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as opposed the MAPK and kainate receptors, NMDA receptors are coincidence detectors that detect the simultaneous presence of
glutamate and GABA
ionotropic receptors differ from metabotropic receptors in which of the following ways
ionotropic receptors form a channel whereas metabotropic receptors couple to channels through intracellular signaling molecules
which of the following is NOT a type of glutamate receptor
GABA(b)
G-protein coupled receptors have how many transmembrane domains
7
acetylcholine is degrade in the synaptic cleft or neurotransmitter junction by which enzyme
acetylcholine esterase
myasthenia gravis is caused by
development of autoantibodies that block the ability of acetylcholine to bind to nicotinic receptors at the neuromuscular junction
muscarinic receptors are
GPCRs that bind acetylcholine
Group I metabotropic glutamate receptors couple to ___ while group II and group III receptors couple to ___
Galphaq, Galphai
Which enzyme converts glutamate to GABA
glutamic acid decarboxylase
in the developing brain GABA is excitatory primarily because
intracellular chloride concentrations are very high
Parkinson's disease is caused by a loss of ___ neurons from the ___
dopamine, substantia nigra
cocaine increase synaptic dopamine by
blocking the dopamine transporter
antidepressant drugs promarily act on the ___ system
serotonergic
the AA precursor for dopamine and norepinepherine is ___ while the amino acid precursor for serotonin is ___
tyrosine, tryptophan
Catecholamines are primarily removed from the synaptic cleft by
reuptake transporters found on the presynaptic membrane
tolerance refers to
a decrease in the effect of the drug after repeated dosing
the ion channel receptor for serotonin is called
5-HT3
which of the following best describes the difference between Paracrine signaling and synaptic signaling
synaptic signaling is isolated to single pre and post synaptic pairs while paracrine signaling can affect multiple cells
which of the following are examples of extra cellular signaling molecules
lipid mediators, peptides, diffusable gasses
GPCRs couplr directly to
heterotrimeric G proteins
Which of the following proteins has intrinsice GTPase activity and sets the duration of signaling after activation of a GPCR
Galpha proteins
GalphaS proteins produce which of the following cellular responses
stimulation of adenylyl cyclase and stimulation of cAMP accumulation
GalphaI proteins produce which of the following cellular responses
inhibition of adenylyl cyclase and inhibition of cAMP accumulation
the GPCR cycle is terminate when Galpha subunit
hydrolyzes GTP to GDP and rebinds beta-gamma subunits
the most commong downstream transcription regulatory target of cAMP/PKA signaling is
CREB
GalphaQ proteins couple to
phospholipase C
Which of the following mechanisms can allow for calcium entry into the postsynaptic terminal to induce a signaling response
activation of IP3, activation of NMDA, activation of voltage gated calcium
When PKA binds cAMP molecules this causes a conformation shift in the kinase htat
changes the shape of the regulatory domain such that it bends away from the catalytic domain allowing the catalytic subunit to associate with substrates
most kinases in the human or other mammal genomes are ___ kinases
serine and theronine
the action of PKA is terminated by
cAMP hydrolysis and phosphodiesterase
Ligands fro receptor tyrosine kinases include
neurotrophic factors, synaptic adhesion, soluble extracellular proteins
downstream signaling through tyrosine kinase receptors is mediated largely by ___ that stimulate the ___ pathway
small G proteins, MAPK
transcription factors are important signaling molecules because
they recruit RNA polymerase to cause gene transcription in adult neurons
postsynaptic densities in dendritic spines are remarkable because they
contain a broad variety of signaling molecules that enable synaptic plasticity
PKC activity is most commonly associated with GPCRs that couple through which of the following alpha subunits
GalphaQ
pre-propetides are
peptide neurotransmitter precursors that must be processed before they can be released as active molecules
endorphin peptides bind predominantly to which type of receptor
Mu opioid receptors
the primary sites of action of endogenous opioids to produce analgesia are located in
the periaqueductal grey
the G protein coupled receptor with the highest expression density in the brain is
CB1 cannabinoid receptor
as opposed to most other NTs in theb rain, endocannabinoids and 2-arachidonyl glycerol act as
retrograde NTs
the cellular action of anadamide is terminated by
fatty acid amide hydroxylase
the primary location and physiological role of CB1 receptors appear to be
presynaptic, inhbition of NT release
the primary sensor for noxious heat, which is also a receptor for the chili peper derived compound cpsaicin is
TRPV1
Mice that lack TRPV1 have which phenotype
they have deficits in noxious thermal snesation
transient receptor potential channels, or TRPs, are often referred to as thermosensores. TRPM8 senes
cold