Drug pathways Flashcards

1
Q

Thiazide diuretics e.g. bendroflumethiazide

A

Blocks NaCl reabsorption at the distal tubule in the kidneys by blocking the NaCl co-transporter

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2
Q

Loop diuretics e.g. furosemide

A

Inhibits Na reabsorption in the loop of Henle

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3
Q

Potassium sparing diuretics e.g. spironolactone

A

Blocks the action of aldosterone

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4
Q

Bisoprolol

A

Block B1 adrenoreceptors antagonising the sympathetic nervous system

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5
Q

Atenolol

A

Blocks B1 and B2 adrenoreceptors

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6
Q

Ca2+ channel blockers e.g. amlodipine

A

Binds to L-type Ca2+ channels in smooth muscle causing relaxation

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7
Q

Nitrates e.g GTN or Isosorbide

A

metabolism releases nitric oxide dilating vascular smooth muscle and reducing preload to the heart

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8
Q

Potassium channel openers e.g. nicorandil

A

Vasodilator

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9
Q

Ivabradine

A

Lowers HR

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10
Q

Aspirin

A

Blocks cyclo-oxygenase enzyme preventing the production of thromboxane A2

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11
Q

Clopidogril

A

Blocks ADP binding to its receptor on platelet blocking platelet aggregation

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12
Q

Heparin

A

Inactivates thrombin and activated factor x by biding to antithrombin

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13
Q

Low molecular weight heparin e.g. Dalteparin

A

forms a complex with antithrombin converting it into an inactivator of factor Xa

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14
Q

Streptokinase

A

Binds to circulating plasminogen to form an activator complex that converts further plasminogen to plasmin

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15
Q

Class IA anti-arrhythmic drugs e.g. procainamide

A

dissociated from Na channels at a moderate rate

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16
Q

Class IB anti-arrhythmic drugs e.g. Lidocaine

A

dissociates from Na channels at a rapid rate

17
Q

Class IC anti-arrhythmic drugs e.g. Flecainide

A

dissociates from Na channels at a rapid rate

18
Q

Class II anti-arrhythmic drugs e.g. propranolol

A

B-adrenoreceptor antagonist - decreases rate of depolarisation

19
Q

Class III anti-arrhythmic drugs e.g. amiodarone

A

Voltage activated K+ channels - prolong AP duration increasing refractory period

20
Q

Class IV anti-arrhythmic drugs e.g. verapamil

A

voltage activated Ca2+ channels - slow conduction in SA and AV nodes

21
Q

Class V anti-arrhythmic drugs e.g. adenosine

A

activates A1-adenosine receptors coupled to Gi, opens ACh sensitive K+ channels (GIRK)

22
Q

Adrenaline

A

increases contractility, HR, dilates coronary arteries and redirects blood flow away from the gut and skin