Title of article :
The effect of titanium dioxide nanoparticles on mice midbrain substantia nigra
Author/Authors :
Heidari, Zahra Department of Anatomy and Cell Biology - School of Medicine - Mashhad University of Medical Sciences , Mohammadipour, Abbas Department of Anatomy and Cell Biology - School of Medicine - Mashhad University of Medical Sciences, Mashhad - Microanatomy Research Center - School of Medicine - Mashhad University of Medical Sciences , Haeri, Parisa Department of Anatomy and Cell Biology - School of Medicine - Mashhad University of Medical Sciences , Ebrahimzadeh-bideskan, Alireza Department of Anatomy and Cell Biology - School of Medicine - Mashhad University of Medical Sciences, Mashhad - Microanatomy Research Center - School of Medicine - Mashhad University of Medical Sciences
Abstract :
Objective(s): Widely used Titanium dioxide nanoparticles (TiO2) enter into the body and cause various
organ damages. Therefore, we aimed to study the effect of TiO2 on the substantia nigra of midbrain.
Materials and Methods: 40 male BALB/c mice were randomly divided into five groups: three groups
received TiO2 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.
Results: The results showed that the time recorded for mice to turn completely downward on the
pole in the TiO2-50 group increased and also the time recorded for animals to hang on the wire in
the hanging test significantly decreased (P<0.05) in comparison with other groups. Also, the average
number of tyrosine hydroxylase positive neurons in TiO2-25 and TiO2-50 groups significantly
decreased as compared to the TiO2-10 and control groups (P<0.05). The total number of dark neurons
in the TiO2-25 and TiO2-50 groups was substantially higher than the TiO2-10, control and normal
saline groups (P<0.05).
Conclusion: Our findings indicated that TiO2, depending on dose, can cause the destruction of
dopaminergic neurons and consequently increase the risk of Parkinson’s disease.
Keywords :
Dark neurons , Mice , Substantia nigra , Titanium dioxide nanoparticles , Tyrosine hydroxylase neurons
Journal title :
Astroparticle Physics