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Attenuation of Endoplasmic Reticulum Stress, Impaired Calcium Homeostasis, and Altered Bioenergetic Functions in MPP + -Exposed SH-SY5Y Cells Pretreated with Rutin.

Authors :
Enogieru AB
Haylett WL
Miller HC
van der Westhuizen FH
Hiss DC
Ekpo OE
Source :
Neurotoxicity research [Neurotox Res] 2019 Nov; Vol. 36 (4), pp. 764-776. Date of Electronic Publication: 2019 May 04.
Publication Year :
2019

Abstract

Parkinson's disease (PD) is a common neurodegenerative disorder that affects approximately 1% of the population over the age of 65 years. While treatment options for PD are limited, reports show that plant-derived bioactive compounds such as rutin possess numerous pharmacological benefits, including antioxidant and antiapoptotic activities. This study aimed to investigate the potential role of rutin in MPP <superscript>+</superscript> -treated SH-SY5Y neuroblastoma cells, an established cell model of PD. Our findings reveal increased concentrations of Ca <superscript>2+</superscript> and endoplasmic reticulum (ER) stress as well as impaired mitochondrial membrane potential and bioenergetic status in SH-SY5Y cells treated with MPP <superscript>+</superscript> only. This is demonstrated by a significant reduction in the expression levels of BiP, significantly reduced basal respiration, maximal respiration, and spare respiratory capacity as well as a significant increase in the expression levels of CHOP; however, these effects were significantly attenuated following pretreatment with rutin. Also, rutin significantly improved basal and compensatory glycolysis as a response to an impaired oxidative phosphorylation system triggered by MPP <superscript>+</superscript> , characterized by deficient ATP production. In conclusion, our findings provide the first evidence on the ability of rutin to maintain Ca <superscript>2+</superscript> homeostasis, inhibit ER stress, and protect the mitochondria in MPP <superscript>+</superscript> -treated SH-SY5Y cells.

Details

Language :
English
ISSN :
1476-3524
Volume :
36
Issue :
4
Database :
MEDLINE
Journal :
Neurotoxicity research
Publication Type :
Academic Journal
Accession number :
31055769
Full Text :
https://doi.org/10.1007/s12640-019-00048-4