Na Wei, Luo-Man Zhang, Jing-Jing Xu, Sheng-Lei Li, Rui Xue, Sheng-Li Ma, Cai Li, Miao-Miao Sun, Kui-Sheng Chen
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引用次数: 0
Abstract
Vascular dementia (VaD) is a cognitive disorder characterized by a decline in cognitive function resulting from cerebrovascular disease. The hippocampus is particularly susceptible to ischemic insults, leading to memory deficits in VaD. Astaxanthin (AST) has shown potential therapeutic effects in neurodegenerative diseases. However, the mechanisms underlying its protective effects in VaD and against hippocampal neuronal death remain unclear. In this study, We used the bilateral common carotid artery occlusion (BCCAO) method to establish a chronic cerebral hypoperfusion (CCH) rat model of VaD and administered a gastric infusion of AST at 25 mg/kg per day for 4 weeks to explore its therapeutic effects. Memory impairments were assessed using Y-maze and Morris water maze tests. We also performed biochemical analyses to evaluate levels of hippocampal neuronal death and apoptosis-related proteins, as well as the impact of astaxanthin on the PI3K/Akt/mTOR pathway and oxidative stress. Our results demonstrated that AST significantly rescued memory impairments in VaD rats. Furthermore, astaxanthin treatment protected against hippocampal neuronal death and attenuated apoptosis. We also observed that AST modulated the PI3K/Akt/mTOR pathway, suggesting its involvement in promoting neuronal survival and synaptic plasticity. Additionally, AST exhibited antioxidant properties, mitigating oxidative stress in the hippocampus. These findings provide valuable insights into the potential therapeutic effects of AST in VaD. By elucidating the mechanisms underlying the actions of AST, this study highlights the importance of protecting hippocampal neurons and suggests potential targets for intervention in VaD. There are still some unanswered questions include long-term effects and optimal dosage of the use in human. Further research is warranted to fully understand the therapeutic potential of AST and its application in the clinical treatment of VaD.
血管性痴呆(VaD)是一种认知障碍疾病,其特点是因脑血管疾病导致认知功能下降。海马体特别容易受到缺血性损伤,从而导致 VaD 的记忆障碍。虾青素(AST)对神经退行性疾病具有潜在的治疗作用。然而,其对 VaD 和海马神经元死亡的保护作用的机制仍不清楚。在这项研究中,我们采用双侧颈总动脉闭塞(BCCAO)法建立了慢性脑灌注不足(CCH)的VaD大鼠模型,并以每天25毫克/千克的剂量向胃中输注AST,持续4周,以探索其治疗效果。我们使用Y迷宫和莫里斯水迷宫测试评估了大鼠的记忆损伤。我们还进行了生化分析,以评估海马神经元死亡和凋亡相关蛋白的水平,以及虾青素对PI3K/Akt/mTOR通路和氧化应激的影响。我们的研究结果表明,虾青素能明显缓解VaD大鼠的记忆损伤。此外,虾青素还能防止海马神经元死亡,减少细胞凋亡。我们还观察到,虾青素调节了PI3K/Akt/mTOR通路,表明其参与了促进神经元存活和突触可塑性的过程。此外,AST 还具有抗氧化特性,可减轻海马中的氧化应激。这些发现为 AST 对 VaD 的潜在治疗作用提供了宝贵的见解。通过阐明 AST 的作用机制,该研究强调了保护海马神经元的重要性,并提出了干预 VaD 的潜在靶点。目前仍有一些悬而未决的问题,包括对人体的长期影响和最佳使用剂量。要充分了解 AST 的治疗潜力及其在 VaD 临床治疗中的应用,还需要进一步的研究。