Department of Physiology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Neurophysiology Research Center, Department of Physiology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Physiol Behav. 2023 Oct 1;269:114286. doi: 10.1016/j.physbeh.2023.114286. Epub 2023 Jul 2.
Social communication and interaction deficits, memory impairment, and anxiety-like behavior are characterized in many people identified with autism spectrum disorder (ASD). A thorough understanding of the specific aspects that contribute to the deficiencies associated with ASD can aid research into the etiology of the disorder while also providing targets for more effective intervention. As part of the ASD pathophysiology, alterations in synaptogenesis and abnormal network connections were seen in high-order brain areas, which control social behavior and communication. The early emergence of microglia during nervous system development may contribute to synaptic dysfunction and the pathobiology of ASD. Since aquaporin-4 (AQP4) appears to be required for the basic procedures of synapse activation, certain behavioral and cognitive impairments as well as disturbance in water homeostasis might likely arise from AQP4 deficiency. Here, through the measurement of the water content of the hippocampus and behavioral experiments we aim to explore the contribution of astrocytic AQP4 to the autism-like behavior induced by prenatal valproic acid (VPA) exposure and whether inhibition of AQP4 per se can induce autistic-like behavior in control rats. Microinjection of TGN-020 (10 µM, i.c.v), a specific AQP4 inhibitor, for 7 successive days before behavioral tasks from postnatal day 28 to 35 revealed that inhibition of AQP4 in the control offspring caused lower social interaction and locomotor activity, higher anxiety, and decreased ability to recognize novel objects, very similar to the behavioral changes observed in offspring prenatally exposed to VPA. However, VPA-exposed offspring treated with TGN-020, showed no further remarkable behavioral impairments than those detected in the autistic-like rats. Furthermore, both control offspring treated with TGN-020 and offspring exposed to VPA had a considerable accumulation of water in their hippocampi. But AQP4 inhibition did not affect the water status of the autistic-like rats. The findings of this study revealed that control offspring exhibited similar hippocampal water retention and behavioral impairments that were observed in maternal VPA-exposed offspring following inhibition of astrocytic AQP4, whereas, in autistic-like rats, it did not produce any significant change in water content and behaviors. Findings suggest that AQP4 deficiency could be associated with autistic disorder and may be a potential pharmaceutical target for treating autism in the future.
社交沟通和互动障碍、记忆障碍和类似焦虑的行为是许多被诊断为自闭症谱系障碍(ASD)的人的特征。深入了解导致 ASD 相关缺陷的具体方面,可以帮助研究该疾病的病因,同时为更有效的干预提供目标。作为 ASD 病理生理学的一部分,在控制社交行为和交流的高级大脑区域中观察到突触发生和异常网络连接的改变。神经发育过程中早期出现的小胶质细胞可能有助于突触功能障碍和 ASD 的病理生物学。由于水通道蛋白-4(AQP4)似乎是突触激活基本过程所必需的,因此某些行为和认知障碍以及水动态平衡紊乱可能是由于 AQP4 缺乏引起的。在这里,我们通过测量海马体的含水量和行为实验,旨在探讨星形胶质细胞 AQP4 对产前丙戊酸(VPA)暴露诱导的类似自闭症行为的贡献,以及 AQP4 本身的抑制是否会导致对照大鼠出现自闭症样行为。从出生后第 28 天到第 35 天,连续 7 天每天在行为任务前向对照组幼鼠侧脑室注射 TGN-020(10 μM),一种特异性 AQP4 抑制剂,结果表明,在对照组幼鼠中抑制 AQP4 会导致较低的社交互动和运动活性、较高的焦虑和识别新物体的能力下降,与产前暴露于 VPA 的幼鼠观察到的行为变化非常相似。然而,用 TGN-020 处理的暴露于 VPA 的幼鼠没有表现出比自闭症样大鼠更显著的行为障碍。此外,用 TGN-020 处理的对照组幼鼠和暴露于 VPA 的幼鼠的海马体中都有相当数量的水积聚。但是 AQP4 抑制并没有影响自闭症样大鼠的水状态。这项研究的结果表明,抑制星形胶质细胞 AQP4 后,对照组幼鼠表现出与母体 VPA 暴露幼鼠相似的海马水潴留和行为障碍,而在自闭症样大鼠中,AQP4 缺乏并未导致水含量和行为产生任何显著变化。这些发现表明,AQP4 缺乏可能与自闭症有关,并且可能成为未来治疗自闭症的潜在药物靶点。