Drugs Flashcards
What is an example of a nicotinic and muscarinic agonist?
pilocarpine/isoptocarpine
What is a muscarinic agonist?
Duvoid - broad M agonist, but remember M2 and M3 are associated with the bladder. M2 allows the internal sphincter to relax, and M3 allows the detrussor to contract. Duvoid is prescribed to anesthesia-induced urinary continence, “can’t go”
What is a nicotinic agonist?
Nicotine, has a biphasic nature, at low doses it is a activator of N-2, and at hi doses it is inhibitor of N-2. Hi enough and it will effect N-1
What is an N-2 receptor antagonist?
These block the CG Na+ channels at the neuro-neuron and neuromuscular junction. Curare/d-tubocurare/tubadil. Succinylcholine/Sux/Anectine used in intubation
What is the warning for anesthesiologists using Sux?
too hi dosage and you will relax the diaphragm and suffocate the patient
What is a N1 receptor antagonist?
at the pre-ganglionic/post-ganglionic synapse on both sympathetic and parasympathetic sides. Trimethaphan/Arfonad. Used in a surgical setting to create a controlled HYPOtension. Has a much greater effect on the sympathetic side.
What are muscarinic antagonists?
parasympathetic drug, neuro-effector. Belladonna/Atropine comes from the deadly nightshade. It blocks the PSNS desire to constrict the pupil. Allows for eye dilation. Not used anymore bc long to wear off.
Mydriacyl -M blocker, used for eye dilation now bc quick to wear off
Detrol - M blocker, hinders PSNS desire to relax sphincter and contract detrussor. Allows sphincter to constrict and detrussor to relax. Used to treat incontinence. Opposite of Duvoid
GI muscarinic antagonist
Bentyl prescribed for irritable bowel syndrome.
Scopolamines is also a derivative of deadly nightshade. twilight labor
Scop and Transderm are prescribed in the treatment of motion sickness. the goal is to target M1 and M3, the muscarininc receptors in charge of long phasic contractions at the gut wall.
anti-cholinesterases
prolong the half life of Ach in the synaptic cleft
neostigmine, physostigmine, eserine - used in the treatment of myasthenia gravis
Insecticides malathion, parathion
War gas Sarin
Sympathetic NS drugs - subtype presynaptic effect
blockage of NT synthesis (Demser), creation of fase T (Aldomet), blocking the release of NT (Ismelin) block transport back into protective vesicles (Serpasil, protected from MAOs) false displacement of NT (Dextradrine)
Demser
blocks the synthesis of NE (also E by default) by blocking tyrosine hydroxylase (no tyrosine, no L-DOPA). This is a bad HBP drug bc it is so wide-ranging, decreases sympathetic effect
Aldomet (methyl DOPA)
is a sub for L-DOPA, M-DOPA gets converted to alpha-methyl-NE. This does not bind alpha 1, but does bind alpha 2. Overall decrease of SNS response.
Ismelin
blocks the release of Ne/E. HBP treatment
Serpasil (Reserpine)
blocks the transport of NE back into the synaptic vesicles. Thus NE is more susceptible to MAOs. Less NE, decrease sympathetic effect.
Amphetamines. Ephedrine, Dexadrine
function in the displacement of the neurotransmitter without an action potential. Also directly activates alpha and beta receptors. Dexadrine used in the treatment of narcolepsy and hypotension. Makes NE more available, more active. Amphetamines enhance effect of Ne/E…not sure if they bind or just make Ne/E more available…controversial