Pharmacology Quizzes Flashcards
Hypertension treatment with the a 2 agonist, clonidine, works by _________.
acting at autoreceptors to decrease sympathetic outflow
Direct-acting sympathomimetics ________________________.
bind to post- (or pre-) synaptic receptors
___________ is an example of a non-selective sympathomimetic drug.
Epinephrine
Vasoconstriction via epinephrine is a useful means to _____________________.
reduce bleeding surfaces
prolong actions of local anesthetics
shrink mucosa during surgical procedures
Vasoconstriction effects of a-agonists include:
decongestant
lowering IOP
“red eye” reduction
Indirect-acting sympathomimetics act by
facilitating catecholamine (e.g., DA and NE) release blocking NE reuptake
As an alternate approach to treating ADHD, the actions of guanafacine [Intuniv] include _____________.
central inhibitory actions that decrease NE release
Relaxation of bronchial and uterine smooth muscle is achieved through _________.
β2 agonists
Methamphetamine actions for treatment of ADD include _____________________.
actions on α2a,2b,2c receptors
blocking reuptake of DA and NE
blocking reuptake of 5-HT
Modafinil currently has FDA use approval for _______________________.
narcolepsy
Modafinil has low abuse potential
True
Modafinil has no side effects
False
Allergic reactions to bee stings can be treated with ______________.
epinephrine
Atropine competes with _____________ for a binding site on the muscarinic receptor.
Acetylcholine
Atropine Sensitivity Curve, ___________ are most sensitive to the effects of muscarinic antagonism, while the _____________ is least sensitive.
salivary glands; gastrointestinal tract
Scopolamine is a _________ and a(n) ___________that is used for _____________.
belladonna alkaloid - muscarinic antagonist - motion sickness
Muscarinic antagonists treat peptic ulcer by ____________________.
reducing gastric motility and gastric acid secretion
Atropine, __________ and ____________ are components of an antidote for nerve gas poisoning
pralidoxime – diazepam
Muscarinic antagonists constrict pupils (miosis) and increase lung secretions
False
Tolterodine tartrate [Detrol LA] is a ___________ used as treatment for ____________.
muscarinic antagonist; overactive bladder
Ipratropium Bromide [Atrovent] and Tiotropium Bromide [Spiriva ] are most effective for ______________.
preventing bronchospasm
Which of the following is NOT a likely side effect of a muscarinic antagonist: mydriasis, diarrhea, constipation, xerostomia
diarrhea
Which of the following effects would require the lowest dosage of atropine? dry mouth, pupil dilation, increased heart rate, decreased gastric secretions and motility
dry mouth
Atropine is an antidote for all types of mushroom poisoning.
False
Which of the following is NOT a clinical use of a muscarinic antagonist? motion sickness & vertigo, dilate pupils for ocular exam, dilate airways in COPD patients, glaucoma
glaucoma
Carbidopa actions include ________________.
inhibiting synthesis of dopamine
The actions of a 1 - antagonists that decrease hypertension include _____________.
relaxing smooth muscle in bladder neck, prostate and urethra OR reducing peripheral resistance in vasculature OR slowing down heart rate OR intracavernous vasodilation
reducing peripheral resistance in vasculature
The actions of a 1 - antagonists that treat BPH include _____________.
relaxing smooth muscle in bladder neck, prostate and urethra
b-antagonists treat glaucoma by ____________________________.
inhibiting aqueous formation via β2-receptor antagonism on nonpigmented ciliary epithelium
The a s -antagonist, yohimbine, increases blood pressure and heart rate by an action on:
pre-synaptic autoreceptors
Non-selective b-antagonists have utility in treating _______________
cardiac arrhythmias
acute dissecting aortic aneurysm
hyperthyroidism
b 1 -antagonists are most selective for receptors located ________________.
on cardiac muscle
In general, the older the man, the larger his _________________.
prostate gland
The actions of a b1-receptor antagonist in treating panic symptoms are due to __________________.
blocking certain fight-or- flight reactions
The sympathetic nervous system is part of the
peripheral nervous system
Acetylcholine is the neurotransmitter at:
- the preganglionic synapse of the parasympathetic nervous system
- the postganglionic synapse of the parasympathetic nervous system
- the preganglionic synapse of the sympathetic nervous system
Preganglionic parasympathetic nerves exit the spinal cord at the:
cranial & sacral level
Pre-ganglionic neurons of the sympathetic nervous system:
- synapse on a ganglionic chain
- are short and myelinated
- release ACh
After release into the synapse, acetylcholine:
interacts with muscarinic and nicotinic receptors
Adrenergic receptors consist of:
α and β subtypes
After release into the synapse, norepinephrine:
- is broken down in the synapse to inactive metabolites that can be detected in blood and urine
- is recycled back into the terminal vesicles for subsequent release
- is taken back up into the terminal and broken down by MAO
Which of the following statements is true about the “Fight or Flight” response:
- it is facilitated by diverging preganglionic sympathetic neurons synapsing on multiple postganglionic sympathetic neurons
- it functions to maintain steady organ functions
- it is also referred to as the “Feed or Breed” response
it is facilitated by diverging preganglionic sympathetic neurons synapsing on multiple postganglionic sympathetic neurons
Nicotinic cholinergic receptors are:
ligand gated ion channels
Postganglionic release of acetylcholine from parasympathetic nerves activates ______________ on
exocrine glands, smooth muscle and cardiac muscle.
muscarinic receptors
Preganglionic __________ neurons can diverge and synapse with many postganglionic ________
neurons, while preganglionic __________ neurons generally form only single synaptic connections with
postganglionic _____________ neurons.
sympathetic, sympathetic, parasympathetic, parasympathetic
What is the rate-limiting factor of the production of all catecholamines?
tyrosine hydroxylase