From the Department of Neurosurgery and Neurobiology, Barrow Aneurysm and AVM Research Center, Barrow Neurological Institute, Phoenix, AZ.
Hypertension. 2019 Feb;73(2):491-496. doi: 10.1161/HYPERTENSIONAHA.118.11804.
Gut microbiota modulates metabolic and immunoregulatory axes and contributes to the pathophysiology of diseases with inflammatory components, such as atherosclerosis, diabetes mellitus, and ischemic stroke. Inflammation is emerging as a critical player in the pathophysiology of an intracranial aneurysm. Therefore, we hypothesized that the gut microbiota affects aneurysm formation by modulating inflammation. We induced intracranial aneurysms in mice by combining systemic hypertension and a single injection of elastase into the cerebrospinal fluid. Depletion of the gut microbiota was achieved via an oral antibiotic cocktail of vancomycin, metronidazole, ampicillin, and neomycin. Antibiotics were given 3 weeks before aneurysm induction and either continued until the end of the experiment or stopped 1 day before aneurysm induction. We also assessed the effects of the gut microbiota depletion on macrophage infiltration and mRNA levels of inflammatory cytokines. Gut microbiota depletion by antibiotics reduced the incidence when antibiotics were started 3 weeks before aneurysm induction and continued until the end of the experiment (83% versus 6%, P<0.001). Even when antibiotics were stopped 1 day before aneurysm induction, the gut microbiota depletion significantly reduced the incidence of aneurysms (86% versus 28%, P<0.05). Both macrophage infiltration and mRNA levels of inflammatory cytokines were reduced with gut microbiota depletion. These findings suggest that the gut microbiota contributes to the pathophysiology of aneurysms by modulating inflammation. Human studies are needed to determine the exact contribution of the gut microbiota to the pathophysiology of aneurysm formation and disease course in humans.
肠道微生物群调节代谢和免疫调节轴,并有助于具有炎症成分的疾病的病理生理学,如动脉粥样硬化、糖尿病和缺血性中风。炎症正在成为颅内动脉瘤病理生理学的关键因素。因此,我们假设肠道微生物群通过调节炎症影响动脉瘤的形成。我们通过将系统性高血压和单次脑脊髓液弹性酶注射相结合在小鼠中诱导颅内动脉瘤。通过万古霉素、甲硝唑、氨苄西林和新霉素的口服抗生素鸡尾酒来耗尽肠道微生物群。抗生素在动脉瘤诱导前 3 周给予,并在实验结束前继续使用或在动脉瘤诱导前 1 天停止使用。我们还评估了肠道微生物群耗竭对巨噬细胞浸润和炎症细胞因子 mRNA 水平的影响。抗生素开始于动脉瘤诱导前 3 周并持续到实验结束时,肠道微生物群耗竭可降低发生率(83%对 6%,P<0.001)。即使在动脉瘤诱导前 1 天停止使用抗生素,肠道微生物群耗竭也显著降低了动脉瘤的发生率(86%对 28%,P<0.05)。巨噬细胞浸润和炎症细胞因子的 mRNA 水平均随肠道微生物群耗竭而降低。这些发现表明,肠道微生物群通过调节炎症促进动脉瘤的病理生理学。需要进行人类研究来确定肠道微生物群对人类动脉瘤形成和疾病过程的病理生理学的确切贡献。