FORM & FUNCTION (Starvation 2) Flashcards
Late (severe) phase of starvation:
-begins once fatty acid, ketones deplete
*utilize proteins
Protein utilization:
-from tissues are broken down to provide AA
-AA to alpha-keto acids
>gluconeogenesis
>ketogenesis
>NOT lipogenesis
Body protein depletion order:
- Digestive enzymes (stomach, pancreas, small intestine)
- Liver enzymes that process incoming nutrients form the intestine (ex. bile acid formation)
- Muscle
Muscle:
-body’s largest supply of protein
-animal becomes inactive (breakdown of contractile fibers)
Ubiquitin-proteasome system:
- Protein substance is tagged with ubiquitin (requires ATP)
- Proteasome recognizes the protein+ubiquitin and starts breaking down the quaternary protein
- Polypeptides are further broken down by proteases into AA
AA catabolism overview:
-60% of AA released will be alanine and glutamine
-AA to alpha-keto acid + glutamate
>alpha-keto A to Alanine (then to pyruvate)
>glutamate to Alanine or glutamine
Alanine and glutamine:
-alanine goes to liver: gluconeogenesis and get urea (nitrogenous waste)
-glutamine goes to kidney: gluconeogenesis and get ammonium (nitrogenous waste)
*mechanism to generate glucose and to remove nitrogen waste
AA deamination results in:
-high levels of glutamate
-muscle sacrifices pyruvate to recycle these into alanine (sent to liver)
-pyruvate + glutamate=alanine and alpha-ketoglutarate
Additional glutamate:
-converted to glutamine and exported to kidney
>NH3+ added with ATP
Alanine processing:
-transported to liver for gluconeogenesis
- high levels of alanine aminotransferase (ALT) in the liver
>alanine to pyruvate: by-product of NH3+ goes to urea cycle
Urea cycle:
-primary site is in the liver
-a process to remove toxic nitrogen buildup
Glutamate processing:
-glutamine is transported to the kidney to support gluconeogenesis
-glutaminase activity is high in the kidney (glutamine to glutamate)
-most NH4+ is excreted in urine/filtrate, even though kidney can perform the urea cycle
Late starvation summary:
-fat store depletion
-increase gluconeogenesis
-increase muscle wasting/proteolysis
-compromised liver function
Complications of late starvation:
-edema
-shock
-coma
Role of liver:
-gets AA
1. gluconeogenesis (to brain, RBC)
2. Ketones (to extrahepatic tissues)
3. Protein synthesis (to plasma proteins)
*these processes compete for AA
*maintaining glucose and ketones production hinders protein synthesis