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21 Cards in this Set

  • Front
  • Back
How is nitrogen balanced in the body?
uptake by protein, lost in urine (mostly as urea, to a small extent by creatinine, uric acid, and ammonia)
What is obligatory nitrogen loss?
loss of nitrogen through amino acid catabolism, growing hair and nails, sloughing cells
How are amino acids produced?
digestion and hydrolysis of dietary protein, hydrolysis of body protein, de novo synthesis of non-essential amino acids
How are amino acids used?
body protein synthesis, gluconeogenesis, synthesis of other nitrogen containing compounds
What makes a protein a high-quality protein?
combination and quantity of essential amino acids, digestibility
What is protein digestibility?
the amount of nitrogen that was absorbed into the body relative to the amount of nitrogen that was consumed
What is biological value (BV)(of proteins)?
a scale to measure protein quality, measured as the amount of retained nitrogen as proportion of the amount of absorbed nitrogen, corrected by fecal loss of nitrogen (the lower the excreted nitrogen, the higher the BV)
What is the protein recommended dietary allowance for adults?
0.8 g per kg body weight per day
What is the average protein turnover in the human body and what factors affect this rate?
400g/day are degraded and replenished, rate depends on half life of protein, and tissue type, age, growth, disease
How are body proteins degraded (pathways)?
ubiquitin-proteasome pathway degrades short-lived proteins (very ATP dependent),
autophagy-lysosome pathway degrades most long-lived intracellular proteins (less energy consuming)
How are protein degradation pathways regulated?
low insulin levels activate pathways, starvation (lack of dietary amino acids) increases the rate of autophagy, limiting amino acids activate protein degradation, stress hormones lead to hypercatabolism
Which hormones contribute to hypercatabolism of body proteins?
stress hormones; cortisol, epinephrine
What is glutamine's role during severe stress?
acts as the preferred respiratory fuel for lymphocytes, hepatocytes, intestinal mucosal cells (it is a conditionally-essential amino acid)
What enzymes are responsible for dietary protein digestion and where are they found?
1st: pepsin - stomach
2nd: proteases - pancreas
3rd: aminopeptidases - brush border of enterocytes
How are pancreatic proteases activated?
enteropeptidase converts trypsinogen to trypsin, then trypsin activates additional trypsin, chymotrypsinogen, proelastase, procarboxypeptidase
How does pepsin become active?
HCl and other pepsin molecules convert pepsinogen to pepsin
What is celiac sprue?
immune mediated inflammation and damage of the mucosa in the small intestine, a result of ingestion of gluten, causes malabsorption, diarrhea, vomiting
How are free amino acids absorbed into the enterocyte?
Sodium dependent transporters
How are di- and tri- peptides absorbed into the enterocyte?
Hydrogen dependent transporters
What is Hartnup disease?
a defect in apical amino acid absorption (a defective transporter for neutral amino acids), usually involves tryptophan deficiency
What is Cystinuria?
defective membrane carrier for dibasic amino acids (cysteine, ornithine, arginine, lysine - COAL), these are usually excreted in urine