vitamins and minerals -Squier Flashcards

1
Q

What is a vitamin?

A

small organic molecules that cannot be synthesized

ex: enzyme cofactors, antioxidants and other functions

fat soluble: vitamin A, D, E, K

  • -> stored in liver and adipose tissue
  • difficult to absorb and excrete
  • excess intake can cause toxicity

water soluble: thiamine, riboflavin, vitamin B’s folate, vitamin C, biotin, pantothenic acid, choline

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2
Q

What can lead to megaloblastic anemia?

A

thiamine or B12 deficiencies

there is an inability to synthesize DNA resulting in an inability of cells to divide

-vit B12 is needed to maintain FH4 –> needed for methyl transfer reactions important in DNA synthesis
a deficiency in vit B12 can cause a deficiency in FH4

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3
Q

What is the function of folic acid (B9)?

What can a deficiency of Folic acid lead to?

A

folic acid is responsible for 1 C transfers in the synthesis of AAs, purines and thymidine

-forms tetrahydrofolate (TH4) that is critical for DNA synthesis (movement of 1C groups)

  • folic acid deficiency can lead to megaloblastic anemia —> large immature RBC precursors
  • rapidly dividing cells are affected (bone marrow and gut)
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4
Q

What can a Vitamin B12 deficiency lead to?

A

accumulation of odd-numbered fatty acids
which may be incorporated into cell membranes of nerves
Neurological abnormalities (dementia) & degeneration of
spinal cord
Glossitis, diarrhea, weight loss
Causes secondary folate deficiency leading to
megaloblastic anemia

causes:
insufficient dietary intake
pernicious anemia
pancreatic insufficiency

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5
Q

What are the two enzymes that Vitamin B12 are cofactors for?

A
  1. methylmalonyl CoA mutase
    - -> critical for the breakdown of odd-numbered FA’s
  2. homocysteine methyltransferase necessary for methionine synthesis
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6
Q

What carries vitamin B12 in circulation?

A

dietary B12 is released from food in the stomach and then binds IF (intrinsic factor) is the carrier of B12 in the lumen to the endothelial cells there it can be taken up into the blood and then stored in the liver

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7
Q

What is the function of Vitamin C?

A

Vitamin C plays an important role in collagen synthesis
–> important in normal connective tissue and wound healing

-binds to collagen to carry it into the cell –> facilities in the absorption of dietary iron

Vitamin C maintains VItamin E in a reduced state –> important in maintaining membranes
–> vit C is a reducing factor –> an tx e-s to keep metals reduced

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8
Q

What can vitamin C deficiency cause?

A

Scurvy (symptoms due to decrease in collagen synthesis)

- swollen, sore & spongy gums with bleeding & loose teeth
- anemia
- spontaneous bruising
- poor wound healing
- swollen joints & muscle pain
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9
Q

What are the two components of collagen that vitamin C is important in maintaining? And how?

A

hydroxyproline and hydroxylysine
–> vit C keeps the iron in the Fe2+ state (reduced)

vit c prevents the auto-oxidation of active site metals needed for the oxidation of proline and collagen cross linking .

Proline hydroxylase (iron active sites) and lysyl oxidase (copper active sites) are critical for collage cross-linking

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10
Q

What is the significance of vitamin B6?

A

-precursor to PLP (pyridoxyl phosphate)
required for glycogen phosphorylase (breakdown of glycogen) –> used in transamination, deamination, decarboxylation, condensation
-required for heme synthesis (ALA synthase)
-required for amino acid metabolism (ex: histamine formation)
-*conversion of tryptophan to niacin

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11
Q

What are the symptoms of B6 deficiency?

A

Symptoms of Deficiency (Rare):
Abnormal amino acid metabolism
Secondary pellagra (due to inability to synthesize niacin)
Microcytic anemia

Deficiencies Have Been Observed For: 
Women on oral contraceptives
 Alcoholics & elderly
 Newborns on certain types of formula
 Treatment with isoniazid (for tuberculosis infection) inactivates PLP & causes B6 deficiency
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12
Q

What are the functions of thiamine (vitamin B1)?

A
cofactor for enzymes (thiamine pyrophosphate, TPP) 
important in 
1. pyruvate dehydrogenase complex
2. alpha-ketoglutarate dehydrogenase
3. transketolase 
4. branched chain AA 
--> alpha-ketoacid dehydrogenase 

TPP breaks C bonds (ex: 3C private –> 2 C acetyl CoA)

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13
Q

What can thiamine deficiency cause?

A

Decreased ATP production which affects nervous system activity
Accumulation of lactate & pyruvate (lactic acidosis)
Decreased NADPH formation via HMP & affects fatty acid synthesis
(myelin synthesis affected & peripheral neuropathy)
Causes Beri-beri
- dry skin
- irritability
- progressive paralysis
Causes Wernicke’s encephalopathy
- confusion, ataxia
- nystagmus & eye paralysis
- peripheral neuropathy
If untreated, may progress into Korsakoff ‘s psychosis
- irreversible syndrome
- amnesia & deficits in learning & memory

Causes of Deficiency:
 Alcoholism
 Systemic disease (cancer , AIDS)
 Insufficient dietary intake
 Severe liver disease
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14
Q

What is the function of Niacin (vitamin B3) and what does a deficiency lead to?

