Clinical Uses of Drugs Altering the ANS Flashcards

1
Q

what are some muscarinic agonists?

A
  • pilocarpine: used to treat glaucoma and dry mouth, used in sweat tests
  • bethanecol: used to occasionally aid bladder and gastric emptying
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2
Q

what are examples of some nicotine agonists?

A

-succinylcholine: is a high affinity agonist used in surgery for depolarising paralysis

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3
Q

what are cholinesterase inhibitors and what are some examples?

A

-they inhibit the break down of Ach so there is an increase in [Ach] so there is a greater stimulation of AchRs

  • there are short lasting or long lasting (parathion insecticide)
  • tacrine, donezepil, rivastigmine: used for dementia, neuromuscular diseases
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4
Q

when are muscarinic blockers/antagonists used?

A
  • in premedication before anaesthesia: to decrease secretions and to sedate
  • in the heart: to increase AV conduction
  • to cure motion sickness
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5
Q

when are nicotinic blockers/antagonists used and what are some examples?

A
  • muscle relaxants are direct nAchR blockers: tubocurarine

- depolarising blockers are direct nAchR agonists: suxamethonium

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6
Q

what are adrenoreceptor agonists used for?

A
  • eye drops: ephedrine are βa blockers
  • prolongation of local anaesthetic action: adrenaline
  • nasal decongestation: ephedrine
  • asthma inhalers: salbutamol are β2 agonists
  • premature labour: they are β agonists
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7
Q

what are the main uses of βa receptor blockers?

A
  • for the heart: atenolol slows down HR which improves profusion, reduces the demands dn reduces arrhythmia
  • in kidneys: atenolol triggers the JGA mechanism
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8
Q

what are the main used of αa receptor blockers?

A
  • to reduce high BP: prazosin

- to increase urination: αa1 selective

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9
Q

what is prazosin more commonly used for?

A
  • for male urinary problems: benign prostate hyperplasia
  • the prostate gland enlarges which narrows the urethra
  • this causes for the development of weak, slow urinary stream
  • straining to urinate, dribbling at end, inability to empty bladder completely, uncontrollable need to void
  • blocking tha α1a receptors causes relaxation of SM in bladder neck, urethra and prostrate gland
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10
Q

talk about he generation of α-a blockers used to treat prostatic hyperplasia

A
  • 1st + 2nd gen: (prazosin + terazosin) orally taken once a day, but side effects include low BP, wooziness and dizziness
  • 3rd gen: (tamsulosin) is uroselective and have minimal effects on BP but experience ejaculatory dysfunction
  • 4th gen: (alfuzosin) has comparable efficacy as 3rd gen but no effect of ejaculation
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11
Q

how do drugs have an indirect enhancement of endogenous NA?

A
  • cocaine, meth, MOA inhibitors (tranylcypromine)
  • cocaine inhibits the NA uptake mechanism at the neuronal cell which increases the amount of NA interacting w receptors
  • meth has a similar effect as cocaine but competed w NA for uptake and displaces NA in vesicles
  • MOA inhibitors inhibit enzymes that break down NA which increases NA circulating: sympathetic overdrive
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