Targeting autophagy using small-molecule compounds to improve potential therapy of Parkinson's disease
Acta Pharmaceutica Sinica B
; (6): 3015-3034, 2021.
Article
ي En
| WPRIM
| ID: wpr-922781
المكتبة المسؤولة:
WPRO
ABSTRACT
Parkinson's disease (PD), known as one of the most universal neurodegenerative diseases, is a serious threat to the health of the elderly. The current treatment has been demonstrated to relieve symptoms, and the discovery of new small-molecule compounds has been regarded as a promising strategy. Of note, the homeostasis of the autolysosome pathway (ALP) is closely associated with PD, and impaired autophagy may cause the death of neurons and thereby accelerating the progress of PD. Thus, pharmacological targeting autophagy with small-molecule compounds has been drawn a rising attention so far. In this review, we focus on summarizing several autophagy-associated targets, such as AMPK, mTORC1, ULK1, IMPase, LRRK2, beclin-1, TFEB, GCase, ERR
النص الكامل:
1
الفهرس:
WPRIM
نوع الدراسة:
Prognostic_studies
اللغة:
En
مجلة:
Acta Pharmaceutica Sinica B
السنة:
2021
نوع:
Article