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Cleistocalyx nervosum var. paniala berry fruit protects neurotoxicity against endoplasmic reticulum stress-induced apoptosis
被引:33
作者:
Sukprasansap, Monruedee
[1
]
Chanvorachote, Pithi
[2
,3
]
Tencomnao, Tewin
[4
]
机构:
[1] Chulalongkorn Univ, Fac Allied Hlth Sci, Dept Clin Chem, PhD Program Clin Biochem & Mol Med, Bangkok, Thailand
[2] Chulalongkorn Univ, Fac Pharmaceut Sci, Dept Physiol & Pharmacol, Bangkok 10330, Thailand
[3] Chulalongkorn Univ, Fac Pharmaceut Sci, Cell Based Drug & Hlth Prod Dev Res Unit, Bangkok, Thailand
[4] Chulalongkorn Univ, Fac Allied Hlth Sci, Dept Clin Chem, Bangkok 10330, Thailand
关键词:
Cleistocalyx nervosum var. paniala;
Anthocyanin;
ROS;
glutamate;
ER stress;
Neuroprotective effect;
OXIDATIVE STRESS;
ALZHEIMERS-DISEASE;
HT22;
CELLS;
NEURODEGENERATIVE DISORDERS;
ANTIOXIDANT ACTIVITY;
PHENOLIC-COMPOUNDS;
ANTHOCYANINS;
CASPASE-12;
DEATH;
SUPPLEMENTATION;
D O I:
10.1016/j.fct.2017.03.025
中图分类号:
TS2 [食品工业];
学科分类号:
0832 ;
摘要:
Oxidative and endoplasmic reticulum (ER) stresses cause neuronal damage leading to neurodegenerative disorders. Cleistocalyx nervosum var. paniala (CNP) berry fruit has been shown to possess powerful antioxidant properties. Here, we investigated the neuroprotective effect of CNP extract against glutamate-mediated oxidative/ER stress-induced cell death in mouse hippocampal neuronal HT22 cells. CNP extract was clarified for its radical scavenging activities, total phenolic and anthocyanin contents. The key anthocyanin cyanidin-3-glucoside was used as a marker to standardize the extract used in the study. We found that pretreated cells with CNP extract (0.05-1 mu g/ml) prevented neuronal cell death in response to 5 mM glutamate evaluated by cell viability Nur, LDH and apoptosisinecrosis Annexin V/ propidium iodide co-staining assays. For mechanistic approach, glutamate-induced cell death through reactive oxygen species (ROS)-mediated ER stress pathways, indicating the increase of ROS and ER stress signature molecules including calpain, caspases-12 and C/EBP homologous proteins (CHOP). CNP extract inhibited ROS production. Moreover, the extract also suppressed the specific-ER stress apoptotic proteins level in glutamate-induced cells by upregulating the gene expression of cellular antioxidant enzymes (SODS, CAT, GPx and GSTs). Taken together, our results provide information about and the molecular mechanism of CNP extract as a promising neuroprotectant and antioxidant. (C) 2017 Elsevier Ltd. All rights reserved.
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页码:279 / 288
页数:10
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