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        | Term 
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        | Term 
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        | Term 
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        | Term 
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        | Term 
 | Definition 
 
        | sympathomimetic mixed alpha agonist |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | beta 2 agonists used to calm uterus in dangerous pregnancies
 |  | 
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        | Term 
 | Definition 
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        | Term 
 | Definition 
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        | Term 
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        | Term 
 | Definition 
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        | Term 
 
        | cholinesterase degredation
 susceptibility
 |  | Definition 
 
        | acetylcholine +++ methacholine +
 carbachol 0
 bethanachol 0
 |  | 
        |  | 
        
        | Term 
 
        | comparative potency for muscarinics in cardiovascular |  | Definition 
 
        | methacholine +++ acetylcholine ++
 carbachol +
 bethanechol 0
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | bethanachol +++ carbachol +++
 methacholine ++
 Acetylcholine ++
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | quaternary ammonium muscarinic antagonist |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | quaternary ammonium muscarinic antagonist |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | quaternary ammonium muscarinic antagonist |  | 
        |  | 
        
        | Term 
 
        | homatropine methylbromide |  | Definition 
 
        | quaternary ammonium muscarinic antagonist |  | 
        |  | 
        
        | Term 
 
        | scopalamine methylbromide |  | Definition 
 
        | quaternary ammonium muscarine antagonist |  | 
        |  | 
        
        | Term 
 
        | alpha-methylnorepinephrine |  | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 
        | low dose epinephrine response |  | Definition 
 
        | beta 1 agonism predominates |  | 
        |  | 
        
        | Term 
 
        | high dose epinephrine response |  | Definition 
 
        | tachycardia, positive inotrope, increased peripheral resistance |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | acetylcholinesterase inhibitor, uncharged (CNS) 
 targets Parkinson's and Alzheimer's
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | edrophonium is used to determine between cholinergic attack and myasthenia gravis |  | 
        |  | 
        
        | Term 
 
        | differences in sensitivity of muscarinic sites (most sensitive/responsive to least) |  | Definition 
 
        | 1)  salivation, bronchial, sweating 2)  pupil dilation, accomodation, cardiac
 3)  urinary bladder, GI tract
 4) gastric secretion
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | anticholinergic respiratory muscarinic blocker
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | nicotinic agonist / deactivates nicotinic receptors with chronic use |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | muscarinic antagonist CNS effects
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | muscarinic antagonist CNS effects and sedation/motion sickness
 |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
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        | Term 
 | Definition 
 | 
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        | Term 
 | Definition 
 
        | name brand for tolteridine muscarinic antagonist
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | indirect parasympathomimetic effects on nicotinic receptors as well
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | indirect parasympathomimetic |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | muscarinic agonist 
 reverse ester, works at nicotinic receptors as well as muscarinic
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | acetycholinesterase inhibitor quaternary amine
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | monamine oxidase inhibitor |  | 
        |  | 
        
        | Term 
 
        | prototype nicotinic agonist |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | prototype muscarinic agonist |  | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | isoproterenol epinephrine
 norepinephrine
 dobutamine
 |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 
        | prototype alpha 2 agonist |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | prototype alpha 1 agonists |  | Definition 
 
        | epinephrine norepinephrine
 phenylephrine
 |  | 
        |  | 
        
        | Term 
 
        | tricyclic antidepressant action
 |  | Definition 
 
        | inhibits reuptake of NE and serotonin |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | destroys adrenergic nerves taken up by dopaminergic and noradrenergic nerves
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | inhibits reuptake of NE also probably inhibits reuptake of DA
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | binds to adrenergic vesicles preventing NE storage/ competes with NE for reuptake quaternary ammonium
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | binds to storage vesicles preventing storage of NE uncharged molecule, crosses BBB
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | used as local anesthetic w/local vasoconstrictor (a-1 agonist).  inhibits Na channels and prevents signal cascade from traversing nerve |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | choline uptake inhibitor, limits synthesis of acetylcholine |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | used in NE producing tumors of the medulla 
 inhibits tyrosine - dobutamine pathway
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | metyrosine 
 used in adrenal medulla tumors
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | inhibits release of acetylcholine causing flaccid paralysis |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | promotes release of norepinephrine  effectively the opposite of botulin toxin except in adrenergic nerves |  | 
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        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 
        | prototype muscarinic antagonist |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | prototype nicotinic antagonists |  | Definition 
 
