传统中医药的化合物调节信号通路,以改善与心脏相关的病理
Luwen Zhang1,2, Wei Wang3, Xincan Liu2
1The First Clinical Medical College of Henan University of Chinese Medicine, Zhengzhou, Henan, China.
Frontiers in pharmacology
|April 17, 2025
概括
传统中国医学 (TCM) 通过向炎症,氧化应激和纤维化,为心血管疾病 (CVD) 提供有前途的治疗方法. 本综述探讨了TCM化合物如何调节有效的CVD管理的关键途径.
科学领域:
- 生物医学科学 生物医学科学
- 药理学 药理学是指药理学的学科.
- 心脏病学 心脏病学
背景情况:
- 心血管疾病 (CVD) 是全球主要的死亡原因,发病率越来越高.
- 心血管疾病的病理生理机制包括炎症,氧化应激,自和心肌纤维化.
- 传统中医 (TCM) 对心血管疾病提出了潜在的治疗策略.
研究的目的:
- 审查了解TCM在治疗心血管疾病中的作用的最新进展.
- 探索TCM化合物如何调节涉及心血管疾病的关键信号通路.
主要方法:
- 关于TCM和心血管疾病的最新研究的文献综述.
- 对TCM对炎症,氧化应激,自和纤维化的影响进行分析.
- 检查TCM化合物对相关信号通路的影响.
主要成果:
- 通过针对多个组件和途径,TCM表现出协同效应.
- 在心血管疾病模型中,TCM可以调节炎症反应并减轻氧化应激.
- TCM有助于调节自和促进心肌纤维化修复.
结论:
- TCM化合物为管理心血管疾病提供了一种多目标的方法.
- 对TCM机制的进一步研究可以为心血管健康带来新的治疗策略.
- 在解决心血管疾病复杂的病理生理学方面,TCM显示出显著的潜力.
相关概念视频
Heart Failure Drugs: Inhibitors of Renin-Angiotensin System
315
The activation of the sympathetic nervous system and the renin-angiotensin-aldosterone system (RAAS) contributes to cardiac remodeling, and inhibiting the RAAS is a pharmacological target in heart failure management. As a result, neurohumoral modulation is a crucial treatment principle for managing heart failure. This approach involves using medications like ACE inhibitors (ACEIs), angiotensin receptor blockers (ARBs), β-blockers, mineralocorticoid receptor antagonists (MRAs), and neutral...
315
Pathophysiology of Cardiac Performance
488
Typical heart performance is influenced by heart rate, rhythm, myocardial contraction, and metabolism or blood flow. The cardiac muscle exhibits distinct electrophysiological features, including pacemaker activity and calcium channel control, which play a vital role in the heart's response to various drugs. The autonomic nervous system, comprising the sympathetic and parasympathetic branches, regulates heart rate. Sympathetic activation increases heart rate, while parasympathetic activation...
488
Heart Failure Drugs: Inotropic Agents
414
Positive inotropic agents are commonly used as the first line of treatment for heart failure. One such agent is digoxin, derived from the genus Digitalis, which has been known for centuries but effectively utilized since 1785. However, these cardiac glycosides can have potentially toxic effects due to their mechanism of action, which involves inhibiting Na+/K+-ATPase and increasing contractility. Digoxin is absorbed orally and distributed in various tissues, including the CNS. It has a long...
414
Transducer Mechanism: Enzyme-Linked Receptors
2.3K
Enzyme-linked receptors are cell-surface receptors acting as an enzyme or associating with an enzyme intracellularly. They make excellent drug targets. Drugs can bind to the extracellular ligand-binding domain or directly affect their enzymatic domain and alter their activity.
Major types that are helpful drug targets include:
Major types that are helpful drug targets include:
2.3K


