解开多糖的结构性质与抗炎活性之间的联系:一篇综述
Yuanhao Qiu1, Aoying Zhang2, Xiuning Lian3
1College of Medicine, Pingdingshan University, Pingdingshan, Henan, 467000, China; Traditional Chinese Medicine (Zhong Jing) School, Henan Key Laboratory of Chinese Medicine for Polysaccharides and Drugs Research, Henan University of Chinese Medicine, Zhengzhou, Henan, 450046, China.
Carbohydrate research
|June 21, 2025
概括
自然的多糖,复杂的碳水化合物,通过调节免疫力和肠道细菌,表现出抗炎作用. 它们的结构,包括分子量和联系,决定了这种活动,有助于药物开发.
科学领域:
- 生物化学 生物化学
- 免疫学 免疫学 免疫学
- 药理学 药理学是指药理学的学科.
背景情况:
- 多糖是具有显著抗炎潜力的天然大分子.
- 它们的治疗作用通过与免疫系统和肠道微生物群相互作用来准炎症性疾病.
- 了解多糖的结构是利用其抗炎性能的关键.
研究的目的:
- 审查多糖的结构性质和它们的抗炎活性之间的关系.
- 要突出了解多糖介导炎症调节的分子机制的最新进展.
- 为开发基于多糖的新型抗炎疗法提供见解.
主要方法:
- 关于具有抗炎作用的天然多糖类最近研究的文献综述.
- 对生物活性多糖的结构特征的研究分析.
- 检查详细介绍分子机制和向作用器官的研究.
主要成果:
- 多糖的抗炎活性受分子量,单糖组成,甘油酸链接和分支的影响.
- 已经确定了天然抗炎多糖的多种分子机制和向器官.
- 结构性特征对于理解多糖如何调节炎症通路至关重要.
结论:
- 多糖的结构特征是它们抗炎功效的关键决定因素.
- 对多糖体结构-活性关系的进一步研究可以指导开发有效的抗炎药物.
- 本综述为多糖在治疗炎症疾病中的应用提供了有价值的见解.
相关概念视频
Glycosaminoglycans
5.2K
Glycosaminoglycans (GAGs), also known as mucopolysaccharides, are long and linear polymers comprising of specific repeating disaccharides - the amino sugar that can be N-acetylglucosamine or N-acetylgalactosamine, and a uronic acid that is usually glucuronic acid or iduronic acid.
GAGS are found in the extracellular matrix of vertebrates, invertebrates, and bacteria. Due to their polar nature they attract water, and serve as excellent lubricants or shock absorbers in an animal body.
Hyaluronic...
GAGS are found in the extracellular matrix of vertebrates, invertebrates, and bacteria. Due to their polar nature they attract water, and serve as excellent lubricants or shock absorbers in an animal body.
Hyaluronic...
5.2K
Cellulose and Pectic Polysaccharides
3.9K
Every plant cell has a cell wall that protects the cell, provides structural support, and gives the cell shape. Cellulose, the main structural component of the plant cell wall, makes up over 30% of plant matter. It is the most abundant organic compound on earth. Cellulose is an unbranched polysaccharide composed of linear chains of glucose molecules linked by β (1→4) glycosidic bonds.
As a cell matures, its cell wall specializes according to its type. For example, the...
As a cell matures, its cell wall specializes according to its type. For example, the...
3.9K
Chemistry of Carbohydrates
75.9K
Carbohydrates are an essential part of the diet in humans and animals. Grains, fruits, and vegetables are natural sources of carbohydrates that provide energy to the body, particularly through glucose, a simple sugar that is a component of starch and an ingredient in many staple foods. The stoichiometric formula (CH2O)n, where n is the number of carbons in the molecule represents carbohydrates. In other words, the ratio of carbon to hydrogen to oxygen is 1:2:1 in carbohydrate molecules. This...
75.9K
Biosynthesis of Polysaccharides
100
Polysaccharides such as glycogen and starch are synthesized from nucleoside diphosphate sugars, primarily uridine diphosphate glucose (UDPG) and adenosine diphosphate glucose (ADPG). These activated glucose donors act as key intermediates in carbohydrate metabolism and biosynthesis. UDPG primarily involves glycogen synthesis in animals and many bacteria, while ADPG plays a fundamental role in starch synthesis in plants and certain bacteria.UDPG is formed when glucose-1-phosphate reacts with...
100
Proteoglycans
4.0K
Glycans, a class of complex heterogeneous molecules, can be covalently attached to proteins to form glycosylated proteins that regulate various physiological and pathological processes. Glycosylated proteins or glycoproteins comprise N-linked and O-linked oligosaccharides. O-glycosylation is the most common type of protein glycosylation. Here, glycans attach to the oxygen atom of the hydroxyl groups of Serine or Threonine residues. O-linked glycosylation occurs later in protein processing,...
4.0K
Oligosaccharide Assembly
3.0K
Protein glycosylation starts in the ER lumen and continues in the Golgi apparatus. Glycosyltransferases catalyze the addition of sugar molecules or glycosylation of proteins. Usually, these enzymes add sugars to the hydroxyl groups of selected serine or threonine residues to form O-linked glycans or the amino groups of asparagine residues to form N-linked glycans. Different positions on the same polypeptide chain can contain differently linked glycans.
Multiple sugar molecules that may or may...
Multiple sugar molecules that may or may...
3.0K