        | tuburcurarine hexamathonium
 |  | 
        |  | 
        
        | Term 
 
        | prototype B agonist (nonselective) |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | cevimeline contraindication |  | Definition 
 
        | CYP2D6 substrate, accumulation can occur in CYP2D6 impaired |  | 
        |  | 
        
        | Term 
 
        | hyperthyroidism and parasympathomimetics |  | Definition 
 
        | may cause atrial fibrillation |  | 
        |  | 
        
        | Term 
 
        | preferred therapies for Sjogrens |  | Definition 
 
        | cimetidine or pilocarpine |  | 
        |  | 
        
        | Term 
 
        | preferred therapies for Xerostoma |  | Definition 
 
        | cimetidine or pilocarpine |  | 
        |  | 
        
        | Term 
 
        | preferred therapies for urinary retention |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | preferred therapies for GI reflux |  | Definition 
 
        | bethanachol or metoclopramide 
 increases lower esophageal tone, increases gastric emptying
 |  | 
        |  | 
        
        | Term 
 
        | mechanism of actetylcholine topical in advance of opthalmic surgery |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | pilocarpine or carbachol mechanism of action in glaucoma |  | Definition 
 
        | improves ureoscleral outflow |  | 
        |  | 
        
        | Term 
 
        | reduction of aqueous humor formation via alpha-1 agonism |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | reduction of aqueous humor formation via alpha-2 agonist |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | reduction of aqueous humor formation via beta 1 antagonism |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | classes of drugs to treat glaucoma via aqueous humor drainage |  | Definition 
 
        | parasympathomimetics or acetylcholinesterase inhibitors |  | 
        |  | 
        
        | Term 
 
        | parasympathomimetic used in in vivo diagnostic for bronchial spasms |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | which parasympathomimetic does atropine have poor antagonistic effects |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | depolarizing neuromuscular blockers |  | Definition 
 
        | succinyl choline or decamethonium (decamethonium not used therapeutically)
 |  | 
        |  | 
        
        | Term 
 
        | ganglionic blocker effects |  | Definition 
 
        | heart:  tachycardia vasculature:  dilation, hypotension
 eyes:  mydriasis, cycloplegia
 GI: decreased tone and motility, urinary retention
 secretory: anhidrosis, xerostomia
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | a direct muscle relaxant only antidote for malignant hyperthermia
 
 occasionally causes drowsiness, rare hepatotoxicity or respiratory depression w/brain lesion
 |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | peripheral depolarizing NM blocker 
 not used therapeutically
 |  | 
        |  | 
        
        | Term 
 
        | tubocurarine site of action and drug class |  | Definition 
 
        | peripheral acting non depolarizing NM blocker works at skeletal endplate |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | nondepolarizing NM blocker |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | nondepolarizing NM blocker |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | nondepolarizing NM blocker |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | nondepolarizing NM blocker |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | aminosteroid, works at cellular endplate nondepolarizing NM blocker
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | aminosteroid, nondepolarizing NM blocker |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | amino steroid, nondepolarizing NM blocker |  | 
        |  | 
        
        | Term 
 
        | the more potent compounds:  aminosteroids or benzylsoquinolinium |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | adverse effects of tubocurarine administration |  | Definition 
 
        | ganglionic block histamine release
 |  | 
        |  | 
        
        | Term 
 
        | adverse effects of metocurine administration |  | Definition 
 
        | ganglionic block histamine release
 |  | 
        |  | 
        
        | Term 
 
        | adverse effects of alcuronium administration |  | Definition 
 
        | ganglionic block histamine release
 |  | 
        |  | 
        
        | Term 
 
        | adverse effect of succinylcholine administration |  | Definition 
 
        | histamine release vagal stimulation
 postoperative muscle pain
 increased intraocular pressure
 hyperkalemia
 malignant hyperthermia (idiosyncrocy)
 apnea (ideosyncracy)
 |  | 
        |  | 
        
        | Term 
 
        | adverse effect of pancuronium administration |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | specific caution for succinylcholine |  | Definition 
 
