Lycium ruthenicum Murr polysaccharide protects cortical neurons against oxygen-glucose deprivation/reperfusion in neonatal hypoxic-ischemic encephalopathy

被引:35
作者
Deng, Kewei [1 ]
Li, Yanling [2 ]
Xiao, Mi [3 ]
Wang, Fanghui [3 ]
Zhou, Ping [4 ]
Zhang, Wei [3 ]
Heep, Axel [5 ]
Li, Xiaoquan [3 ]
机构
[1] Northwest Womens & Childrens Hosp, Dept Neonatol, Xian 710061, Peoples R China
[2] Qujiang Matern Hosp, Dept Neonatol, Xian 710060, Peoples R China
[3] Xi An Jiao Tong Univ, Dept Neonatol, Affiliated Hosp 1, 277 Yanta West Rd, Xian 710061, Peoples R China
[4] Xi An Jiao Tong Univ, Clin Lab, Affiliated Hosp 1, Xian 710061, Peoples R China
[5] North Bristol NHS Trust, Neonatal Unit, Southmead Hosp, Bristol, Avon, England
关键词
Neonatal hypoxic-ischemic encephalopathy (HIE); L. ruthenicum polysaccharide 3 (LRP3); Hypoxic-ischemic injury; Oxidative stress; Nrf2/HO-1 signaling pathway; NRF2/HO-1; PATHWAY; OXIDATIVE STRESS; BRAIN-INJURY; STRUCTURAL-CHARACTERIZATION; DEATH; FRUIT; ACID; RATS;
D O I
10.1016/j.ijbiomac.2020.04.122
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Neonatal hypoxic-ischemic encephalopathy (HIE) is a complex condition that remains the leading cause of mortality and morbidity among infants. Polysaccharide has been reported to possess diverse biological activities, however, the neuro-protective activity of polysaccharide isolated from Lycium ruthenicum remains unknown so far. However, the role of Lycium ruthenicum polysaccharide 3 (LRP3) in HIE has not been evaluated. Herein, we investigated the effect of LRP3 on oxygen-glucose deprivation/reoxygenation (OGD/R)-induced primary cortical neurons. Our results demonstrated that LRP3 significantly improved the cell viability of OGD/R-induced cortical neurons. The OGD/R-caused increase in ROS production and decrease in the activities of anti-oxidative enzymes including catalase (CAT), superoxide dismutase (SOD) and glutathione peroxidase (GPx) were miti-gated by LRP3. Besides, the caspase-3 activity in OGD/R-induced cortical neurons was markedly decreased after LRP3 treatment. The increased bax expression and decreased bcl-2 expression caused by OGD/R stimulation were alleviated by pretreatment with LRP3. In addition, LRP3 significantly induced the expressions of nuclear factor erythroid 2-related factor (Nrf2) and heme oxygenase-1 (HO-1) in OGD/R-induced cortical neurons. However, inhibition of Nrf2/HO-1 signaling pathway through transfection with siRNA targeting Nrf2 reversed the protective effects of LRP3. In conclusion, LRP3 exerts a neuroprotective effect against OGD/R-induced neuronal injury in rat primary cortical neurons. (c) 2020 Elsevier B.V. All rights reserved.
引用
收藏
页码:562 / 568
页数:7
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