在动脉样硬化内皮功能障碍中的PPARγ:调节性化合物和PTMs
Jinwen Luan1, Xiaohui Ji1, Longhua Liu1
1School of Exercise and Health, Shanghai University of Sport, Shanghai 200082, China.
International journal of molecular sciences
|October 14, 2023
概括
过酶增殖器激活受体- (PPARγ) 对于内皮功能至关重要,可以治疗动脉样硬化. 这篇评论探讨了PPARγ的研究.
科学领域:
- 心血管研究研究心血管研究
- 分子生物学分子生物学
- 内分泌学 在内分泌学.
背景情况:
- 动脉样硬化是心血管疾病的主要原因,涉及到内皮功能障碍.
- 过氧体增殖器激活受体- (PPARγ) 对于维持内皮功能至关重要.
- PPARγ在内皮功能障碍中的确切作用尚不清楚.
研究的目的:
- 审查PPARγ在调节内皮功能中的机制.
- 探索PPARγ调控化合物和翻译后修改 (PTM) 的影响.
- 评估针对动脉样硬化的内皮PPARγ的治疗潜力.
主要方法:
- 对PPARγ,内皮功能和动脉样硬化等研究的文献综述.
- 对PPARγ调节器的作用机制的分析.
- 检查影响PPARγ活性的PTM.
主要成果:
- PPARγ在内皮细胞中起着保护作用.
- 调节性化合物和PTM显著影响PPARγ对内皮功能的控制.
- 内皮PPARγ是动脉样硬化治疗的有希望的标.
结论:
- 了解PPARγ机制是开发新动脉样硬化疗法的关键.
- 向内皮PPARγ提供了预防和治疗心血管疾病的潜在策略.
- 对PPARγ调节器和PTM进行进一步研究是有必要的.
相关概念视频
Atherosclerosis I: Introduction
9
Atherosclerosis is a progressive disorder characterized by the buildup of plaques on the arterial inner wall, causing them to narrow and harden over time. These plaques comprise lipids, calcium, blood components, carbohydrates, and fibrous tissue. The process primarily affects the intima of large and medium-sized arteries, reducing blood flow in any artery.Etiology and risk factorsThe cause of atherosclerosis is multifactorial, involving a complex interplay among endothelial injury, lipid...
9
Coronary Artery Disease II: Pathophysiology
12
Coronary Artery Disease (CAD) originates from a series of events that impair the function of coronary arteries, the blood vessels responsible for delivering oxygen-rich blood to the heart muscle. The pathophysiology of CAD is closely linked to atherosclerosis, a chronic inflammatory and lipid-driven condition affecting the vascular endothelium.1. Endothelial DamageThe process begins with damage to the vascular endothelium, which serves as a protective barrier between the blood and the vessel...
12
Transducer Mechanism: Nuclear Receptors
1.4K
Nuclear receptors, or NRs, are unique transcription factors that regulate gene transcription and affect the cellular pathways involved in reproduction, development, or metabolism. Their ability to be stimulated by small lipophilic ligands and control vital cellular processes makes them ideal drug targets. Nearly 10-15% of currently prescribed drugs target these receptors.
About 48 different soluble family members of nuclear receptors are identified that can be divided into two main classes:
About 48 different soluble family members of nuclear receptors are identified that can be divided into two main classes:
1.4K
Covalently Linked Protein Regulators
6.8K
Proteins can undergo many types of post-translational modifications, often in response to changes in their environment. These modifications play an important role in the function and stability of these proteins. Covalently linked molecules include functional groups, such as methyl, acetyl, and phosphate groups, and also small proteins, such as ubiquitin. There are around 200 different types of covalent regulators that have been identified.
These groups modify specific amino acids in a protein....
These groups modify specific amino acids in a protein....
6.8K
Peripheral Artery Disease I: Introduction
9
Peripheral artery disease (PAD) predominantly results from atherosclerosis, which involves the accumulation of fatty deposits, or plaques, within the walls of arteries. This causes them to narrow and harden, significantly reducing blood flow. PAD predominantly affects the legs but also impacts other areas, such as the arms, thereby impairing overall circulation and organ function.Etiology of PAD:The principal cause of PAD is atherosclerosis, which results from fatty deposits inside the arterial...
9
GPCRs Regulate Adenylyl Cylase Activity
5.6K
Some GPCRs transmit signals through adenylyl cyclase (AC), a transmembrane enzyme. AC helps synthesize second messenger cyclic adenosine monophosphate (cAMP). AC catalyzes cyclization reaction and converts ATP to cAMP by releasing a pyrophosphate. The pyrophosphate is further hydrolyzed to phosphate by the enzyme pyrophosphatase, which drives cAMP synthesis to completion. However, cAMP is rapidly degraded to 5′ AMP by the enzymes phosphodiesterase (PDE), preventing overstimulation of...
5.6K


