Proteins Metabolism Flashcards

(37 cards)

1
Q

Kwashiorkor

A

Protein deficiency but adequate calories

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2
Q

Famine edema

A

Inadequate synthesis of plasma proteins, mostly albumin, so fluid escape into tissues

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3
Q

Marasmus

A

Protein energy malnutrition
Protein calorie deficiency
Starvation

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4
Q

Protein malnutrition causes in developed countries

A
Prégnant and lactating mothers 
Eating disorders 
Alcoholism 
Drug addicts 
Hospital patients 
Elderly and chronically ill
Genetic disorders
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5
Q

Essential amino acids

A

Mnemonic PVT TIM HALL

Arg
His
Île
Leu
Lys
Met
Phy
Thr
Trp 
Val
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6
Q

Non essential amino acids

A
Ala
Asn 
Asp
Cys 
Glu 
Gln 
Gly 
Pro 
Ser 
Tyr
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7
Q

Amino acids requirements

A

No significant storage

Depends on age sex and activity

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8
Q

2 fates of amino acids degradation

A

Amino acids can produce NH4 or carbon skeleton

NH4 can

  • enter biosynthesis of AA, nucleotides, amines
  • enter urea cycle

Carbon skeleton become a-ketoacids which can enter citric acid cycle —> OAA can be formed and undergo gluconeogenesis

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9
Q

What is glycogenic AA

A

Product of AA degradation can enter gluconeogenesis

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10
Q

Ketogenic AA degradation

A

Ketogenic AA degradation products are intermediates of lipid metabolism or ketone bodies

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11
Q

AA purely ketogenic

A

Leucine

Lysine

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12
Q

AA both ketogenic and glucogenic

A

Isoleucine
Phenylalanine
Tyrosine
Tryptophan

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13
Q

Products of glucogenic AA breakdown

A
Pyruvate 
a-ketoglutarate
Succinyl coa 
Fumarate 
OAA
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14
Q

Products of ketogenic AA breakdown

A

Acetyl coa

Acetoacetate

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15
Q

Healthy adult nitrogen balance

A

Excretion of nitrogen equals intake

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16
Q

4 majors reaction of AA

A

Transamination

Oxidative deamination

Decarboxylation

Transdeamination

17
Q

Transamination

A

Transfer of NH2 to form another AA

18
Q

Enzyme in transamination

A

Transaminase

AA1+ aketoacid 2<===> aketoacid1+ AA 2

19
Q

Transaminase cofactor

A

Pyridoxal phosphate derived from vit b6

20
Q

Major AA In AA metabolism

A

aketoglutarate
Gln
Glutamate

21
Q

Most abundant AA serving as neural transport and storage form of ammonia

22
Q

Glutamate dehydrogenase action

A

Glutamate + NADP+ H2O <==> aketoglutarate+ NADPH + NH4+

23
Q

Glutamine synthétase action

A

Glutamate + ATP + NH4+ —-> glutamine + ADP + pi

24
Q

Glutaminase action

A

Glutamine —-> glutamate

25
Amino Acid oxidase
Amino acid + FAD + H2O —-> aketo acid +NH3 + FADH2 FADH2 + O2 —-catalase—> FAD + H2O2
26
Decarboxylation
CO2 removed from glutamate to form GABA
27
Transdeamination
Coupling of aminotransferase with glutamate dehydrogenase Lead to formation of pyruvate
28
Tryptophan metabolized to
Alanine Acetyl coa CO2 Formate Small amount to serotonin , niacin, melatonin
29
AA precursors of
Protein synthesis Active metabolites Metabolic fuels
30
Serotonin
Neurotransmitter which impacts behavior such as appetite , aggression, sleep, sensory perception, depression Potent vasoconstrictir of Blood vessels’ Helps in circadian cycle
31
Antidepressants that inhibits serotonin reuptake
Paxil Prozac Zoloft
32
...... is a structural agonist that potential es effect of serotonin
LSD
33
Hartnups disease
Defect in transportation or absorption of AA in intestines Defect in reabsorption un renal tubules of kidney High urine concentration of essential amino acids Symptoms : Hereditary pellagra like skin rash Cerebellar ataxia temporary Constant renal amino aciduria 3 D Dermatitis Dementia (20%) Diarrhea
34
Direct source of ammonia in liver
Glutamate Glutamine ( from other tissues) Alanine ( from muscles )
35
Major contributor to waste nitrogen
Muscle
36
Nitrogen waste products
Urea in vertebrates Uric acid in birds and reptiles
37
Carbamoyl phosphate synthesis and entry into urea cycle
HCO3- + NH4+ gives carbamoyl phosphate