What are the major functions of the α1 receptor? - ANSWER Increase vascular smooth muscle contraction, increase pupillary dilator muscle contraction
... [Show More] (mydriasis), increase intestinal and bladder sphincter muscle contraction
What are the major functions of the α2 receptor? - ANSWER Decrease sympathetic outflow, decrease insulin release, decrease lipolysis, increase platelet aggregation, decrease aqueous humor production
What are the major functions of the β1 receptor? - ANSWER Increase heart rate, increase contractility, increase renin release, increase lipolysis
What are the major functions of the β2 receptor? - ANSWER Vasodilation, bronchodilation, increase lipolysis, increase insulin release, decrease uterine tone (tocolysis), ciliary muscle relaxation, increase aqueous humor production
What are the major functions of the M1 receptor? - ANSWER CNS, enteric nervous system
What are the major functions of the M2 receptor? - ANSWER Decrease heart rate and contractility of atria
What are the major functions of the M3 receptor? - ANSWER Increase exocrine gland secretions (e.g., lacrimal, salivary, gastric acid), increase gut peristalsis, increase bladder contraction, increase bronchoconstriction, pupillary sphincter muscle contraction (miosis), ciliary muscle contraction (accommodation)
What are the major functions of the D1 receptor? - ANSWER Relaxes renal vascular smooth muscle
What are the major functions of the D2 receptor? - ANSWER Modulates transmitter release, especially in the brain
What are the major functions of the H1 receptor? - ANSWER Increase nasal and bronchial mucus production, increase vascular permeability, contraction of bronchioles, pruritis, pain
What are the major functions of the H2 receptor? - ANSWER Increase gastric acid secretion
What are the major functions of the V1 receptor? - ANSWER Increase vascular smooth muscle contraction
What are the major functions of the V2 receptor? - ANSWER Increase H2O permeability and reabsorption in collecting tubules of kidney (V2 is found in the "2" kidneys)
What receptors are associate with Gq? - ANSWER H1, α1, V1, M1, and M3
What receptors are associated with Gs? - ANSWER H2, B1, B2, V2, D1
What receptors are associated with Gi? - ANSWER M2, α2, D2
Bethanechol - ANSWER -Direct cholinergic agonist
-Activates bowel and bladder smooth muscle
-Used in postoperative and neurogenic ileus
-Resistant to AChE
Carbachol - ANSWER -Direct cholinergic agonist
-Carbon copy of acetylcholine
-Constricts pupils and relieves intraocular pressure in glaucoma
Methacholine - ANSWER -Direct cholinergic agonist
-Stimulates muscarinic receptors in airways when inhaled
-Used as a challenge test for diagnosis of asthma
Pilocarpine - ANSWER -Direct cholinergic agonist
-Contracts ciliary muscle of eye (open angle glaucoma), contracts pupillary sphincter (closed angle glaucoma)
-Potent stimulator of sweat, tears and saliva
-AChE resistant
Donepezil - ANSWER -Anticholinesterse - increases ACh
-Alzheimer disease
Galantamine - ANSWER -Anticholinesterse - increases ACh
-Alzheimer disease
Rivastigmine - ANSWER -Anticholinesterse - increases ACh
-Alzheimer disease
Edrophonium - ANSWER -Anticholinesterse - increases ACh
-Historically used to diagnose myasthenia gravis (MG is now diagnosed by anti-AChR Ab test.
