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Nrf2调控网络与骨质疏松症的相关性及中医药干预研究     被引量:1

Research progress on the correlation between Nrf2 regulatory network and osteoporosis and Chinese medicine intervention

文献类型:期刊文献

中文题名:Nrf2调控网络与骨质疏松症的相关性及中医药干预研究

英文题名:Research progress on the correlation between Nrf2 regulatory network and osteoporosis and Chinese medicine intervention

作者:刘沛[1];蒋宜伟[1,2];周玉英[2];张夏阳[1];海云翔[1];旷武龙[1];江朔轩[1]

第一作者:刘沛

机构:[1]甘肃中医药大学,甘肃兰州730000;[2]甘肃中医药大学附属医院,甘肃兰州730000

第一机构:甘肃中医药大学

年份:2024

卷号:30

期号:2

起止页码:240

中文期刊名:中国骨质疏松杂志

外文期刊名:Chinese Journal of Osteoporosis

收录:CSTPCD;;北大核心:【北大核心2023】;CSCD:【CSCD2023_2024】;

基金:国家自然科学基金(82160916);兰州市科技计划项目(2021-1-95);甘肃中医药大学“课程思政”项目(2020年);甘肃中医药大学中医学一级学科“岐黄英才”导师专项基金项目(2021)。

语种:中文

中文关键词:Nrf2;氧化应激;炎症;自噬;铁死亡;骨质疏松症;中医药

外文关键词:Nrf2;oxidative stress;inflammation;autophagy;ferroptosis;osteoporosis;traditional Chinese medicine

摘要:随着社会人口老龄化程度的不断加剧,骨质疏松症所带来的危害日益得到人们的重视。由于机体氧化应激导致的炎症水平升高以及进一步诱导的铁死亡是引起骨质疏松症的关键危险因素。核因子E2相关因子2(Nrf2)作为主要调节氧化应激的关键因子,能够通过调节炎症、自噬以及铁死亡等多方面而构成一个调控网络,与骨质疏松症密切相关。目前已有大量研究证实中医药能够通过Nrf2调控网络发挥抗氧化、抗炎等多种作用,在治疗骨质疏松症方面效果明显。本文通过总结Nrf2调控网络与骨质疏松症的相关性以及中医药干预的研究成果,为今后中医药精准防治骨质疏松症提供新的方向。
With the increasing aging of society and population,people pay more and more attention to the harm caused by osteoporosis.Increased inflammation caused by oxidative stress and further induced ferroptosis are key risk factors for osteoporosis.Nuclear factor E2-related factor 2(Nrf2),as a key factor mainly regulating oxidative stress,can also regulate inflammation.Autophagy and ferroptosis constitute a regulatory network and are closely related to osteoporosis.At present,a large number of studies have confirmed that traditional Chinese medicine exerts various functions such as antioxidant and anti-inflammatory through Nrf2 regulatory network,and has obvious effects in the treatment of osteoporosis.By summarizing the correlation between Nrf2 regulatory network and osteoporosis and the research result of TCM intervention,this paper provides a new direction for the accurate prevention and treatment of osteoporosis by TCM in the future.

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