        | K+ loss and hyperkalemia.  avoid use with soft tissue trauma |  | 
        |  | 
        
        | Term 
 
        | metabolic pathways for NM blockers |  | Definition 
 
        | all are hepatic or renal except for succinycholine which uses a plasma cholinesterase.  succinylcholine preferred for patients with hepatic/renal problems |  | 
        |  | 
        
        | Term 
 
        | skeletal muscle relaxants therapeutic purposes |  | Definition 
 
        | adjunct to anesthesia adjunct to electroshock therapy
 |  | 
        |  | 
        
        | Term 
 
        | dantrolene therapeutic uses (dantrium)
 |  | Definition 
 
        | malignant hyperthermia or muscle spasticities 
 binds calcium to sarcoplasmic reticulum; inhibits calcium movement in response to depolarization
 |  | 
        |  | 
        
        | Term 
 
        | botulin type B (myoblock)
 therapeutic uses
 |  | Definition 
 
        | blepharospasm, strabismus cervical distonia
 |  | 
        |  | 
        
        | Term 
 
        | botulinum adverse effect with tuburcararine |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | botulinum adverse effects |  | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | direct acting skeletal muscle relaxant |  | 
        |  | 
        
        | Term 
 
        | SAR for muscarine agonists |  | Definition 
 
        | 1)  molecule must contain nitrogen capable of bearing a positive charge, preferably a quaternary ammonium salt 
 2)  for maximum potency the substituents off the nitrogen must not exceed the size of a methyl group
 
 3)  there should be an oxygen atom, preferable an ester-like oxygen capable of participating in hydrogen bonding
 
 4)  there should be exactly two carbons between oxygen and nitrogen (ethylene bridge)
 |  | 
        |  | 
        
        | Term 
 
        | 5 member versus 6 member lactam when determining efficacy of synthetic muscarinic |  | Definition 
 
        | 6 member lactam will have no activity, affinity only (antagonist) |  | 
        |  | 
        
        | Term 
 
        | essential structure for quaternary ammonium when post-acetyl bonded carbons |  | Definition 
 
        | pyrolidine ring, secondary or tertiary amine would lose all activity |  | 
        |  | 
        
        | Term 
 
        | synthetic choline esters   |  | Definition 
 
        | carbachol, methacholine, bethanachol |  | 
        |  | 
        
        | Term 
 
        | uncharged reversible AChE inhibitors |  | Definition 
 
        | physostigme, rivastigme, tacrine, donepezil |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | non-polar acetylcholinesterase inhibitor |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | non-polar acetylcholinesterase inhibitor |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | non-polar acetylcholinesterase inhibitor |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | non-polar acetylcholinesterase inhibitor |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | selective alpha-2 agonist |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | pilocarpine, acetylcholine, bethanachol, cevimeline, methacholine, |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | parasympathomimetic muscarinic agonist |  | 
        |  | 
        
        | Term 
 
        | diisopropyl fluorophosphate |  | Definition 
 
        | irreversible AChE inhibitor |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | irreversible AChE inhibitor |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | irreversible AChE inhibitor |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | irreversible AChE inhibitor |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | irreversible AChE inhibitor |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | irreversible AChE inhibitor |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | irreverisble AChE inhibitor |  | 
        |  | 
        
        | Term 
 
        | polar reversible AChE inhibitors |  | Definition 
 
        | pyridostigmine, neostigmine, demecarium, ambenomium, adrophonium |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | polar AChE inhibitor, parasympathomimetic, used in myesthenia gravis |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | polar AChE inhibitor, used in tensilon test to distinguish MG from cholinergic crisis |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | mixed alpha and beta agonist, sympathomimetic |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 
        | potency difference between atropine and scopalamine in parasympathetically innervated organs |  | Definition 
 
        | atropine more potent in heart and intestine, scopalamine more potent in iris, ciliary, secretory |  | 
        |  | 
        
        | Term 
 
        | atropine cardiovascular effects |  | Definition 
 
        | tachycardia, abolish reflex vagal slowing, decrease AV refractory period, atropine flush |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | peripheral nicotinic ganglion blocker, non-depolarizing and charged |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | tertiary amine muscarinic antagonist |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | tertiary amine muscarinic antagonist |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | tertiary amine muscarinic antagonist |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | nicotine, trimethephan, mecamylamine, hexamethonium |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | nicotine agonist, ganglionic blocker |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 
        | adrenergics used for ciliary body A-2 agonism |  | Definition 
 
