Battaglini Denise, Pimentel-Coelho Pedro Moreno, Robba Chiara, Dos Santos Claudia C, Cruz Fernanda Ferreira, Pelosi Paolo, Rocco Patricia Rieken Macedo
Anesthesia and Intensive Care, San Martino Policlinico Hospital, IRCCS for Oncology and Neuroscience, Genoa, Italy.
Department of Surgical Sciences and Integrated Diagnostics, University of Genoa, Genoa, Italy.
Front Neurol. 2020 Jun 25;11:598. doi: 10.3389/fneur.2020.00598. eCollection 2020.
The microbiota-gut-brain axis is considered a central regulator of the immune system after acute ischemic stroke (AIS), with a potential role in determining outcome. Several pathways are involved in the evolution of gut microbiota dysbiosis after AIS. and signaling pathways involve bidirectional communication between the hypothalamic-pituitary-adrenal axis, the autonomic nervous system, the enteric nervous system, and the immune cells of the gut. Alterations in gut microbiome can be a risk factor and may also lead to AIS. Both risk factors for AIS and gut-microbiome composition are influenced by similar factors, including diabetes, hypertension, hyperlipidemia, obesity, and vascular dysfunction. Furthermore, the systemic inflammatory response after AIS may yield liver, renal, respiratory, gastrointestinal, and cardiovascular impairment, including the multiple organ dysfunction syndrome. This review focus on biochemical, immunological, and neuroanatomical modulation of gut microbiota and its possible systemic harmful effects after AIS, as well as the role of ischemic stroke on microbiota composition. Finally, we highlight the role of gut microbiota as a potential novel therapeutic target in acute ischemic stroke.
微生物群-肠-脑轴被认为是急性缺血性卒中(AIS)后免疫系统的核心调节因子,在决定预后方面具有潜在作用。AIS后肠道微生物群失调的演变涉及多种途径。 和 信号通路涉及下丘脑-垂体-肾上腺轴、自主神经系统、肠神经系统和肠道免疫细胞之间的双向通信。肠道微生物组的改变可能是一个危险因素,也可能导致AIS。AIS的危险因素和肠道微生物组组成均受相似因素影响,包括糖尿病、高血压、高脂血症、肥胖和血管功能障碍。此外,AIS后的全身炎症反应可能导致肝脏、肾脏、呼吸、胃肠道和心血管损害,包括多器官功能障碍综合征。本综述重点关注AIS后肠道微生物群的生化、免疫和神经解剖学调节及其可能的全身有害影响,以及缺血性卒中对微生物群组成的作用。最后,我们强调肠道微生物群作为急性缺血性卒中潜在新治疗靶点的作用。