Ch 11 - Lipid and Amino Acid Metabolism Flashcards

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1
Q

Where does mechanical digestion of lipids occur?

A

primarily in the mouth and stomach

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2
Q

Where does chemical digestion of lipids occur and what is it facilitated by?

A

the small intestines

- facilitated by bile, pancreatic lipase, colipase, and cholesterol esterase

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3
Q

Why do digested lipids form micelles?

A

for absorption or to be absorbed directly

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4
Q

Where are short chain fatty acids absorbed?

A

across the intestine into the blood

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5
Q

Where are long chain fatty acids absorbed?

A

as micelles and assembled into chylomicrons for release into the lymphatic system

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6
Q

How are lipids mobilized from adipocytes? from lipoproteins?

A
  • hormone sensitive lipase

- lipoprotein lipase

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7
Q

What are chylomicrons and how are they transported?

A

the transport mechanism for dietary triacylglycerol molecules and are transported via the lymphatic system

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8
Q

What do VLDL do?

A

transports newly synthesized triacylglycerol molecules from the liver to peripheral tissues in the bloodstream

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9
Q

What is IDL?

A
  • a VLDL remnant in transition between triacylglycerol and cholesterol transport
  • picks up cholesteryl esters from HDL
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10
Q

What does LDL transport?

A

primarily cholesterol for use by tissues

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11
Q

What is HDL involved in?

A

involved in the reverse transport of cholesterol

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12
Q

What do apoproteins control?

A

interactions between lipoproteins

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13
Q

How is cholesterol obtained?

A

through dietary sources or through de novo synthesis in the liver

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14
Q

What is the key enzyme in cholesterol biosynthesis?

A

HMG-CoA reductase

- inhibition of this enzyme lowers production of cholesterol

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15
Q

What does LCAT catalyze?

A

the formation of cholesteryl esters for transport with HDL

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16
Q

What does CETP catalyze?

A

the transition of IDL to LDL by transferring cholesteryl esters from HDL

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17
Q

What are fatty acids?

A

carboxylic acids, typically with a single long chain, although they can be branched

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18
Q

What is the difference between saturated and unsaturated fatty acids?

A
  • saturated have no double bonds between carbons

- unsaturated have one or more double bonds

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19
Q

Where are fatty acids synthesized?

A

in the cytoplasm from acetyl-CoA transported out of the mitochondria

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20
Q

What are the 5 steps of fatty acid synthesis?

A
  • activation (attach to acyl carrier protein), bond formation, reduction (of carbonyl group), dehydration, and a second reduction (of double bond)
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21
Q

What is the only fatty acid that humans can synthesize and how is it synthesized?

A

palmitic acid, formed after 8 repeats of synthesis

  • fully saturated, so with no double bonds
  • ha 16 carbons and is synthesized from 8 molecules of acetyl-CoA (16:0)
22
Q

Where does fatty acid oxidation occur?

A

in the mitochondria following transport by the carnitine shuttle

23
Q

What are the steps of beta oxidation?

A

occurs in mitochondria

  • oxidation of the FA to form a double bond
  • hydration of the double bond to form a hydroxyl group
  • oxidation of the hydroxyl group to form a carbonyl (beta-ketoacid)
  • cleavage of the beta-ketoacid into a shorter acyl-CoA and acetyl-CoA
24
Q

How does beta oxidation of unsaturated fatty acids differ from that of saturated fatty acids?

A

an additional isomerase and an additional reductase for unsaturated that provides the stereochemistry needed for further oxidation

25
Q

When do ketone bodies (ketogenesis) form?

A

during a prolonged starvation state due to excess acetyl-CoA in the liver

26
Q

What does ketolysis do?

A

regenerates acetyl-CoA for use as an energy source in peripheral tissues

27
Q

Where does the brain derive its energy from during prolonged starvation?

A

can derive up to 2/3rds of its energy from ketone bodies

28
Q

Where does protein digestion occur?

A

primarily in small intestines

29
Q

When does catabolism of cellular proteins occur?

A

only under conditions of starvation

30
Q

What are carbon skeletons of amino acids used for in protein catabolism?

A
  • energy, either through gluconeogenesis or ketone body formation
  • amino groups are fed into the urea cycle for excretion
  • the fate of a side chain depends on its chemistry
31
Q

When lipids leave the stomach, what stages of digestion have been accomplished? What enzymes are added to accomplish the next phase?

A
  • physical digestion is accomplished in the mouth and the stomach, reducing the particle size
  • beginning in the small intestine, pancreatic lipase, colipase, cholesterol esterase, and bile assist in the chemical digestion of lipids
  • in the more distal portion of the small intestine, absorption occurs
32
Q

Do all lipids enter the circulation through the lymphatic system?

