Difference between revisions of "Team:UST Beijing/Background"
| Line 127: | Line 127: | ||
<div class="pad15"></div> | <div class="pad15"></div> | ||
<div class="row"> | <div class="row"> | ||
| − | <blockquote><p>Ginseng triterpenes' structure is similar to that of cholesterol, | + | <blockquote><p>Ginseng triterpenes' structure is similar to that of cholesterol, therefore it has the potential of regulating LXRs. |
| − | LXRs is a typical nuclear receptor. In the presence of co- | + | LXRs is a typical nuclear receptor. In the presence of co-regulators, bound by agonists (such as ginsenosides), LXRs could bind to specific site on target gene promoter region to activate transcription of the target gene. Ginsenosides or like could regulate the metabolism of cholesterol. </p></blockquote> |
| − | + | ||
| − | + | ||
| − | + | ||
</div> | </div> | ||
<div class="pad15"></div> | <div class="pad15"></div> | ||
Revision as of 02:56, 14 October 2018
Cholesterol
an essential component of membrane structure, but gradually accumulates in arteries of human body, which results in the number one killer mechanism of human life:
atherosclerosis
An alarming health threat: Atherosclerosis
Shown on the right are the cholesterol structure and pie charts of epidemic statistics of atherosclerosis-related mortality (black area: atherosclerosis-related death) in China
Pathology of Atheroscleosis
Artery atherosclerosis refers to arteries accumulated with cholesterol resulting in blockage of blood flow. Cholesterol is the main culprit of cardio-cerebrovascular disease. In heart it causes heart attack. In brain it causes blockage stroke.
Molecular Mechanism of Atherosclerosis Formation
Because of foam cell apoptosis, which is formed by macrophages overloading cholesterol, cholesterol is deposited on the inner wall of artery.
Nuclear receptor LXR as therapeutic target against atherosclerosis
Live X receptor(LXR) functions as a master regulation switch, which can accelerate the transport of cholesterol and prevent the formation of foam cells.
Ginseng triterpenes' structure is similar to that of cholesterol, therefore it has the potential of regulating LXRs. LXRs is a typical nuclear receptor. In the presence of co-regulators, bound by agonists (such as ginsenosides), LXRs could bind to specific site on target gene promoter region to activate transcription of the target gene. Ginsenosides or like could regulate the metabolism of cholesterol.
Ginsenoside TR1 modulates
LXR biological activity
