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Amino acid neurotransmitters
Examples include Glutamate, GABA, and Glycine.
Biogenic amines
Includes Dopamine, Serotonin, Norepinephrine, and Histamine.
Purine neurotransmitters
Adenosine and ATP are key examples.
Neuropeptides
Examples include Endorphins, Substance P, and Oxytocin.
Unique neurotransmitter
Acetylcholine (ACh) is distinct from other classes.
NMDA receptor
Requires glutamate and depolarization for activation.
Inhibition of inhibition
Endocannabinoids reduce GABA release, increasing excitability.
Biogenic amines characteristics
Synthesized from amino acids, modulate behaviors.
Peptide neurotransmitter synthesis
Synthesized as pre-propeptides in rough ER.
Peptide processing
Cleaved into active forms in Golgi apparatus.
Endocannabinoids synthesis
Synthesized on demand, not stored in vesicles.
Nitric oxide synthesis
Gaseous neurotransmitter synthesized on demand.
Retrograde signaling
Endocannabinoids act on presynaptic cells post-release.
Vesicular transporters
Some amino acids share transport mechanisms.
Metabotropic receptors
G-protein-coupled receptors initiating signaling cascades.
Tyrosine hydroxylase
Key enzyme for catecholamine synthesis, not all amines.
Serotonin synthesis
Derived from tryptophan, not tyrosine.
GABA
An inhibitory neurotransmitter involved in neural signaling.
Calcium influx
Triggers exocytosis of neurotransmitters at synapses.
Synaptic plasticity
Involves NMDA receptors in memory formation.
Recycling
Recycling is via EAATs.
Acetylcholine breakdown
Acetylcholine is broken down in the synaptic cleft by acetylcholinesterase, not recycled via excitatory amino acid transporters (EAATs), which are involved in glutamate recycling.
Cholinesterase
Acetylcholine is degraded by acetylcholinesterase.
Acetylcholine synthesis
Pyruvate is a key component in acetylcholine synthesis.
VAChT
VAChT is the transporter responsible for packaging acetylcholine into synaptic vesicles.
Acetylcholine receptors
Acetylcholine acts on both nicotinic (ionotropic) and muscarinic (metabotropic) receptors.
Nicotinic and AMPA receptors
Both nicotinic and AMPA receptors are ionotropic receptors that function via a ligand-gated mechanism.
Muscarinic receptor
This is a metabotropic receptor, not ionotropic, so it does not operate via a direct gate mechanism.
Neuropeptides secretion
Neuropeptides are secreted by neurons, not glial cells.
Neuropeptides as hormones
Many neuropeptides, such as oxytocin and vasopressin, also function as hormones.
Neuropeptides packaging
Neuropeptides are packaged into large, dense-core vesicles.
Neuropeptides synthesis
Neuropeptides are synthesized as large precursor molecules.
Neuropeptides behavior
Neuropeptides often play roles in regulating mood, pain, and social behaviors.
GABA packaging
GABA is packaged into vesicles using the vesicular inhibitory amino acid transporter (VIAAT).
Glutamate packaging
Glutamate is packaged by vesicular glutamate transporters (VGLUTs), not VIAAT.
Serotonin packaging
Serotonin is packaged by vesicular monoamine transporters (VMATs).
Endogenous opioids packaging
These are neuropeptides and are packaged into large, dense-core vesicles rather than through VIAATs.
Adrenalin signaling
Adrenalin (epinephrine) can act through both ionotropic and metabotropic mechanisms, depending on the type of receptor.
Serotonin receptors
Serotonin predominantly uses metabotropic receptors but does have one ionotropic receptor (5-HT3).
Norepinephrine receptors
Acts primarily through metabotropic receptors.
Histamine receptors
Uses only metabotropic receptors.
Dopamine receptors
Uses only metabotropic receptors.
NMDA receptor requirements
The NMDA receptor requires glycine or D-serine as a co-agonist.
Inhibitory neurotransmitter
The presynaptic terminal releases an inhibitory neurotransmitter, such as GABA.
Endocannabinoids release
Endocannabinoids are released from the postsynaptic terminal, not the presynaptic terminal.
Neurotransmitter packaging
Neuropeptides are generally packaged in large, dense-core vesicles, not clear-core ones.
Rimonabant action
Rimonabant blocks cannabinoid receptors, not opioid receptors.