医学
药理学
氧化应激
PI3K/AKT/mTOR通路
半胱氨酸蛋白酶
KEAP1型
信号转导
生物
细胞凋亡
癌症研究
生物信息学
细胞生物学
程序性细胞死亡
生物化学
转录因子
基因
作者
Mohammad Hossein Zamanian,Gholamreza Bazmandegan,Antoni Sureda,Eduardo Sobarzo-Sánchez,Hasan Yousefi-Manesh,Samira Shirooie
出处
期刊:Current Neuropharmacology
[Bentham Science]
日期:2020-12-31
卷期号:19 (1): 97-110
被引量:9
标识
DOI:10.2174/1570159x18666200510020744
摘要
: Troxerutin (TRX), a semi-synthetic bioflavonoid derived from rutin, has been reported to exert several pharmacological effects including antioxidant, anti-inflammatory, antihyperlipidemic, and nephroprotective. However, the related molecular details and its mechanisms remain poorly understood. In the present review, we presented evidences from the diversity in vitro and in vivo studies on the therapeutic potential of TRX against neurodegenerative, diabetes, cancer and cardiovascular diseases with the purpose to find molecular pathways related to the treatment efficacy. TRX has a beneficial role in many diseases through multiple mechanisms including, increasing antioxidant enzymes and reducing oxidative damage, decreasing in proapoptotic proteins (APAF-1, BAX, caspases-9 and-3) and increasing the antiapoptotic BCL-2, increasing the nuclear translocation of nuclear factor erythroid 2-related factor 2 (Nrf2) and downregulating the nuclear factor κB (NFκ). TRX also reduces acetylcholinesterase activity and upregulates phosphoinositide 3- kinase/Akt signaling pathway in Alzheimer’s disease models. Natural products such as TRX may develop numerous and intracellular pathways at several steps in the treatment of many diseases. Molecular mechanisms of action are revealing novel, possible combinational beneficial approaches to treat multiple pathological conditions.
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