Narirutin Attenuates Cerebral Ischemia-Reperfusion Injury by Suppressing the TXNIP/NLRP3 Pathway

被引:2
|
作者
Luo, Li [1 ]
Wang, Saiying [1 ]
Liu, Wenna [1 ]
Zhang, Zimei [2 ]
Zhao, Minggao [1 ]
Liu, An [1 ]
机构
[1] Air Force Med Univ, Tangdu Hosp, Precis Pharm & Drug Dev Ctr, Dept Pharm, Xian 710038, Peoples R China
[2] Univ Sci & Technol China, Div Life Sci & Med, Hefei 230026, Anhui, Peoples R China
关键词
Narirutin; Cerebral ischemic-reperfusion injury; Blood-brain barrier; Inflammation; NOD-like receptor protein 3 inflammasome; Thioredoxin interacting protein; NLRP3 INFLAMMASOME ACTIVATION; OXIDATIVE STRESS; BRAIN; STROKE; BARRIER; DAMAGE;
D O I
10.1007/s11064-023-04062-z
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
Narirutin (Nar) is a flavonoid that is abundantly present in citrus fruits and has attracted considerable attention because of its diverse pharmacological activities and low toxicity. Here, we evaluated the preventive effects of Nar in middle cerebral artery occlusion/reperfusion (MCAO/R)-injured mice and oxygen-glucose deprivation/reperfusion (OGD/R)-injured bEnd.3 cells. Pretreatment with Nar (150 mg/kg) for 7 days effectively reduced infarct volume, improved neurological deficits, and significantly inhibited neuronal death in the hippocampus and cortex in MCAO/R-injured mice. Moreover, anti-apoptotic effects of Nar (50 mu M) were observed in OGD/R-injured bEnd.3 cells. In addition, Nar pre-administration regulated blood-brain barrier function by increasing tight junction-related protein expression after MCAO/R and OGD/R injury. Nar also inhibited NOD-like receptor protein 3 (NLRP3) inflammasome activation by reducing the expression of thioredoxin-interacting protein (TXNIP) in vivo and in vitro. Taken together, these results provide new evidence for the use of Nar in the prevention and treatment of ischemic stroke.
引用
收藏
页码:692 / 705
页数:14
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