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chemical signaling
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direct communication is through ____ _______
gap junctions
a ____ is a protein channel that connects 2 cells in a gap junction
connexon
indirect communication is via ____ _______
chemical messengers
direct communication is good for ____ distance only and is very ____
short distance, fast
during indirect communication, a secretory cell releases a chemical messenger that binds to a receptor on a ____ ______
target cell
______ signaling involves 2 cells that are very close to each other but not touching
paracrine
_____ signaling is similar to paracrine signaling but the secretory cells will always be a nueron
neurotransmitter
in neurotransmitter signalling the target cell will be another ____, _____, or _____ and is very ______.
neuron, gland, or muscle, fast
_______ singaling involves a hormone being released into the bloodstream
endocrineen
endocrine signaling is good for ____ distances and is very ____ to take effect
long, slow
Paracrines, neurotrasmitters, and hormones are ____ that bind to receptors
ligands
is the endocrine messenger is ____ it will dissolve in the bloodstream
hydrophillic
the ____ ___ _______ determines where the receptor is found on the target cell
type of messenger
_____ _______ molecules such as steriods or hormones will bind on receptors inside of the cell
nonpolar signal
the receptor for ____ messegeners will be on the outside of the plasma membrane on a target cell
polar
receptor affinity is based on ____ and affinity is based on _____/______
shape, strength/charge
receptor activation depends on _____ of _____, adding more ligand increases liklihood that ligand will bind to receptor, once all receptors are bound adding more ligands will not have any effect
concentration of ligand
receptor activation depends on _______ ______ of receptors, adding more receptors will increase the chance of a ligand attaching
expression of receptors
receptor activation depends on _____ __ ______ ____ ______, increase the attraction, more likely for binding
affinity of receptor for ligand
how can the number of receptors change?
receptor synthesis or receptor turnover
______ means receptor synthesis is happening more quickly, ________ means receptor synthesis is happenign more slowly
upregulation, downregulation
usually the number of receptors is _________ the number of lignad. if there is more ligand the cell will _____________, if there is less ligand there will be _________________.
similar to, make extra receptors, less receptors made by the cell.
addictive drugs are __________ that bind ot receptors already in the body
artificial ligands
binding of an addictive drug to the receptors in the body activates a network of dopaminergic cells in the mesolimbic region of the brain that is involved in ______________, produces excessive ______. this is a _________________.
emotional reward, dopamine, postitive feedback mechanism
_____ are painkillers such as codeine, morphine, oxycodone, oxycontin, and heroin
opiates
opiates activate natural ________________ for endorphins in the brain. endorphin concetration is usually extremely ____.
G-protein coupled receptors, low
______ help with minor pain
endorphins
opiates in the body bind to ALL endorphin receptors which triggers receptor _______ and _____ because we arent supposed to be pain free
turnover and downregulation
____________ occurs from functional uncoupling of G-protein receptors to their effector molecule, this is what leads to people taking more opiates and becoming addicted
desensitization
nicotine has an extremly high affinity for _____ receptors and outcompetes ________ for these receptors
acetylcholine, acetylcholine
to combat nicotine, the cells that need acetylcholine for signalling respond by making more _____ and releasing more ______. this leads to addiction becuase you need more nicotine to get the same effect
receptors, acetylcholine
nicotine is also extremely addictive becuase your body gets better at breaking it down before it reaches the receptors, nicotine ________ _______ ______ for __________________.
upregulates cellular mechanisms for degrading the drug
_______ intolerance is the result of lower concetrations of a drug actually reaching the receptor, caused by degradation (opiates) or increased metabolism of the drug (nicotine)
pharmacokinetic
_________ tolerance is the cellular mechanism that results in receptor downregulation/turnover (opiates) or upregulation (nicotine)
pharmacodynamic
why is nicotine more addictive than heroine
nicotine results in both pharmacokinetic and pharmacodynamic tolerances, opiates are only pharmacokinetic
______ are lignads that bind to a receptor and cause a biological response, a normal physiological response
agonist
_____ is a ligand that bind to receptors and do not cause a biological response and may block a ____ from binding, descreasing cellular response
antagonist, agonist
______ ________ refers to intracellular mechanisms that mediate the response of target cells to the chemical messenger
signal transduction
_______ ______ are intracellular messengers produced by the binding of an extracellular messenger, carries the signal to the nucleus
second messengers
second messengers are not needed for ______/_______ messengers because they can cross the membrane and get to the nucleus
hydrophobic/lipophillic
______ messenger binds to a receptor directly in the cytoplasm or enters the nucleus directly - both produce the same response, the cell increases _____ / ______
lipophillic, gene expression/protein synthesis
in order for a receptor on the membrane to have an effect on the cell it has to be connected to some sort of pathway _______, ________or ________
fast linked ion channel, enzyme linked, or g-protein linked
in a ____________ ion channnel, when the ligand binds, the channel opens and allows ions to cross, the cellular response is ________________.
fast linked ion channel, changing the membrane potential of the cell.
calcium, sodium, chloride, and potassium cross the cell membrane through _____________.
fast linked ion channels
when a receptor is ________ linked, it is connected to the production of a second messenger, epecially _______
enzyme, kinase
_____ is an enzyme that adds a phosphate group to another protein and activates that protein
kinase
when the ligand binds to the enzyme linked receptor, it causes two more receptors to come together to form a ______, called ________. thsi activates the kinase which __________ many proteins in the cell that produce some effect in the cell
dimer, dimerization, phosphorylates
the receptor can be linked to ______ which are small intracellular proteins that link receptors with effector proteins
g-proteins
receptors linked to g-proteins are called __________ aka __________
g-protein coupled receptors, GPCRs
_____________ proteins bridge the gap between the receptor nad another protein inside the cell that does something
effector
the effector protein will either be an __________ or ____________ that produces a second messenger
ion channel or enzyme
effector proteins have three subunits _____, __________ and _________, and 3 types __________, _________, and ______
alpha, beta, and gamma; ion channel regulating, enzyme inhibiting, and enzyme stimulating
g-proteins are referred to as _________________ turned off or turned on depending on what the g-protein is attached to
molecular switches
when the g-protein is bound to _____ it can bind to the effector protein
GTP
for g-protein to turn off, it breaks down GTP to _____ and it cannot bind to the effector protein
GDP
g-protein linked __________ can open and close and do this _________ to stay open longer
ion channels, slowly
______________ channels can only be opened
fast ligand gated
when the effector protein is not an ion channel it is an ______ that controls the production of second messengers
enzyme
the 5 major second messenger pathways regulated by g-proteins are _______, _______, _______, _____, and ______
cAMP, cGMP, IP3, DAG, and calcium