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A Cleaning Crew: The Pursuit of Autophagy in Parkinson's Disease.
Parekh, Pathik; Sharma, Nishant; Gadepalli, Anagha; Shahane, Abhishekh; Sharma, Monika; Khairnar, Amit.
Afiliação
  • Parekh P; Department of Pharmacology and Toxicology , National Institute of Pharmaceutical Education and Research (NIPER) , Ahmedabad , Gandhinagar 382355 , Gujarat India.
  • Sharma N; Department of Pharmacology and Toxicology , National Institute of Pharmaceutical Education and Research (NIPER) , Ahmedabad , Gandhinagar 382355 , Gujarat India.
  • Gadepalli A; Department of Pharmacology and Toxicology , National Institute of Pharmaceutical Education and Research (NIPER) , Ahmedabad , Gandhinagar 382355 , Gujarat India.
  • Shahane A; Department of Pharmacology and Toxicology , National Institute of Pharmaceutical Education and Research (NIPER) , Ahmedabad , Gandhinagar 382355 , Gujarat India.
  • Sharma M; Department of Pharmacology and Toxicology , National Institute of Pharmaceutical Education and Research (NIPER) , Ahmedabad , Gandhinagar 382355 , Gujarat India.
  • Khairnar A; Department of Pharmacology and Toxicology , National Institute of Pharmaceutical Education and Research (NIPER) , Ahmedabad , Gandhinagar 382355 , Gujarat India.
ACS Chem Neurosci ; 10(9): 3914-3926, 2019 09 18.
Article em En | MEDLINE | ID: mdl-31385687
ABSTRACT
Parkinson's disease (PD) is the second-most common neurodegenerative disorder, neuropathologically characterized by the aggregation of misfolded α-synuclein (α-syn) protein, which appears to be central to the onset and progression of PD pathology. Evidence from pioneering studies has highly advocated the existence of impaired autophagy pathways in the brains of PD patients. Autophagy is an evolutionarily conserved, homeostatic mechanism for minimizing abnormal protein aggregates and facilitating organelle turnover. Any aberration in constitutive autophagy activity results in the aggregation of misfolded α-syn, which, in turn, may further inhibit their own degradation-leading to a vicious cycle of neuronal death. Despite the plethora of available literature, there are still lacunas existing in our understanding of the exact cellular interplay between autophagy impairment and α-syn accumulation-mediated neurotoxicity. In this context, clearance of aggregated α-syn via up-regulation of the autophagy-lysosomal pathway could provide a pharmacologically viable approach to the treatment of PD. The present Review highlights the basics of autophagy and detrimental cross-talk between α-syn and chaperone-mediated autophagy, and α-syn and macroautophagy. It also depicts the interaction between α-syn and novel targets, LRRK2 and mTOR, followed by the role of autophagy in PD from a therapeutic perspective. More importantly, it further updates the reader's understanding of various newer therapeutic avenues that may accomplish disease modification via promoting clearance of toxic α-syn through activation of autophagy.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Autofagia / Lisossomos Limite: Animals / Humans Idioma: En Revista: ACS Chem Neurosci Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Autofagia / Lisossomos Limite: Animals / Humans Idioma: En Revista: ACS Chem Neurosci Ano de publicação: 2019 Tipo de documento: Article