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Parkinson’s disease (PD) has caused most economy to lose their active human capital. Due to poor understanding
of the pathophysiology of PD, PD animal models were developed to aid with the investigation of PD pathogenesis and
therapy. Currently, the toxin induced and the genetic animal models are being used for most PD research.
Most neurotoxin animal model’s studies on PD are focused on the motor features and economic importance associated with
dopamine depletion; however, the molecular pathways for cell loss by these models and its usefulness in PD drug development have not been reported fully. In this review, we provided a summary of the toxic mechanism and shortcomings of four
neurotoxins (6-OHDA, MPTP, Rotenone and, Paraquat) that are frequently used to mimic PD in animal models. This review
will give readers basic knowledge on the best toxin to select for a specific PD experiment and also provide information that
will help in development of future toxins with fewer shortcomings. This review also summarizes the mechanism and features
of some PD genetic models.