Neostigmine - ANSWER -Anticholinesterse - increases ACh
-Used in postoperative and neurogenic ileus and urinary retention, myasthenia gravis, and postoperative reversal of neuromuscular junction blockade
Physostigmine - ANSWER -Anticholinesterse - increases ACh
-Used in anticholinergic toxicity
-Crosses the blood-brain barrier (CNS)
Pyridostigmine - ANSWER -Anticholinesterse - increases ACh
-Increases muscle strength
-Used in myasthenia gravis (long acting)
-Does not penetrate CNS
Atropine - ANSWER -Muscarinic antagonist
-Used in bradycardia and for ophthalmic applications
-Also used as antidote for cholinesterase inhibitor poisoning
-Actions include increase pupil dilation, cycloplegia, decreased airway secretions, decreased acid secretions, decreased gut motility, decreased bladder urgency in cystitis
-Toxicity: increased body temp (due to decreased sweating), rapid pulse, dry mouth, dry and flushed skin, cycloplegia, constipation, disorientation;
-Can cause acute angle-closure glaucoma in elderly (due to mydriasis), urinary retention in men with prostatic hyperplasia, and hyperthermia in infants
-See also homatropine and tropicamide
Benztropine - ANSWER -Muscarinic antagonist
-Works in CNS
-Used in Parkinson disease and acute dystonia
Glycopyrrolate - ANSWER -Muscarinic antagonist
-Parental use: preoperative use to reduce airway secretions
-Oral use: drooling, peptic ulcer
Hyoscyamine - ANSWER -Muscarinic antagonist
-Antispasmodics for IBS
Dicyclomide - ANSWER -Muscarinic antagonist
-Antispasmodics for IBS
Ipratropium - ANSWER -Muscarinic antagonist
-Used in COPD and asthma
Tiotropium - ANSWER -Muscarinic antagonist
-Used in COPD and asthma
Oxybutynin - ANSWER -Muscarinic antagonist
-Reduced bladder spasms and urge urinary incontinence
Solifenacin - ANSWER -Muscarinic antagonist
-Reduced bladder spasms and urge urinary incontinence
Tolterodine - ANSWER -Muscarinic antagonist
-Reduced bladder spasms and urge urinary incontinence
Scopalamine - ANSWER -Muscarinic antagonist
-Motion sickness
Tetrodotoxin - ANSWER -Poisoning can result from ingestion of poorly prepared puffer fish (exotic sushi)
-Highly potent toxin that binds fast voltage-gated Na+ channels in cardiac and nerve tissue, preventing depolarization - blocks action potential without changing resting potential (same mechanism as Lidocaine)
-Causes nausea, diarrhea, paresthesias, weakness, dizziness, loss of reflexes.
-Treatment is primarily supportive.
Ciguatoxin - ANSWER -Consumption of reef fish (e.g. barracuda, snapper, eel...)
-Causes ciguatera fish poisoning.
-Opens Na+ channels causing depolarization. Symptoms easily confused with cholinergic poisoning.
-Temperature-related dysesthesia (e.g., "cold feels hot; hot feels cold") is regarded as a specific finding of ciguatera.
-Treatment is primarily supportive.
Scombroid poisoning - ANSWER -Caused by consumption of dark-meat fish (e.g., bonito, mackerel, mahi-mahi, tuna) improperly stored at warm temperature.
-Bacterial histidine decarboxylase converts histidine to histamine. Histamine is not degraded by cooking.
-Acute-onset burning sensation of the mouth, flushing of face, erythema, urticaria, pruritus, headache. May cause anaphylaxis-like presentation (i.e., bronchospasm, angioedema, hypotension).
-Frequently misdiagnosed as allergy to fish.
-Treat supportively with antihistamines; if needed, antianaphylactics (e.g., bronchodilators, epinephrine).
Albuterol - ANSWER -β2 > β1 direct agonist
-Acute asthma
Salmterol - ANSWER -β2 > β1 direct agonist
-Long term asthma or COPD control
Dobutamine - ANSWER -β1 > β2, α direct agonist
-Uses: heart failure (HF) (inotropic > chronotropic), cardiac stress testing.
Dopamine - ANSWER -D1 = D2 > β > α direct agonist
-Uses: unstable bradycardia, HF, shock; inotropic and chronotropic α effects predominate at high doses.
Epinephrine - ANSWER -β > α direct agonist
-Uses: anaphylaxis, asthma, open-angle glaucoma;
α effects predominate at high doses. Significantly stronger effect at β2-receptor than norepinephrine.
Isoprterenol - ANSWER -β1 = β2 direct agonist
-Uses: electrophysiologic evaluation of tachyarrhythmias. Can worsen ischemia
Norepinephrine - ANSWER -α1 > α2 > β1 direct agonist
-Hypotension (butrenal perfusion). Significantly weaker effect at β2-receptor than epinephrine.
