4.5 Article

Neuroprotective approaches to halt Parkinson?s disease progression

期刊

NEUROCHEMISTRY INTERNATIONAL
卷 158, 期 -, 页码 -

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.neuint.2022.105380

关键词

Disease progression; Dopa-resistant; Neuroprotective agents; Parkinson?s disease

资金

  1. Lady Tata Memorial Trust, Mumbai
  2. Department of Science and Technology- Fund for Improvement of Science and Technology Infrastructure in Univer-sities and Higher Educational Institutions (DST-FIST) , New Delhi [SR/FST/LSI-574/2013]

向作者/读者索取更多资源

Neurodegeneration is a significant threat in Parkinson's disease and is responsible for both motor and non-motor symptoms. Current treatments aim to increase dopamine levels but have limited effectiveness in halting disease progression. Therefore, the development of neuroprotective agents is necessary for better management of Parkinson's disease.
One of the most significant threats in Parkinson's disease (PD) is neurodegeneration. Neurodegeneration at both nigral as well as non-nigral regions of the brain is considered responsible for disease progression in PD. The key factors that initiate neurodegeneration are oxidative stress, neuroinflammation, mitochondrial complex-1 inhibition, and abnormal alpha-synuclein (SNCA) protein aggregations. Nigral neurodegeneration results in motor symptoms (tremor, bradykinesia, rigidity, shuffling gait, and postural instability) whereas; non-nigral neurodegeneration is responsible for non-motor symptoms (depression, cognitive dysfunctions, sleep disorders, hallucination, and psychosis). The available therapies for PD aim at increasing dopamine levels. The medications such as Monoamine oxidase B (MAO-B) inhibitors, catechol o-methyltransferase (COMT) inhibitors, Dopamine precursor (Levodopa), dopamine agonists, and dopamine reuptake inhibitors drastically improve the motor symptoms and quality of life only in the early stages of the disease. However, dopa resistant motor symptoms (abnormality in posture, speech impediment, gait, and balance problems), dopa resistant non-motor signs (sleep problems, autonomic dysfunction, mood, and cognitive impairment, pain), and drug-related side effects (motor fluctuations, psychosis, and dyskinesias) are considered responsible for the failure of these therapies. Further, none of the treatments, alone or in combination, are capable of halting the disease progression in the long run. Therefore, there is a need to develop safe and efficient neuroprotective agents, which can slow or stop the disease progression for the better management of PD. In this review, an effort has been made to discuss the various mechanisms responsible for progressive neurodegeneration (disease progression) in PD and also multiple strategies available for halting disease progression.

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