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Hemoglobin

Hemoglobin
76問 • 1年前
  • Almira Coleen
  • 通報

    問題一覧

  • 1

    RBC is composed of _____ hemoglobin

    95%

  • 2

    has mitochondria and nucleus

    Hemoglobin

  • 3

    Lacks mitochondria and nucleus

    RBC

  • 4

    Total of iron that is found in the hemoglobin

    90%

  • 5

    Composition of Hemoglobin

    4 globin chains, 4 heme groups, Fe2+ -4 molecules Hb molecules, with a central ferrous ions (Fe2+)

  • 6

    Low concentration of hemoglobin will results low oxygen levels which can cause ________ which forms ______

    Tissue Hypoxia, Anemia

  • 7

    The biosynthesis of hemoglobin takes place in the _______ to __________ erythrocyte stage

    Normoblast, Polychromatophilic

  • 8

    Heme synthesis occurs in the?

    Mitochondria, Cytoplasm of RBC

  • 9

    Globin synthesis occurs in the?

    Ribosomes

  • 10

    To transport oxygen from the lungs to tissues and transport carbon dioxide from the tissues to the lungs for exhalation

    Hemoglobin

  • 11

    Heme synthesis consists of:

    Protoporphyrin IX, Ferrous Iron

  • 12

    Heme synthesis is consists of:

    Enzymes, Coenzymes, Precursor Substances

  • 13

    Heme synthesis produce

    Blast Cells

  • 14

    SuccinylcoenzymeA condenses with?

    Glycine

  • 15

    SuccinylcoenzymeA condenses with glycine to form?

    Alpha-amino Acid, Beta-Ketoacidic Acid

  • 16

    SuccinylcoenzymeA is decarboxylated in the?

    Delta-aminolevulinic acid (ALA)

  • 17

    4 molecules of PBG react to form?

    Uroporphyrinogen III or I

  • 18

    Uroporphyrinogen III is converted to __________ ----> _________ ---> __________

    Coproporphyrinogen III, Protoporphyrinogen, Protoporphyrin

  • 19

    It is an enzyme where ferrous sulfate is inserted into an protoporphyrin, to form the finished heme moiety.

    Ferrochelatase

  • 20

    Heme Synthesis: Mitochondria --> Succinyl CoA ---> ?

    ALA Synthase

  • 21

    Takes place in the cytoplasm --> ribosomes clustered as polyribosomes in the cytoplasm of normoblast and reticulocytes

    Globin Synthesis

  • 22

    Assembled from 2 polypeptide chains

    Alpha, Beta

  • 23

    4 Primary Chains - It is different by only a few amino acids substitutions.

    Alpha, Beta, Gamma, Delta

  • 24

    Transcription of the globin genes to messenger ribonucleic acid (mRNA)

    Nucleus

  • 25

    Translation of mRNA to the globin polypeptide chain

    Ribosomes

  • 26

    Chains are released from the ribosomes in the cytoplasm

    After Translation

  • 27

    Alpha and Zeta Globin Chains

    Chromosome 16

  • 28

    Beta, Zeta, Delta, Gamma

    Chromosome 11

  • 29

    Embryonic HgB: Goer 1 --> Configuration:

    2 zeta, 2 epsilon

  • 30

    Embryonic HgB: Goer 2 -->

    2 alpha, 2 epsilon

  • 31

    Portland -->

    2 zeta, 2 gamma

  • 32

    Fetal Hemoglobin

    2 alpha, 2 gamma

  • 33

    Adult Hemoglobin

    2 alpha, 2 beta

  • 34

    During this timeline, the dominant hemoglobin is the Embryonic hemoglobin.

    10th week of gestation

  • 35

    Zeta Chain and Epsilon Chain were silenced/degranulated

    10th week of Gestation

  • 36

    In the 10th week of gestation, the alpha and gamma is?

    Upregulated

  • 37

    Alpha switch

    Zeta

  • 38

    Gamma switch

    Epsilon

  • 39

    The downregulation and upregulation of these genes is for the preparation for the activation of?

    Fetal Hb

  • 40

    Occurs during the hepatic hematopoiesis.

    2nd month of gestation

  • 41

    In 2nd month of gestation, it is a globin gene is activated in preparation for the adult hemoglobin.

    Beta

  • 42

    In 2nd month of gestation, the dominant gene in this period is the?

    Fetal Hemoglobin

  • 43

    Dominant gene is still the Fetal hemoglobin.

