| Term 
 | Definition 
 | 
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        | Term 
 | Definition 
 
        | competitive alpha antagonist |  | 
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        | Term 
 | Definition 
 
        | non-selective alpha antagonist |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
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        | Term 
 | Definition 
 | 
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        | Term 
 | Definition 
 | 
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        | Term 
 
        | are antagonists more effective against exogenous or endogenous agonists? |  | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | alpha antagonism to reduce release of epinephrine |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | alpha antagonist to treat |  | 
        |  | 
        
        | Term 
 
        | dually innervated part of eye and its control |  | Definition 
 
        | spincter muscle (PS) and radial muscle (A-1) control dilation.  Muscarinic tone tries to close aperture (nearsightedness) |  | 
        |  | 
        
        | Term 
 
        | singly innervated portion of eye |  | Definition 
 
        | ciliary muscle (PS) increase agonism for nearsightedness, decrease agonism for farsightedness |  | 
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        | Term 
 
        | paralysis of accomodation cause |  | Definition 
 
        | muscarinic antagonism (only) |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 
        | kidney receptors and response |  | Definition 
 
        | B-1 JGA leads to renin release and hypertension |  | 
        |  | 
        
        | Term 
 
        | uterine sympathetic receptors |  | Definition 
 
        | B-2, prevents contraction |  | 
        |  | 
        
        | Term 
 
        | liver sympathetic receptors, response |  | Definition 
 
        | B-2, glyconeogenesis, glycolysis |  | 
        |  | 
        
        | Term 
 
        | catecholamine synthetic pathway |  | Definition 
 
        | phenylalanine, tyrosine, dihydroxyphenylalanine (DOPA), dopamine, norepinephrine, epinephrine |  | 
        |  | 
        
        | Term 
 
        | function of tyrosine hydroxylase |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | aromatic amino acid decarboxylase function |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | dopamine B-hydroxylase function |  | Definition 
 
        | oxidize dopamine to norepinephrine |  | 
        |  | 
        
        | Term 
 
        | non adrenergics that prevent aqueous humor formation |  | Definition 
 
        | prostaglandins and carbonic anhydrase inhibitors |  | 
        |  | 
        
        | Term 
 
        | tertiary amine muscarinic antagonists |  | Definition 
 
        | trihexyphenidyl; tropicamide; benztropine |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | tertiary amine anticholinergic |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | tertiary amine anticholinergic |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | tertiary amine anticholinergic |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | nicotine, trimethaphan, hexamethonium, mecamylamine |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | emergency BP lowering; dissecting aortic aneurism |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | neostigme, pyridostigme, adrephonium, ambenomium, demecarium |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | physostigme, rivastigme, tacrin, donepezil, edrophonium |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | MG, paralytic ileum, alzheimers (rivastigme), urinary |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | antidote non-depolarizing NM blockers, terminate paroxysmal superventricular tachycardia, antidote atropine intoxication (physostigmine) |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | reactivators of AChE; not effective against carbamylated molecules |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | aminosteroid nondepolarizing neuromuscular blocker |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | aminosteroid nondepolarizing nueromuscular blocker |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | aminosteroid nondepolarizing neuromuscular blocker |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | benzo nondepolarizing neuromuscular blocker |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | benzo nondepolarizing neuromuscular blocker |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | benzo nondepolarizing neuromuscular blocker |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | benzo nondepolarizing neuromuscular blocker |  | 
        |  | 
        
        | Term 
 
        | nondepolarizing benzylosiquinolinium neuromuscular blockers |  | Definition 
 
        | d-tuburcurarine, mivacurium, metocurine, atracurium, alcuronium |  | 
        |  | 
        
        | Term 
 
        | aminosteroid nondepolarizing neuromuscular blockers |  | Definition 
 
        | vecuronium, pancuronium, rocuronium |  | 
        |  | 
        
        | Term 
 
        | succinyl choline ganglionic blockade? |  | Definition 
 
        | no, but histamine release yes |  | 
        |  | 
        
        | Term 
 
        | pancuronium and succinylcholine ANS effects |  | Definition 
 
        | pancuronium sympathetic stimulation, succinylcholine vagal stimulation |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | plasma esterase plus spontaneous degredation |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | direct neuromuscular blocker; locks up calcium and prevents neurotransmitter release; interferes with phasic contractions (spasms) only.  no effect on tettanic contractions |  | 
        |  | 
        
