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Question 1
Correct
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Where is Vitamin B 12 absorbed?
Your Answer: Terminal ileum
Explanation:Protein-bound vitamin B12 must be released from the proteins by the action of digestive proteases in both the stomach and small intestine. Gastric acid releases the vitamin from food particles; therefore antacid and acid-blocking medications (especially proton-pump inhibitors) may inhibit absorption of B12. B12 must be attached to Intrinsic Factor (IF) for it to be efficiently absorbed, as receptors on the enterocytes in the terminal ileum of the small bowel only recognize the B12-IF complex; in addition, intrinsic factor protects the vitamin from catabolism by intestinal bacteria.
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This question is part of the following fields:
- Haematology
- Medicine
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Question 2
Incorrect
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Select one true statement about haemoglobin synthesis…
Your Answer: Is dependant on the coenzyme vit B12 in the major rate limiting step.
Correct Answer: Occurs in the cytosol of developing red cells.
Explanation:Haemoglobin (Hb) is synthesized in a complex series of steps. The haem part is synthesized in a series of steps in the mitochondria and the cytosol of immature red blood cells, while the globin protein parts are synthesized by ribosomes in the cytosol. Production of Hb continues in the cell throughout its early development from the proerythroblast to the reticulocyte in the bone marrow.
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This question is part of the following fields:
- Haematology
- Medicine
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Question 3
Correct
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What is the main function of vitamin E?
Your Answer: It is an antioxidant
Explanation:Vitamin E has many biological functions, the antioxidant function being the best known. Other functions include enzymatic activities, gene expression, and neurological function(s).
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This question is part of the following fields:
- Haematology
- Medicine
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Question 4
Correct
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Which of the following is a function of Vitamin C?
Your Answer: Hydroxylation of proline to hydroxyproline for collagen synthesis
Explanation:Vitamin C acts as an electron donor for eight different enzymes: Three enzymes (prolyl-3-hydroxylase, prolyl-4-hydroxylase, and lysyl hydroxylase) that are required for the hydroxylation of proline and lysine in the synthesis of collagen.
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This question is part of the following fields:
- Haematology
- Medicine
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Question 5
Correct
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The actions of thrombin result directly in the release of:
Your Answer: Fibrin monomers
Explanation:Thrombin in turn acts as a serine protease that converts soluble fibrinogen into insoluble strands of fibrin, as well as catalysing many other coagulation-related reactions.
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This question is part of the following fields:
- Haematology
- Medicine
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Question 6
Correct
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The extrinsic coagulation pathway is initiated by activation of which clotting factor?
Your Answer: Factor VII
Explanation:The tissue factor pathway (extrinsic) begins following damage to the blood vessel. FVII leaves the circulation and comes into contact with tissue factor (TF) expressed on tissue-factor-bearing cells (stromal fibroblasts and leukocytes), forming an activated complex (TF-FVIIa).
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This question is part of the following fields:
- Haematology
- Medicine
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Question 7
Correct
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Iron absorption occurs primarily in which part of the GIT?
Your Answer: Duodenum
Explanation:Like most mineral nutrients, the majority of the iron absorbed from digested food or supplements is absorbed in the duodenum by enterocytes of the duodenal lining.
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This question is part of the following fields:
- Haematology
- Medicine
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Question 8
Correct
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What is the average life span of neutrophils?
Your Answer: 24 hours
Explanation:The average lifespan of inactivated human neutrophils in the circulation has been reported by different approaches to be between 5 and 90 hours.
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This question is part of the following fields:
- Haematology
- Medicine
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Question 9
Correct
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Why is tissue plasminogen activator (tPa) a valuable treatment used in myocardial infarction and stroke?
Your Answer: It forms plasmin from its inactive precursor
Explanation:tPA is a serine protease involved in the breakdown of blood clots. It functions by converting plasminogen, an inactive precursor, into plasmin, an active enzyme. Plasmin then degrades fibrin, the main protein component of blood clots, leading to clot dissolution. This mechanism is particularly valuable in the treatment of myocardial infarction (heart attack) and ischemic stroke, where timely dissolution of the clot can restore blood flow to affected tissues and reduce damage.
Therefore, the correct answer is:
- It forms plasmin from its inactive precursor
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This question is part of the following fields:
- Haematology
- Medicine
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Question 10
Correct
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The following occurs as a result of 2,3 Bisphosphoglycerate binding to deoxyhaemoglobin
Your Answer: A reduction in deoxyhaemoglobin's affinity for oxygen
Explanation:2,3-BPG acts as a heteroallosteric effector of haemoglobin, lowering haemoglobin’s affinity for oxygen by binding preferentially to deoxyhaemoglobin. An increased concentration of BPG in red blood cells favours formation of the T, low-affinity state of haemoglobin and so the oxygen-binding curve will shift to the right.
