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首页> 外文期刊>Toxicology: An International Journal Concerned with the Effects of Chemicals on Living Systems >Changes of cytoskeletal proteins in nerve tissues and serum of rats treated with 2,5-hexanedione.
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Changes of cytoskeletal proteins in nerve tissues and serum of rats treated with 2,5-hexanedione.

机译:2,5-己二酮处理后大鼠神经组织和血清中细胞骨架蛋白的变化。

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摘要

To investigate the mechanisms and biomarker of the neuropathy induced by 2,5-hexanedione (HD), male Wistar rats were administrated HD at dosage of 200 or 400mg/kg for 8 weeks (five-times per week). All rats were sacrificed after 8 weeks of treatment and the cerebrum cortex (CC), spinal cord (SC) and sciatic nerves (SN) were dissected, homogenized and used for the determination of cytoskeletal proteins by western blotting. The levels of neurofilaments (NFs) subunits (NF-L, NF-M and NF-H) in nerve tissues of 200 and 400mg/kg HD rats significantly decreased in both the supernatant and pellet fractions. Furthermore, significant negative correlations between NFs levels and gait abnormality were observed. As for microtubule (MT) and microfilament (MF) proteins, the levels of alpha-tubulin, beta-tubulin and beta-actin in the supernatant and pellet fraction of SN significantly decreased in 200 and 400mg/kg HD rats and correlated negatively with gait abnormality. However, the contents of MT and MF proteins in CC and SC were inconsistently affected and had no significant correlation with gait abnormality. The levels of NF-L and NF-H in serum significantly increased, while NF-M, alpha-tubulin, beta-tubulin and beta-actin contents remain unchanged. A significant positive correlation (R=0.9427, P<0.01) was observed between gait abnormality and NF-H level in serum as the intoxication went on. These findings suggested that HD intoxication resulted in a progressive decline of cytoskeletal protein contents, which might be relevant to the mechanisms of HD-induced neuropathy. NF-H was the most sensitive index, which may serve as a good indicator for neurotoxicity of n-hexane or HD.
机译:为了研究2,5-己二酮(HD)诱导的神经病变的机制和生物标志物,以200或400mg / kg的剂量对雄性Wistar大鼠HD进行8周(每周5次)。处理8周后,处死所有大鼠,解剖大脑皮层(CC),脊髓(SC)和坐骨神经(SN),均质化,并通过蛋白质印迹法测定细胞骨架蛋白。在200和400mg / kg HD大鼠的神经组织中,神经丝(NFs)亚基(NF-L,NF-M和NF-H)的水平在上清液和沉淀级分中均显着降低。此外,观察到NFs水平与步态异常之间的显着负相关。至于微管(MT)和微丝(MF)蛋白,在200和400mg / kg HD大鼠中,上清液和SN的沉淀级分中的α-微管蛋白,β-微管蛋白和β-肌动蛋白水平显着降低,并且与步态呈负相关紊乱ETC。然而,CC和SC中MT和MF蛋白的含量受到不一致的影响,并且与步态异常无显着相关性。血清中NF-L和NF-H的水平显着增加,而NF-M,α-微管蛋白,β-微管蛋白和β-肌动蛋白含量保持不变。随着中毒的进行,步态异常与血清中NF-H水平之间存在显着的正相关(R = 0.9427,P <0.01)。这些发现提示HD中毒导致细胞骨架蛋白含量的逐渐下降,这可能与HD诱导的神经病的机制有关。 NF-H是最敏感的指标,可以作为正己烷或HD神经毒性的良好指标。

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