Heidari Zahra, Mohammadipour Abbas, Haeri Parisa, Ebrahimzadeh-Bideskan Alireza
Department of Anatomy and Cell Biology, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Microanatomy Research Center, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Iran J Basic Med Sci. 2019 Jul;22(7):745-751. doi: 10.22038/ijbms.2019.33611.8018.
Widely used Titanium dioxide nanoparticles (TiO) enter into the body and cause various organ damages. Therefore, we aimed to study the effect of TiO on the substantia nigra of midbrain.
40 male BALB/c mice were randomly divided into five groups: three groups received TiO at doses of 10, 25, and 50 mg/kg, the fourth group received normal saline for 45 days by gavage, and control group (without intervention). Then, Motor tests including pole and hanging tests were done to investigate motor disorders. The animal brain was removed for histological purposes. Accordingly, immunohistochemistry was performed to detect tyrosine hydroxylase positive cells, and then toluidine blue staining was done to identify dark neurons in the substantia nigra. Eventually, the total number of these neurons were counted using stereological methods in different groups.
The results showed that the time recorded for mice to turn completely downward on the pole in the TiO-50 group increased and also the time recorded for animals to hang on the wire in the hanging test significantly decreased (0.05) in comparison with other groups. Also, the average number of tyrosine hydroxylase positive neurons in TiO-25 and TiO-50 groups significantly decreased as compared to the TiO-10 and control groups (0.05). The total number of dark neurons in the TiO-25 and TiO-50 groups was substantially higher than the TiO-10, control and normal saline groups (0.05).
Our findings indicated that TiO, depending on dose, can cause the destruction of dopaminergic neurons and consequently increase the risk of Parkinson's disease.
广泛使用的二氧化钛纳米颗粒(TiO)进入人体并导致各种器官损伤。因此,我们旨在研究TiO对中脑黑质的影响。
将40只雄性BALB/c小鼠随机分为五组:三组分别接受10、25和50mg/kg剂量的TiO,第四组通过灌胃给予生理盐水45天,对照组(无干预)。然后,进行包括杆试验和悬挂试验在内的运动测试以研究运动障碍。取出动物大脑用于组织学研究。相应地,进行免疫组织化学检测酪氨酸羟化酶阳性细胞,然后进行甲苯胺蓝染色以识别黑质中的深色神经元。最终,使用体视学方法对不同组中的这些神经元总数进行计数。
结果显示,与其他组相比,TiO-50组小鼠在杆上完全向下翻转的记录时间增加,并且在悬挂试验中动物悬挂在铁丝上的记录时间显著减少(P<0.05)。此外,与TiO-10组和对照组相比,TiO-25组和TiO-50组中酪氨酸羟化酶阳性神经元的平均数量显著减少(P<0.05)。TiO-25组和TiO-50组中深色神经元的总数明显高于TiO-10组、对照组和生理盐水组(P<0.05)。
我们的研究结果表明,TiO根据剂量不同,可导致多巴胺能神经元的破坏,从而增加帕金森病的风险。