Old wine in new bottles: Kaempferol is a promising agent for treating the trilogy of liver diseases

脂肪性肝炎 肝癌 肝病 癌症研究 自噬 医学 脂肪肝 Wnt信号通路 炎症 纤维化 肝损伤 药理学 信号转导 生物 疾病 免疫学 细胞生物学 病理 内科学 生物化学 肝细胞癌 细胞凋亡
作者
Xiaolin Xiao,Qichao Hu,Xinyu Deng,Kaiyun Shi,Wenwen Zhang,Yinxiao Jiang,Xiao Ma,Jinhao Zeng,Xiaoyin Wang
出处
期刊:Pharmacological Research [Elsevier]
卷期号:175: 106005-106005 被引量:43
标识
DOI:10.1016/j.phrs.2021.106005
摘要

As a source of various compounds, natural products have long been important and valuable for drug development. Kaempferol (KP) is the most common flavonol with bioactive activity and has been extracted from many edible plants and traditional Chinese medicines. It has a wide range of pharmacological effects on inflammation, oxidation, and tumour and virus regulation. The liver is an important organ and is involved in metabolism and activity. Because the pathological process of liver diseases is extremely complicated, liver diseases involving ALD, NASH, liver fibrosis, and HCC are often complicated and difficult to treat. Fortunately, there have been many reports that KP has a good pharmacological effect on a series of complex liver diseases. To fully understand the mechanism of KP and provide new ideas for its clinical application in the treatment of liver diseases, this article reviews the pharmacological mechanism and potential value of KP in different studies involving various liver diseases. In the trilogy of liver disease, high concentrations of ROS stimulate peroxidation and activate the inflammatory signal cascade, which involves signalling pathways such as MAPK/JAK-STAT/PERK/Wnt/Hipp, leading to varying degrees of cell degradation and liver damage. The development of liver disease is promoted in an inflammatory environment, which is conducive to the activation of TGF-β1, leading to increased expression of pro-fibrosis and pro-inflammatory genes. Inflammation and oxidative stress promote the formation of tumour microenvironments, and uncontrolled autophagy of cancer cells further leads to the development of liver cancer. The main pathway in this process is AMPK/PTEN/PI3K-Akt/TOR. KP can not only protect liver parenchymal cells through a variety of antioxidant and anti-apoptotic mechanisms but also reduces the immune inflammatory response in the liver microenvironment, thereby preventing cell apoptosis; it can also inhibit the ER stress response, prevent inflammation and inhibit tumour growth. KP exerts multiple therapeutic effects on liver disease by regulating precise signalling targets and is expected to become an emerging therapeutic opportunity to treat liver disease in the future.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
大幅提高文件上传限制,最高150M (2024-4-1)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
刚刚
车厘子水门汀完成签到 ,获得积分10
刚刚
畅快宛丝应助wang5945采纳,获得10
1秒前
4秒前
背后半烟完成签到,获得积分10
5秒前
6秒前
香蕉觅云应助小鹿斑斑比采纳,获得10
6秒前
6秒前
Biu完成签到,获得积分10
7秒前
脑洞疼应助光亮元枫采纳,获得10
7秒前
嘿嘿完成签到,获得积分10
8秒前
能干涵瑶完成签到,获得积分10
9秒前
李李发布了新的文献求助10
11秒前
喵喵完成签到 ,获得积分10
11秒前
12秒前
13秒前
汉堡包应助liang采纳,获得10
13秒前
14秒前
xyy关注了科研通微信公众号
14秒前
Hellowa发布了新的文献求助10
17秒前
Lucas应助地狱跳跳虎采纳,获得10
18秒前
18秒前
小科发布了新的文献求助10
19秒前
沐浴清风发布了新的文献求助30
21秒前
英喆完成签到 ,获得积分10
21秒前
ljc完成签到 ,获得积分10
23秒前
23秒前
酷波er应助传统的海露采纳,获得30
23秒前
24秒前
夏侯乐枫发布了新的文献求助10
25秒前
28秒前
28秒前
28秒前
哎嘿应助沐浴清风采纳,获得10
29秒前
jychen85完成签到 ,获得积分10
30秒前
31秒前
ever1997完成签到,获得积分10
31秒前
lcc完成签到 ,获得积分10
31秒前
充电宝应助芹菜煎蛋采纳,获得10
32秒前
夏侯乐枫完成签到,获得积分10
33秒前
高分求助中
Evolution 10000
ISSN 2159-8274 EISSN 2159-8290 1000
Becoming: An Introduction to Jung's Concept of Individuation 600
Ore genesis in the Zambian Copperbelt with particular reference to the northern sector of the Chambishi basin 500
A new species of Coccus (Homoptera: Coccoidea) from Malawi 500
A new species of Velataspis (Hemiptera Coccoidea Diaspididae) from tea in Assam 500
PraxisRatgeber: Mantiden: Faszinierende Lauerjäger 500
热门求助领域 (近24小时)
化学 医学 生物 材料科学 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 基因 遗传学 催化作用 物理化学 免疫学 量子力学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 3161275
求助须知:如何正确求助?哪些是违规求助? 2812718
关于积分的说明 7896398
捐赠科研通 2471562
什么是DOI,文献DOI怎么找? 1316052
科研通“疑难数据库(出版商)”最低求助积分说明 631098
版权声明 602112