/CIRCRESAHA.119.316394. Epub 2020 Feb 13.

Abstract

RATIONALE

High-salt diet is one of the most important risk factors for hypertension. Intestinal flora has been reported to be associated with high salt-induced hypertension (hSIH). However, the detailed roles of intestinal flora in hSIH pathogenesis have not yet been fully elucidated.

OBJECTIVE

To reveal the roles and mechanisms of intestinal flora in hSIH development.

METHODS AND RESULTS

The abovementioned issues were investigated using various techniques including 16S rRNA gene sequencing, untargeted metabolomics, selective bacterial culture, and fecal microbiota transplantation. We found that high-salt diet induced hypertension in Wistar rats. The fecal microbiota of healthy rats could dramatically lower blood pressure (BP) of hypertensive rats, whereas the fecal microbiota of hSIH rats had opposite effects. The composition, metabolism, and interrelationship of intestinal flora in hSIH rats were considerably reshaped, including the increased corticosterone level and reduced and arachidonic acid levels, which tightly correlated with BP. The serum corticosterone level was also significantly increased in rats with hSIH. Furthermore, the above abnormalities were confirmed in patients with hypertension. The intestinal could inhibit the production of intestinal-derived corticosterone induced by high-salt diet through its metabolite arachidonic acid.

CONCLUSIONS

hSIH could be transferred by fecal microbiota transplantation, indicating the pivotal roles of intestinal flora in hSIH development. High-salt diet reduced the levels of and arachidonic acid in the intestine, which increased intestinal-derived corticosterone production and corticosterone levels in serum and intestine, thereby promoting BP elevation. This study revealed a novel mechanism different from inflammation/immunity by which intestinal flora regulated BP, namely intestinal flora could modulate BP by affecting steroid hormone levels. These findings enriched the understanding of the function of intestinal flora and its effects on hypertension.

摘要

背景

高盐饮食是高血压最重要的危险因素之一。据报道,肠道菌群与高盐诱导的高血压(hSIH)有关。然而,肠道菌群在 hSIH 发病机制中的详细作用尚未完全阐明。

目的

揭示肠道菌群在 hSIH 发展中的作用和机制。

方法和结果

使用包括 16S rRNA 基因测序、非靶向代谢组学、选择性细菌培养和粪便微生物群移植在内的各种技术研究了上述问题。我们发现高盐饮食可诱导 Wistar 大鼠发生高血压。健康大鼠的粪便微生物群可显著降低高血压大鼠的血压(BP),而 hSIH 大鼠的粪便微生物群则有相反的作用。hSIH 大鼠的肠道菌群组成、代谢和相互关系发生了显著重塑,包括皮质酮水平升高和 及花生四烯酸水平降低,这与 BP 密切相关。hSIH 大鼠的血清皮质酮水平也显著升高。此外,这些异常在高血压患者中得到了证实。肠道 可通过其代谢产物花生四烯酸抑制高盐饮食诱导的肠道来源的皮质酮产生。

结论

hSIH 可通过粪便微生物群移植传递,表明肠道菌群在 hSIH 发展中起关键作用。高盐饮食降低了肠道中 及花生四烯酸的水平,增加了肠道来源的皮质酮产生和血清及肠道中的皮质酮水平,从而促进 BP 升高。本研究揭示了一种不同于炎症/免疫的肠道菌群调节 BP 的新机制,即肠道菌群通过影响类固醇激素水平来调节 BP。这些发现丰富了对肠道菌群功能及其对高血压影响的理解。

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