Metformin reduces neuroinflammation and improves cognitive functions after traumatic brain injury

被引:27
作者
DiBona, Victoria L. [1 ]
Shah, Mihir K. [1 ]
Krause, Kayla J. [1 ]
Zhu, Wenxin [1 ]
Voglewede, Mikayla M. [1 ]
Smith, Dana M. [1 ]
Crockett, David P. [1 ]
Zhang, Huaye [1 ]
机构
[1] Rutgers State Univ, Robert Wood Johnson Med Sch, Dept Neurosci & Cell Biol, Piscataway, NJ USA
关键词
Metformin; TBI; Neuroinflammation; Microglia; Par1; MARK; ACTIVATED PROTEIN-KINASE; SYNAPTIC PLASTICITY; KAPPA-B; PHOSPHORYLATION; MEMORY; LKB1; NEUROGENESIS; EPIDEMIOLOGY; ASTROCYTES; BEHAVIOR;
D O I
10.1016/j.neures.2021.05.007
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Within the brain, traumatic brain injury (TBI) alters synaptic plasticity and increases neuroinflammation and neuronal death. Yet, there lacks effective TBI treatments providing pleiotropic beneficial effects on these diverse cellular processes necessary for functional recovery. Here, we show the diabetes drug, metformin, significantly improves cognitive functions after controlled cortical impact (CCI) injury in mice, showing improved spatial learning and nest building. Furthermore, injured animals treated with metformin exhibit increased ramification of microglia processes, indicating reduced neuroinflammation. Finally, metformin treatment in vitro increased neuronal activation of partitioning defective 1 (Par1), a family of Ser/Thr kinases playing a key role in synaptic plasticity and neuroinflammation. These results suggest metformin is a promising therapeutic agent for targeting multiple cellular processes necessary for functional TBI recovery. (c) 2021 Elsevier B.V. and Japan Neuroscience Society. All rights reserved.
引用
收藏
页码:99 / 109
页数:11
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