        | Term 
 
        | sympathetic endocrine effects |  | Definition 
 
        | modulation of renin secretion, modulation of pancreatic secretions, secretion of anterior pituitary (dopamine) |  | 
        |  | 
        
        | Term 
 
        | alpha methyl norepinephrine |  | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | alpha 2 agonist   creates dry mouth as type "b" effect |  | 
        |  | 
        
        | Term 
 
        | clonidine-specific therapeutic use |  | Definition 
 
        | reduces withdrawal symptoms without opiate effects |  | 
        |  | 
        
        | Term 
 
        | sympathomimetic CNS effects |  | Definition 
 
        | decreased appetite, increased wakefulness |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | none, it has an isomer that agonizes beta-2 and alpha-1 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | DOPAMINE, alpha-1, beta-1 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | beta 1 and beta 2 agonism |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | increased PR, +inotrop, +chronotrope |  | 
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        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | alpha-2 agonist for glaucoma |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | shock by continuous infusion, increase JGD filtration |  | 
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        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | some types of shock w/oliguria   adverse:  10% tachycardia |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 
        | reuptake inhibition and indirect sympathomimetic activity |  | Definition 
 
        | no agonistic activity; indirect sympathomimetic must get into the nerve to have an effect |  | 
        |  | 
        
        | Term 
 
        | histamine and vagal nerve |  | Definition 
 
        | decreases firing/increases heartrate |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 
        | epinephrine's metabolic effects |  | Definition 
 
        | increases lactate in muscle; inhibits insulin release (A-2); promotes glucagon release (B-2); increase cAMP; increase phosphorylase in liver; glycolysis; G-1-P; G-6-P; increase adipose lipase; |  | 
        |  | 
        
        | Term 
 
        | noncetecholamine alpha agonists (4) |  | Definition 
 
        | phenylephrine, menoxamine, metaraminol, mephentermine |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | IAS is its major classification but it has mixed properties as well as CNS effects |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | more CNS acting than amphetamine |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | false transmitter, full agonist on A-2, affinity but no other activity on other receptors |  | 
        |  | 
        
        | Term 
 
        | more potent methylated carbon on choline esters |  | Definition 
 
        | beta.  the carbamate ester of beta methyl choline is bethanacol |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | BPH, pheochromocytoma, autonomic hyperreflexia in spinal cord transection |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | ergonavine, ergotamine, ergotoxine; partial agonists
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | powerful oxytocic; used to treat Prinzmetal's Angina |  | 
        |  | 
        
        | Term 
 
        | ergonavine adverse events |  | Definition 
 
        | gangarene, ergotism, can lead to infarct due to vasoconstriction, |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | more antagonistic properties: dihidroergotamine; dihidroergotoxin |  | 
        |  | 
        
        | Term 
 
        | nonselective beta antagonists (4) |  | Definition 
 
        | propranolol, timolol, nadolol, pindolol |  | 
        |  | 
        
        | Term 
 
        | selective beta-1 antagonists |  | Definition 
 
        | metoproplol, atenolol, acebutolol, esmolol |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | non selective beta 2 antagonist, not metabolized in vivo; mostly PNS, particularly compared to propranolol; used for heart disease and angina |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | can mask hypoglycemia; non-specific beta antagonist |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | beta-1 selective antagonist; can mask tachycardia due to hypoglycemia |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | for exam purposes is nonselective beta antagonist |  | 
        |  | 
        
        | Term 
 
        | which beta antagonist has the most intrinsic sympathomimetic activity |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | which beta antagonist has the greatest lipid solubility |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | which beta antagonist has the greatest membrane stabilizing capacity |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | which beta antagonists have the longest/shortest half lives |  | Definition 
 
        | nadolol 10+ hours; esmolol 0.1 hours |  | 
        |  | 
        
        | Term 
 
        | carvedilol specific therapy with cardiac insufficiency |  | Definition 
 
        | has some inverse agonistic properties which lead to reverse inotrope and chronotrope benefits |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | in tachycardia after cardiac surgery when other beta blockers have worn off; administered by continuous infusion |  | 
        |  |