Lecture 7 - Carbohydrate, lipid and amino acid metabolism Flashcards

1
Q

What is the absorptive state

A

Energy comes from oxidizing nutrients that enter bloodstream from gut

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2
Q

What is the postabsorptive state

A

Nutrients mobilized from body’s stores (NOT starvation)

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3
Q

How many hours does it take for absorption after a meal for carnivores and omnivores?

A

4 hours

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4
Q

How long does it take for absorption in ruminants

A

Digestion/absorption more continuous

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5
Q

What is energy stored as

A

Glycogen and fat

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6
Q

The process of making glycogen is called..

A

Glycogenesis

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7
Q

What happens to aa in the liver

A

They are modified (created and broken down)

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8
Q

What amino acids can be synthesized by the body?

A

Non-essential amino acids

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9
Q

Amino acid composition of diet matters less in…

A

ruminants

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10
Q

What is converted to glucose in the liver

A

Galactose and fructose

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11
Q

What processes is the liver a key player in

A

Anabolic and catabolic

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12
Q

What happens to glucose in the liver

A

Phosphorylated in cell (accumulates until dephosphorylation). Glucose-6-phosphatase allows it to exit

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13
Q

Lack of glucose-6-phosphatase in dogs is…

A

Glycogen storage disease (hypoglycemia + mental depression)

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14
Q

What takes up glucose and converts it to triglycerides

A

Adipocytes

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15
Q

What % of liver mass does glycogen need to be for glycogenesis to stop

A

5%

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16
Q

What happens to excess glucose once we reach 5% liver mass

A

Converted to triglycerides, released as lipoproteins, taken up by adipose and mammary

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17
Q

What is equine polysaccharide storage myopathy

A

Genetic glycogen storage disease
Incurable but manageable (diet and exercise)

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18
Q

Two types of PSSM

A

Type 1: increase expression of glycogen synthase (GSY1), but not branching enzyme (glycogen with no branches harder to breakdown)
Type 2: Abnormal glycogen deposition without GSY1 or GBE1 mutation

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19
Q

Where are lipoproteins produced? What do they do

A

Liver
Transport triglycerides to rest of body

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20
Q

What are lipoproteins made of

A

Triglycerides, phospholipids, cholesterol, transport proteins, apolipoprotein

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21
Q

Role of apolipoprotein

A

Tell lipoprotein where to go, recognized by specific cell membrane receptors

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22
Q

Main enzyme of lipoproteins

A

Lipoprotein lipase

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23
Q

What happens to triglycerides after lipid degradation? Fa?

A

TG stored
Some fa used as energy source, most ffa diffuse into adipose, mammary and other cells (or converted back to TG)

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24
Q

What happens to chylomicron remnants after lipid degradation

A

Back to liver = liver enriched with cholesterol

25
How are ffa transported? Other lipids?
FFA = albumin Other = lipoproteins
26
Where are lipoproteins synthesized
Liver
27
What is VLDL? LDL? HDL?
VLDL = very low density lipoprotein LDL = low density lipoprotein HDL = high density lipoprotein
28
What are "bad cholesterol" what does it do
LDL and VLDL Transport cholesterol to cells (taken up by endocytosis)
29
What is "good cholesterol" what does it do
HDL Collects cholesterol from cells and transports to liver (then excreted as bile)
30
Slide 13
HDL, VLDL, LDL
31
What happens to aa in the liver
Used to make many things (e.g. albumin, fibrinogen, complement) Some converted to keto acids, converted to glucose and FAs Low glucose = used as cellular fuel
32
Deamination is when...
amino group is separated from organic acids
33
What part of the aa is used as an energy source
organic acids
34
How do liver cells replenish glycogen stores
Glucose and aa's
35
What does the liver do with lipids
Exports them around the body
36
Slide 18***
CHO, lipid and aa metabolism
37
What is glycogenolysis
If glucose concentrations fall below a certain level, liver mobilizes glycogen reserves
38
Why can't skeletal muscle release glucose in to the blood
Lack glucose-6-phosphate (needed to dephosphorylate and release glucose from cell)
39
What does skeletal muscle do to get glucose out
Produce pyruvate and lactate
40
What is gluconeogenesis? What organs are involves? What are the sources?
Making glucose from non-carbohydrate sources Liver and kidney Pyruvate from aa breakdown, lactate and glycerol
41
Precursor of glucose
Propionic acid
42
What is the cori cycle
Lactate produced in muscle cells is converted to glucose in the liver and can return to muscle cells
43
Slide 21
Cori cycle
44
What is utilized as the main energy source in a postabsorptive state? Referred to as..
Lipids (glucose sparing) TGs broken down, FA diffuse in blood, taken up by tissues, oxidized to make energy
45
Insulin is secreted by __________ in response to _________________
Beta cells High blood glucose
46
What does insulin do (4)
Increase uptake of glucose in the cells of organs Stimulates synthesis of glycogen, inhibits degradation Increases consumption of glucose for ATP production Inhibits gluconeogenesis
47
Glucagon is secreted by _____________ in response to ____________________
Alpha cells Low blood glucose
48
What does glucagon do
Stimulates glycogenolysis in the liver Stimulates gluconeogenesis in the liver Stimulates lipolysis in adipose
49
Keys to regulating blood glucose levels
Insulin and glucagon
50
Slide 26**
Insulin and glucagon and proteins/aa
51
What is lipolysis
Lysing lipoproteins
52
Slide 27**
Glucagon effects
53
___________________ causes mobilization of glucose from glycogen
Epinephrine
54
What is fatty liver
Occurs when excessive fa mobilization occurs, or impaired ability to export it via apolipoproteins (VLDL packaging low) Excessive mobilization from adipose
55
Severe fatty liver can...
impair liver function
56
Fatty liver most common in
Early lactation dairy cows Late gestation beef cattle
57
Slide 30, 31**
Glucose metabolism
58
What does hormone sensitive lipase do
Break down TG into ffa and glycerol