Lipids and amino acids Flashcards

(44 cards)

1
Q

Why are amino acids which arent used as building blockd degraded?

A

No storage for amino acids

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2
Q

Where is the major site for amino acid degradation?

A

Liver

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3
Q

Where is proteolytic enzymes absorbed and released? What do they produce?

A

Absorbed into intestinal cells and released into blood for absorption by other tissues

Produce- single smino acids, di/tri peptides

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4
Q

What happens in a protein turnover?

A

Tightly regulated
Takes place at different rates
Damaged proteins have to be removed

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5
Q

Some amino acids also contain nitrogen in the side chain which can be toxic when built up. Is ammonia or ammonium the toxic part?

A

Ammonium

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6
Q

After removal of the a-amino group the remaining carbon skeletons are converted into major metabolic intermediates. What can these be converted into?

A

Glucose or oxidised in the TCA cycle

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7
Q

What are ketogenic amino acids degraded into?

A
  • Degraded to acetyl-CoA or acetoacetyl-CoA

- Can give rise to ketpne bodies or fatty acids

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8
Q

What are glycogenic amino acids degraded to?

A
  • Degraded to pyruvate or TCA cycle intermediates

- Can be converted into phosphoenolpyruvate and then into glucose

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9
Q

What happens to amino acids in Alcaptonuria disorder?

A

Degradation of phenylalanine and tyrosine is blocked

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10
Q

What happens to amino acids in maple syrup urine disease?

What are the affects of the disease?

A

Degradation of valine, isoleucine, and leucine is blocked

Urine smells like maple syrup
Mental and physical retardation
Prevented by appropriate diet

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11
Q

What happens to amino acids in phenylketonuria disorder? How can it be treated?

A
  • Phenylaline accumulates in all body fluids
  • Leads to severe mental retardation if untreated

Therapy- Low phenylaline diet

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12
Q

What does an increased fat intake wihtout appropriate energy expenditure lead to?

A
  • Increase in number of adipocytes
  • More fat in adipocytes
  • Obesity
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13
Q

What does control of energy balance depend on?

A

-Genetically linked factors
(protein messengers regulating appetite)
-Environmental factors
(food abundance, fashionable foods)

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14
Q

How is BMI calculated?

A

weight/(height)^2

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15
Q
What is an:
Overweight (grade I obesity)
Clinical (grade II obesity)
Morbid (grade III obesity)
BMI number
A

Overweight 25-30kg/m2
Clinical >30kg/m2
Morbid >40kg/m2

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16
Q

What is diabetes mellitus associated with?

A

Obesity

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17
Q

List medical complications associated with obesity?

A
Coronary heart disease
Hypertension
Stroke
Arthritis
Gall bladder disease
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18
Q

What polyunsaturated fatty acids can not be made by the body?

A

Linoleic acid, Linolenic acid, arachidonic acid

19
Q

What are some fat soluble lipids?

A

Vitamins- A, D, E, K

20
Q
  • Main energy source in adipose tissue
  • Comapact (dont require concomitant storage of water)
  • Hydrophoic
  • High energy yield per gram

What is this?

A

Triglycerides

21
Q

What does aliphatic mean?

A

No ring structure

22
Q

What are the main products of fat digestion?

A

Glycerol
Fatty acids
Monoglycerides

23
Q

Where do short and medium length fatty acids enter?

24
Q

Where do longer chain FAs and monoglycerides go?

A

Re-synthesised to triglycerides

25
What are coated with a layer of protein, phospholipid and cholestoral
Chylomicrons
26
Where do chylomicrons enter the body?
Lymph, then the blood stream
27
At muscle and adipose tissue what happens to chylomicrons?
Attacked and cleaved by lipoprotein lipases
28
What happens to free fatty acids?
- Resynthesised into triacylglycerols | - Oxidised to provide energy in muscle
29
What is lipolysis?
Breakdown of lipids
30
In lipolysis of stored fat what happens in the initial cleavage by hormone sensitive lipase?
Releases free fatty acids and glycerol, occurs when energy is released
31
What must happen before fatty acids can be oxidised to generate energy? Where does it occur
They have to be converted to CoA derivatives In the cytoplasm
32
Where does further oxidation of fatty acids occur? How does this happen
In the mitochondrial matrix Special carrier mechanism- The carnitine shuttle
33
What happens during the carnitine shuttle?
Fatty acids are transferred from acyl-CoA to carnitine The machanism facilitates antipode of acyl-carnitine into the mitochondrion and carnitine out
34
Where is the acyl-carnitine transporter located?
Inner membrane
35
What is the net result of the carnitine shuttle?
acyl-CoA located in the mitochondriol matrix
36
Where does beta oxidation take place | How many steps in this cycle?
Mitochondrial matrix | Four steps
37
What are the products of the B oxidation cycle?
1 acetyl CoA 1 FADH2 1 NADH + H+ 1 fatty acyl-CoA, shortened by 2 carbon atoms
38
How many times doe sthe b oxidation cycle occur?
8 times
39
What happens during the breakdown of glycerol?
Activated by glycerol-3-phosphate by glycerol kinase Dehydrogenated to dihydroxyacetone phosphate
40
What is the other name for fatty acid synthesis?
Lipogenesis
41
Where does de novo synthesis of fatty acids mainly occur?
Liver, kidney, mammary glands, adipose tissue and brain
42
What kind of process is lipogenesis?
Reductive
43
What is the translation of post prandial?
After food
44
What happens during the prolonged period of fasting?
Glycogen depleted, utilisation of other energy sources