Hypoxic Preconditioning Mitigates Acute Hypoxia Induced MS/VDB Cholinergic Cell Loss and Memory Impairments.

IF 7 2区 医学 Q1 GERIATRICS & GERONTOLOGY
Linhui Qin, Yong Yang, Houdi Zhang, Sijie Li, Xi Wu, Minjie Wang, Simeng Liu, Heguan Fu, Xunming Ji, Cong Han, Changhong Ren
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Abstract

Cholinergic cells originating from the medial septal nucleus (MS) and the vertical and horizontal limbs of the diagonal band of Broca (VDB and HDB, respectively) are critical for supporting a variety of memory and cognitive functions. However, the viability of cholinergic cells has not been explored in the context of acute hypoxia (AH). This study aimed to investigate the effects of AH on cholinergic cells in these nuclei and to test whether hypoxic preconditioning (HPC)-a previously established neuroprotective therapy-could prevent cholinergic cell loss, cognitive dysfunction, and hippocampal synaptic dysfunction in mice exposed to AH. We found that cholinergic cell loss occurred in the MS/DB after AH. HPC prevented this effect and also improved AH-induced cognitive dysfunction and hippocampal synaptic dysfunction. Overall, our findings highlight the significant role of cholinergic cells in AH-induced memory impairments and suggest that the preservation of cholinergic cell viability may provide a mechanism by which HPC improves memory impairments and preserves the function of memory-processing brain structures after AH.

缺氧预处理减轻急性缺氧诱导的MS/VDB胆碱能细胞丧失和记忆障碍。
来源于中隔核(MS)和Broca斜带的垂直和水平分支(分别为VDB和HDB)的胆碱能细胞对支持各种记忆和认知功能至关重要。然而,在急性缺氧(AH)的情况下,胆碱能细胞的活力尚未得到探讨。本研究旨在研究AH对这些细胞核中胆碱能细胞的影响,并测试缺氧预处理(HPC)-一种先前建立的神经保护疗法-是否可以预防暴露于AH的小鼠胆碱能细胞丢失,认知功能障碍和海马突触功能障碍。我们发现AH后MS/DB出现胆碱能细胞丢失。HPC阻止了这种作用,并改善了ah诱导的认知功能障碍和海马突触功能障碍。总的来说,我们的研究结果强调了胆碱能细胞在AH诱导的记忆障碍中的重要作用,并表明保留胆碱能细胞活力可能提供了一种机制,通过这种机制,HPC可以改善AH后的记忆障碍,并保留记忆处理脑结构的功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Aging and Disease
Aging and Disease GERIATRICS & GERONTOLOGY-
CiteScore
14.60
自引率
2.70%
发文量
138
审稿时长
10 weeks
期刊介绍: Aging & Disease (A&D) is an open-access online journal dedicated to publishing groundbreaking research on the biology of aging, the pathophysiology of age-related diseases, and innovative therapies for conditions affecting the elderly. The scope encompasses various diseases such as Stroke, Alzheimer's disease, Parkinson’s disease, Epilepsy, Dementia, Depression, Cardiovascular Disease, Cancer, Arthritis, Cataract, Osteoporosis, Diabetes, and Hypertension. The journal welcomes studies involving animal models as well as human tissues or cells.
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