        | epinephrine, dipivephrine, apraclonidine |  | 
        |  | 
        
        | Term 
 
        | prototype alpha-1 agonists |  | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | Epi, NE, Isoproterenol, Dobutamine |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | isoproterenol, epinephrine |  | 
        |  | 
        
        | Term 
 
        | prototype muscarinic agonist |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | prototype nicotinic agonist |  | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | pilocarpine, muscarine, arecholine |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 
        | indirect parasympathomimetics |  | Definition 
 
        | carbachol, metoclopramide |  | 
        |  | 
        
        | Term 
 
        | muscarinic antagonists (4) |  | Definition 
 
        | atropine, scopalamine, homotropine, tolteridine (detrol) |  | 
        |  | 
        
        | Term 
 
        | anticholinergics (charged, muscarine antagonists) (5)
 |  | Definition 
 
        | ipratropium, tiotropium, methscopalamine, homotropine methylbromide, scopalamine methylbromide |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | anticholinergic, polar antagonist |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | anticholinergic, polar antagonist |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | anticholinergic, polar antagonist |  | 
        |  | 
        
        | Term 
 
        | homotropine methylbromide |  | Definition 
 
        | anticholinergic, polar antagonist |  | 
        |  | 
        
        | Term 
 
        | scopalamine methylbromide |  | Definition 
 
        | anticholinergic, polar antagonist |  | 
        |  | 
        
        | Term 
 
        | differential sensitivity of muscarinic sites |  | Definition 
 
        | 1)  salivation, bronchial, sweat 2) pupil dilation, accomodation, cardiac
 3) urinary bladder, GI tract
 4) gastric secretion
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | edrophonium to distinguish MG from cholinergic crisis |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | nonpolar AChE inhibitor targeting Parkinson's and Alzheimer's |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 
        | chronotropic and inotropic effects of dobutamine |  | Definition 
 
        | inotropic only, isomerization prevents chronotropic effects |  | 
        |  | 
        
        | Term 
 
        | low dose epinephrine systemic effects |  | Definition 
 
        | tachycardia and hypotension |  | 
        |  | 
        
        | Term 
 
        | likely outcome for epinephrine administration in angina patient |  | Definition 
 
        | increased angina due to decreased cardiac efficiency (work/oxygen uptake) |  | 
        |  | 
        
        | Term 
 
        | peripheral resistance expectation with Epi, NE and Iso |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | pulse rate differences with epinephrine, NE and Iso administration |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | Systolic BP with administration of Epi, NE, Iso |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | Diastolyic BP with administration of Epi, NE, Iso |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | MABP differences with administration of Epi, NE, Iso |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | halogenated hydrocarbons or cyclopropane cautions with epinephrine |  | Definition 
 
        | epinephrine sensitizes the myocardium to the effects of these drugs and arrhythmias can occur |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | muscarinic receptor antagonist |  | 
        |  | 
        
        | Term 
 
        | succinyl choline and psuedocholinesterase |  | Definition 
 
        | pse metabolizes succinyl choline, atypical pse leads to apne (idiosyncratic outcome) |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | non-depolarizing NM blocker |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | non-depolarizing NM blocker |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | non-depolarizing NM blocker |  | 
        |  | 
        
        | Term 
 
        | norepinephrine precautions |  | Definition 
 
        | tissue necrosis at extreme periphery, hyperthyroidism, sensitization of myocardium, causes contractions |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | beta-1, increases renin secretion, ultimatlely increases BP |  | 
        |  | 
        
        | Term 
 
        | uterus receptors and presentation |  | Definition 
 
        | alpha - contraction, beta-2, relaxation |  | 
        |  | 
        
        | Term 
 
        | skeletal muscle receptors |  | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | alpha - ejaculation, muscarinic - erection |  | 
        |  | 
        
        | Term 
 
        | adrenal medulla receptors |  | Definition 
 
        | nicotinic - epinephrine secretion |  | 
        |  | 
        
        | Term 
 
        | lacrimal glands receptors |  | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | B-2, glycogenolysis, etc. |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | pilo erector muscles, alpha; sweat glands muscarinic |  | 
        |  | 
        