    Before birth

  • 44

    Before birth the _____ globin chains are down regulated, while ________, chains are upregulated.

    gamma (y), beta (β) and delta (δ)

  • 45

    Before birth, there is a what type of switch?

    Gamma → Beta

  • 46

    Dominant gene is now the Adult Hemoglobin.

    6th month after birth

  • 47

    In 6 months after birth , the dominant gene is now the?

    Adult Hemoglobin

  • 48

    Complete hemoglobin molecule

    Tetramer

  • 49

    Found in normal human embryos and fetuses with a gestational stage of less than 3 months

    Embryonic Hemoglobin

  • 50

    3 types of embryonic HgB: - All of these are absent at birth because starting the third month of gestation, the synthesis of these will be seized and HbF will begin to reproduced.

    Hb Gower 1, Hb Gower 2, Portland

  • 51

    Becomes the major intrauterine and neonatal form of Hb which persist up to birth

    Fetal Hemoglobin

  • 52

    Major Hb of the fetuses and newborns produced _____ after conception

    4 months

  • 53

    total Hb content at birth

    80%

  • 54

    In Fetal Hemoglobin, there is less than __ by 6 months of age?

    8%

  • 55

    A condition where an individual still has high amount of HbF at an adult age.

    Hereditary Persistence of Fetal Hemoglobin (HPFH)

  • 56

    Higher O2 affinity than that of adult Hb because lungs are still developing, O2 tension is a little low compared to O2 tension in normal adult.

    True

  • 57

    The substance responsible for regulating affinity of O2 (HbA).

    2,3 DPG

  • 58

    Its weakly bind to HbF, meaning, if 2, 3 DPG binds, it lowers the affinity because it does not accept O2.

    True

  • 59

    Produced by 1 year of age and onwards

    HbA1

  • 60

    Sub-fraction of HbA which includes the separate fractions A1a, A1b, and A1c

    Hb A1 or Glycosylated/Glycated HbA

  • 61

    the most common

    HbA1c

  • 62

    The only difference is that Hb A1 has a binding attachment to a carbohydrate group which is?

    Glucose

  • 63

    ↑ glucose content, ↑ HbA1 for about ____ in a normal individual that don’t suffer with DM. ____ to those with DM.

    3-6%, 6-12%

  • 64

    α2δ2 (2 alpha and 2 delta); constitutes <3.5% of the total Hb content

    HbA2

  • 65

    Not produce in reticulocyte only in normoblasts

    HbA2

  • 66

    In HbA2, there is an increased in?

    β-thalassemia and sickle cell anemia

  • 67

    In HbA2, there will be a decreased in?

    α-thalassemia and IDA (Iron Deficiency Anemia)

  • 68

    degradation product of HbA2

    HbA3

  • 69

    major Hb in fetuses and newborn but one of the minor Hb in adults; comprising <2% of total Hb; ↑ in Hereditary Persistence of Fetal Hb (HPFH)

    HbF

  • 70

    NORMAL HEMOGLOBIN IN BLOOD Hb A2: Hb F: Hb A:

    <3.5%, 1–2%, 95%

  • 71

    Found in RBCs that have just come from the lungs. This is where the Oxygen and Hemoglobin binds together. Once it leaves the lungs, this is what is known as? o Gives a pinkness to the skin

    Oxyhemoglobin (HbO2)

  • 72

    Reduced or deoxygenated Hb (without oxygen) Found in RBCs after releasing O2 in the tissues. After the Hemoglobin has given up its oxygen to the tissues, it becomes?

    Deoxyhemoglobin (HbCO2)

  • 73

    Causes Hypoxic – cyanotic (very low O2)  But this is still normal. It only becomes abnormal when the level of deoxyhemoglobin is elevated.

    Deoxyhemoglobin (HbCO2)

  • 74

    In deoxyhemoglobin, in cases of hypoxia, it gives a? hue to the skin. You can check this in the gums.

