Cardiovascular Flashcards
What are the two phases that make up the blood? Give their proportions also.
Cellular phase 45%
Fluid phase 55%
What makes up the majority of the cellular component of the blood?
RBCs (44%)
Define heamatorcrit and give its usual value
The proportion of the cellular component of the blood, 0.45.
Define serum
Fluid component of blood with all the clotting factors removed
What happens to the haematocrit during acute anaemic (bleeding) and why?
Stays the same, 0.45. Cellular and fluid components of blood lost in the same proportion
What happens to the haematocrit during chronic anaemia?
Decreases (0.2)
Define haematopoesis
Production of blood cells
Where are a haemopoetic stem cells in an adult?
Bone marrow at axial skeleton
Where are haemopoetic stem cells found in a child?
Bone marrow at all bone
Where are haemopoetic stem cells found in utero?
Yolk sac, liver and spleen
What growth factor causes haemopoetic stem cells to proliferate into RBCs? And where is the factor secreted?
Erythropoetin (EPo)
Kidneys
Where are mature blood cells found?
In circulation
What growth factor causes haemopoetic stem cells to proliferate into WBCs?
Granulocyte-colony stimulating factor (GCSF)
What growth factor caused haemopoetic stem cells to proliferated into platelets?
Thrombopoetin (TPo)
Give the average life span of RBCs
120 days
Give the average life span of WBCs
6 hours
Give the average life span of platelets
7-10 days
Which of the blood cells are anucleate/ have no membrane bound organelles?
RBCs and platelets
Erythrocyte is the proper name for which type of blood cell?
RBC
Describe the shape of RBCs and state why they are this shape?
Biconcave
Increases SA:V for rapid diffusion of O2/CO2
What is a reticulocyte?
A young erythrocyte still containing its ribosomes (1% of circulating erythrocytes)
What are the main sites of RBC breakdown?
Liver and spleen
What is the major breakdown product of haemoglobin (and therefore RBCs)?
Bilirubin
What is the function of RBCs?
Contain haemoglobin to allow the transport of gases O2/CO2
Describe the structure of Hb
4 polypeptide chains (2 alpha and 2 beta)
4 haem groups each with an Fe 2+ (ferrous group)
How does the presence of CO2 affect the binding of O2 to Hb? What is the name of the shift that results on an oxygen dissociation curve and in which direction does it occur?
Increase in CO2 Decrease in pH Conformational change of Hb Decreased affinity for O2 Increased unloading of O2
Bohr shift
To the right
What is the proper name for WBCs?
Leukocytes
What are the two main types of leukocytes
Granulocytes
Agranulocytes
Give the normal range of Hb
12.5-15.5g/dL
Give the 3 types of granulocyte, give in order of most to least abundant
Neutrophil
Eosinophil
Basophil
State the 2 types of agranuolocyte, giving the most abundant type first
Lymphocyte
Monocyte
Describe the features and role of a neutrophil
Multi-lobar (4) lobes
Phagocytic
Release cytokines in inflammatory response
Describe the features and role of eosinophils
2-3 lobes
Pink staining granules
Protect against parasite infection
Describe the structure and function of basophils
Blue staining granules
Secrete histamine and anticlotting factors that increase blood flow and therefore attracts infection fighting cells to accumulate at site of infection
Describe the features and role of lymphocytes
Small, darkly stained nucleus, & very little cytoplasm
Role in specific/adaptive immunity
T - thymus - cyctotoxic
B - bone marrow - antibodies/immunoglobulins
Describe the features and role of monocytes
Kidney shaped nucleus
Phagocytes in blood
Migrate and mature at tissue - macrophages
Define haemostasis
The prevention of blood loss
Give the 3 mechanisms of haemostasis when an injury to a blood vessel occurs
Vasoconstriction
Platelet plug formation
Coagulation/clotting cascade
Define what is meant by a haematoma
Accumulation of blood within tissues (increase interstitial pressure prevents continues blood loss)
Where are the majority of clotting factors synthesised? Which of the clotting factors are synthesised here?
Liver I II V VII VII IX X XI
What is clotting factor I?
Fibrinogen
What is clotting factor II?
Prothrombin
Describe the platelet plug formation
Exposure of collagen
von Willerbrand factor bind to collagen
Platelets bind to vWF by GP1b receptor
Binding causes the release of alpha and dense granules
ADP (from dense granules) binds to P2 (purinergic receptors) which activates the cell
Activation
- change in shape to psuedopodia
- change in metabolism
- change in surface membrane
* activation of GPIIb/IIIa receptor, increased affinity for fibrin
* thromboxane A2 release, derived from arachidonic acid
Thromboxane A2 and ADP stimulate platelet aggregation
Fibrinogen forms bridges between aggregating platelets
PLATELET PLUG
Surrounding non-damaged cells release prostaglandin and NO that inhibit aggregation and stop the platelet plug spreading any further
Define thrombosis
The formation of a clot inside a vessel
What is the proper name for platelets
Thrombocytes
Describe the features and role of platelets
Cytoplasmic fragment of megakaryocytes Anucleate Circulate in the inactive form Alpha and dense granules (also lysosomes and peroxisomes) Role in heamostatis
What have if the no. of platelets are decreased to less than 20% of their normal amount
Spontaneous bleeding
What is the importance of cascade reactions?
Bio amplification
Tight regulation/graduated response
What is the penultimate step in the coagulation cascade? And what is this step catalysed by?
Prothrombin to thrombin
Prothrombinase (Xa) (Also requires Ca2+)
What is the final step in the coagulation cascade? And what is it catalysed by?
Fibrinogen to fibrin
Thrombin (Also requires Ca2+)