Lipid droplets deposition in perihematoma tissue is associated with neurological dysfunction after intracerebral hemorrhage.

IF 1.6 4区 医学 Q4 NEUROSCIENCES
Neuroreport Pub Date : 2025-03-19 Epub Date: 2025-02-26 DOI:10.1097/WNR.0000000000002136
Zhangze Wu, Quan Zhao, Ziqi Hu, Dongsheng Jiao
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引用次数: 0

Abstract

Secondary brain injury following intracerebral hemorrhage (ICH) significantly reduces patients' quality of life due to impaired neurological function. Lipid droplets are implicated in secondary brain injury in various central nervous system diseases. Thus, the role and mechanisms of lipid droplets in secondary brain injury post-ICH require further investigation. We analyzed the changes of genes related to lipid metabolism in brain tissue of ICH mice. Lipid droplets around the hematoma were detected by BODIPY staining. Mice received intraperitoneal injections of Triacsin C (10 mg/kg, once daily) after ICH. Subsequently, neuronal damage was evaluated using TUNEL and Nissl staining, and ethological tests assessed sensorimotor function. After ICH, notable changes occurred in lipid metabolism pathways and genes (Plin2, Ucp2, Apoe), and a large number of lipid droplets accumulated around the hematoma. Triacsin C significantly reduced lipid droplets deposition, decreased neuronal damage, and improved sensory and motor functions. Peripheral administration to prevent lipid droplets formation can greatly reduce nerve damage and enhance nerve function. Our findings indicate that targeting lipid droplets could be a promising treatment for ICH.

脑出血后血肿周围组织脂滴沉积与神经功能障碍有关。
脑出血后继发性脑损伤因神经功能受损而显著降低患者的生活质量。脂滴与各种中枢神经系统疾病的继发性脑损伤有关。因此,脂滴在脑出血后继发性脑损伤中的作用和机制有待进一步研究。我们分析了脑出血小鼠脑组织脂质代谢相关基因的变化。BODIPY染色检测血肿周围脂滴。脑出血后小鼠腹腔注射丙三嗪C (10 mg/kg,每日1次)。随后,用TUNEL和尼氏染色评估神经元损伤,并用行为学测试评估感觉运动功能。ICH后脂质代谢途径和基因(Plin2、Ucp2、Apoe)发生明显变化,血肿周围积聚大量脂滴。Triacsin C显著减少脂滴沉积,减轻神经元损伤,改善感觉和运动功能。外周给药防止脂滴形成,可大大减轻神经损伤,增强神经功能。我们的研究结果表明,靶向脂滴可能是一种有希望的治疗脑出血的方法。
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来源期刊
Neuroreport
Neuroreport 医学-神经科学
CiteScore
3.20
自引率
0.00%
发文量
150
审稿时长
1 months
期刊介绍: NeuroReport is a channel for rapid communication of new findings in neuroscience. It is a forum for the publication of short but complete reports of important studies that require very fast publication. Papers are accepted on the basis of the novelty of their finding, on their significance for neuroscience and on a clear need for rapid publication. Preliminary communications are not suitable for the Journal. Submitted articles undergo a preliminary review by the editor. Some articles may be returned to authors without further consideration. Those being considered for publication will undergo further assessment and peer-review by the editors and those invited to do so from a reviewer pool. The core interest of the Journal is on studies that cast light on how the brain (and the whole of the nervous system) works. We aim to give authors a decision on their submission within 2-5 weeks, and all accepted articles appear in the next issue to press.
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