Pharmacology Flashcards

1
Q

describe the mechanism by which beta 1 adrenoceptors become activated: the sympathetic system

A

noradrenaline and adrenaline activate the b1 receptors in nodal cells and myocardial cells.
coupling through G proteins activate adenylyl cyclase to increase cAMP which causes an increase in the L type calcium channels which results in an increases the calcium coming in, triggering the Sarcoplasmic reticulum calcium injection

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2
Q

Name effects of sympathetic system on HR, contractility, conduction and automaticity

A

HR increase
Contract increase
Conduction INCREASE
Automaticity increase

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3
Q

What is an increase in HR mediated by and what is it due to?

A

mediated by SA node and due to increase in slope of the pacemaker potential

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4
Q

What is an increase in contractility due to?

A

an increase in phase 2 of cardiac potential in atrial and ventricular myocytes and enhanced Ca2+ influx

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5
Q

Describe the process by which the parasympathetic system monitors the heart

A

acetylcholine (post ganglionic transmitter) activates M2 muscarinic cholinoceptors, largely in nodal cells which triggers the recruitment of Potassium channels decreasing the slope resulting in slower HR but no effect on the contraction of the heart

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6
Q

Describe the effect of the parasympathetic system on HR, contractility, AV node conductance

A

Decrease HR
decrease Contractility
Decrease AV node conductance

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7
Q

Parasympathetic/sympathetic stimulation may cause arrhythmias to occur in the atria?

A

parasympathetic

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8
Q

What may be used in atrial flutter or AF to suppress impulse conduction through the AV node?

A

vagal manoeuvres

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9
Q

name some vagal manoeuvres

A

aortic baroreceptors, massage carotid bifurcation

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10
Q

what is the function of the Ivabradine drug?

A

anti anginal drug

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11
Q

p: Ivabradine

A
  • Selective blocker of HCN leading to greater channel slows HR by decreasing the slope of the pacemaker potential
    By decreasing the amount of effective potassium channels slowing everything down
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12
Q

Describe excitation contraction in cardiac muscle: contraction

A
  • Opening of Ca++ L type channels during phase 2 of action potential
    Ca++ influx into cytoplasm
    Calcium release from Sarcoplasmic reticulum (CICR calcium induced calcium release)
    Ca++ binds to troponin C and shifts tropomyosin out of the actin cleft > so cross bridge formation resulting in contraction.
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13
Q

Describe excitation contraction in cardiac muscle: relaxation

A
  • Repolarisation in phase 3 to 4, so L type channels close
  • Ca++ influx ceases, NCX1 causes Ca++ efflux
  • Sarcoplasmic Reticulum ceases to release Ca++
  • Ca++ dissociates from troponin C = broken cross bridges between actin and myosin so relaxation
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14
Q

describe the mechanism by which B1-adrenoceptors activation increases the force of contraction on the heart

A
  • B1 activation activates adenylyl cyclase which converts ATP to cAMP
    leads to phosphorylation by PKA which initiates L type channels, that enhance contractility.
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15
Q

Name some things B1-adrenoceptor agonists generally do to the heart and body?

A
increase:
HR
Force
Rate
CO2 AND O2 consumption

Decreases:
cardiac efficacy
Arrhythmias

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16
Q

What is dobutamine used for?

A

acute Heart Failure

17
Q

is dobutamine A/B selective?

A

Beta

18
Q

What way is dobutamine administered and half life?

A

IV and 2 min

19
Q

What is adrenaline used for?

A

anaphylaxis

cardiac arrest

20
Q

Is adrenaline A/B ant/agonist?

A

a or beta agonist

21
Q

How is adrenaline administered and half life?

A

IM, SC, IVE

2 min

22
Q

Name one other B1-adrenoceptor agonist used on the heart and its use?

A

noradrenaline

the rate and force of contraction of the heart.

23
Q

What is the general effect of B1 RECEPTOR ANATGONISTS?

A

Blocks B adrenoceptors

non-selectively or selectively

24
Q

name non selective B antagonists

A

B 1+2 propanolol

25
Q

name the selective B1 antagonists

A

atenolol, bisoprolol, metoprolol

26
Q

how do B1 antagonists help arrhythmias?

A

decrease excessive sympathetic drive (in stress or emotion), delay conduction through AV node restore sinus rhythm (AF and SVT)

27
Q

how do B1 antagonists help angina?

A

can be alternate 1st line to CCB

28
Q

how do B1 antagonists help HF?

A

paradoxical but low doses reduce excessive sympathetic drive not in short term, wait a couple of days

29
Q

how do B1 antagonists help hypertension?

A

only if comorbidities (angina) present

30
Q

name some adverse effects of b adrenoceptor antagonists

A

Bronchospasm (asthma)
can aggravate cardiac failure
bradycardia, hypoglycaemia (release of glucose in liver controlled by B2), fatigue
cold extremities

31
Q

Name the Muscarinic receptor agonist

A

Atropine

32
Q

what is atropine used for?

A

Used 1st line in severe or symptomatic bradycardia (following MI).

33
Q

How does atropine work?

A

Increase in HR (blocks parasympathetic stimulation), No effect on BP (resistance vessels lack parasympathetic innervation).

34
Q

p: Inotropic agents eg Digoxin in therapy of heart failure

A

Digoxin inhibits Na+/K+ ATPase,
less Na+ and Ca++ is exchanged (increasing Intracellular Ca++),
greater storage of Ca++ in SR,

35
Q

How is Digoxin used?

A

IV in acute HF, orally in chronic HF, especially HF with AF

36
Q

name the adverse effects of Digoxin

A

Depression of AV node (heart block), Arrhythmias
nausea/ vomiting
diarrhoea
disturbs colour vision yellow vision.