A comprehensive review on adaptive plasticity and recovery mechanisms post-acquired brain injury.

IF 4.1
Neuroprotection Pub Date : 2025-06-08 eCollection Date: 2025-09-01 DOI:10.1002/nep3.70006
Ravi Kumar Rajan
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Abstract

Adaptive plasticity, the brain's ability to reorganize and form new neural connections after injury, is crucial for recovery following acquired brain injury (ABI). This process involves axonal sprouting, dendritic remodeling, and neurogenesis, which restore neural connections and compensate for lost functions. While neuroinflammation and reactive astrocytes aid tissue repair, optimizing these responses to minimize secondary damage remains a challenge. Brain-derived neurotrophic factor (BDNF) plays a vital role in neurogenesis and dendritic growth, positioning it as a potential therapeutic target for brain repair. Rehabilitation strategies that stimulate these adaptive changes can enhance neuroplasticity and functional recovery. The complexity of ABI recovery is influenced by factors such as injury severity, age, and genetic and epigenetic factors, which regulate neuronal repair and synaptic plasticity. Maladaptive plasticity refers to compensatory mechanisms that initially aid recovery but ultimately become harmful. Severe injuries like traumatic brain injury (TBI) and stroke can trigger adaptive responses, such as axonal sprouting, but excessive reliance on these processes may become maladaptive. In contrast, mild TBIs offer greater recovery potential. Age-related differences in plasticity complicate recovery, with younger individuals exhibiting greater plasticity and older adults experiencing reduced plasticity and increased likelihood of maladaptive changes. Genetic factors, such as BDNF gene polymorphisms and DNA methylation, influence recovery outcomes. Neuroinflammation plays a dual role: acute inflammation supports recovery, while chronic inflammation can exacerbate damage. Precision medicine, tailored to an individual's genetic and epigenetic profile, offers promising strategies to optimize recovery. Growth factors like BDNF and insulin-like growth factor 1 (IGF-1) are essential for neurogenesis, synaptic plasticity, and neural network reorganization, supporting both structural and functional recovery. However, maladaptive plasticity must be managed carefully for effective recovery. Targeted rehabilitation therapies, along with pharmacological agents and neuromodulation techniques, offer insights into personalized treatment strategies to enhance adaptive plasticity and optimize ABI recovery outcomes. This review explores the mechanisms of adaptive plasticity following ABI and discusses therapeutic interventions to support and optimize recovery, offering promising avenues for improving patient outcomes.

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后天性脑损伤后适应性可塑性及其恢复机制综述
适应性可塑性是指大脑在损伤后重组和形成新的神经连接的能力,对后天性脑损伤(ABI)后的恢复至关重要。这一过程包括轴突发芽、树突重塑和神经发生,这些过程可以恢复神经连接并补偿失去的功能。虽然神经炎症和反应性星形胶质细胞有助于组织修复,但优化这些反应以减少继发性损伤仍然是一个挑战。脑源性神经营养因子(BDNF)在神经发生和树突生长中起着至关重要的作用,是脑修复的潜在治疗靶点。刺激这些适应性变化的康复策略可以增强神经可塑性和功能恢复。ABI恢复的复杂性受损伤严重程度、年龄、遗传和表观遗传等因素的影响,这些因素调节着神经元修复和突触可塑性。不适应的可塑性是指最初有助于恢复但最终变得有害的补偿机制。创伤性脑损伤(TBI)和中风等严重损伤可引发适应性反应,如轴突发芽,但过度依赖这些过程可能会导致适应不良。相比之下,轻度创伤性脑损伤具有更大的恢复潜力。与年龄相关的可塑性差异使恢复变得复杂,年轻人表现出更强的可塑性,而老年人的可塑性降低,适应不良变化的可能性增加。遗传因素,如BDNF基因多态性和DNA甲基化,影响恢复结果。神经炎症起着双重作用:急性炎症有助于恢复,而慢性炎症会加剧损伤。根据个人的遗传和表观遗传特征量身定制的精准医学,为优化康复提供了有希望的策略。生长因子如BDNF和胰岛素样生长因子1 (IGF-1)对神经发生、突触可塑性和神经网络重组至关重要,支持结构和功能恢复。然而,为了有效的恢复,必须仔细管理适应不良的可塑性。有针对性的康复治疗,以及药物和神经调节技术,为个性化治疗策略提供了见解,以增强适应性可塑性和优化ABI恢复结果。这篇综述探讨了ABI后适应性可塑性的机制,并讨论了支持和优化康复的治疗干预措施,为改善患者的预后提供了有希望的途径。
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