感觉剥夺后,雄性Rett模型小鼠的长期皮质可塑性降低。

IF 1.3 4区 医学 Q4 NEUROSCIENCES
Somatosensory and Motor Research Pub Date : 2023-12-01 Epub Date: 2022-12-24 DOI:10.1080/08990220.2022.2158799
Farnoosh Farhoomand, Kerry R Delaney
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引用次数: 0

摘要

目的/目的:Rett (RTT)综合征是一种神经发育障碍,由甲基cpg结合蛋白2的功能丧失突变引起。我们研究了早期有症状的雄性突变小鼠通过须修剪引起的感觉剥夺诱导的活动依赖性可塑性,以评估神经重新连接的能力。方法:修剪1根须0 ~ 14天,将须残端摆动1秒引起的神经激活引起的脑血氧瞬间减少的内在光学成像与未修剪的对照须进行比较。结果:大脑皮层对未修剪须摆动的诱发反应在14天内保持不变,野生型(n = 14)修剪须减少49.0±4.3%,而突变型仅减少22.7±4.6% (n = 18, p = 0.001)。结论:由于感觉剥夺后须桶皮层神经激活的减少依赖于诱发和基础神经活动,因此须修剪后皮层重新布线的损害为探索RTT突触建立和维持缺陷的机制提供了一个合适的范例,这可能是治疗的潜在目标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Long-term cortical plasticity following sensory deprivation is reduced in male Rett model mice.

Purpose/aim: Rett (RTT) syndrome, a neurodevelopmental disorder, results from loss-of-function mutations in methyl-CpG-binding protein 2. We studied activity-dependent plasticity induced by sensory deprivation via whisker trimming in early symptomatic male mutant mice to assess neural rewiring capability.

Methods: One whisker was trimmed for 0-14 days and intrinsic optical imaging of the transient reduction of brain blood oxygenation resulting from neural activation by 1 second of wiggling of the whisker stump was compared to that of an untrimmed control whisker.

Results: Cortical evoked responses to wiggling a non-trimmed whisker were constant for 14 days, reduced for a trimmed whisker by 49.0 ± 4.3% in wild type (n = 14) but by only 22.7 ± 4.6% in mutant (n = 18, p = 0.001).

Conclusion: As the reduction in neural activation following sensory deprivation in whisker barrel cortex is known to be dependent upon evoked and basal neural activity, impairment of cortical re-wiring following whisker trimming provides a paradigm suitable to explore mechanisms underlying deficiencies in the establishment and maintenance of synapses in RTT, which can be potentially targeted by therapeutics.

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来源期刊
Somatosensory and Motor Research
Somatosensory and Motor Research 医学-神经科学
自引率
0.00%
发文量
4
审稿时长
>12 weeks
期刊介绍: Somatosensory & Motor Research publishes original, high-quality papers that encompass the entire range of investigations related to the neural bases for somatic sensation, somatic motor function, somatic motor integration, and modeling thereof. Comprising anatomical, physiological, biochemical, pharmacological, behavioural, and psychophysical studies, Somatosensory & Motor Research covers all facets of the peripheral and central processes underlying cutaneous sensation, and includes studies relating to afferent and efferent mechanisms of deep structures (e.g., viscera, muscle). Studies of motor systems at all levels of the neuraxis are covered, but reports restricted to non-neural aspects of muscle generally would belong in other journals.
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