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This question is part of the following fields:
- Haematology
- Medicine
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Question 11
Correct
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Platelets are stored in this body organ.
Your Answer: Spleen
Explanation:Megakaryocyte and platelet production is regulated by thrombopoietin. Each megakaryocyte produces between 1,000 and 3,000 platelets during its lifetime. An average of 1011 platelets are produced daily in a healthy adult. Reserve platelets are stored in the spleen, and are released when needed by splenic contraction induced by the sympathetic nervous system.
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This question is part of the following fields:
- Haematology
- Medicine
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Question 12
Correct
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Which one of the following is necessary to activate plasminogen to plasmin?
Your Answer: tPA
Explanation:In circulation, plasminogen adopts a closed, activation resistant conformation. Upon binding to clots, or to the cell surface, plasminogen adopts an open form that can be converted into active plasmin by a variety of enzymes, including tissue plasminogen activator (tPA), urokinase plasminogen activator (uPA), kallikrein, and factor XII (Hageman factor).
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This question is part of the following fields:
- Haematology
- Medicine
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Question 13
Correct
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Bone marrow barrier is important to:
Your Answer: Allow mature red blood cells to pass into circulation
Explanation:The blood vessels of the bone marrow constitute a barrier, inhibiting immature blood cells from leaving the marrow. Only mature blood cells contain the membrane proteins, such as aquaporin and glycophorin, that are required to attach to and pass the blood vessel endothelium.
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This question is part of the following fields:
- Haematology
- Medicine
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Question 14
Correct
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Choose the correct statement regarding the protein C/S system?
Your Answer: The protein C/S complex inactivates factor Va and VIIIa
Explanation:The best characterized function of Protein S is its role in the anti coagulation pathway, where it functions as a cofactor to Protein C in the inactivation of Factors Va and VIIIa.
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This question is part of the following fields:
- Haematology
- Medicine
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Question 15
Correct
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Choose the most correct answer, what reduces affinity for oxygen in haemoglobin?
Your Answer: All the options are true
Explanation:The strength with which oxygen binds to haemoglobin is affected by several factors. These factors shift or reshape the oxyhaemoglobin dissociation curve. A rightward shift indicates that the haemoglobin under study has a decreased affinity for oxygen. The causes of shift to right can be remembered using the mnemonic, CADET, face Right! for CO2 and CO, Acid (H+), 2,3-DPG, Exercise and Temperature.
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This question is part of the following fields:
- Haematology
- Medicine
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Question 16
Correct
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From which of the following can niacin be synthesized in humans
Your Answer: Tryptophan
Explanation:Niacin, is also known as vitamin B3. The liver can synthesize niacin from the essential amino acid tryptophan, requiring 60 mg of tryptophan to make one mg of niacin.
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This question is part of the following fields:
- Haematology
- Medicine
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Question 17
Correct
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Which vitamin plays a major role in the metabolism of many amino acids?
Your Answer: Vitamin B6
Explanation:Vitamin B6 is part of the vitamin B group, and its active form, pyridoxal 5′-phosphate (PLP) serves as a coenzyme in many enzyme reactions in amino acid, glucose, and lipid metabolism.
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This question is part of the following fields:
- Haematology
- Medicine
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Question 18
Correct
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Regarding Iron stores, which of the following contains the highest proportion of total body iron?
Your Answer: Haemoglobin
Explanation:Most well-nourished people in industrialized countries have 4 to 5 grams of iron in their bodies. Of this, about 2.5 g is contained in the haemoglobin needed to carry oxygen through the blood, and most of the rest (approximately 2 grams in adult men, and somewhat less in women of childbearing age) is contained in ferritin complexes that are present in all cells, but most common in bone marrow, liver, and spleen.
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This question is part of the following fields:
- Haematology
- Medicine
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Question 19
Correct
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All of the following are Vitamin K-dependent clotting factors except:
Your Answer: Factor XI
Explanation:Activated Vitamin K is used to gamma carboxylate (and thus activate) certain enzymes involved in coagulation: Factors II, VII, IX, X, and protein C and protein S. Inability to activate the clotting cascade via these factors leads to the bleeding symptoms
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This question is part of the following fields:
- Haematology
- Medicine
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Question 20
Correct
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Which of the following conditions is procoagulant?
Your Answer: Factor V Leiden
Explanation:Factor V Leiden is a genetic mutation of one of the clotting factors in the blood, Factor V. This mutation makes Factor V resistant to inactivation by activated Protein C, which normally helps to regulate clot formation. As a result, individuals with Factor V Leiden are at increased risk of developing abnormal blood clots (thrombophilia), making it a procoagulant condition.