        | Term 
 
        | GI tract sympathetic innervation |  | Definition 
 
        | alpha 1 - decreased motility |  | 
        |  | 
        
        | Term 
 
        | histamine receptors on arteriolar smooth muscle cause ... |  | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | non-selective competitive alpha antagonist; |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | selective alpha-1 antagonist |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | selective alpha-1 antagonist |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | selective alpha-1 antagonist |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | alpha-1 antagonism can reduce BPH, also can lead to apoptosis of prostate |  | 
        |  | 
        
        | Term 
 
        | doxazasin preferred therapy |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | do antagonists work better against exogenous or endogenous agonists? |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | phenylephrine and n-methyl substituent |  | Definition 
 
        | structural oddity, still alpha-specific agonist |  | 
        |  | 
        
        | Term 
 
        | potency effects by substitution of hydroxyls on catechol |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | metaproterenol and terbutaline hydroxyl positions |  | Definition 
 
        | 3 and 5, lead to beta-2 preferential binding |  | 
        |  | 
        
        | Term 
 
        | catecholamine substitution on alpha carbon |  | Definition 
 
        | eliminates MAO binding site |  | 
        |  | 
        
        | Term 
 
        | catecholamine substitution on beta carbon |  | Definition 
 
        | reduces lipid solubility, decreases CNS effects |  | 
        |  | 
        
        | Term 
 
        | l-isomerization on Beta carbon |  | Definition 
 
        | greater peripheral activity |  | 
        |  | 
        
        | Term 
 
        | isomerization of alpha carbon |  | Definition 
 
        | dextrarotary generally more potent than levoratory, d-amphetimine more potent in CNS |  | 
        |  | 
        
        | Term 
 
        | atherosclerosis and baroreceptors |  | Definition 
 
        | atherosclerosis can limit reflex, increasing impact of sympathomimetics |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | parallels long term administration of MAO inhibitors; tyramine doesn't get metabolized leading to ocotopamine synthesis and displacement of NE from adrenergic vesicles |  | 
        |  | 
        
        | Term 
 
        | MAO inhibitors "cheese" crisis |  | Definition 
 
        | severe hypertensive crisis, tyramine induces large decrease of NE and with impaired MAO infarction can result |  | 
        |  | 
        
        | Term 
 
        | epinephrine and renal performance |  | Definition 
 
        | filtration fraction decreased, retention of K+, Na+ and Cl- increased |  | 
        |  | 
        
        | Term 
 
        | systole response with epinephrine |  | Definition 
 
        | shortened in preference to shortening diastole |  | 
        |  | 
        
        | Term 
 
        | epinephrine uterus interaction in last trimester of pregnancy |  | Definition 
 
        | inhibits alpha stimulation (to an extent) preventing contraction |  | 
        |  | 
        
        | Term 
 
        | epinephrine and metabolism |  | Definition 
 
        | increases glucose and lactate in blood, inhibits insulin release |  | 
        |  | 
        
        | Term 
 
        | epinephrine and circulating volume |  | Definition 
 
        | decreases volume by increasing intracellular fluid; increases hematocrit |  | 
        |  | 
        
        | Term 
 
        | dopamine therapeutic uses |  | Definition 
 
        | severe congestive failure; acute improvement in severe renal or cardiac failure, no long term benefit |  | 
        |  | 
        
        | Term 
 
        | two major disease states for beta agonism |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | dobutamine therapeutic uses |  | Definition 
 
        | acute relief post cardiac surgery; myocardial infarction; congestive heart failure |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 
        | beta agonists and asthma risk |  | Definition 
 
        | chronic tolerance and death or near death |  | 
        |  | 
        
        | Term 
 
        | amphetamine and blood pressure |  | Definition 
 
        | raises both systolic and diastolic blood pressure |  | 
        |  | 
        
        | Term 
 
        | adverse effects of alpha-1 antagonists |  | Definition 
 
        | first use effects causing orthostatic hypotension; first use should be at bedtime |  | 
        |  | 
        
        | Term 
 
        | alpha-2 antagonist ergot alkaloid |  | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | also paralysis of accomodation; muscarinic agonists |  | 
        |  |