Title:A Systematic Review of Various In-vivo Screening Models as well as the
Mechanisms Involved in Parkinson's Disease Screening Procedures
Volume: 19
Issue: 2
Author(s): Ankita Wal, Pranay Wal*, Himangi Vig, Abdul Samad, Madhusmruti Khandai and Sachin Tyagi
Affiliation:
- Pranveer Singh Institute of Technology (Pharmacy), Kanpur, India
Keywords:
Parkinson’s disease, 6-hydroxydopamine model, 1-methyl 4-phenyl-1, 2, 3, 6-tetrahydropyridine model, reserpine antagonism, chlorpromazine antagonism, tremorine, oxotremorine antagonism.
Abstract:
Background: Parkinson's disease is the second most common neurological ailment. It is also
known that it affects practically all other brain components, although only gradually. Animal models
are mostly used to test the efficacy of treatment against a specific enzyme and aid in creating a new
drug dose.
Objective: The purpose of this review is to highlight in vivo Parkinson's disease screening approaches,
as well as the mechanism of action of each drug involved in Parkinson's disease development, and discuss
the limitations of each model. In addition, it also sheds light on Parkinson's disease genetic models.
Methods: The data for the publication was gathered from databases, such as PubMed, Bentham Science,
Elsevier, Springer Nature, Wiley, and Research Gate, after a thorough examination of diverse
research findings linked to Parkinson’s disease and its screening models.
Results: Each chemical or drug has a unique mechanism for causing disease, whether through the production
of reactive oxygen species or the blockage of the dopamine receptor. Almost every disease
symptom, whether physical or behavioral, is covered by each of the constructed models' unique set of
indicators and symptoms.
Conclusion: Animal models are typically used to assess a medicine's activity against a specific enzyme
and aid in the creation of a new drug dose. The process, restrictions, and mechanisms interfering
with the screening, as well as the level of animal suffering, must all be thoroughly reviewed before
any model for screening for Parkinson's disease can be implemented.