Nutrition Flashcards

1
Q

Thiamine is

A

B1

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2
Q

Riboflavin is

A

B2

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3
Q

Niacin is

A

B3

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4
Q

Pantothenic acid is

A

B5

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5
Q

Pyridoxine is

A

B6

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6
Q

Biotin is

A

B7

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7
Q

Folate is

A

B9

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8
Q

Cobalamin is

A

B12

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9
Q

Ascorbic acid is

A

Vitamin C

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10
Q

Retinol is

A

Vitamin A

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11
Q

Tocopherol/tocotrienol is

A

Vitamin E

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12
Q

Phytomenadione/phylloquinone/phytonadione is

A

Vitamin K

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13
Q

Vitamin used in measles

A

Vitamin A

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14
Q

Vitamin used in AML subtype M3

A

Vitamin A

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15
Q

Prevents squamous metaplasia

A

Vitamin A

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16
Q

Vitamin A deficiency (4)

A

Night blindness
Dry, scaly skin
Keratomalacia/Bitot spots
Immunosuppression

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17
Q

Teratogenic vitamin?

A

Vitamin A

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18
Q

Acute vitamin A toxicity? (4)

A

Nausea
Vomiting
Vertigo
Blurred vision

19
Q

Chronic vitamin A toxicity? (2)

A

Hepatic toxicity/HM

Pseudotumor cerebri

20
Q

B1 function? (4)

A

TPP is a cofactor for:

1) Pyruvate dehydrogenase (glycolysis–>TCA cycle)
2) α-ketoglutarate dehydrogenase (TCA cycle)
3) Transketolase (HMP–>glycolysis)
4) Branched chain ketoacid dehydrogenase (BC amino acid excretion)

21
Q

Wernicke-Korsakoff syndrome

1) Cause?
2) Classic triad?
3) Other Sxs?
4) Structures damaged?
5) Tx?

A

Cause: B1 (thiamine) deficiency

Classic triad: confusion, ophthalmoplegia, ataxia

Other Sxs: confabulation, serious memory loss, personality change

Damaged: medial dorsal nucleus of the thalamus, mammillary bodies

Tx: prompt administration of IV thiamine

22
Q

Beri-beri

1) Cause?
2) Types and Sxs?

A

Cause: B1 (thiamine) deficiency

Dry Beri-beri: polyneuritis, symmetric muscle wasting

Wet Beri-beri: heart failure and edema

23
Q

B2 function?

A

Makes FAD and FMN; utilized in redox rxns–e.g. in TCA

24
Q

B2 deficiency?

A

Cheilosis, corneal vascularization (2 C’s)

25
B3 function?
Makes NAD+ and NADP+; utilized in redox reactions
26
Vitamin used to treat dyslipidemia?
B3 (Niacin). Lowers VLDL, raises HDL
27
Hartnup disease: 1) Defect? 2) Sxs? 3) Treatment?
Defect: autosomal recessive deficiency of neutral amino acid transporters in proximal renal tubule and enterocytes, causing excretion and poor absorption of tryptophan Sxs: Pellagra (Diarrhea, dementia, dermatitis) Tx: high protein diet and niacin supplementation
28
Mild B3 deficiency?
Glossitis
29
Severe B3 deficiency?
Pellagra (3 D's) 1) Diarrhea 2) Dementia (+ hallucinations) 3) Dermatitis (C3/C4 distribution "broad collar rash", hyperpigmentation of sun exposed limbs)
30
B3 toxicity? (3)
Flushing (via PGs; take aspirin) Hyperglycemia Hyperuricemia
31
Causes of pellagra? (3)
1) Hartnup disease (Trp excretion/malabsorption) 2) Carcinoid syndrome (↑Trp → serotonin) 3) Isoniazid (B6 required for synthesis)
32
B5 function? (3 major)
Component of CoA: Fatty acid/cholesterol synthesis, ACh synthesis, glycolysis-->TCA
33
B5 deficiency? (1)
Adrenal insufficiency
34
B6 function? (4 major)
As PLP, cofactor in: 1) Neurotransmitter synthesis 2) Heme synthesis 3) Niacin (B3) synthesis 4) Conversion of homocysteine to cysteine
35
B6 deficiency?
1) Neuro: peripheral neuropathy, hyper-irritability, convulsions 2) Sideroblastic anemia (↓heme production + ↑free Fe)
36
B7 function?
Cofactor in carboxylation reactions
37
B7 deficiency can be caused by?
``` Antibiotic use (endogenous production in gut) Excessive ingestion of raw egg whites (Avidin binding) ```
38
B9 function?
As THF: | 1) synthesis of DNA/RNA bases
39
Where is B9 absorbed?
Jejunum
40
B9 deficiency?
1) Megaloblastic anemia (w/hypersegmented neutrophils and macrocytes) 2) Glossitis 3) NO NEURO Sxs
41
Vitamin given to expecting mothers to prevent neural tube defects?
B9
42
Labs differentiating B9 and B12 deficiency?
B9: ↑homocysteine, NL methylmalonic acid B12: ↑homocysteine, ↑ methylmalonic acid
43
B12 function? (2)
1) Replenishes THF (B9) | 2) Generates methionine from homocysteine, which participates in myelination/DNA synthesis