Exam 1 Flashcards

1
Q

Most folate in the body is found in the reduced form of ________ which is oxidized by_________.

A

Tetrahydrofolate (FH4)

dihydrofolate reductase

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2
Q

Three Structural Features of Folate and their importances

A
  1. Peteridine Ring: site of oxidation/reduction
  2. Para-aminobenzoic acid (PABA): sulfa drugs are analogs of this, which are antimicrobial. (bacteria make folate)
  3. Polyglutamate Tail: cleaved to n=1 in brush border of lumen
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3
Q

Diseases that can damage intestinal mucosa and, thus inhibit folate synthesis? (3)

A
  • Crohn’s Disease
  • Alcoholism
  • Celiac Disease
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4
Q

Cause of a functional folate deficiency? Note: serum levels seem fine.

A

Stuck in most reduced form (N5-methyl-FH4)

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5
Q

What is the major carbon source for the one carbon pool (which forms FH4)

A

Serine

FH4 is needed for purine synthesis!! <— needed for cell division

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6
Q

Major source of Vitamin B12?

A

Meats

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7
Q

Major source of Folate?

A

Leafy Green Vegetables

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8
Q

Deficiency of intrinsic factor which leads to Vitamin B12 deficiency.

A

Pernicious Anemia

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9
Q

Three possible routes of Vitamin B12 deficiency?

A

R-Binder Absent
Intrinsic Factor Deficient
Dietary Decrease

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10
Q

Name of test which helps specify the cause of a Vitamin B12 deficiency. (Involves several steps and urine collection)

A

Schilling Test

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11
Q

What is SAM made up of? (~2)

A

Methionine (made from B12)

ATP

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12
Q

Function of SAM?

A

Important in Neurotransmittters Synthesis

Adds methyl groups to nitrogen or oxygen atoms (it is converted to SAH when it does this)

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13
Q

Function of Folate?

A

The one Carbon Pool (FH4/Purine Synthesis)

Adds one carbon groups (from serine) to carbon or sulfur atoms

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14
Q

Pt. with limited DNA synthesis, and RBCs do not work properly causing anemia. Can be caused by B12 or Folate deficiency. Enlarged Cells.

A

Megoblastic Anemia

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15
Q

Fancy term for “made from scratch”

A

de novo

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16
Q

Molecule that contributes both carbons and nitrogen to purine synthesis?

17
Q

Disease where enzyme involved in protein salvage is defective and purines are not salvaged and instead converted into uric acid?

A

Lesch-Nyhan syndrome

18
Q

Disease with is associated with inability to produce T or B cells due to build up of toxic materials, which is caused by lack of protein salvage. (lymphocytes are known to use the salvage pathway for synthesis)

A

Adenosine Deaminase Deficiency

19
Q

What is an important enzyme in the production of uric acid from the breakdown of GMP and AMP (purine degradation)

A

Xanthine Oxidase - xanthine is the product of AMP/GMP degradation. It is then made into uric acid and hopefully excreted.

20
Q

Inhibition of the enzymes which help produce OMP and UMP causing an excess of Orotic Acid in the urine is called?

A

Orotic Aciduria