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Heme Metabolism

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Deficiency porphyria. Acute intermittent. porphyria. Congenital ... Acute intermittent porphyria. Laboratory tests. Major Symptoms. Enzyme Involved. Type ... – PowerPoint PPT presentation

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Title: Heme Metabolism


1
Heme Metabolism
  • Heme biosynthesis and Porphyrias
  • Heme degradation Jaundice

2
Heme Biosynthesis Porphyrias
  • Cruelly referred to as a Vampires disease.
    Thought to be a cause of the madness of King
    George III.
  • Can be caused by lead poisoning The fall of the
    Roman Empire!

3
Not a vampires disease
  • Some symptoms of porphyrias have lead people to
    believe that these diseases provide some basis
    for vampire legends
  • Extreme sensitivity to sunlight
  • Anemia
  • This idea has been discarded both for scientific
    reasons
  • Porphyrias do not cause a craving for blood.
  • Drinking blood would not help a victim of
    porphyria.

And for compasionate reasonsPorphyria is a rare,
but frightening condition hard to diagnose and
there is no cure.
4
The Madness of Inbreeding
George III Severe abdominal pain, mental
confusion, dark urine.
5
PORPHYRIAS
Mitochondria
GLYCINE SuccinylCoA
Agent Orange
ALA synthase
3p21/Xp11.21
d-aminolevulinic acid(ALA)
ALA-dehydratase Deficiency porphyria
ALA dehydratase
9q34
Porphobilinogen(PBG)
Acute intermittent porphyria
PBG deaminase
11q23
hydroxymethylbilane
Congenital erythropoietic porphyria
Uroporphyrinogen III cosynthase
10q26
uroporphyrinogen III
Uroporphyrinogen decarboxylase
Prophyria cutanea tarda
1q34
coprophyrinogene III
Coproporphyrinogen oxidase
Herediatary coproporphyria
9
Protoporphyrinogene IX
Protoporphyrinogen oxidase
Variegate porphyria
protoporphyrin IX
1q14
Ferrochelatase
Erythropoietic protoporphyria
Heme
18q21.3
6
COORDINATED REGULATION OF HEME AND GLOBIN
SYNTHESIS
  • Heme
  • inhibits activity of pre-existing ?-ALA
    synthase
  • diminishes the transport of ?-ALA synthase from
    cytoplasm to mitochondria after synthesis of the
    enzyme.
  • represses the production of ?-ALA synthase by
    regulating gene transcription.
  • stimulates globin synthesis to ensure that
    levels of free heme remain low in concentration.

Inhibition of the synthase and stimulation of
globin synthesis are the most important aspects
in balancing hemoglobin production.
7
Heme Catabolism
Heme Degradation
HEME
O2
(opens the porphyrin ring)
Fe3
BILIVERDIN
BILIRUBIN
BILIRUBIN diglucuronide
BILE
8
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9
Jaundice
Hyperbilirubinemia Two forms Direct bilirubin
Conjugated with glucoronic acid Indirect
bilirubin unconjugated, insoluble in water.
10
Whats the cause of jaundice?
  • 1- Increased production of bilirubin by hemolysis
    or blood disease
  • Increase in blood indirect bilirubin
  • Called pre-hepatic jaundice
  • Stool color remains normal.
  • 2- Abnormal uptake or conjugation of bilirubin
  • Leads to non-hemolytic unconjugated
    hyperbilirubinemia
  • Increased indirect bilirubin.
  • Stool color turns gray.
  • Caused by liver damage or disease.

11
Whats the cause of jaundice?
  • 3- Cholestasis Problems with bile flow.
  • a Intrahepatic cholestasis hyper
    conjugated bilirubinemia
  • Increase in blood indirect and direct bilirubin
  • Caused by liver damage or disease eg cirrhosis,
    hepatitis
  • Can also occur in pregnancy
  • bExtrahepatic cholestasis
  • Blockage of bilirubin transport in the bilary
    tract.
  • Increased direct bilirubin.
  • Stool color turns gray.
  • Caused by Tumors or gall stones.

12
CLINICAL PREMISE Newborns often have a yellowish
tint to their skin. This condition is known as
jaundice and results from the infant ridding
itself of "fetal" hemoglobin which will be
replaced by "adult" hemoglobin. As you will learn
in this lecture, catabolic products from
hemoglobin are removed by the liver. However, the
infant's liver is often too immature to handle
the excessive breakdown products. Instead they
accumulate giving the yellowish tint. Exposure to
mild UV light from the sun is usually sufficient
to destroy these compounds, although in very
severe cases blood dialysis may become necessary
as these byproducts can be toxic.
13
Table 1- The porphyrias. You are responsible for
the enzyme defects in red
14
BLOOD CELLS
KIDNEY
reabsorbed into blood
INTESTINE
via bile duct to intestines
LIVER
Figure 2. Catabolism of hemoglobin
15
Figure 3. Examples of hyperbilirubinemia
16
Table 2- Genetic Disorders of Bilirubin Metabolism
17
Formation of porphobilinogenLead Poisoning
18
Cyclization to the porphyrin
19
Cyclization to the porphyrin
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