昆虫蜡中聚多糖醇对秀丽隐杆线虫帕金森病模型的潜在治疗作用。

IF 6.2
Chenjing Ma, Ying Feng, Xian Li, Long Sun, Zhao He, Jin Gan, Minjie He, Xin Zhang, Xiaoming Chen
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引用次数: 2

摘要

帕金森病是世界上第二常见的神经退行性疾病。帕金森病的标准治疗方法侧重于症状缓解,而不是试图完全解决潜在的退行性过程。本研究旨在通过研究秀丽隐杆线虫PD模型中所表现的疾病症状的改善来评估昆虫蜡来源的聚多糖醇(PIW)的潜在治疗效果。在我们的评估中,我们使用了以下三个模型:NL5901,这是一个α-突触核蛋白聚集的转基因模型;用6-羟基多巴胺(6-OHDA)诱导的野生型N2;和6-OHDA诱导的BZ555作为多巴胺能神经元(DNs)损失的模型。具体而言,我们研究了PIW处理对α-突触核蛋白聚集、DNA损失、脂质丰度和处理生物体寿命的影响。此外,我们检测了活性氧(ROS)、丙二醛(MDA)、三磷酸腺苷(ATP)、谷胱甘肽S-转移酶(GST)和超氧化物歧化酶(SOD)水平的治疗相关变化,以及相关基因的mRNA生产谱。10µg/mL剂量的PIW减少了NL5901中α-突触核蛋白的聚集,并抑制了6-OHDA诱导的BZ555中DNs的损失。总体而言,在所有三种模型中,PIW处理降低了ROS和MDA水平,恢复了脂质丰度,延长了蠕虫的寿命,这可能与细胞存活和氧化应激反应途径相关基因的表达谱变化有关。我们的研究结果表明,在这些模型中,PIW减轻了PD的症状,可能是通过调节损伤引发的应激反应,如α-突触核蛋白聚集或6-OHDA治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Potential Therapeutic Effects of Policosanol from Insect Wax on Caenorhabditis elegans Models of Parkinson's Disease.

Potential Therapeutic Effects of Policosanol from Insect Wax on Caenorhabditis elegans Models of Parkinson's Disease.

Parkinson's disease (PD) is the second most common neurodegenerative disease worldwide. The standard treatments for PD focus on symptom relief rather than attempting to address the underlying degenerative processes completely. This study aimed to evaluate the potential therapeutic effects of policosanol derived from insect wax (PIW) by investigating improvements in disease symptoms represented in Caenorhabditis elegans models of PD. For our assessments, we used the following three models: NL5901, which is a transgenic model for α-synuclein aggregation; wild-type N2 induced with 6-hydroxydopamine (6-OHDA); and 6-OHDA-induced BZ555 as a model for loss of dopaminergic neurons (DNs). Specifically, we examined the effects of PIW treatment on α-synuclein aggregation, the loss of DNs, lipid abundance, and the lifespan of treated organisms. Further, we examined treatment-related changes in the levels of reactive oxygen species (ROS), malondialdehyde (MDA), adenosine triphosphate (ATP), glutathione S-transferase (GST), and superoxide dismutase (SOD), as well as the mRNA production profiles of relevant genes. A 10 µg/mL dose of PIW reduced the aggregation of α-synuclein in NL5901 and suppressed the loss of DNs in 6-OHDA-induced BZ555. Overall, PIW treatment decreased ROS and MDA levels, restored lipid abundance, and prolonged the lifespans of worms in all the three models, which may be associated with changes in the expression profiles of genes related to cell survival and oxidative stress response pathways. Our findings show that PIW alleviated the symptoms of PD in these models, possibly by regulating the stress responses initiated by injuries such as α-synuclein aggregation or 6-OHDA treatment.

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