FORM & FUNCTION (Starvation 2) Flashcards

1
Q

Late (severe) phase of starvation:

A

-begins once fatty acid, ketones deplete
*utilize proteins

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2
Q

Protein utilization:

A

-from tissues are broken down to provide AA
-AA to alpha-keto acids
>gluconeogenesis
>ketogenesis
>NOT lipogenesis

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3
Q

Body protein depletion order:

A
  1. Digestive enzymes (stomach, pancreas, small intestine)
  2. Liver enzymes that process incoming nutrients form the intestine (ex. bile acid formation)
  3. Muscle
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4
Q

Muscle:

A

-body’s largest supply of protein
-animal becomes inactive (breakdown of contractile fibers)

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5
Q

Ubiquitin-proteasome system:

A
  1. Protein substance is tagged with ubiquitin (requires ATP)
  2. Proteasome recognizes the protein+ubiquitin and starts breaking down the quaternary protein
  3. Polypeptides are further broken down by proteases into AA
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6
Q

AA catabolism overview:

A

-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

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7
Q

Alanine and glutamine:

A

-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

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8
Q

AA deamination results in:

A

-high levels of glutamate
-muscle sacrifices pyruvate to recycle these into alanine (sent to liver)
-pyruvate + glutamate=alanine and alpha-ketoglutarate

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9
Q

Additional glutamate:

A

-converted to glutamine and exported to kidney
>NH3+ added with ATP

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10
Q

Alanine processing:

A

-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

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11
Q

Urea cycle:

A

-primary site is in the liver
-a process to remove toxic nitrogen buildup

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12
Q

Glutamate processing:

A

-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

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13
Q

Late starvation summary:

A

-fat store depletion
-increase gluconeogenesis
-increase muscle wasting/proteolysis
-compromised liver function

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14
Q

Complications of late starvation:

A

-edema
-shock
-coma

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15
Q

Role of liver:

A

-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

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16
Q

Serum albumin (protein);

A

-plasma protein is 60% serum albumin
-transports protein and fatty acid
-maintain plasma colloid osmotic pressure

17
Q

Hydrostatic pressure;

A

-pushes out of vessel

18
Q

Osmotic pressure:

A

-pulls in

19
Q

Starvation compromised liver function:

A

-decrease serum albumin (decrease FFA transport)
-decrease osmotic pressure (hydrostatic pressure is greater and pushes liquid out of vessel)
-increase plasma fluid LOSS

20
Q

Physiological consequences of decreased serum albumin:

A

-plasma fluid enters interstitial space (edema)
OR
-abdominal cavity (ascites)
*leads to blood volume depletion (hypovolemia) and impairs O2 delivery to organs
*then results in shock or coma leading to death

21
Q

Risk of pneumonia:

A

-immune system compromised
-protein degradation can lead to loss of myofibrillar proteins in muscles that function in respiration

22
Q

Muscles that function in respiration:

A

-diaphragm and integral costal (inspiration)
-abdominal and external muscles (power force expiration, ex. coughing)

23
Q

Unable to cough:

A

-leads to increase risk of lunch and bronchioles infection
*high risk of infection leads to respiratory failure