    Bluish

  • 75

    High Oxygen Saturation High Oxygen Tension High Oxygen Affinity Partial Pressure of Oxygen (PO2) – 100 mmHg Hgb will pick up Oxygen

    Lungs

  • 76

    Low Oxygen Saturation Low Oxygen Tension Low Oxygen Affinity Hgb will release Oxygen Partial Pressure of Oxygen (PO2) – 20 mmHg

    Tissue

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    Regulation of Body Iron

    Regulation of Body Iron

    Almira Coleen · 17問 · 1年前

    Regulation of Body Iron

    Regulation of Body Iron

    17問 • 1年前
    Almira Coleen

    問題一覧

  • 1

    RBC is composed of _____ hemoglobin

    95%

  • 2

    has mitochondria and nucleus

    Hemoglobin

  • 3

    Lacks mitochondria and nucleus

    RBC

  • 4

    Total of iron that is found in the hemoglobin

    90%

  • 5

    Composition of Hemoglobin

    4 globin chains, 4 heme groups, Fe2+ -4 molecules Hb molecules, with a central ferrous ions (Fe2+)

  • 6

    Low concentration of hemoglobin will results low oxygen levels which can cause ________ which forms ______

    Tissue Hypoxia, Anemia

  • 7

    The biosynthesis of hemoglobin takes place in the _______ to __________ erythrocyte stage

    Normoblast, Polychromatophilic

  • 8

    Heme synthesis occurs in the?

    Mitochondria, Cytoplasm of RBC

  • 9

    Globin synthesis occurs in the?

    Ribosomes

  • 10

    To transport oxygen from the lungs to tissues and transport carbon dioxide from the tissues to the lungs for exhalation

    Hemoglobin

  • 11

    Heme synthesis consists of:

    Protoporphyrin IX, Ferrous Iron

  • 12

    Heme synthesis is consists of:

    Enzymes, Coenzymes, Precursor Substances

  • 13

    Heme synthesis produce

    Blast Cells

  • 14

    SuccinylcoenzymeA condenses with?

    Glycine

  • 15

    SuccinylcoenzymeA condenses with glycine to form?

    Alpha-amino Acid, Beta-Ketoacidic Acid

  • 16

    SuccinylcoenzymeA is decarboxylated in the?

    Delta-aminolevulinic acid (ALA)

  • 17

    4 molecules of PBG react to form?

    Uroporphyrinogen III or I

  • 18

    Uroporphyrinogen III is converted to __________ ----> _________ ---> __________

    Coproporphyrinogen III, Protoporphyrinogen, Protoporphyrin

  • 19

    It is an enzyme where ferrous sulfate is inserted into an protoporphyrin, to form the finished heme moiety.

    Ferrochelatase

  • 20

    Heme Synthesis: Mitochondria --> Succinyl CoA ---> ?

    ALA Synthase

  • 21

    Takes place in the cytoplasm --> ribosomes clustered as polyribosomes in the cytoplasm of normoblast and reticulocytes

    Globin Synthesis

  • 22

    Assembled from 2 polypeptide chains

    Alpha, Beta

  • 23

    4 Primary Chains - It is different by only a few amino acids substitutions.

    Alpha, Beta, Gamma, Delta

  • 24

    Transcription of the globin genes to messenger ribonucleic acid (mRNA)

    Nucleus

  • 25

    Translation of mRNA to the globin polypeptide chain

    Ribosomes

  • 26

    Chains are released from the ribosomes in the cytoplasm

    After Translation

  • 27

    Alpha and Zeta Globin Chains

    Chromosome 16

  • 28

    Beta, Zeta, Delta, Gamma

    Chromosome 11

  • 29

    Embryonic HgB: Goer 1 --> Configuration:

    2 zeta, 2 epsilon

  • 30

    Embryonic HgB: Goer 2 -->

    2 alpha, 2 epsilon

  • 31

    Portland -->

    2 zeta, 2 gamma

  • 32

    Fetal Hemoglobin

    2 alpha, 2 gamma

  • 33

    Adult Hemoglobin

    2 alpha, 2 beta

  • 34

    During this timeline, the dominant hemoglobin is the Embryonic hemoglobin.

    10th week of gestation

  • 35

    Zeta Chain and Epsilon Chain were silenced/degranulated

    10th week of Gestation

  • 36

    In the 10th week of gestation, the alpha and gamma is?

    Upregulated

  • 37

    Alpha switch

    Zeta

  • 38

    Gamma switch

    Epsilon

  • 39

    The downregulation and upregulation of these genes is for the preparation for the activation of?

    Fetal Hb

  • 40

    Occurs during the hepatic hematopoiesis.

    2nd month of gestation

  • 41

    In 2nd month of gestation, it is a globin gene is activated in preparation for the adult hemoglobin.

    Beta

  • 42

    In 2nd month of gestation, the dominant gene in this period is the?

