The effects of aqueous cinnamon bark extract and cinnamaldehyde on neurons of substantia nigra and behavioral impairment in a mouse model of Parkinson's disease

Abstract:
Background And Objective
Parkinson's disease (PD) is characterized by a progressive loss of dopaminergic neurons in substantia nigra. In recent years, there have been interests in the role of the free radical damage in PD. Cinnamon and its derivative, cinnamaldehyde acts as powerful antioxidant and anti-inflammatory agents. This research focused on the effects of cinnamon extract and cinnamaldehyde on neurons of SNc of a mouse model of Parkinson’s disease.
Materials And Methods
45 adult male mice with an average weight of 25-35 g were divided into 9 groups of 5 each: group 1: control PBS, group 2: control serum, group 3: 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP), group 4: MPTP low dose of cinnamon extract pretreatment (20 mg/kg), group 5: MPTP high dose of cinnamon extract pretreatment (40 mg/kg), group 6: MPTP low dose of cinnamon extract treatment (20 mg/kg), group7: MPTP high dose of cinnamon extract treatment (40 mg/kg), group 8: MPTP cinnamaldehyde pretreatment (30 mg/kg), group 9: MPTP cinnamaldehyde treatment (30 mg/kg). Rotarod test was used to assess motor and balance of the mice. After behavioral studies, all mice were anesthetized and perfused transcardially with 0.1 M PBS (PH=7.4) followed by 4% buffered paraformaldehyde fixative. The brain of the mice were removed and fixed in the paraformaldehyde and stained for Nissl and the number of Nissl-stained neurons were counted. Data was analyzed using SPSS software by one way ANOVA.
Results
Aqueous cinnamon extract and cinnamaldehyde improved rotarod performance of MPTP-lesioned mice and prevented loss of Nissl-stained neurons of SNc of the midbrain.
Conclusion
These findings suggest that cinnamaldehye as a natural antioxidant may protect neurons of SNc neurons against Parkinson’s disease.
Language:
English
Published:
Journal of Basic & Clinical Pathophysiology, Volume:5 Issue: 1, Winter-Spring 2017
Page:
27
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