Crosstalk between gut microbiome and immunology in the management of ischemic brain injury

被引:17
|
作者
Rahman, Ziaur [1 ]
Dandekar, Manoj P. [1 ]
机构
[1] Natl Inst Pharmaceut Educ & Res NIPER, Dept Pharmacol & Toxicol, Hyderabad, Telangana, India
关键词
Stroke; Immune system; Gut microbiota; SCFAs; Inflammation; REGULATORY T-CELLS; CHAIN FATTY-ACIDS; FOCAL CEREBRAL-ISCHEMIA; INTESTINAL MICROBIOTA; IMMUNE-SYSTEM; MICROGLIAL ACTIVATION; INTERFERON-GAMMA; PROINFLAMMATORY CYTOKINES; HISTONE DEACETYLASES; EXPERIMENTAL STROKE;
D O I
10.1016/j.jneuroim.2021.577498
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Ischemic brain injury is a serious neurological complication, which accrues an immense activation of neuroinflammatory responses. Several lines of research suggested the interconnection of gut microbiota perturbation with the activation of proinflammatory mediators. Intestinal microbial communities also interchange information with the brain through various afferent and efferent channels and microbial by-products. Herein, we discuss the different microelements of gut microbiota and its connection with the host immune system and how change in immune-microbial signatures correlates with the stroke incidence and post-injury neurological sequelae. The activated inflammatory cells increase the production of proinflammatory cytokines, chemokines, proteases and adhesive proteins that are involved in the systemic inflammation, blood brain barrier disruption, gut dysbiosis and aggravation of ischemic brain injury. We suggest that fine-tuning of commensal gut microbiota (eubiosis) may regulate the activation of CNS resident cells like microglial, astrocytes, mast cells and natural killer cells.
引用
收藏
页数:10
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