    Fetal Hemoglobin

  • 43

    Dominant gene is still the Fetal hemoglobin.

    Before birth

  • 44

    Before birth the _____ globin chains are down regulated, while ________, chains are upregulated.

    gamma (y), beta (β) and delta (δ)

  • 45

    Before birth, there is a what type of switch?

    Gamma → Beta

  • 46

    Dominant gene is now the Adult Hemoglobin.

    6th month after birth

  • 47

    In 6 months after birth , the dominant gene is now the?

    Adult Hemoglobin

  • 48

    Complete hemoglobin molecule

    Tetramer

  • 49

    Found in normal human embryos and fetuses with a gestational stage of less than 3 months

    Embryonic Hemoglobin

  • 50

    3 types of embryonic HgB: - All of these are absent at birth because starting the third month of gestation, the synthesis of these will be seized and HbF will begin to reproduced.

    Hb Gower 1, Hb Gower 2, Portland

  • 51

    Becomes the major intrauterine and neonatal form of Hb which persist up to birth

    Fetal Hemoglobin

  • 52

    Major Hb of the fetuses and newborns produced _____ after conception

    4 months

  • 53

    total Hb content at birth

    80%

  • 54

    In Fetal Hemoglobin, there is less than __ by 6 months of age?

    8%

  • 55

    A condition where an individual still has high amount of HbF at an adult age.

    Hereditary Persistence of Fetal Hemoglobin (HPFH)

  • 56

    Higher O2 affinity than that of adult Hb because lungs are still developing, O2 tension is a little low compared to O2 tension in normal adult.

    True

  • 57

    The substance responsible for regulating affinity of O2 (HbA).

    2,3 DPG

  • 58

    Its weakly bind to HbF, meaning, if 2, 3 DPG binds, it lowers the affinity because it does not accept O2.

    True

  • 59

    Produced by 1 year of age and onwards

    HbA1

  • 60

    Sub-fraction of HbA which includes the separate fractions A1a, A1b, and A1c

    Hb A1 or Glycosylated/Glycated HbA

  • 61

    the most common

    HbA1c

  • 62

    The only difference is that Hb A1 has a binding attachment to a carbohydrate group which is?

    Glucose

  • 63

    ↑ glucose content, ↑ HbA1 for about ____ in a normal individual that don’t suffer with DM. ____ to those with DM.

    3-6%, 6-12%

  • 64

    α2δ2 (2 alpha and 2 delta); constitutes <3.5% of the total Hb content

    HbA2

  • 65

    Not produce in reticulocyte only in normoblasts

    HbA2

  • 66

    In HbA2, there is an increased in?

    β-thalassemia and sickle cell anemia

  • 67

    In HbA2, there will be a decreased in?

    α-thalassemia and IDA (Iron Deficiency Anemia)

  • 68

    degradation product of HbA2

    HbA3

  • 69

    major Hb in fetuses and newborn but one of the minor Hb in adults; comprising <2% of total Hb; ↑ in Hereditary Persistence of Fetal Hb (HPFH)

    HbF

  • 70

    NORMAL HEMOGLOBIN IN BLOOD Hb A2: Hb F: Hb A:

    <3.5%, 1–2%, 95%

  • 71

    Found in RBCs that have just come from the lungs. This is where the Oxygen and Hemoglobin binds together. Once it leaves the lungs, this is what is known as? o Gives a pinkness to the skin

    Oxyhemoglobin (HbO2)

  • 72

    Reduced or deoxygenated Hb (without oxygen) Found in RBCs after releasing O2 in the tissues. After the Hemoglobin has given up its oxygen to the tissues, it becomes?

    Deoxyhemoglobin (HbCO2)

  • 73

    Causes Hypoxic – cyanotic (very low O2)  But this is still normal. It only becomes abnormal when the level of deoxyhemoglobin is elevated.

    Deoxyhemoglobin (HbCO2)

  • 74

    In deoxyhemoglobin, in cases of hypoxia, it gives a? hue to the skin. You can check this in the gums.

    Bluish

  • 75

    High Oxygen Saturation High Oxygen Tension High Oxygen Affinity Partial Pressure of Oxygen (PO2) – 100 mmHg Hgb will pick up Oxygen

    Lungs

  • 76

    Low Oxygen Saturation Low Oxygen Tension Low Oxygen Affinity Hgb will release Oxygen Partial Pressure of Oxygen (PO2) – 20 mmHg

    Tissue