老年小鼠的海马神经动态和术后谵妄样行为

IF 9.1 1区 医学 Q1 ANESTHESIOLOGY
Shiqi Guo, Liuyue Yang, Weihua Ding, Tewodros Mulugeta Dagnew, Yuting Gao, Wei Wang, Pei Wang, Song Huang, Chongzhao Ran, Changning Wang, Le Shen, Qian Chen, Oluwaseun Akeju, Shiqian Shen
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引用次数: 0

摘要

背景:术后谵妄(POD)是麻醉/手术后常见且严重的临床症状。虽然其临床影响是公认的,但潜在的电生理机制仍然很大程度上未知,为有效治疗带来了挑战。本研究旨在研究具有POD发生倾向的老年小鼠麻醉/手术前后的海马神经动力学。方法:采用成年和老年小鼠建立POD模型。在基线(手术前一天)以及麻醉/手术后9小时和24小时对N = 10只小鼠进行pod样行为评估。行为学测试包括空地测试、y型迷宫测试、埋藏食物测试和新物体识别测试。在相同的时间间隔内,使用高密度硅探针(HSP)对清醒、受限的小鼠进行体内慢性脑记录。为了进一步研究海马神经动力学,还进行了体内双光子钙成像。此外,用吲哚- 3-丙酸(IPA)预处理老龄小鼠,通过电生理和钙显像评价其对pod样行为和神经活动的影响。结果:我们首先观察到,与麻醉/手术后的成年小鼠相比,老年小鼠表现出明显的pod样行为(通过z分数测量)。我们的分析揭示了海马神经元活动与年龄相关的显著差异。在手术后9小时,老年小鼠与成年小鼠相比,锥体细胞活性明显增加,中间神经元活性明显减少。这些神经元动力学的变化与老年小鼠pod样症状的发生有关。手术后24小时,老年小鼠的锥体细胞和中间神经元的活动都恢复到手术前的水平,这与pod样行为的改善相吻合。此外,IPA预处理可以调节老年小鼠的神经元活动,减轻锥体细胞的过度活跃,部分改善中间神经元功能障碍,这些变化与pod样行为的减轻有关。结论:海马神经活动的改变可能与脑功能障碍和pod样行为有关。IPA预处理可以调节老年小鼠的神经回路失衡,潜在地减轻POD的发病率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hippocampal Neural Dynamics and Postoperative Delirium-like Behavior in Aged Mice.

Background: Postoperative delirium (POD) is a common and serious clinical condition that occurs after anesthesia/surgery. While its clinical impact is well recognized, the underlying electrophysiologic mechanisms remain largely unknown, posing challenges for effective treatment. This study aims to investigate hippocampal neural dynamics before and after anesthesia/surgery in aged mice, which have a tendency to develop POD.

Methods: This study included adult and aged mice with a POD model. POD-like behavior was assessed in N = 10 mice at baseline (the day before surgery), as well as at 9 h and 24 h after anesthesia/surgery. A behavioral battery, including the open field test, Y maze, buried food test, and novel object recognition, was used for assessment. In vivo chronic brain recordings were performed on awake, restrained mice using a high-density silicon probe during the same time intervals. To further investigate hippocampal neural dynamics, in vivo two-photon calcium imaging was also conducted. Additionally, aged mice were pretreated with indole-3-propionic acid (IPA), and its effects on POD-like behavior and neural activity were evaluated using electrophysiology and calcium imaging.

Results: The first observation was that aged mice exhibited significant POD-like behavior, as measured by Z scores, compared to adult mice after anesthesia/surgery. Analysis revealed significant age-related differences in hippocampal neuronal activities. At 9 h after surgery, aged mice exhibited a marked increase in pyramidal cell activity and a reduction in interneuron activity compared to adult mice. These changes in neuronal dynamics were associated with the onset of POD-like symptoms in aged mice. By 24 h after surgery, both pyramidal cell and interneuron activity in aged mice had returned to presurgery levels, which coincided with an improvement in POD-like behavior. Additionally, IPA pretreatment modulated neuronal activity in aged mice, attenuating pyramidal cell hyperactivity and partially ameliorating interneuron dysfunction, changes associated with mitigated POD-like behavior.

Conclusions: Alterations in hippocampal neural activity may significantly contribute to brain dysfunction and POD-like behavior. IPA pretreatment may modulate neural circuit imbalances in aged mice, potentially mitigating POD incidence.

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来源期刊
Anesthesiology
Anesthesiology 医学-麻醉学
CiteScore
10.40
自引率
5.70%
发文量
542
审稿时长
3-6 weeks
期刊介绍: With its establishment in 1940, Anesthesiology has emerged as a prominent leader in the field of anesthesiology, encompassing perioperative, critical care, and pain medicine. As the esteemed journal of the American Society of Anesthesiologists, Anesthesiology operates independently with full editorial freedom. Its distinguished Editorial Board, comprising renowned professionals from across the globe, drives the advancement of the specialty by presenting innovative research through immediate open access to select articles and granting free access to all published articles after a six-month period. Furthermore, Anesthesiology actively promotes groundbreaking studies through an influential press release program. The journal's unwavering commitment lies in the dissemination of exemplary work that enhances clinical practice and revolutionizes the practice of medicine within our discipline.
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