Biochemistry Flashcards

(93 cards)

1
Q

Water soluble vitamins

A

B complex and C

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2
Q

Lipid soluble vitamins

A

A, D, E and K

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3
Q

B1 (Thiamine)

A

Def causes BeriBeri (Increased pyruvate conc)

  • Weakness
  • Memory Loss
  • Neuritis
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4
Q

B2 (Riboflavin)

A

FAD (Active form)

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5
Q

B3 (Niacin)

A

NAD (Active form)
Converts lactate to pyruvate using LDH
Def causes pellagra (Dementia, Diarrhea and Dermatitis)

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6
Q

B6 (Pyridoxine)

A

Causes decarboxylation of :

  1. Glutamate -> GABA
  2. Histidine -> Histamine
  3. Tryptophan -> Serotonin
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7
Q

Vit C (Ascorbic Acid)

A
Def = Scurvy 
* Gingavitis 
* Ptechial hemorrhage 
* Bleeding gums 
Causes hydroxylation of lysine and proline 
Helps with collagen formation
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8
Q

Vit A ( Retinol)

A
Cis = night blindness 
Trans = regeneration of epithelial tissue
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9
Q

Vit D3 (Calciferol)

A

Active form = calcitriol

Def = Rickets (children) / Osteomalacia (adults)

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10
Q

Vit E (Alpha Tocopherol)

A

Strongest antioxidant = protects from cancers etc

Given to pregnant women

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11
Q

Vit K (Menaquionone)

A

Activates/carboxylates coagulation factors
Def = Hemorrhage
Carboxylates glutamic acid

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12
Q

Methotrexate

A

Inhibits dihydrofolate reductase (THF isnt produced and cell division stops)
Used to treat leukemia

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13
Q

B9 in bacteria

A

Decrease under treatment with sulphonamides (Inhibits PABA)

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14
Q

Cause of pernicious anemia

A

Decrease of intrinsic factors

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15
Q

Lysosyloxidase deficiency causes?

A

Collagen destruction

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16
Q

Antioxidant vitamins

A

E, C and A

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17
Q

Vikasol treats?

A

Vit K deficiencies

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18
Q

Liver failure due to ?

A

1,25 dihydroxycholecalciferol deficiency

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19
Q

Alanine

A

Alanine -> Pyruvate (E= Alanine amino transferase)

Transports ammonia to the liver

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20
Q

Tyrosine deficiency?

A
  1. Parkinsons (decreased dopamine)
  2. Depression (decreased dop/epi/nor)
  3. Alkaptonuria (abnormal catabolism of tyrosine)
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21
Q

Dopamine synthesis occurs where?

A

Substantia nigra

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22
Q

What causes an increase of AST/ ALT?

A

Liver pathologies (e.g. Hepatitis)
Starvation (ALT increases)
MI (AST increases)

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23
Q

Malabsorption of tryptophan

A

Hartnap disease

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24
Q

Tryptophan

A

Deficiency = Pellegra
* Vit B6 converts tryptophan to B3 and serotonin
Increases serotonin

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25
Erythropoietic porphyria
Incr/Decr of uroporphyrinogen 1
26
Cardiac arrhythmia
Hypokalemia
27
Hepatic cirrhosis
Increase hippuric acid in urine
28
What does MOA (Monoamine Oxidase) inhibit ?
Serotonin and noradrenaline
29
Presence of hydroxyproline/hydroxylysine
Collagenosis
30
Deficiency of phenyalanine?
Albinism | * Phenyalanine -> tyrosine -> melanin
31
Where is citrullenne found?
Ornithinic cycle
32
Carnitine
Transports FA from cytosol to mitochondria
33
Phenylketonuria
Olive green urine
34
Glycated hemoglobin
Allows to estimate glycemia rate
35
Presence of ketone bodies
Metabolic acidosis
36
Where is carbon labelled glucose found?
Palmitic Acid
37
Kalikine
Protein inhibited by contrical
38
Dark yellow feces
Unconjugated bilirubin (Jaundice)
39
Colorless feces
Conjugated bilirubin (Jaundice)
40
Cushings syndrome
Increase gluconeogenesis
41
Timaline
Given for bronchopenumonia
42
Creatine vs creatinine ?
Creatine in urine = Muscle dystrophy | Creatinine in urine = Kidney pathology (K for Kidneys - Kreatinine in krok)
43
Hyperlipoproteinanemia Type 11a
Increased LDL
44
Bile acid deficiency
Steatorrhoea
45
Glycogenosis
Glycogen phosphorylase deficiency
46
Insulin
Activates glycogen synthesis | Deactivates glycogen phosphorylase
47
Haemolytic anemia
Due to G6P dehydrogenase deficiency
48
Xanthine oxidase deficiency
Increased accumulation of xanthine and hypoxanthine
49
Isomers
Same function but different function (catalyze the same reactions)
50
Aldosteronism
Affects adrenal glands
51
Endonuclease
Restores native DNA structure in cells
52
MI
Increased LDH, AST and creatine phosphokinase
53
Cataract
Glycosylation of eye proteins
54
Pagets disease
Destroys collagen | * Increased oxyproline in urine
55
Glycolysis
Causes lactate accumulation in muscles
56
Disturbed purine metabolism
Increased urate conc
57
Glutamic acid
Detoxifies NH4 in brain tissue
58
Cyanide
Affects cytochrome oxidase in mitochondria
59
CRP (C Reactive Protein) in blood
Rheumatism
60
Ceruloplasmin
Carries Copper (E.g. Wilsons Disease)
61
Bence Jones Proteins
Myeloma | aka paraproteins
62
Infiltration of fat steatosis
Loss of phosphatidylcholine
63
Calcitonin
Stimulates tooth mineralization
64
Vit D, E, K
Affected by gallbladder removal / bile reduction
65
Trans retoinic acid
Penetrates nuclear membrane
66
Lysyl oxidase
Causes collagen issues
67
Gastromucoprotein
Absorbs Vit B12
68
Isoniazid
Affects VitB3 (NAD) and B6
69
Choline
Causes fatty liver infiltration
70
Purines
Increase uric acid
71
Valine, Leucine, Isoleucine
BCAAs | Maple syrup disease
72
Perioxidase
Breaks down H2O2
73
Tyrosine deficiency
Increased homogenistic acid formation
74
LDH1,2 LDH3 LDH4 LDH5
Heart damage Lung damage Kidney damage Liver/smooth muscle damage
75
S.Sonne
Dysentry
76
Precursors for POMC
Lipotropin,corticotropin etc
77
Cyanide
Affects cytochrome oxidase (aa3)
78
No mitochondria
Anaerobic glycolysis
79
No ATP synthesis
Membrane rest potential disappears
80
Atopy
Asthmatic attack
81
Hepatic steatosis
Disrupts phosphatidylcholine
82
Protein starvation
Decreased albumins
83
Lysyl oxidase
Issues with collagen
84
Streptokinase
Induces platelet lysis
85
Chronic alcoholism
Thiamine deficiency
86
Deficiency of B9/B12
Megaloblastic anemia | Atrophy of tongue
87
Absent glycogene phosphorylase in liver
Causes low glucose in blood stream
88
Co enzyme A
Derived from pantothenic acid
89
Cortisol
Glucocorticoid
90
Niemann-Pick disease
Sphingomyelinase deficiency
91
Von Gierke's Disease
Absence of G6P,hypoglycemia, and hepatomegaly.
92
Bromide poisoning
Use NaCl
93
Alkaptonuria
Black urine