The other conditions listed are associated with bleeding tendencies rather than increased clotting:
- Afibrinogenemia: A rare genetic disorder where there is a complete lack of fibrinogen, leading to bleeding problems.
- Hemophilia: A group of inherited bleeding disorders where blood does not clot properly due to the lack of sufficient blood-clotting proteins (factors VIII or IX).
- Hypothrombinemia: A condition characterized by low levels of prothrombin, leading to increased bleeding.
- Christmas disease (Hemophilia B): A form of hemophilia caused by a deficiency of factor IX, resulting in a bleeding tendency.
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This question is part of the following fields:
- Haematology
- Medicine
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Question 21
Correct
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Which of these vitamins is not found in plants?
Your Answer: Vitamin B12
Explanation:No fungi, plants, nor animals (including humans) are capable of producing vitamin B12. Only bacteria and archaea have the enzymes needed for its synthesis. Proved food sources of B12 are animal products (meat, fish, dairy products).
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This question is part of the following fields:
- Haematology
- Medicine
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Question 22
Correct
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Question 23
Correct
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Which of the following is true regarding platelets?
Your Answer: Normally have a half-life of about 8 days
Explanation:Platelets have no cell nucleus: they are fragments of cytoplasm that are derived from the megakaryocytes of the bone marrow, and then enter the circulation. They have a half life of 5-9 days.
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This question is part of the following fields:
- Haematology
- Medicine
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Question 24
Correct
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With regard to the spleen which of the following has the correct match?
Your Answer: Periarteriolar lymphoid sheets - T lymphocytes
Explanation:The spleen consists of:Red pulp – responsible for mechanical filtration of red blood cells. Red pulp contains sinusoids, which are filled with blood, splenic cords of reticular fibers and a marginal zoneWhite pulp – responsible for active immune response through humoral and cell-mediated pathways. Composed of nodules, called Malpighian corpuscles. These are composed of: lymphoid follicles, rich in B-lymphocytes and periarteriolar lymphoid sheaths, rich in T-lymphocytes
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This question is part of the following fields:
- Haematology
- Medicine
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Question 25
Correct
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Vitamin B12 is transported from the enterocytes to the bone marrow by which factor?
Your Answer: Transcobalamin II (TC IIi)
Explanation:B12 must be attached to IF for it to be efficiently absorbed, as receptors on the enterocytes in the terminal ileum of the small bowel only recognize the B12-IF complex. Once the IF/B12 complex is recognized by specialized ileal receptors, it is transported into the portal circulation. The vitamin is then transferred to transcobalamin II (TC-II/B12), which serves as the plasma transporter.
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This question is part of the following fields:
- Haematology
- Medicine
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Question 26
Correct
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One of the functions of the spleen with regards to red blood cells is:
Your Answer: To filter and remove aged and abnormal red blood cells
Explanation:The spleen plays important roles in regard to red blood cells (also referred to as erythrocytes) and the immune system. It removes old red blood cells and holds a reserve of blood, which can be valuable in case of haemorrhagic shock, and also recycles iron. As a part of the mononuclear phagocyte system, it metabolizes haemoglobin removed from senescent erythrocytes. The globin portion of haemoglobin is degraded to its constitutive amino acids, and the haem portion is metabolized to bilirubin, which is removed in the liver.
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This question is part of the following fields:
- Haematology
- Medicine
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Question 27
Correct
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Question 28
Correct
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Regarding transportation of iron in the body, the process in which iron is transported from the enterocyte into the blood occurs using which transporter protein:
Your Answer: Ferroportin
Explanation:Divalent metal transporter 1 (DMT1) transport several divalent metals including iron across the enterocyte’s cell membrane into the cell. The cell can then release it into the body via the only known iron exporter in mammals, ferroportin.
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This question is part of the following fields:
- Haematology
- Medicine
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Question 29
Correct
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In the clotting mechanism, activation of factor IX can occur through the direct actions of:
Your Answer: Factor VIIa & XIa
Explanation:Factor IX is processed to remove the signal peptide, glycosylated and then cleaved by factor XIa (of the contact pathway) or factor VIIa (of the tissue factor pathway). When activated into factor IXa, in the presence of Ca2+, membrane phospholipids, and a Factor VIII cofactor, it hydrolyses one arginine-isoleucine bond in factor X to form factor Xa. Factor IX is inhibited by antithrombin.
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This question is part of the following fields:
- Haematology
- Medicine
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Question 30
Correct
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In the normal adult, haematopoiesis is present
Your Answer: Axial skeleton and proximal ends of long bones
Explanation:In children, haematopoiesis occurs in the marrow of the long bones such as the femur and tibia. In adults, it occurs mainly in the pelvis, cranium, vertebrae, and sternum.
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This question is part of the following fields:
- Haematology
- Medicine
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