Neuropathology of Parkinson's Disease: An Update of the Recent Findings

Neuropathology of Parkinson's Disease: An Update of the Recent Findings

Bilal El-Mansoury, Omar El Hiba, Mustapha Agnaou, Arumugam Radhakrishan Jayakumar, Abdelaati El Khiat, Kholoud Kahim, Samira Boulbaroud, Nadia Zouhairi, Oumaima Tibssirte, Hayat Bouighajd, Moulay Abdelmonaim El Hidan, Abdesslam Ferssiwi, Abdelali Bitar
DOI: 10.4018/978-1-6684-5156-4.ch006
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Abstract

Parkinson's disease (PD) is a progressive neurodegenerative movement disorder of great concern of which no proven neuroprotective or neurorestorative therapies are available. It is characterized mainly by the degeneration of dopamine (DA) producing neurons in the substantia nigra (SN) pars compacta (SNpc) resulting in nigrostriatal pathway dysregulation and eventually disturbed subcortico-cortical interactions. The pathophysiological mechanisms leading to PD development are not completely understood. Several mechanisms and pathway dysfunctions have been proposed as they play a critical role in the pathogenesis of PD. These include oxidative stress, dysfunctional mitochondria, neuroinflammation, ubiquitin proteasomal dysfunction, and α-synuclein protein aggregation. This chapter will provide an overview on neuropathology, pathogenesis, and the recent pathophysiological mechanisms involved in PD.
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The History And Clinical Manifestations Of Parkinson’S Disease

James Parkinson was published “An essay on the shaking palsy” (1817), in which he described in a clear and detailed manner for the first time six patients with the disease. Further, the disease bears his name after Jean-Martin Charcot, who first used the term “Maladie de Parkinson” or Parkinson’s disease (PD) five decades later (in the mid-1800s) (Mcdonald et al., 2018). Jean-Martin Charcot distinguished PD from multiple sclerosis and other conditions marked by tremor, and he identified cases that would subsequently possibly be included among the Parkinsonism-plus syndromes.

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