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10 Cards in this Set

  • Front
  • Back
What was the first clinically viable beta blocker?
pronanolol
What happened with first generation beta blockers?
they were non-selective, antagonized both Beta1 and Beta2 subtypes
Why would you have a selective beta blocker?
so that you can avoid bronchoconstrictive and vasoconstrictive effects of Beta2 blockade
What's up with second generation beta blockers?
subtype selective, more potent at antagonizing beta1 than beta2
What's up with third generation beta blockers?
selective with additional cardiovascular actions, also alpha1 receptor antagonists so that they are more potent anti-hypertensive agents, successful heart failure drugs
What do intrinsic sympathomimetic effect drugs do?
partial agonists, counteract an increase in adrenergic stimulation, doesn't affect resting heart rate
preserves BP
Why wouldn't you give intrinsic sympathomimetic effect drugs?
not as good at treating myocardial ischemia or in improving post-MI survival
What are the other effects of beta-blockers?
anesthetic, membrane stabilizer, produce NO, activate beta2 receptors, block Ca entry, open K channels, antioxidant activity
How often do you have to give a newer beta-blocker?
once or twice daily
How often do you give propranalol?
four times daily