Chapter 4 Flashcards
(40 cards)
exogenous vs. endogenous substances:
exogenous is from an external source; endogenous from an internal source
discovery of acetylcholine involved:
frog hearts
the basal forebrain is the major source of ___ in the brain
ACh
acetylcholine is sent from:
the basal forebrain
acetylcholine is sent to:
the cortex, amygdala, hippocampus, skeletal muscles, the PNS
acetylcholine’s major roles in the CNS are:
learning and memory modulation
acetylcholine’s major roles in the PNS are:
motor control, parasympathetic activity
dopamine is sent from:
the midbrain: the VTA and the SN
dopamine is sent to:
the cortex, basal ganglia, and nucleus accumbens
dopamine’s major roles are:
reward processing, learning, motivation
the ventral segmental area is a portion of the midbrain that:
sends dopamine to the nucleus accumbens
glutamate is sent from:
everywhere
glutamate is sent to:
everywhere
glutamate’s major role is:
the most predominant excitatory neurotransmitter in the brain
GABA is sent from:
everywhere
GABA is sent to:
everywhere
GABA’s major role is:
the most predominant inhibitory neurotransmitter in the brain
metabolic tolerance:
form of drug tolerance that arises when repeated exposure to the drug causes the metabolic machinery of the body to become more efficient at clearing the drug
functional tolerance:
the form of drug tolerance that arises when repeated exposure to the drug causes receptors to be up-regulated or down-regulated
possible drug effects on transmitter production:
could inhibit transmitter synthesis; could block axonal transport; could interfere with neurotransmitter storage
possible drug effects on transmitter release:
could prevent synaptic transmission; could alter synaptic transmitter release; could modulate transmitter release by presynaptic receptors
possible drug effects on neurotransmitter clearance:
could inactivate transmitter reuptake; could block transmitter degradation
possible drug effects on receptor activity:
could blockade receptors or activate receptors
possible drug effects on postsynaptic activity
could alter number of receptors or modulate second messengers