新生儿冻伤诱导的皮质畸形改变海马基因表达并导致成年雄性Wistar大鼠持续认知和情绪缺陷

IF 3.4 3区 医学 Q2 NEUROSCIENCES
Olga E. Zubareva, Anna A. Kovalenko, Denis S. Sinyak, Tatyana Y. Postnikova, Marat R. Subkhankulov, Elmira R. Sabirova, Aleksey V. Zaitsev
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引用次数: 0

摘要

皮质畸形,包括小脑回畸形,通常与人类癫痫和认知障碍等神经发育合并症有关。为了研究早期皮质破坏如何导致持续的行为障碍,我们采用雄性Wistar大鼠的新生儿多小回新皮质局灶性冻结病变(FFL)模型。在出生后第0天(P0)诱导单侧皮质病变,并在P21时分析海马基因表达的分子变化(谷氨酸能信号:Grin1、Grin2a、Grin2b、Gria1、Gria2;神经炎症:Nlrp3、Il1b、Il1rn;胶质标志物:Gfap、Aif1;神经营养因子:Bdnf、Fgf2)。行为结果,包括运动活动、探索行为、焦虑样行为、社会互动和识别记忆,在成年期进行评估(P70-P90)。新生儿皮质病变诱导海马基因表达亚区特异性改变:同侧背侧海马Grin2b和Gria1表达减少,而对侧腹侧海马Grin2a、Bdnf和Fgf2表达增加。这些分子变化与成年大鼠随后的认知缺陷(识别记忆受损)和情绪失调(焦虑样行为加剧)以及探索活动减少有关。基本运动功能和社交能力没有受到影响,癫痫易感性(通过最大电击阈值评估)没有变化,突出了观察到的损伤的特异性。我们的研究结果表明,早期皮质畸形与小回形成、海马突触可塑性和神经营养信号失调以及持续的神经行为缺陷之间存在潜在的机制联系。这些结果强调了冷冻损伤模型在研究皮质畸形相关合并症的神经发育轨迹方面的翻译相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Neonatal Freeze Lesion-Induced Cortical Malformation Alters Hippocampal Gene Expression and Leads to Persistent Cognitive and Emotional Deficits in Adult Male Wistar Rats

Neonatal Freeze Lesion-Induced Cortical Malformation Alters Hippocampal Gene Expression and Leads to Persistent Cognitive and Emotional Deficits in Adult Male Wistar Rats

Cortical malformations, including microgyria, are often associated with neurodevelopmental comorbidities such as epilepsy and cognitive impairments in humans. To investigate how early cortical disruption leads to persistent behavioral impairments, we employed a neonatal neocortical focal freeze lesion (FFL) model of polymicrogyria in male Wistar rats. Unilateral cortical lesions were induced at postnatal day 0 (P0), and molecular changes in hippocampal gene expression (glutamatergic signaling: Grin1, Grin2a, Grin2b, Gria1, Gria2; neuroinflammation: Nlrp3, Il1b, Il1rn; glial markers: Gfap, Aif1; neurotrophic factors: Bdnf, Fgf2) were analyzed at P21. Behavioral outcomes, including locomotor activity, exploratory behavior, anxiety-like behavior, social interaction, and recognition memory, were assessed in adulthood (P70–P90). Neonatal cortical lesions induced subregion-specific alterations in hippocampal gene expression: Grin2b and Gria1 expression decreased in the ipsilateral dorsal hippocampus, while Grin2a, Bdnf, and Fgf2 increased in the contralateral ventral hippocampus. These molecular changes were associated with subsequent cognitive deficits (impaired recognition memory) and emotional dysregulation (heightened anxiety-like behavior) in adult rats, alongside reduced exploratory activity. Basic motor functions and sociability remained unaffected, and seizure susceptibility (assessed via maximal electroshock threshold) was unchanged, highlighting the specificity of the observed impairments. Our findings suggest a potential mechanistic link between early-life cortical malformations with microgyrus formation, dysregulation of hippocampal synaptic plasticity and neurotrophic signaling, and persistent neurobehavioral deficits. These results underscore the translational relevance of the freeze lesion model for studying the neurodevelopmental trajectory of cortical malformation-related comorbidities.

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来源期刊
Journal of Neuroscience Research
Journal of Neuroscience Research 医学-神经科学
CiteScore
9.50
自引率
2.40%
发文量
145
审稿时长
1 months
期刊介绍: The Journal of Neuroscience Research (JNR) publishes novel research results that will advance our understanding of the development, function and pathophysiology of the nervous system, using molecular, cellular, systems, and translational approaches. JNR covers both basic research and clinical aspects of neurology, neuropathology, psychiatry or psychology. The journal focuses on uncovering the intricacies of brain structure and function. Research published in JNR covers all species from invertebrates to humans, and the reports inform the readers about the function and organization of the nervous system, with emphasis on how disease modifies the function and organization.
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