A

No, small free fatty acids enter the circulation directly

33
Q

Describe the structure of a micelle.

A
  • micelles are collections of lipids with their hydrophobic ends oriented toward the center and their charged ends oriented towards the aqueous environment
  • micelles collect lipids within their hydrophobic centers
34
Q

What is the expected impact on a patient’s weight when started on insulin injections for management of blood glucose levels?

A

an increase in insulin levels will increase lipid storage and decrease lipid mobilization from adipocytes, leading to weight gain in diabetic patients who being insulin injections

35
Q

What is the ratio of free fatty acids to glycerol produced through lipid mobilization?

A

3:1, a triacylglycerol molecule is composed of glycerol and 3 FA

36
Q

What is the primary method of transporting free fatty acids into the blood?

A

free fatty acids remain in the blood, bonded to albumin and other carrier proteins
- a much smaller amount will remain unbonded

37
Q

Order the lipoproteins from greater percentage of protein to lease percentage of protein. Which are primarily involved in triacylglycerol transport?

A

HDL > LDL > IDL > VLDL > chylomicrons

  • VLDL and chylomicrons are the primary triacylglycerol transporters
  • HDL and LDL are mostly involved in cholesterol transport
38
Q

Lipoproteins are synthesized primarily by which 2 organs?

A

intestine and liver

39
Q

When physicians order a lipid panel to evaluate a patient, which value do they prefer to see over minimum threshold rather than below a maximum?

A

HDL is often considered the “good” cholesterol because it picks up excess cholesterol from blood vessels for excretion, so its values are checked for being over a minimum value

40
Q

Under what conditions is HMG-CoA reductase most active? In what cellular region does it exist?

A
  • HMG-CoA reductase is most active in the absence of cholesterol and when stimulated by insulin
  • cholesterol reduces the activity of HMG-CoA reductase, which is localized in the smooth endoplasmic reticulum
41
Q

What proteins are specific to the formation and transmission of cholesteryl esters and what are their functions?

A

LCAT catalyzes the esterification of cholesterol to form cholesteryl esters
- CETP promotes the transfer of cholesteryl esters from HDL to IDL, forming LDL

42
Q

How does fatty acid synthesis compare to beta oxidation?

A
  • they are reverse processes
  • both involve transport across the mitochondrial membrane, followed by a series of redox reactions, but always in the opposite direction of one another
43
Q

Where are fatty acids synthesized and how are they modified?

A
  • synthesized in the cytoplasm

- modified by enzymes in the smooth endoplasmic reticulum

44
Q

Why are fatty acids used to create ketone bodies instead of creating glucose?

A
  • fatty acid degradation results in large amounts of acetyl-CoA, which cannot enter the gluconeogenic pathway to produce glucose
  • only odd-numbered fatty acids can act as a source of carbon for gluconeogenesis; even then, only the final malonyl-CoA molecule can be used
  • energy is packaged into ketone bodies for consumption by the brain and muslces
45
Q

What conditions and tissues favor ketogenesis? ketolysis?

A
  • ketogenesis is favored by a prolonged fast and occurs in the liver; stimulated by increasing concentrations of acetyl-CoA
  • ketolysis favored during prolonged fast, but is stimulated by low energy state in muscle and brain tissues and does not occur in the liver
46
Q

Are bodily proteins commonly broken down to provide acetyl-CoA for lipid synthesis?

A

No, proteins are more valuable to the cell than lipids, thus they will not commonly be broken down for lipid synthesis

47
Q

Where does the bulk of protein digestion occur?

A

small intestine

48
Q

During protein processing, what is the eventual fate the carbon skeleton, amino group, and side chains?

A
  • carbon skeleton is transported to the liver for processing into glucose or ketone bodies
  • amino group will feed into the urea cycle for excretion
  • side chains are processed depending on their composition (basic side chains will be processed like amino groups, while other functional groups will be treated like the carbon skeleton)
49
Q

What happens during fatty acid mobilization?

A
  • there is a breakdown of triacylglycerols in adipocytes by hormone-sensitive lipase (HSL)
  • this breakdown results in the release of 3 FA and a glycerol molecule
  • the glycerol may be used by the liver for gluconeogenesis, but adipocytes do not have the ability to carry out gluconeogenesis
50
Q

Where does the majority of triacylglycerols stored in adipocytes originate from?

A

synthesis in liver

  • the liver is the major metabolic organ in the body and is responsible for much of the synthesis and interconversion of fuel sources
  • most triacylglycerols that are synthesized in the liver are transported as VLDL to adipose tissue for storage