Harris Sydney A, Sgro Marissa, Salberg Sabrina, Li Crystal, Vlassopoulos Elaina, Smith Madeleine, Semple Bridgette D, Chinnery Holly R, Mychasiuk Richelle
Department of Neuroscience, School of Translational Medicine, Monash University, Melbourne, Australia.
Department of Optometry and Vision Science, University of Western Australia, Lions Eye Institute, Perth, Western Australia, Australia.
Acta Neuropathol Commun. 2025 May 15;13(1):100. doi: 10.1186/s40478-025-02029-5.
Abusive head trauma (AHT) resulting from violent shaking and whiplash-induced brain injury by a caregiver, is the leading cause of abusive mortality and morbidity in children. Cerebral oedema is common in survivors of AHT. While many children may initially appear behaviourally asymptomatic or present with non-specific symptoms following the AHT, deficits often emerge later in childhood. Additionally, AHTs are frequently repetitive, with a single child likely to experience multiple AHTs. Despite the prevalence of AHT, the mechanisms that lead to brain pathology and the latent emergence of behavioural deficits are poorly understood, and there is a paucity of preclinical, small animal models to investigate the biology and cumulative effects of repetitive injuries. This study aimed to develop a preclinical model of repetitive AHT and subsequently examine alterations in gene expression, cell types, and early adolescent behaviour. Mice were placed on a 400 rpm shaking device for 60s. This was repeated one, three, or five times throughout the neonatal development period (postnatal days (P)8-12). Injured mice initially displayed no overt behavioural changes compared to uninjured controls; however, in adolescence (P40-45) they later developed deficits in socialisation and thermal nociception. Further, alterations in the expression of genes involved in growth, cell damage, and development were observed in the brains of injured mice, along with an increase in white matter cells and evidence of blood-brain barrier leakage. This novel preclinical model of AHT provides a valuable platform for exploring diagnostic biomarkers and potential therapeutic interventions for children with an AHT.
由照料者剧烈摇晃和鞭打诱发的脑损伤导致的虐待性头部创伤(AHT),是儿童虐待致死和发病的主要原因。脑水肿在AHT幸存者中很常见。虽然许多儿童在遭受AHT后最初可能在行为上无症状或表现出非特异性症状,但缺陷往往在童年后期出现。此外,AHT经常是重复性的,单个儿童可能会经历多次AHT。尽管AHT很普遍,但导致脑病理和行为缺陷潜在出现的机制仍知之甚少,并且缺乏用于研究重复性损伤的生物学和累积效应的临床前小动物模型。本研究旨在建立重复性AHT的临床前模型,随后检查基因表达、细胞类型和青春期早期行为的变化。将小鼠置于400转/分钟的摇晃装置上60秒。在整个新生儿发育期(出生后第(P)8 - 12天)重复1次、3次或5次。与未受伤的对照组相比,受伤小鼠最初没有表现出明显的行为变化;然而,在青春期(P40 - 45),它们后来出现了社交和热痛觉方面的缺陷。此外,在受伤小鼠的大脑中观察到与生长、细胞损伤和发育相关的基因表达变化,同时白质细胞增加且有血脑屏障渗漏的迹象。这种新型的AHT临床前模型为探索AHT儿童的诊断生物标志物和潜在治疗干预措施提供了一个有价值的平台。