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34 Cards in this Set

  • Front
  • Back
epinephrine
a1,2,b1,b2 (B's MORE)
NE
a1,2 (b1 MOST)
isoproternol
b1,b2
oxymetazoline
a1,a2
terbutaline
albuterol
salmerterol
b2
dobutamin
b1
clonidine
apraclonidine
a2
phenylephrine
a1
release agents
amphetamine
tyramine
uptake inhibitor
cocaine
mao/comt inhibitor
paragyline
entacapone
mix-acting
ephedeine
all of the receptors + Releasing agent
dopamine
D1, d2
b1,b2,b3 mechanism?
gs (cAMP increase)
L type ca+2 channels
a1 mechanism
Gq (phospolipase C, Ca+2 channels)
a2 mechanism
Gi (cAMP decrease, K+ increase, PLC incease)
EPI pharmokinetics
0% oral bioavail
no CNS
metabolized by liver (MAO/COMT)
2 min t1/2
IM faster absorbtion
USES OF EPI
acute hypersenitivity (anaphyalaxi/angioedema)

surgical bleeding

open angle glaucoma (decrease pressure)

cardiopulm resus/ cardiac arrest (a1 activation, reduce BF to renal...back to heart)
NE
causes BRADYcARDIA (w/ baroreflex)

vasodialation on all conornay/pulm vessels

use with HYPOTENSION & VASODILATRY SHOCK (sepsis, spinal anethesisa, spinal trauma)
- use with local anestehesis (to slow absorbtion)
Dopamine
LD d1 receptor (vasodilation/renal, stop Na+ resorb in prox tub)
ID b1 + release of NE (SV and HR UP)
HD a1 + D2 (area postrema) (increase sys vasc resistance, vomiting/nausea)

ALL UNDERGO TOLERANCE

DOES NOT ENTER BRAIN/not active oral
t1/2 = 2mins
IV only

USES - cardiogenic/neurogenic/spetic shock (cuz poor renal perfusion)
Phenlephirine
a1 (selective)
not inact by COMT

adverse affects
hyperten, photophobia

USES
hypotension, nasal decongest, myrdiatics, local vasoconstricters
a2 drugs...control
presyn nerve terminal control NE release
Clondine/apraclonidine
a2 selective

ativates Nucles of Tractus solatarious & rostal ventrolateral medulla

activates Imidazoline receptors

all leads to Decreased firing of reticulospinal tract (central adernergic tone)

Effects.....
hypotension (LD) high does HYPERTENSION (a1/a2 activated)

craving reducing affects, sedative, anaglesic

Decease intraoc pressure (dec aq humor)
increase absorb of fluid in intesttine

USES
hypertension
open angle glaucoma (apraclonaine)

hot flashes, ADD, autism, tourettes
Dobutamine
B1 selective

heart - increase conttract/condction

not active by oral. t1/2 = 2mins

uses - given by IV with severaly depressed left Venct fucntion
albuterol/salmerterol/terbutaline
b2

resp- broncodialation, mucus clearance, supression of inflam mediators (hist/leukotiries)
reduce microvasc perm

oral bioval (first pass maybe high)
BBB limited
t1/2 - 1 to 14 hours
INHALINATION main route
B2 agonist time lasting
1.5 hours (EPI, isoprotenol)
3-6 hours (albuterol)
>12 hours (salmeterol/formoterol)
B2 adverse affects
CNS - tremors/cramps/restlessness

Cardio - tachycardia, hypotension

Resp - hypoxemia (too much dialation, decrease V/Q ratio, paradox broncoconstiction

Othersystems - hypokalemai, stimulates K+ into cells
hyperglycemia
b2 contraindiactions
don't use in eldery
hyperthyroidism
seizures
b2 theraputic uses
asthma (as needed)
COPD
premature LABOR (defer delivey)
hyperkalemia (puts K+ in cells)
Tyramine
Indirect acting
taken up by neurons - changed to octopamine....displaces NE

inactive due to large first pass (oral)

Adverse affects bad with MAO inhibitor (leathal hypertensive crisis, due to NE release)

USE - localize lesion of symp nerves
Methyldopa
taken up by neurons....hcanged to methlyNE...a2 agonist (similar to clondine)
Amphetamines
stimulate release of NE, dope, Seroton

blocks catecholamine reuptake

elevation of mood/euphoria (CNS)

similar to NE in periper

uses - ADD, hyperact disorder/narcolepsy/wt reduction
cocaine
blocks cat reuptake

local ansesteia
perip - same as NE
CNS - similar to amph...more intest/shorter
ephedrine
actives all receptors (adernergic)
enhances release of NE

similar to NE
lower potency
longer duraction
oral activiy

ADverse affects - Restlessness/insomnia/urinary rention

clincial - nasal decongestant