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固体脂质姜黄素颗粒可保护中型棘突神经元形态,并减少亨廷顿病 YAC128 小鼠模型的学习和记忆缺陷。

Solid Lipid Curcumin Particles Protect Medium Spiny Neuronal Morphology, and Reduce Learning and Memory Deficits in the YAC128 Mouse Model of Huntington's Disease.

机构信息

Field Neurosciences Institute Laboratory for Restorative Neurology, Central Michigan University, Mt. Pleasant, MI 48859, USA.

Program in Neuroscience, Central Michigan University, Mt. Pleasant, MI 48859, USA.

出版信息

Int J Mol Sci. 2020 Dec 15;21(24):9542. doi: 10.3390/ijms21249542.

Abstract

Huntington's disease (HD) is a genetic neurodegenerative disorder characterized by motor, cognitive, and psychiatric symptoms, accompanied by massive neuronal degeneration in the striatum. In this study, we utilized solid lipid curcumin particles (SLCPs) and solid lipid particles (SLPs) to test their efficacy in reducing deficits in YAC128 HD mice. Eleven-month-old YAC128 male and female mice were treated orally with SLCPs (100 mg/kg) or equivalent volumes of SLPs or vehicle (phosphate-buffered saline) every other day for eight weeks. Learning and memory performance was assessed using an active-avoidance task on week eight. The mice were euthanized, and their brains were processed using Golgi-Cox staining to study the morphology of medium spiny neurons (MSNs) and Western blots to quantify amounts of DARPP-32, brain-derived neurotrophic factor (BDNF), TrkB, synaptophysin, and PSD-95. We found that both SLCPs and SLPs improved learning and memory in HD mice, as measured by the active avoidance task. We also found that SLCP and SLP treatments preserved MSNs arborization and spinal density and modulated synaptic proteins. Our study shows that SLCPs, as well as the lipid particles, can have therapeutic effects in old YAC128 HD mice in terms of recovering from HD brain pathology and cognitive deficits.

摘要

亨廷顿病(HD)是一种遗传性神经退行性疾病,其特征是运动、认知和精神症状,并伴有纹状体中大量神经元变性。在这项研究中,我们使用固体脂质姜黄素颗粒(SLCP)和固体脂质颗粒(SLP)来测试它们在减少 YAC128 HD 小鼠缺陷方面的功效。11 个月大的 YAC128 雄性和雌性小鼠每隔一天口服 SLCP(100mg/kg)或等量的 SLP 或载体(磷酸盐缓冲盐水),持续八周。在第八周使用主动回避任务评估学习和记忆性能。处死小鼠,用高尔基-考克斯染色处理其大脑,研究中型多棘神经元(MSNs)的形态,并进行 Western blot 定量分析 DARPP-32、脑源性神经营养因子(BDNF)、TrkB、突触小体蛋白和 PSD-95 的含量。我们发现 SLCP 和 SLP 均可改善 HD 小鼠的学习和记忆,如主动回避任务所示。我们还发现,SLCP 和 SLP 治疗可保留 MSNs 的分支和脊髓密度,并调节突触蛋白。我们的研究表明,SLCP 和脂质颗粒均可在 YAC128 HD 老年小鼠中发挥治疗作用,可从 HD 脑病理学和认知缺陷中恢复。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1a1/7765279/b031b25c9adf/ijms-21-09542-g001.jpg

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