Riboflavin (Vitamin B2) Flashcards

(23 cards)

1
Q

what are the sources of riboflavin?

A

found especially in products of animal origin (milk, cheese, yogurt)

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2
Q

how can riboflavin be destroyed in foods?

A

because of exposure to sunlight

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3
Q

what is riboflavin fairly resistant too?

A

heat, oxidation, and acid

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4
Q

what is another source of riboflavin (specifically in the body)?

A

bacterial synthesis in the large intestine

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5
Q

what form of riboflavin is most commonly found in food?

A

free and protein-bound (milk, eggs, and enriched breads and cereals)

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6
Q

what form of riboflavin must be released prior to absorption?

A

riboflavin that is found in foods attached non-covalently to proteins, FAD, FMN and riboflavin phosphate

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7
Q

how is the protein from riboflavin released?

A

accomplished by hydrochloric acid secreted within the stomach and proteases secreted by the stomach , pancreas and small intestine

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8
Q

how is FAD converted to free riboflavin?

A

FAD pyrophosphatase converts FAD to FMN, and FMN, in turn, is converted to free riboflavin by FMN phosphatase

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9
Q

how is free riboflavin absorbed?

A

across the intestinal brush border membrane by energy-dependent riboflavin vitamin transporters (RFVT)

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10
Q

what is the function of RFVT3?

A

transports riboflavin across the brush border membrane of the SI

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11
Q

what is the function of RFVT1?

A

carries riboflavin across the basolateral membrane of he intestinal cell

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12
Q

what are examples of riboflavin transporter deficiency disorders?

A

brown-vialetto-van-laere syndrome and Fazio-Londe syndrome

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13
Q

what impairs both riboflavin digestion and absorption?

A

alcohol

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14
Q

where is riboflavin found?

A

small quantities in a variety of tissues and the greatest concentration in the liver, kidneys and heart

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15
Q

following uptake into cell - what is riboflavin converted too?

A

FMN coenzyme by flavokinase/riboflavin kinase and then to FAD by FAD synthase

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16
Q

what is the major enzyme form?

17
Q

what accelerates the conversion of riboflavin into its coenzyme forms?

A

ACTH, aldosterone, and thyroid hormone

18
Q

what is the function of flavin coenzymes?

A

oxidizing agents

19
Q

what is required in the conversion of both PMP and PNP to PLP?

20
Q

how is riboflavin excreted from the body?

A

to a small extent in the feces, but primarily via the urine

21
Q

what is oculo-orogenital syndrome?

A

condition that affects areas of the skin containing high concentration of sebaceous glands, including the external ear, the nasolabial fold, eyelids, and scrotum (males)

22
Q

what can severe riboflavin deficiency also diminish?

A

the riboflavin-dependent synthesis of the co-enzyme form of vitamin B6 and synthesis of niacin from tryptophan

23
Q

how do you determine riboflavin nutriture?

A

measure the activity of the FAD-dependent enzyme erythrocyte glutathione reductase