Flashcard set 1

(35 cards)

1
Q

What is the homeostasis control process?

A

stimulus -> sensor -> controller -> effector -> response

and negative feedback regulation = effector leads to reduction in stimulus

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2
Q

What is the organisation of the ANS?

A
  • sensory afferent nerve fibres
  • control centres: hypothalamus, brain stem, spinal cord
  • efferent pathways: sympathetic nervous system, parasympathetic nervous system
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3
Q

What are the common features of the efferent pathway?

A
  • 2 neurons in series
  • preganglionic neuron originate in CNS
  • postganglionic neuron originate in autonomic ganglia
  • 1 preganglionic neuron can synapse with many postganglionic neurons (8-9)
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4
Q

What is the flight or fight pathway?

A

sight, sound, smell -> amygdala centre -> osteoblasts -> osteocalcin -> inhibits parasympathetic neuron

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5
Q

Organisation of the sympathetic nervous system?

A
  • preganglionic origin = thoracic 1, Lumbar 2/3
  • postganglionic origin = autonomic ganglia
  • preganglionic neuron is short
  • postganglionic neuron is long
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6
Q

Organisation of the parasympathetic nervous system?

A
  • preganglionic origin = cranial nerve III (eye), VII (facial), IX (parotid), X (vagus)
  • postganglionic origin = autonomic ganglia
  • preganglionic neuron is long
  • postganglionic neuron is short
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7
Q

Neurotransmitters of ANS and their synapses

A

Neurotransmitters:

  • Acetylcholine (Ach)
  • Noradrenaline (NAdr)
  • Adrenaline (Adr)
  • Non-adrenergic non-cholinergic (NANC)

Synapses:

  • Cholinergic = nicotinic or muscarinic
  • Adrenergic = alpha or beta
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8
Q

What is the organisation of the muscarinic receptor?

A
  • target organ in PNS (parasympathetic nervous system)
  • exception is sweat glands in SNS (sympathetic nervous system)
  • blocked by ATROPINE
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9
Q

What is the organisation of the nicotinic receptor?

A
  • ganglia in SNS and PNS
  • located at neuromuscular junction
  • blocked by CURARE
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10
Q

What is the organisation of adrenoreceptor Alpha 1?

A
  • postsynaptic
  • releases NAdr > Adr
  • vasoconstrictor and smooth muscle contraction
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11
Q

What is the organisation of adrenoreceptor Alpha 2?

A
  • presynaptic
  • releases Nadr > Adr
  • reduction in adrenergic and cholinergic transmission
  • blocked by PHENTOLAMINE
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12
Q

What is the organisation of adrenoreceptor Beta 1?

A
  • receptor in the heart
  • releases Adr = NAdr
  • increase in heart rate and force of contraction
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13
Q

What is the organisation of adrenoreceptor Beta 2?

A
  • releases Adr > NAdr
  • vasodilation and smooth muscle relaxation
  • blocked by PROPANOL
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14
Q

What are small and large red blood cells called and where are they found?

A
  • small RBCs = microcytic -> found in iron deficiency anaemia
  • large RBCs = macrocytic -> found in folate (vitamin B9) deficiency anaemia
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15
Q

What happens to ages RBCs after 120 days?

A
  • phagocytized in liver and spleen
  • haemoglobin decomposed into heme and globin
  • heme components are recycled e.g heme = bilirubin, iron = stored in liver
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16
Q

Structure of haemoglobin molecule

A
  • globin = made up of 4 protein chains (alpha, beta, gamma, delta)
  • 4 iron containing haem groups = consists of porphyrin ring with 1 Fe atom
17
Q

What are the types of haemoglobin/globin forms?

A
HbA = 2 alpha, 2 beta
HbA2 = 2 alpha, 2 delta
HbF = 2 alpha, 2 gamma 
HbS = sickle cell anaemia
HbH = alpha thalassemia
18
Q

What are the 2 forms of Hb and what are their characteristics?

A
  • r form (relaxed) = high O2 affinity = firmly binds O2

- t form (taught) = low O2 affinity = releases O2

19
Q

What is sickle cell anemia?

A

genetic disease = mutation in beta globin gene -> glutamic acid residue is replaced by valine = sticky patches

Hb polymerises at low PO2 forming long crystals of HbS

20
Q

What is alpha thalassaemia?

A
  • production of alpha globin is reduced = leads to excess of beta chain
  • unstable tetramer of 4 beta chains = HbH
  • reduced oxygen carrying
21
Q

What is beta thalassemia?

A
  • results in iron overload = organ damage
  • excess of alpha chains
  • bind to and damage RBC membranes
22
Q

How is thalassemia diagnosed?

A

Diagnosed by electrophoresis

  • alpha thalassemia = reduced HbA, presence of HbH
  • beta thalassemia = decreased HbA, beta globin reduced or absent
23
Q

What is haemostasis?

A

arrest of bleeding from a broken blood vessel

24
Q

Where are platelets stored and how are they released?

A

stored in the spleen and released by contraction of the spleen activated by SNS

25
What are the 3 steps of haemostasis?
1. vascular spasm 2. formation of platelet plug 3. blood coagulation
26
What are the 2 pathways for blood clotting and what do they do?
1. INTRINSIC = initial stimulus is exposed collagen | 2. EXTRINSIC = blood contact with damaged tissue outside of blood vessel that exposes tissue factor III
27
What are the anti-clotting systems?
1. Antithrombin 2. Tissue factor pathway inhibitor 3. Thrombin 4. Thrombodulin
28
How is thrombin an anticlotting system?
thrombin binds to its receptor which stimulates production of prostaglandins, nitric oxide and ADP = inhibit platelet aggregation
29
What does antithrombin do?
Inhibits many clotting factors esp. thrombin | -> activity is enhanced by HEPARIN
30
What does thrombodulin do?
Expressed by endothelial cells. Binds thrombin eliminating its coagulant effects. Activates protein C -> activates protein S -> inactivates factor Va and VIIIa
31
What are the inherited coagulation disorders?
Von Willebrands disease = lack of von Willebrands factor -> poor platelet aggregation Haemophilia A = deficiency in factor VIII (X-linked) Haemophilia B = rare deficiency in factor IX (AKA christmas disease)
32
2 examples of anticoagulant
1. WARFARIN = inhibits vitamin K | 2. HEPARIN = activates antithrombin III
33
What makes up the ABO system?
5 sugars: - fucose - galactose - N-acetylgalactosamine - N-acetylglucosamine - Sialic acid 3 enzymes: - FUT-1 - A transferase - B transferase 2 genes: - ABO - H
34
What do the ABO and H genes encode?
encode glycosyltransferase = transfer monosaccharide to polysaccharide chains
35
Organisation of CVS
- 2 circulations in series served by 2 pumps - systemic = high pressure - pulmonary = low pressure - unidirectional flow controlled by valves Atrioventricular valve: right = tricuspid left = bicuspid Semilunar valve: right = pulmonary left = aortic