AMPK signaling in diabetes mellitus, insulin resistance and diabetic complications: A pre-clinical and clinical investigation

医学 糖尿病 内科学 胰岛素抵抗 安普克 内分泌学 AMP活化蛋白激酶 信号转导 PI3K/AKT/mTOR通路 蛋白激酶A 生物信息学 激酶 生物 细胞生物学
作者
Maliheh Entezari,Danial Hashemi,Afshin Taheriazam,Amirhossein Zabolian,Shima Mohammadi,Farima Fakhri,Mehrdad Hashemi,Kiavash Hushmandi,Milad Ashrafizadeh,Ali Zarrabi,Yavuz Nuri Ertaş,Sepideh Mirzaei,Saeed Samarghandian
出处
期刊:Biomedicine & Pharmacotherapy [Elsevier]
卷期号:146: 112563-112563 被引量:176
标识
DOI:10.1016/j.biopha.2021.112563
摘要

Diabetes mellitus (DM) is considered as a main challenge in both developing and developed countries, as lifestyle has changed and its management seems to be vital. Type I and type II diabetes are the main kinds and they result in hyperglycemia in patients and related complications. The gene expression alteration can lead to development of DM and related complications. The AMP-activated protein kinase (AMPK) is an energy sensor with aberrant expression in various diseases including cancer, cardiovascular diseases and DM. The present review focuses on understanding AMPK role in DM. Inducing AMPK signaling promotes glucose in DM that is of importance for ameliorating hyperglycemia. Further investigation reveals the role of AMPK signaling in enhancing insulin sensitivity for treatment of diabetic patients. Furthermore, AMPK upregulation inhibits stress and cell death in β cells that is of importance for preventing type I diabetes development. The clinical studies on diabetic patients have shown the role of AMPK signaling in improving diabetic complications such as brain disorders. Furthermore, AMPK can improve neuropathy, nephropathy, liver diseases and reproductive alterations occurring during DM. For exerting such protective impacts, AMPK signaling interacts with other molecular pathways such as PGC-1α, PI3K/Akt, NOX4 and NF-κB among others. Therefore, providing therapeutics based on AMPK targeting can be beneficial for amelioration of DM.

科研通智能强力驱动
Strongly Powered by AbleSci AI
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
w舟完成签到,获得积分20
1秒前
Shao发布了新的文献求助10
3秒前
3秒前
称心芷天完成签到 ,获得积分10
3秒前
你维好困完成签到,获得积分10
4秒前
seki完成签到,获得积分10
4秒前
科研通AI2S应助风懒懒采纳,获得10
4秒前
旋转木马9个完成签到,获得积分10
5秒前
鉴湖发布了新的文献求助10
5秒前
6秒前
6秒前
7秒前
00279完成签到,获得积分10
8秒前
赫连烙完成签到,获得积分10
8秒前
温柔初晴完成签到 ,获得积分10
9秒前
爱因斯坦那个和我一样的科学家完成签到 ,获得积分10
10秒前
yaya完成签到 ,获得积分10
11秒前
无赖真菌完成签到,获得积分20
11秒前
11秒前
13秒前
量子星尘发布了新的文献求助10
13秒前
dilu完成签到,获得积分10
14秒前
谈笑间应助科研通管家采纳,获得10
15秒前
小二郎应助科研通管家采纳,获得10
15秒前
Orange应助科研通管家采纳,获得10
15秒前
谈笑间应助科研通管家采纳,获得10
15秒前
领导范儿应助科研通管家采纳,获得10
15秒前
15秒前
15秒前
Ava应助科研通管家采纳,获得10
15秒前
田様应助科研通管家采纳,获得10
15秒前
谈笑间应助科研通管家采纳,获得10
15秒前
搜集达人应助科研通管家采纳,获得10
15秒前
桐桐应助科研通管家采纳,获得10
15秒前
15秒前
我是老大应助科研通管家采纳,获得10
15秒前
15秒前
16秒前
酷波er应助科研通管家采纳,获得10
16秒前
共享精神应助科研通管家采纳,获得10
16秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Handbook of pharmaceutical excipients, Ninth edition 5000
Aerospace Standards Index - 2026 ASIN2026 3000
Signals, Systems, and Signal Processing 610
Discrete-Time Signals and Systems 610
Social Work and Social Welfare: An Invitation(7th Edition) 410
Medical Management of Pregnancy Complicated by Diabetes 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 纳米技术 有机化学 物理 生物化学 化学工程 计算机科学 复合材料 内科学 催化作用 光电子学 物理化学 电极 冶金 遗传学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 6055730
求助须知:如何正确求助?哪些是违规求助? 7884643
关于积分的说明 16288346
捐赠科研通 5201046
什么是DOI,文献DOI怎么找? 2782954
邀请新用户注册赠送积分活动 1765760
关于科研通互助平台的介绍 1646683