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胆碱能功能障碍参与大鼠慢性脑灌注不足诱导的内侧隔区-dCA1神经回路损伤。

Cholinergic Dysfunction Involvement in Chronic Cerebral Hypoperfusion-Induced Impairment of Medial Septum-dCA1 Neurocircuit in Rats.

作者信息

Xu Yi, Zhang Shuai, Sun Qiang, Wang Xu-Qiao, Chai Ya-Ni, Mishra Chandan, Chandra Shah Ram, Ai Jing

机构信息

Department of Pharmacology, The State-Province Key Laboratories of Biomedicine-Pharmaceutics of China, College of Pharmacy of Harbin Medical University, Harbin, China.

出版信息

Front Cell Neurosci. 2020 Sep 29;14:586591. doi: 10.3389/fncel.2020.586591. eCollection 2020.

Abstract

Chronic cerebral hypoperfusion (CCH) is considered a preclinical condition of mild cognitive impairment and thought to precede dementia. However, as the principal cholinergic source of hippocampus, whether the septo-hippocampal neurocircuit was impaired after CCH is still unknown. In this study, we established the CCH rat model by bilateral common carotid artery occlusion (2VO). Under anesthesia, the medial septum (MS) of rats was stimulated to evoke the field excitatory post-synaptic potential (fEPSP) in the pyramidal cell layer of dCA1. Consequently, we observed decreased amplitude of fEPSP and increased paired-pulse ratio (PPR) after 8-week CCH. After tail pinch, we also found decreased peak frequency and shortened duration of hippocampal theta rhythm in 2VO rats, indicating the dysfunction of septo-hippocampal neurocircuit. Besides, by intracerebroventricularly injecting GABAergic inhibitor (bicuculline) and cholinergic inhibitors (scopolamine and mecamylamine), we found that CCH impaired both the pre-synaptic cholinergic release and the post-synaptic nAChR function in MS-dCA1 circuits. These results gave an insight into the role of CCH in the impairment of cholinergic MS-dCA1 neurocircuits. These findings may provide a new idea about the CCH-induced neurodegenerative changes.

摘要

慢性脑灌注不足(CCH)被认为是轻度认知障碍的临床前状态,并被认为先于痴呆症出现。然而,作为海马体的主要胆碱能来源,CCH后隔海马神经回路是否受损仍不清楚。在本研究中,我们通过双侧颈总动脉闭塞(2VO)建立了CCH大鼠模型。在麻醉状态下,刺激大鼠的内侧隔区(MS)以诱发背侧海马体1区(dCA1)锥体细胞层的场兴奋性突触后电位(fEPSP)。结果,我们观察到8周CCH后fEPSP的幅度降低,成对脉冲比率(PPR)增加。夹尾刺激后,我们还发现2VO大鼠海马θ节律的峰值频率降低,持续时间缩短,这表明隔海马神经回路功能障碍。此外,通过脑室内注射GABA能抑制剂(荷包牡丹碱)和胆碱能抑制剂(东莨菪碱和美加明),我们发现CCH损害了MS-dCA1回路中突触前胆碱能释放和突触后烟碱型乙酰胆碱受体(nAChR)功能。这些结果深入了解了CCH在胆碱能MS-dCA1神经回路损伤中的作用。这些发现可能为CCH诱导的神经退行性变化提供新的思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0543/7550820/dfb96f918e88/fncel-14-586591-g0001.jpg

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