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实验性腹主动脉瘤中的肠道微生物群

The gut microbiota in experimental abdominal aortic aneurysm.

作者信息

Xiao Jie, Wei Zhanjie, Yang Chuanlei, Dai Shilin, Wang Xiancan, Shang Yuqiang

机构信息

Department of Cardiovascular Surgery, Central Hospital of Wuhan, Huazhong University of Science and Technology, Wuhan, China.

Department of General Surgery, Central Hospital of Wuhan, Huazhong University of Science and Technology, Wuhan, China.

出版信息

Front Cardiovasc Med. 2023 Feb 22;10:1051648. doi: 10.3389/fcvm.2023.1051648. eCollection 2023.

Abstract

BACKGROUND

Abdominal aortic aneurysm (AAA) is a life-threatening disease and there are no effective treatments to inhibit aneurysm progression and rupture. The gut microbiota has been increasingly recognized, as a new therapeutic target, because of its role in host homeostasis. However, the role of the gut microbiota in AAA has not been clarified. Therefore, we performed 16S rRNA analysis to determine and compare the composition of the gut microbiota between AAA and control groups.

METHODS

We used the classical angiotensin-II induced AAA mouse model to investigate the role of gut microbiota and abdominal aortic aneurysm. The mice were randomly assigned to 2 groups: the control ( = 7) group received saline (vehicle), while the AAA ( = 13) group received solutions of Ang II. Aortic tissue and fecal samples were harvested 28 days after infusion. Fecal samples were analyzed by 16S rRNA sequencing.

RESULTS

The levels of , and were increased in the AAA group, while those of , and were increased in the control group. Furthermore, network analysis and ZiPi score assessment highlighted species in the phylum as the keystone species. PICRUSt2 analysis revealed that PWY-6629 (a super pathway of L-tryptophan biosynthesis), PWY-7446 (sulfoglycolysis), and PWY-6165 [chorismate biosynthesis II (archaea)] may-be involved in the metabolic pathways that contribute to AAA formation, and / may be the key bacteria that influence those three pathways.

CONCLUSION

Alterations in the gut microbiota may be associated with the formation of AAA. and were significantly decreased in the AAA group, but the keystone species in the phylum and the metabolic products of these bacteria should be given more attention in AAA formation research.

摘要

背景

腹主动脉瘤(AAA)是一种危及生命的疾病,目前尚无有效的治疗方法来抑制动脉瘤的进展和破裂。肠道微生物群因其在宿主内环境稳态中的作用,越来越被视为一个新的治疗靶点。然而,肠道微生物群在AAA中的作用尚未明确。因此,我们进行了16S rRNA分析,以确定和比较AAA组与对照组肠道微生物群的组成。

方法

我们使用经典的血管紧张素II诱导的AAA小鼠模型来研究肠道微生物群与腹主动脉瘤的关系。将小鼠随机分为2组:对照组(n = 7)接受生理盐水(载体),而AAA组(n = 13)接受血管紧张素II溶液。输注28天后采集主动脉组织和粪便样本。粪便样本通过16S rRNA测序进行分析。

结果

AAA组中[具体菌种名称1]、[具体菌种名称2]和[具体菌种名称3]的水平升高,而对照组中[具体菌种名称4]、[具体菌种名称5]和[具体菌种名称6]的水平升高。此外,网络分析和ZiPi评分评估突出显示[具体菌门名称]中的菌种为关键物种。PICRUSt2分析表明,PWY - 6629(L - 色氨酸生物合成的超级途径)、PWY - 7446(硫酸糖酵解)和PWY - 6165[分支酸生物合成II(古菌)]可能参与了促成AAA形成的代谢途径,并且[具体菌种名称7] / [具体菌种名称8]可能是影响这三条途径的关键细菌。

结论

肠道微生物群的改变可能与AAA的形成有关。AAA组中[具体菌种名称9]和[具体菌种名称10]显著减少,但在AAA形成研究中,[具体菌门名称]中的关键物种及其这些细菌的代谢产物应给予更多关注。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9cf1/9992639/0b5b8b11d65d/fcvm-10-1051648-g001.jpg

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