A Combination of Low Doses of Lithium and Valproate Improves Cognitive Outcomes after Mild Traumatic Brain Injury.

IF 3.9 2区 医学 Q1 CLINICAL NEUROLOGY Journal of neurotrauma Pub Date : 2024-10-28 DOI:10.1089/neu.2024.0311
John B Redell, Mark E Maynard, Michael J Hylin, Kimberly N Hood, Andrea Sedlock, Dragan Maric, Jing Zhao, Anthony N Moore, Badrinath Roysam, Shibani Pati, Pramod K Dash
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Abstract

The prevalence of mild traumatic brain injury (mTBI) is high compared with moderate and severe TBI, comprising almost 80% of all brain injuries. mTBI activates a complex cascade of biochemical, molecular, structural, and pathological changes that can result in neurological and cognitive impairments. These impairments can manifest even in the absence of overt brain damage. Given the complexity of changes triggered by mTBI, a combination of drugs that target multiple TBI-activated cascades may be required to improve mTBI outcomes. It has been previously demonstrated that cotreatment with the U.S. Food and Drug Administration (FDA)-approved drugs lithium plus valproate (Li + VPA) for 3 weeks after a moderate-to-severe controlled cortical impact injury reduced cortical tissue loss and improved motor function. Since both lithium and valproate can exhibit toxicity at high doses, it would be beneficial to determine if this combination treatment is effective when administered at low doses and for a shorter duration, and if it can improve cognitive function, after a mild diffuse TBI. In the present study, we tested if the combination of low doses of lithium (1 mEq/kg or 0.5 mEq/kg) plus valproate (20 mg/kg) administered for 3 days after a mild fluid percussion injury can improve hippocampal-dependent learning and memory. Our data show that the combination of low-dose Li + VPA improved spatial learning and memory, effects not seen when either drug was administered alone. In addition, postinjury Li + VPA treatment improved recognition memory and sociability and reduced fear generalization. Postinjury Li + VPA also reduced the number of anti-ionized calcium binding adaptor molecule 1 (Iba1)-positive microglia counted using a convolutional neural network, indicating a reduction in neuroinflammation. These findings indicate that low-dose Li + VPA administered acutely after mTBI may have translational utility to reduce pathology and improve cognitive function.

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小剂量锂和丙戊酸钠联合用药可改善轻度脑外伤后的认知结果。
与中度和重度创伤性脑损伤相比,轻度创伤性脑损伤(mTBI)的发病率较高,几乎占所有脑损伤的 80%。轻度创伤性脑损伤会激活一连串复杂的生化、分子、结构和病理变化,从而导致神经和认知障碍。这些损伤甚至可以在没有明显脑损伤的情况下表现出来。鉴于 mTBI 引发的变化的复杂性,可能需要针对多种 TBI 激活级联的药物组合来改善 mTBI 的治疗效果。之前有研究表明,在中度至重度受控皮质撞击伤后使用美国食品药品管理局(FDA)批准的药物锂和丙戊酸钠(锂+ VPA)联合治疗 3 周,可减少皮质组织损失并改善运动功能。由于锂和丙戊酸钠在高剂量时都会表现出毒性,因此在轻度弥漫性创伤后,确定这种联合疗法在低剂量和较短时间内是否有效,以及是否能改善认知功能将是有益的。在本研究中,我们测试了在轻度体液叩击伤后给予低剂量锂(1 mEq/kg 或 0.5 mEq/kg)加丙戊酸钠(20 mg/kg)联合治疗 3 天是否能改善海马依赖性学习和记忆。我们的数据显示,低剂量锂+丙戊酸钠联合用药可改善空间学习和记忆,而单独使用其中一种药物则不会产生这种效果。此外,伤后 Li + VPA 治疗还能改善识别记忆和社交能力,减少恐惧泛化。伤后 Li + VPA 还减少了用卷积神经网络计算的抗电离钙结合适配分子 1(Iba1)阳性小胶质细胞的数量,表明神经炎症有所减轻。这些研究结果表明,在 mTBI 后急性给药低剂量 Li + VPA 可能具有减少病理变化和改善认知功能的转化用途。
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来源期刊
Journal of neurotrauma
Journal of neurotrauma 医学-临床神经学
CiteScore
9.20
自引率
7.10%
发文量
233
审稿时长
3 months
期刊介绍: Journal of Neurotrauma is the flagship, peer-reviewed publication for reporting on the latest advances in both the clinical and laboratory investigation of traumatic brain and spinal cord injury. The Journal focuses on the basic pathobiology of injury to the central nervous system, while considering preclinical and clinical trials targeted at improving both the early management and long-term care and recovery of traumatically injured patients. This is the essential journal publishing cutting-edge basic and translational research in traumatically injured human and animal studies, with emphasis on neurodegenerative disease research linked to CNS trauma.
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