Sensory neuropathy and nociception in rodent models of Parkinson's disease

Parkinson's disease (PD) often manifests with prodromal pain and sensory losses whose etiologies are not well understood. Multiple genetic and toxicity-based rodent models of PD partly recapitulate the histopathology and motor function deficits. Although far less studied, there is some evidence...

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Main Authors: Lucie Valek (Author), Georg Auburger (Author), Irmgard Tegeder (Author)
Format: Book
Published: The Company of Biologists, 2019-06-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Lucie Valek  |e author 
700 1 0 |a Georg Auburger  |e author 
700 1 0 |a Irmgard Tegeder  |e author 
245 0 0 |a Sensory neuropathy and nociception in rodent models of Parkinson's disease 
260 |b The Company of Biologists,   |c 2019-06-01T00:00:00Z. 
500 |a 1754-8403 
500 |a 1754-8411 
500 |a 10.1242/dmm.039396 
520 |a Parkinson's disease (PD) often manifests with prodromal pain and sensory losses whose etiologies are not well understood. Multiple genetic and toxicity-based rodent models of PD partly recapitulate the histopathology and motor function deficits. Although far less studied, there is some evidence that rodents, similar to humans, develop sensory manifestations of the disease, which may precede motor disturbances and help to elucidate the underlying mechanisms of PD-associated pain at the molecular and neuron circuit levels. The present Review summarizes nociception and other sensory functions in frequently used rodent PD models within the context of the complex phenotypes. In terms of mechanisms, it appears that the acute loss of dopaminergic neurons in systemic toxicity models (MPTP, rotenone) primarily causes nociceptive hyperexcitability, presumably owing to a loss of inhibitory control, whereas genetic models primarily result in a progressive loss of heat perception, reflecting sensory fiber neuropathies. At the molecular level, neither α-synuclein deposits alone nor failure of mitophagy alone appear to be strong enough to result in axonal or synaptic pathology of nociceptive neurons that manifest at the behavioral level, and peripheral sensory loss may mask central 'pain' in behavioral tests. Hence, allostatic combinations or additional challenges and novel behavioral assessments are needed to better evaluate PD-associated sensory neuropathies and pain in rodents. 
546 |a EN 
690 |a Non-motor Parkinson's disease 
690 |a Synuclein 
690 |a Mitophagy 
690 |a Mitogenesis 
690 |a Protein aggregate 
690 |a Pain 
690 |a Sensory neuropathy 
690 |a Medicine 
690 |a R 
690 |a Pathology 
690 |a RB1-214 
655 7 |a article  |2 local 
786 0 |n Disease Models & Mechanisms, Vol 12, Iss 6 (2019) 
787 0 |n http://dmm.biologists.org/content/12/6/dmm039396 
787 0 |n https://doaj.org/toc/1754-8403 
787 0 |n https://doaj.org/toc/1754-8411 
856 4 1 |u https://doaj.org/article/8d9b91c12c944e1da68a2f11c3408e30  |z Connect to this object online.