Humans have two sources of cholesterol: absorption from ingested food and de novo synthesis by the liver. High levels of cholesterol in the blood correlates with cardiovascular disease, but cholesterol is required to regulate membrane fluidity and is a precursor for important molecules like steroids and bile acids. Thus, humans evolved several types of regulation of cholesterol levels. How does the human body compensate for excess consumption of cholesterol in the diet? Transcription of the HMG-CoA reductase gene decreases in the presence of high intracellular cholesterol. Eating a cholesterol-rich meal causes the hypothalamus, the hunger center of the brain, to signal satiety. High cholesterol concentrations upregulate the number of serum transport proteins that deliver cholesterol to the liver for degradation.

Concepts of Biology
1st Edition
ISBN:9781938168116
Author:Samantha Fowler, Rebecca Roush, James Wise
Publisher:Samantha Fowler, Rebecca Roush, James Wise
Chapter9: Molecular Biology
Section: Chapter Questions
Problem 10RQ: Control of gene expression in eukaryotic cells occurs at which level(s)? a. only the transcriptional...
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Humans have two sources of cholesterol: absorption from ingested food and de novo synthesis by the liver. High levels of
cholesterol in the blood correlates with cardiovascular disease, but cholesterol is required to regulate membrane fluidity and is a
precursor for important molecules like steroids and bile acids. Thus, humans evolved several types of regulation of
cholesterol levels.
How does the human body compensate for excess consumption of cholesterol in the diet?
Transcription of the HMG-CoA reductase gene decreases in the presence of high intracellular cholesterol.
Eating a cholesterol-rich meal causes the hypothalamus, the hunger center of the brain, to signal satiety.
High cholesterol concentrations upregulate the number of serum transport proteins that deliver cholesterol to the liver
for degradation.
Excess cholesterol and a lack of ATP inhibit the activity of HMG-CoA reductase in the liver to decrease
cholesterol synthesis.
Adipose cells switch to using cholesterol instead of glucose to produce ATP.
Transcribed Image Text:Humans have two sources of cholesterol: absorption from ingested food and de novo synthesis by the liver. High levels of cholesterol in the blood correlates with cardiovascular disease, but cholesterol is required to regulate membrane fluidity and is a precursor for important molecules like steroids and bile acids. Thus, humans evolved several types of regulation of cholesterol levels. How does the human body compensate for excess consumption of cholesterol in the diet? Transcription of the HMG-CoA reductase gene decreases in the presence of high intracellular cholesterol. Eating a cholesterol-rich meal causes the hypothalamus, the hunger center of the brain, to signal satiety. High cholesterol concentrations upregulate the number of serum transport proteins that deliver cholesterol to the liver for degradation. Excess cholesterol and a lack of ATP inhibit the activity of HMG-CoA reductase in the liver to decrease cholesterol synthesis. Adipose cells switch to using cholesterol instead of glucose to produce ATP.
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