Phenylephrine - ANSWER -α1 > α2 direct agonist
-Uses: hypotension (vasoconstrictor), ocular procedures (mydriatic), rhinitis (decongestant)
Amphetamine - ANSWER -Indirect general sympathetic agonist
-reuptake inhibitor; also releases stored catecholamines
-Narcolepsy, obesity, ADHD.
Cocaine - ANSWER -Indirect general sympathetic agonist
-Reuptake inhibitor
-Causes vasoconstriction and local anesthesia.
-Never give β-blockers if cocaine intoxication is
suspected (can lead to unopposed α1 activation and extreme hypertension).
Ephedrine - ANSWER -Indirect general sympathetic agonist
-Releases stored catecholamines
-Nasal decongestion, urinary incontinence, hypotension.
Norepinephrine vs. isoproterenol - ANSWER -Norepinephrine increases systolic and diastolic pressures as a result of α1-mediated vasoconstriction causing increased in mean arterial pressure and reflex bradycardia. -However, isoproterenol (no longer commonly used) has little α effect but causes β2-mediated vasodilation, resulting in decreased mean arterial pressure and increased heart rate through β1 and reflex activity.
Clonidine - ANSWER -α2-agonist
-Uses: hypertensive urgency (limited situations); does not decrease renal blood flow; ADHD, Tourette syndrome
-Toxicity: CNS depression, bradycardia, hypotension, respiratory depression, miosis
α-methyldopa - ANSWER -α2-agonist
-Used for hypertension in pregnancy
-Toxicity: Direct Coombs ⊕ hemolysis, SLE-like syndrome
Phenoxybenzamine - ANSWER -Nonselective α-blocker
-Irreversible
-Used preoperatively for pheochromocytoma to prevent catecholamine (hypertensive) crisis
-Toxicity: orthostatic hypotension, reflex tachycardia
Phentolamine - ANSWER -Nonselective α-blocker
-Give to patients on MAO inhibitors who eat tyramine containing foods
-Toxicity: orthostatic hypotension, reflex tachycardia
Prazosin - ANSWER -Selective α1-blocker
-Uses: urinary symptoms of BPH; PSTD
-Hypertension
-Toxicity: 1st-dose orthostatic hypotension, dizziness, headache
Terazosin - ANSWER -Selective α1-blocker
-Uses: urinary symptoms of BPH;
-Hypertension
-Toxicity: 1st-dose orthostatic hypotension, dizziness, headache
Doxazosin - ANSWER -Selective α1-blocker
-Uses: urinary symptoms of BPH;
-Hypertension
-Toxicity: 1st-dose orthostatic hypotension, dizziness, headache
Tamsulosin - ANSWER -Selective α1-blocker
-Uses: urinary symptoms of BPH;
-Toxicity: 1st-dose orthostatic hypotension, dizziness, headache
Mirtazapine - ANSWER -Selective α2-blocker
-Used in depression
-Toxicity: sedation, increased serum cholesterol, increased appetite
α-blockade of epinephrine vs. phenylephrine - ANSWER Shown in the picture are the effects of an α-blocker (e.g., phentolamine) on blood pressure responses to epinephrine and phenylephrine. The epinephrine response exhibits reversal of the mean blood pressure change, from a net increase (the α response) to a net decrease (the β2 response). The response to phenylephrine is suppressed but not reversed because phenylephrine is a "pure" α-agonist without β action.
Effects of β-blockers - ANSWER -Angina pectoris—decrease heart rate and contractility, resulting in decrease O2 consumption
-MI—β-blockers (metoprolol, carvedilol, and bisoprolol) mortality
-SVT (metoprolol, esmolol)—decrease AV conduction velocity (class II antiarrhythmic)
-Hypertension—decrease cardiac output, decrease renin secretion (due to β1-receptor blockade on JGA cells)
-HF—decrease mortality in chronic HF
-Glaucoma (timolol)—decrease secretion of aqueous humor [Show Less]