Potential use of antioxidants for the treatment of chronic inflammatory diseases

氧化应激 超氧化物歧化酶 抗氧化剂 活性氧 炎症 药理学 医学 化学 生物化学 免疫学
作者
Alexander V. Blagov,Volha I. Summerhill,Vasily N. Sukhorukov,Elena B. Zhigmitova,Anton Y. Postnov,Alexander N. Orekhov
出处
期刊:Frontiers in Pharmacology [Frontiers Media]
卷期号:15 被引量:16
标识
DOI:10.3389/fphar.2024.1378335
摘要

The excessive production of various reactive oxidant species over endogenous antioxidant defense mechanisms leads to the development of a state of oxidative stress, with serious biological consequences. The consequences of oxidative stress depend on the balance between the generation of reactive oxidant species and the antioxidant defense and include oxidative damage of biomolecules, disruption of signal transduction, mutation, and cell apoptosis. Accumulating evidence suggests that oxidative stress is involved in the physiopathology of various debilitating illnesses associated with chronic inflammation, including cardiovascular diseases, diabetes, cancer, or neurodegenerative processes, that need continuous pharmacological treatment. Oxidative stress and chronic inflammation are tightly linked pathophysiological processes, one of which can be simply promoted by another. Although, many antioxidant trials have been unsuccessful (some of the trials showed either no effect or even harmful effects) in human patients as a preventive or curative measure, targeting oxidative stress remains an interesting therapeutic approach for the development of new agents to design novel anti-inflammatory drugs with a reliable safety profile. In this regard, several natural antioxidant compounds were explored as potential therapeutic options for the treatment of chronic inflammatory diseases. Several metalloenzymes, such as superoxide dismutase, catalase, and glutathione peroxidase, are among the essential enzymes that maintain the low nanomolar physiological concentrations of superoxide (O 2 •−) and hydrogen peroxide (H 2 O 2 ), the major redox signaling molecules, and thus play important roles in the alteration of the redox homeostasis. These enzymes have become a striking source of motivation to design catalytic drugs to enhance the action of these enzymes under pathological conditions related to chronic inflammation. This review is focused on several major representatives of natural and synthetic antioxidants as potential drug candidates for the treatment of chronic inflammatory diseases.

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
科研通AI2S应助迷路的宛海采纳,获得20
刚刚
甜美迎蓉完成签到,获得积分10
刚刚
1秒前
666完成签到,获得积分10
1秒前
一只小鸮完成签到 ,获得积分10
2秒前
3秒前
3秒前
快乐科研发布了新的文献求助10
3秒前
严锦强发布了新的文献求助30
4秒前
阿喵完成签到,获得积分10
4秒前
5秒前
小马甲应助Demons采纳,获得10
6秒前
ZoeyD完成签到 ,获得积分10
6秒前
胖飞飞完成签到,获得积分10
6秒前
ding应助科研通管家采纳,获得10
7秒前
科研通AI5应助科研通管家采纳,获得10
7秒前
天天快乐应助科研通管家采纳,获得10
7秒前
汉堡包应助科研通管家采纳,获得10
7秒前
丘比特应助科研通管家采纳,获得10
7秒前
7秒前
wanci应助科研通管家采纳,获得10
7秒前
科研通AI5应助科研通管家采纳,获得10
7秒前
李健应助科研通管家采纳,获得10
8秒前
谨慎枫叶发布了新的文献求助10
8秒前
8秒前
赘婿应助科研通管家采纳,获得10
8秒前
8秒前
丘比特应助科研通管家采纳,获得10
8秒前
爱吃冬瓜完成签到,获得积分10
8秒前
乐观的天问完成签到,获得积分10
9秒前
夺命倩倩儿完成签到,获得积分20
9秒前
10秒前
11秒前
啦啦啦完成签到,获得积分10
12秒前
12秒前
赵mz发布了新的文献求助30
13秒前
夏尔完成签到,获得积分10
14秒前
15秒前
谨慎枫叶完成签到,获得积分20
15秒前
waerteyang发布了新的文献求助10
16秒前
高分求助中
Algorithmic Mathematics in Machine Learning 500
Advances in Underwater Acoustics, Structural Acoustics, and Computational Methodologies 400
Getting Published in SSCI Journals: 200+ Questions and Answers for Absolute Beginners 300
Fatigue of Materials and Structures 260
The Monocyte-to-HDL ratio (MHR) as a prognostic and diagnostic biomarker in Acute Ischemic Stroke: A systematic review with meta-analysis (P9-14.010) 240
The Burge and Minnechaduza Clarendonian mammalian faunas of north-central Nebraska 206
An Integrated Solution for Application of Next-Generation Sequencing in Newborn Screening 200
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 物理 生物化学 纳米技术 计算机科学 化学工程 内科学 复合材料 物理化学 电极 遗传学 量子力学 基因 冶金 催化作用
热门帖子
关注 科研通微信公众号,转发送积分 3831882
求助须知:如何正确求助?哪些是违规求助? 3374030
关于积分的说明 10483332
捐赠科研通 3093959
什么是DOI,文献DOI怎么找? 1703241
邀请新用户注册赠送积分活动 819322
科研通“疑难数据库(出版商)”最低求助积分说明 771423