Clinical Uses of Drugs Altering the ANS Flashcards
what are some muscarinic agonists?
- pilocarpine: used to treat glaucoma and dry mouth, used in sweat tests
- bethanecol: used to occasionally aid bladder and gastric emptying
what are examples of some nicotine agonists?
-succinylcholine: is a high affinity agonist used in surgery for depolarising paralysis
what are cholinesterase inhibitors and what are some examples?
-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
when are muscarinic blockers/antagonists used?
- in premedication before anaesthesia: to decrease secretions and to sedate
- in the heart: to increase AV conduction
- to cure motion sickness
when are nicotinic blockers/antagonists used and what are some examples?
- muscle relaxants are direct nAchR blockers: tubocurarine
- depolarising blockers are direct nAchR agonists: suxamethonium
what are adrenoreceptor agonists used for?
- 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
what are the main uses of βa receptor blockers?
- for the heart: atenolol slows down HR which improves profusion, reduces the demands dn reduces arrhythmia
- in kidneys: atenolol triggers the JGA mechanism
what are the main used of αa receptor blockers?
- to reduce high BP: prazosin
- to increase urination: αa1 selective
what is prazosin more commonly used for?
- 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
talk about he generation of α-a blockers used to treat prostatic hyperplasia
- 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
how do drugs have an indirect enhancement of endogenous NA?
- 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