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Hypertension. 2019 Jul;74(1):184-193. doi: 10.1161/HYPERTENSIONAHA.119.13155. Epub 2019 Jun 3.
2
Formyl peptide receptor-1 activation exerts a critical role for the dynamic plasticity of arteries via actin polymerization.甲酰肽受体 1 的激活通过肌动蛋白聚合对动脉的动态可塑性发挥关键作用。
Pharmacol Res. 2019 Mar;141:276-290. doi: 10.1016/j.phrs.2019.01.015. Epub 2019 Jan 10.
3
Dietary metabolism, the gut microbiome, and heart failure.饮食代谢、肠道微生物群与心力衰竭。
Nat Rev Cardiol. 2019 Mar;16(3):137-154. doi: 10.1038/s41569-018-0108-7.
4
Attenuation of Microbiotal Dysbiosis and Hypertension in a CRISPR/Cas9 Gene Ablation Rat Model of GPER1.GPER1 的 CRISPR/Cas9 基因敲除大鼠模型中微生物失调和高血压的衰减
Hypertension. 2018 Nov;72(5):1125-1132. doi: 10.1161/HYPERTENSIONAHA.118.11175.
5
The Mouse Microbiome Is Required for Sex-Specific Diurnal Rhythms of Gene Expression and Metabolism.小鼠微生物组对于性别特异性基因表达和代谢的昼夜节律是必需的。
Cell Metab. 2019 Feb 5;29(2):362-382.e8. doi: 10.1016/j.cmet.2018.09.023. Epub 2018 Oct 18.
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Dysregulated Microbial Fermentation of Soluble Fiber Induces Cholestatic Liver Cancer.可溶性膳食纤维失调的微生物发酵可诱发胆汁淤积性肝癌。
Cell. 2018 Oct 18;175(3):679-694.e22. doi: 10.1016/j.cell.2018.09.004.
7
Salt-Responsive Metabolite, β-Hydroxybutyrate, Attenuates Hypertension.盐反应代谢物 β-羟丁酸可减轻高血压。
Cell Rep. 2018 Oct 16;25(3):677-689.e4. doi: 10.1016/j.celrep.2018.09.058.
8
Disparate effects of antibiotics on hypertension.抗生素对高血压的不同影响。
Physiol Genomics. 2018 Oct 1;50(10):837-845. doi: 10.1152/physiolgenomics.00073.2018. Epub 2018 Aug 10.
9
To Be, or Nox to Be, Endoplasmic Reticulum Stress in Hypertension.存在,还是不存在,内质网应激与高血压
Hypertension. 2018 Jul;72(1):59-60. doi: 10.1161/HYPERTENSIONAHA.118.10940. Epub 2018 May 29.
10
Hypertension Induced Morphological and Physiological Changes in Cells of the Arterial Wall.高血压引起的动脉壁细胞形态和生理变化。
Am J Hypertens. 2018 Sep 11;31(10):1067-1078. doi: 10.1093/ajh/hpy083.

微生物组对血管生理学至关重要:无菌状态会削弱小鼠的收缩力并诱导性别特异性血管重塑。

Microbiota are critical for vascular physiology: Germ-free status weakens contractility and induces sex-specific vascular remodeling in mice.

机构信息

Microbiome Consortium, Center for Hypertension and Precision Medicine, Department of Physiology and Pharmacology, University of Toledo College of Medicine & Life Sciences, Toledo, OH, USA.

Microbiome Consortium, Center for Hypertension and Precision Medicine, Department of Physiology and Pharmacology, University of Toledo College of Medicine & Life Sciences, Toledo, OH, USA.

出版信息

Vascul Pharmacol. 2020 Feb-Mar;125-126:106633. doi: 10.1016/j.vph.2019.106633. Epub 2019 Dec 13.

DOI:10.1016/j.vph.2019.106633
PMID:31843471
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7036036/
Abstract

Commensal microbiota within a holobiont contribute to the overall health of the host via mutualistic symbiosis. Disturbances in such symbiosis is prominently correlated with a variety of diseases affecting the modern society of humans including cardiovascular diseases, which are the number one contributors to human mortality. Given that a hallmark of all cardiovascular diseases is changes in vascular function, we hypothesized that depleting microbiota from a holobiont would induce vascular dysfunction. To test this hypothesis, young mice of both sexes raised in germ-free conditions were examined vascular contractility and structure. Here we observed that male and female germ-free mice presented a decrease in contraction of resistance arteries. These changes were more pronounced in germ-free males than in germ-free females mice. Furthermore, there was a distinct change in vascular remodeling between males and females germ-free mice. Resistance arteries from male germ-free mice demonstrated increased vascular stiffness, as shown by the leftward shift in the stress-strain curve and inward hypotrophic remodeling, a characteristic of chronic reduction in blood flow. On the other hand, resistance arteries from germ-free female mice were similar in the stress-strain curves to that of conventionally raised mice, but were distinctly different and showed outward hypertrophic remodeling, a characteristic seen in aging. Interestingly, we observed that reactive oxygen species (ROS) generation from bone marrow derived neutrophils is blunted in female germ-free mice, but it is exacerbated in male germ-free mice. In conclusion, these observations indicate that commensal microbiota of a holobiont are central to maintain proper vascular function and structure homeostasis, especially in males.

摘要

共生体中的共生微生物通过互利共生为宿主的整体健康做出贡献。这种共生关系的紊乱与多种影响现代人类社会的疾病显著相关,包括心血管疾病,它是人类死亡率的首要原因。鉴于所有心血管疾病的一个标志是血管功能的变化,我们假设从共生体中去除微生物群体会诱导血管功能障碍。为了验证这一假设,我们研究了在无菌条件下饲养的雌雄幼鼠的血管收缩性和结构。在这里,我们观察到雄性和雌性无菌小鼠的阻力动脉收缩能力下降。与无菌雌性小鼠相比,无菌雄性小鼠的这种变化更为明显。此外,无菌雄性和雌性小鼠之间的血管重塑也有明显的变化。雄性无菌小鼠的阻力动脉表现出血管僵硬增加,这表现为应力-应变曲线向左移位和内向萎缩性重塑,这是慢性血流减少的特征。另一方面,无菌雌性小鼠的阻力动脉的应力-应变曲线与常规饲养的小鼠相似,但明显不同,表现出外向性肥大性重塑,这是衰老的特征。有趣的是,我们观察到骨髓来源的中性粒细胞的活性氧(ROS)生成在无菌雌性小鼠中受到抑制,但在无菌雄性小鼠中则加剧。总之,这些观察结果表明,共生体的共生微生物群对于维持适当的血管功能和结构稳态至关重要,特别是在男性中。