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

被引:18
作者
Enogieru, Adaze Bijou [1 ]
Haylett, William Lloyd [2 ,3 ]
Miller, Hayley Christy [4 ]
van der Westhuizen, Francois Hendrikus [4 ]
Hiss, Donavon Charles [1 ]
Ekpo, Okobi Eko [1 ]
机构
[1] Univ Western Cape, Dept Med Biosci, Robert Sobukwe Rd,Private Bag X17, ZA-7535 Bellville, South Africa
[2] Stellenbosch Univ, Div Mol Biol & Human Genet, Dept Biomed Sci, Fac Med & Hlth Sci, Cape Town, South Africa
[3] Stellenbosch Univ, Div Endocrinol, Dept Med, Fac Med & Hlth Sci, Cape Town, South Africa
[4] North West Univ, Focus Area Human Metabol, Fac Nat Sci, Potchefstroom, South Africa
关键词
Parkinson's disease; Rutin; ER stress; Oxidative phosphorylation; Glycolysis; UNFOLDED PROTEIN RESPONSE; IN-VITRO; MITOCHONDRIAL DYSFUNCTION; PARKINSONS-DISEASE; ANTIOXIDANT PROPERTIES; INDUCED APOPTOSIS; ANIMAL-MODELS; GLYCOLYSIS; NEURONS; NEUROTOXICITY;
D O I
10.1007/s12640-019-00048-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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+-treated SH-SY5Y neuroblastoma cells, an established cell model of PD. Our findings reveal increased concentrations of Ca2+ and endoplasmic reticulum (ER) stress as well as impaired mitochondrial membrane potential and bioenergetic status in SH-SY5Y cells treated with MPP+ 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+, characterized by deficient ATP production. In conclusion, our findings provide the first evidence on the ability of rutin to maintain Ca2+ homeostasis, inhibit ER stress, and protect the mitochondria in MPP+-treated SH-SY5Y cells.
引用
收藏
页码:764 / 776
页数:13
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