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环境强化增强了低氧缺血性脑病中 Ca2.1 通道介导的突触前可塑性。

Environmental Enrichment Enhances Ca 2.1 Channel-Mediated Presynaptic Plasticity in Hypoxic-Ischemic Encephalopathy.

机构信息

Department and Research Institute of Rehabilitation Medicine, Yonsei University College of Medicine, Seoul 03722, Korea.

Graduate Program of NanoScience and Technology, Yonsei University, Seoul 03722, Korea.

出版信息

Int J Mol Sci. 2021 Mar 26;22(7):3414. doi: 10.3390/ijms22073414.

Abstract

Hypoxic-ischemic encephalopathy (HIE) is a devastating neonatal brain condition caused by lack of oxygen and limited blood flow. Environmental enrichment (EE) is a classic paradigm with a complex stimulation of physical, cognitive, and social components. EE can exert neuroplasticity and neuroprotective effects in immature brains. However, the exact mechanism of EE on the chronic condition of HIE remains unclear. HIE was induced by a permanent ligation of the right carotid artery, followed by an 8% O hypoxic condition for 1 h. At 6 weeks of age, HIE mice were randomly assigned to either standard cages or EE cages. In the behavioral assessments, EE mice showed significantly improved motor performances in rotarod tests, ladder walking tests, and hanging wire tests, compared with HIE control mice. EE mice also significantly enhanced cognitive performances in Y-maze tests. Particularly, EE mice showed a significant increase in Ca 2.1 (P/Q type) and presynaptic proteins by molecular assessments, and a significant increase of Ca 2.1 in histological assessments of the cerebral cortex and hippocampus. These results indicate that EE can upregulate the expression of the Ca 2.1 channel and presynaptic proteins related to the synaptic vesicle cycle and neurotransmitter release, which may be responsible for motor and cognitive improvements in HIE.

摘要

缺氧缺血性脑病(HIE)是一种由缺氧和血流量有限引起的毁灭性新生儿脑疾病。环境丰富(EE)是一种经典的范式,具有物理、认知和社会成分的复杂刺激。EE 可以在不成熟的大脑中发挥神经可塑性和神经保护作用。然而,EE 对 HIE 慢性期的确切机制仍不清楚。HIE 通过永久性结扎右侧颈总动脉,然后在 8% O 缺氧条件下 1 小时来诱导。在 6 周龄时,HIE 小鼠被随机分配到标准笼或 EE 笼中。在行为评估中,与 HIE 对照组相比,EE 组的小鼠在转棒试验、梯级行走试验和悬挂线试验中运动表现明显改善。EE 组的小鼠在 Y 迷宫测试中的认知表现也明显提高。特别是,通过分子评估,EE 组的 Ca 2.1(P/Q 型)和突触前蛋白的表达显著增加,在大脑皮层和海马体的组织学评估中 Ca 2.1 也显著增加。这些结果表明,EE 可以上调与突触囊泡循环和神经递质释放相关的 Ca 2.1 通道和突触前蛋白的表达,这可能是 HIE 运动和认知改善的原因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/70ef/8037860/0acff946a75b/ijms-22-03414-g001.jpg

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