IF 1.6 Q3 CLINICAL NEUROLOGY
NeuroSci Pub Date : 2025-03-12 DOI:10.3390/neurosci6010025
Amaya L Street, Vedant P Thakkar, Sean W Lemke, Liza M Schoenbeck, Kevin M Schumacher, Monica Sathyanesan, Samuel S Newton, Alexander D Kloth
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摘要

自闭症谱系障碍(ASD)是一种神经发育障碍,影响着全球超过 2% 的人口,其特点是行为重复、兴趣领域受限、社交沟通障碍和高度焦虑。目前,针对 ASD 的核心特征还没有已知的有效治疗方法。以往的文献已证实,促红细胞生成素(EPO)是一种很有前景的抗抑郁剂,它是一种具有造血副作用的强效神经原和神经营养剂。氨基甲酰化促红细胞生成素(CEPO)是促红细胞生成素的一种化学工程非造血衍生物,似乎保留了促红细胞生成素的神经保护因子,但没有血液学特性。最近的证据显示,CEPO能纠正BALB/cJ(BALB)小鼠与压力相关的抑郁行为,而BALB小鼠也可作为ASD小鼠模型。与 C57BL/6J 对照组相比,我们研究了 CEPO 是否能恢复社交和焦虑相关的行为缺陷。给小鼠注射 CEPO(40 μg/kg 磷酸盐缓冲盐水)或载体 21 天后,我们分析了小鼠在三室社交法、空地、高架加迷宫和波尔索尔特强迫游泳任务中的表现。CEPO似乎将小鼠在三室社会接近任务中的社会性纠正到了C57的水平,增加了小鼠与新的、社会性小鼠互动的时间,而不是改变小鼠在迷宫中探索活动的总量。与这一发现相一致的是,小鼠在空旷场地中行进的距离并没有随之增加,任务中与焦虑相关的测量指标也没有发生任何变化。另一方面,CEPO能改善高架加迷宫中的探索行为。这项研究首次证明了非促红细胞生成素 EPO 衍生物对自闭症小鼠模型的社会行为有益,值得进一步研究其作用机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Carbamoylated Erythropoietin Rescues Autism-Relevant Social Deficits in BALB/cJ Mice.

Autism spectrum disorder (ASD) is a neurodevelopmental disorder that affects over 2% of the population worldwide and is characterized by repetitive behaviors, restricted areas of interest, deficits in social communication, and high levels of anxiety. Currently, there are no known effective treatments for the core features of ASD. The previous literature has established erythropoietin (EPO) as a promising antidepressant, working as a potent neurogenic and neurotrophic agent with hematopoietic side effects. Carbamoylated erythropoietin (CEPO), a chemically engineered non-hematopoietic derivative of EPO, appears to retain the neuroprotective factors of EPO without the hematologic properties. Recent evidence shows that CEPO corrects stress-related depressive behaviors in BALB/cJ (BALB) mice, which also have face validity as an ASD mouse model. We investigated whether CEPO can recover deficient social and anxiety-related behavioral deficits compared to C57BL/6J controls. After administering CEPO (40 μg/kg in phosphate-buffered saline) or vehicle over 21 days, we analyzed the mice's performance in the three-chamber social approach, the open field, the elevated plus maze, and the Porsolt's forced swim tasks. CEPO appeared to correct sociability in the three-chamber social approach task to C57 levels, increasing the amount of time the mice interacted with novel, social mice overall rather than altering the overall amount of exploratory activity in the maze. Consistent with this finding, there was no concomitant increase in the distance traveled in the open field, nor were there any alterations in the anxiety-related measures in the task. On the other hand, CEPO administration improved exploratory behavior in the elevated plus maze. This study marks the first demonstration of the benefits of a non-erythropoietic EPO derivative for social behavior in a mouse model of autism and merits further investigation into the mechanisms by which this action occurs.

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