A

Functions:
Cofactor for oxidase & dehydrogenase enzymes (active forms are NAD+ & NADP+)
Repair of UV light damage in DNA in skin
Treatment of hyperlipidemia in high doses
(nicotinic acid inhibits lipolysis & leads to decrease in VLDL synthesis)

Deficiency:
Causes pellagra (skin, GI & nervous system symptoms)
- photosensitive dermatitis
- diarrhea
- dementia (apathy, confusion, disorientation, lethargy)
- can lead to death

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15
Q

What is the function of vitamin B2 (riboflavin)?

what does a deficiency cause?

A

cofactors for oxidase and dehydrogenase enzymes (active forms are FAD and FMN)

Deficiency:
 Causes ariboflavinosis
	- glossitis
	- cheilosis (fissures at corners of mouth)
	- dermatitis
	- angular stomatitis
	- cataracts
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16
Q

What is the function of biotin?

A

Coenzyme for CARBOXYLATION reactions (transfers CO2)

1) Pyruvate carboxylase (gluconeogenesis & TCA anaplerotic reaction)
2) Acetyl CoA carboxylase (fatty acid synthesis)
3) Propionyl CoA carboxylase (b-oxidation of odd numbered fatty acids)
4) Branched-chain amino acid metabolism

17
Q

What is the function of pantothenic acid?

A

transfer of acyl groups as a component of CoA (acetyl CoA, succinyl CoA, fatty acyl CoA)
-component of FA synthase

deficiency can cause burning foot syndrome

18
Q

What are the functions of Vitamin A?

A

Important in vision (retinal pigment) and hormonal regulation (acts as steroid hormone important in epithelial cell differentiation)

retinoic acid regulates gene expression:
- transcriptional regulator

signal transduction in vision:

  • retinol and light –> isomerization
  • transducin activated–> cGMP lowered, hyper polarization due to closing of Na+ channels
19
Q

What is the function of Vitamin D?

A

Maintains adequate plasma levels of Ca2+ by:

1) Increasing uptake of calcium & phosphorus from intestine
2) Increasing reabsorption of calcium from kidney
3) Increasing resorption of bone

vitamin D regulates gene expression
vitamin D will promote calbindin formation ==> calbindin is important for Ca2+ to be transported across epithelial cells

20
Q

what is the function of vitamin K? What can a vitamin K deficiency cause?

A
  • Coenzyme for g-carboxylation of glutamate residues of clotting factors II, VII, IX, X & prothrombin
  • activates clotting factors and clotting cascade

-deficiency:
Causes poor clotting & bleeding disorders
May result in hemorrhagic disease of newborn
(prophylactic administration of Vitamin K to all newborns)

21
Q

What is the function of Vitamin E? What can deficiency lead to?

A

antioxidant (along with Vitamin C)

transported from liver to adipose via VLDLs to be stores in adipose tissue

deficiency:
hemolytic anemia in newborns (increased oxidative stress in RBCs)
-muscle weakness, ataxia, peripheral neuropathy, nystagmus

22
Q

What forms of iron are typically found in the body?

A
  • transported in the blood stream as a complex with transferrin to sites of storage
  • stored as ferritin (mostly) and some as hemosiderin (27%)
  • unbound iron can make free radicals

heme iron is preferentially absorbed, facilitated by vitamin C

23
Q

What is caused by iron deficiency?

A

iron deficiency anemia –> decreased production of hemoglobin and decrease in O2 to tissues
-pallor, tiredness, SOB, palpitations

24
Q

What is the function of iodine? What does an iodine deficiency cause?

A

required for the synthesis of thyroid hormone

deficiency causes goiter –> overproduction of TSH

25
Q

What is the function of zinc? What does a deficiency in zinc cause?

A

Cofactor for enzymes
- dehydrogenases (ex. lactate dehydrogenase)
- peptidases
- superoxide dismutase
- carbonic anhydrase
- certain enzymes involved in DNA & protein synthesis
Component of zinc finger DNA binding domains in certain transcription factors–> structure of transcription factors

Deficiency:
Caused by malabsorption in SI in acrodermatitis enteropathica (rare autosomal disorder)
Acrodermatitis enteropathica characterized by
- growth retardation
- hypogonadism
- delayed wound healing
- lesions around orifices & on hands/ feet
Completely cured by zinc therapy

26
Q

What is the function of copper and what causes copper deficiency?

A

Functions:
Cofactor for enzymes
- lysyl oxidase (crosslinks collagen & elastin)
- tyrosinase (melanin production)
- dopamine b-hydroxylase (catecholamine production)
- cytochrome c oxidase (ETC)
- superoxide dismutase (scavenges superoxide radicals & prevents membrane damage)
- ceruloplasmin (promotes absorption of iron)

Causes of Deficiency:
Menke’s kinky hair syndrome (rare X-linked disorder) caused by defective absorption of copper from SI (life expectancy < 2 yrs)
Clinical features
- depigmentation of hair
- arterial degeneration
- neuronal degeneration & mental retardation
- growth failure & anemia

Causes of Overload:
Wilson’s disease (rare autosomal recessive disorder) resulting in failure of liver to excrete copper in bile, leading to copper accumulation
Specific pumps that pump Ca2+ (out of the cell) that can allow copper to accumulate if mutated

Copper deposition in

- liver (cirrhosis)
- brain (severe progressive neurological disability, mental deterioration)
- eyes (yellow-brown rings around corneal limbus)