Affiliation:
1. Chitkara College of Pharmacy, Chitkara University, Rajpura, Punjab, India
2. Government College of Pharmacy, Shimla, India
3. Department of Biology, Faculty of Science, Selcuk University Campus, Konya, Turkey
Abstract
:
The limitations of conventional treatment therapies in Parkinson’s disorder, a common neurodegenerative
disorder, lead to the development of an alternative gene therapy approach. Multiple
treatment options targeting dopaminergic neuronal regeneration, production of enzymes linked with
dopamine synthesis, subthalamic nucleus neurons, regulation of astrocytes and microglial cells and
potentiating neurotrophic factors, were established. Viral vector-based dopamine delivery, prodrug
approaches, fetal ventral mesencephalon tissue transplantation and dopamine synthesizing enzyme encoding
gene delivery are significant therapies evidently supported by numerous trials. The review
primarily elaborates on the significant role of glial cell-line derived neurotrophic factor in alleviating
motor symptoms and the loss of dopaminergic neurons in Parkinson’s disease. Neuroprotective and
neuroregenerative effects of GDNF were established via preclinical and clinical study outcomes. The
binding of GDNF family ligands with associated receptors leads to the formation of a receptor-ligand
complex activating Ret receptor of tyrosine kinase family, which is only expressed in dopaminergic
neurons, playing an important role in Parkinson’s disease, via its association with the essential protein
encoded genes. Furthermore, the review establishes delivery aspects, like ventricular delivery of recombinant
GDNF, intraparenchymal and intraputaminal delivery using infusion catheters. The review
highlights problems and challenges of GDNF delivery, and essential measures to overcome them, like
gene therapy combinations, optimization of delivery vectors, newer targeting devices, motor symptoms
curbing focused ultrasound techniques, modifications in patient selection criteria and development
of novel delivery strategies based on liposomes and encapsulated cells, to promote safe and effective
delivery of neurotrophic factor and establishment of routine treatment therapy for patients.
Publisher
Bentham Science Publishers Ltd.
Subject
Genetics(clinical),Drug Discovery,Genetics,Molecular Biology,Molecular Medicine
Cited by
11 articles.
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