BIOL 1260 Lecture 3: Cell Excitability and Drug Receptors

16 views7 pages

Document Summary

Channel-linked receptors (ionotropic) = direct receptor control ligand-gated. Bind to ion channels hyper/depolarization cellular effects. Ex. nicotinic ach receptor, gaba-alpha receptor: voltage-sensitive. G-protein coupled receptors (metabotropic) = slow transmitters/hormones: bind to ec or transmembrane surface change in excitability second messengers cellular effects, ex. muscarinic ach receptor. Kinase-linked receptors: protein phosphorylation cellular effects, ex. insulin receptor, tgf-beta. Receptors linked to gene transcription (nuclear) = for steroid hormones: mna synthesis protein synthesis cellular effects, ex. estrogen receptor (er) intracellular enzymes: antimitotic drugs, rnai. Extracellular enzymes: ace inhibitors, acetylcholinesterase cholinergic pharmacology nerve agents. Class of organophosphates that block ache (enzyme which destroys ach) Tabun: originally insecticide designed to disrupt the insect"s nervous system: very potent, miosis, dizziness, severe shortness of breath in humans. Sarin: 2x as potent as tabun. Nerve gas poisoning: miosis, salivation, convulsion, involuntary urination, death by asphyxiasion as respiratory muscle control is lost: dumbel (diarrhea, urination, miosis, bronchoconstriction, excitation, lacrimation) botulinum toxin.

Get access

Grade+
$40 USD/m
Billed monthly
Grade+
Homework Help
Study Guides
Textbook Solutions
Class Notes
Textbook Notes
Booster Class
10 Verified Answers
Class+
$30 USD/m
Billed monthly
Class+
Homework Help
Study Guides
Textbook Solutions
Class Notes
Textbook Notes
Booster Class
7 Verified Answers

Related Documents

Related Questions