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小剂量 LPS 预处理对百草枯诱导的神经毒性、小胶质细胞激活以及多巴胺能系统中α-突触核蛋白和 synphilin-1 表达的影响。

The influence of preconditioning with low dose of LPS on paraquat-induced neurotoxicity, microglia activation and expression of α-synuclein and synphilin-1 in the dopaminergic system.

机构信息

Department of Neuropsychopharmacology, Maj Institute of Pharmacology, Polish Academy of Sciences, 12 Smetna St., 31-343, Kraków, Poland.

Department of Neurobiology, Maj Institute of Pharmacology, Polish Academy of Sciences, Kraków, Poland.

出版信息

Pharmacol Rep. 2022 Feb;74(1):67-83. doi: 10.1007/s43440-021-00340-1. Epub 2021 Nov 11.

Abstract

BACKGROUND

Prolonged inflammation, oxidative stress, and protein aggregation are important factors contributing to Parkinson's disease (PD) pathology. A known ROS generator, pesticide paraquat (PQ), was indicated as an environmental substance potentially increasing the incidence of PD and is used to model this disease. We investigated if a combination of inflammation and oxidative stress in subthreshold doses would exacerbate the modelled neuropathology.

METHODS

We examined the late effects of acute or repeated peripheral inflammation induced by low dose of LPS (10 μg/kg, ip) on PQ toxicity in the rat nigrostriatal dopaminergic pathway, microglial activation markers and expression of major Lewy bodies proteins, α-synuclein and synphilin-1.

RESULTS

We observed that LPS increased, while PQ decreased body temperature and microglia CD11b expression in the SN. Single LPS pretreatment, 3 h before repeated weekly PQ injections (4×) slightly aggravated neuronal degeneration in the SN. Moreover, degeneration of dopaminergic neurons after weekly repeated inflammation itself (4×) was observed. Interestingly, repeated LPS administration combined with each PQ dose counteracted such effect. The expression of α-synuclein decreased after repeated LPS injections, while only combined, repeated LPS and PQ treatment lowered the levels of synphilin-1. Therefore, α-synuclein and synphilin-1 expression change was influenced by different mechanisms. Concomitantly, decreased levels of the two proteins correlated with decreased degeneration of dopaminergic neurons and with a normalized microglia activation marker.

CONCLUSIONS

Our results indicate that both oxidative insult triggered by PQ and inflammation caused by peripheral LPS injection can individually induce neurotoxicity. Those factors act through different mechanisms that are not additive and not selective towards dopaminergic neurons, probably implying microglia. Repeated, but small insults from oxidative stress and inflammation when administered in significant time intervals can counteract each other and even act protective as a preconditioning effect. The timing of such repetitive insults is also of essence.

摘要

背景

长期的炎症、氧化应激和蛋白质聚集是导致帕金森病(PD)病理的重要因素。已知的 ROS 生成剂百草枯(PQ)被认为是一种潜在的增加 PD 发病率的环境物质,并被用于模拟这种疾病。我们研究了亚阈值剂量的炎症和氧化应激的组合是否会加剧模拟的神经病理学。

方法

我们检查了低剂量 LPS(10μg/kg,ip)诱导的急性或重复外周炎症对大鼠黑质纹状体多巴胺能通路中 PQ 毒性、小胶质细胞激活标志物和主要路易体蛋白α-突触核蛋白和突触核蛋白-1表达的晚期影响。

结果

我们观察到 LPS 增加,而 PQ 降低 SN 中的体温和小胶质细胞 CD11b 表达。单次 LPS 预处理,在每周重复 PQ 注射(4×)前 3 小时,轻微加重 SN 中的神经元变性。此外,每周重复炎症本身(4×)也观察到多巴胺能神经元的变性。有趣的是,每周重复 LPS 给药与每次 PQ 剂量结合反而拮抗了这种作用。重复 LPS 注射后α-突触核蛋白表达降低,而只有重复 LPS 和 PQ 联合治疗降低了突触核蛋白-1的水平。因此,α-突触核蛋白和突触核蛋白-1表达的变化受不同机制的影响。同时,两种蛋白质水平的降低与多巴胺能神经元变性的减少以及小胶质细胞激活标志物的正常化相关。

结论

我们的结果表明,PQ 引发的氧化应激和外周 LPS 注射引起的炎症都可以单独诱导神经毒性。这些因素通过不同的机制起作用,这些机制不是累加的,对多巴胺能神经元也不是选择性的,可能涉及小胶质细胞。当在显著的时间间隔内给予重复的、但较小的氧化应激和炎症损伤时,它们可以相互拮抗,甚至作为预处理效应发挥保护作用。这种重复损伤的时间也是至关重要的。

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