Proteasome Activity in Parkinsonism through D1 Dopamine Receptor

Authors

  • R. B. Jiménez Neuroscience and Biotechnology Laboratory, School of Medicine, Universidad Panamericana, México DF, México
  • J.E. Telich-Tarriba Neuroscience and Biotechnology Laboratory, School of Medicine, Universidad Panamericana, México DF, México
  • J.D. Carrillo-Ruíz Department of Neuroscience and Psychophysiology, Universidad Anahuac, Mexico, Neurosurgery Clinic of Spasticity, Service Functional Neurosurgery and Radiosurgery Hospital General de México
  • G. Rivera-Silva Tisular Engineering and Regenerative Medicine Laboratory, University of Monterrey, San Pedro Garza García, NL, México

Keywords:

L-DOPA, Antiparkinsonian drugs, Ubiquitine-proteosome system, Akinetic symtoms

Abstract

As of today, L-DOPA is recognized as the most efficacious drug to alleviate the typical signs and symptoms of Parkinson disease (PD). It is most effective for the akinetic symtoms, and its use is indicated when the disease becomes disabling or it cannot be controlled by other antiparkinsonian drugs. Unfortunately, response to medication changes during the progression of the disease, with the patients developing tolerance to treatment and the need for higher doses that lead to the development of side effects. The Ubiquitine-proteosome system (UPS) is key in regulating the degradation of normal and abnormal intracellular proteins linked to signal transduction, cell cycle progression, apoptosis and differenciation; therefore it dysregulation would be expected to impact several systems. UPS dysregulation has been implicated in cancer, neurodegenerative and autoimmune diseases.

References

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Published

2013-01-29

How to Cite

B. Jiménez, R., Telich-Tarriba, J. ., Carrillo-Ruíz, J. ., & Rivera-Silva, G. . (2013). Proteasome Activity in Parkinsonism through D1 Dopamine Receptor. Scientific Journal of Pure and Applied Sciences, 2(1), 54-56. Retrieved from http://sjournals.com/index.php/sjpas/article/view/1009

Issue

Section

Medicine