FORM & FUNCTION (Synaptic Transmission) Flashcards
Sensory input: mechanosensitive channels example
-when patellar tendon is tapped with a reflex hammer, it causes the muscle to stetch
-stretching opens a population of mechanosensitive channels that allow positive ions to flow in and generate a RECEPTOR CURRENT
Receptor potential magnitude correlates with:
-stimulus strength
-when receptor potential threshold, VG Na+ channels open=initiating an AP
If receptor potential surpasses the threshold value:
-triggers multiple Aps
-higher receptor potential intensity leads to more FREQUENT APs
AP frequency is limited by:
-duration of the absolute refractory period
Synaptic transmission at neural junction:
-AP reaches end of presynaptic neuron
-VG Ca2+ channels open in response
-influx of Ca2+ ions causes synaptic vesicles to release NTs
-NTs bind to receptors on postsynaptic neuron
-binding opens ligand-gated ion channels, leading to influx of ions
-if induces a significant change in potential, a new AP can be initiated in the postsynaptic neuron
NT vesicles moving and release of NTs:
- Minor increase in Ca2+ promotes vesicles to move to Active Zone via actin
- Several proteins participate in attaching vesicle to the active zone
- Docking: complex of SNARE proteins docks vesicle to membrane
- Fusion between vesicle and membrane requires an increase in Ca2+ in cytoplasm
- Ca2+ binds with synaptotagmin and interacts with SNARE complex and cause fusion
Proteins involved in NT vesicles release:
-synaptotagmin
-v-SNARES: on the vesicle surface
-t-SNARES: on membrane
*SNARE is a neurotoxin target
Chemical synapses:
-AP causes opening of VG Ca2+ channels in pre-synaptic terminal
-quantal release of NT: each AP releases the same amount of NT into the synaptic cleft
-‘on signal’ for post-synaptic neuron is binding of NT to receptors
-‘off signal’ is some mechanism of removing the NT from the synaptic cleft
Mechanisms of NTs removal:
- Enzymatic breakdown of enzymes
- Reuptake
- Diffusion
Enzymatic breakdown of enzymes:
-Ach is broken down into choline and acetic acid by AChE (Ach esterase) at the synaptic cleft
>AChE is on membrane of post-synaptic neuron
Reuptake of NT:
-NT taken up by specific transporters on the presynaptic neuron (ex. serotonin, NE) or on astrocytes (ex. glutamate)
Diffusion:
-occurs to a certain extent with all NTs
-only mechanism of removal of peptide NTs
-slow=long duration of action if this is only mechanism of removal
Substance P:
-neuropeptide involved in pain
-can use it as a potential biomarker of pain assessment in dogs
Response initiation on postsynaptic neuron:
-NTs influence cellular activated based on receptor type, altering MP directly or indirectly through a secondary messenger system
Receptor diversity:
-a single NT can elicit varied responses by bind to different receptor subtypes
Receptor types:
-ionotropic receptors (fast)
-metabotropic receptors (slow)
Ionotropic receptors:
-fast
-directly coupled to ion channels, causing IMMEDIATE MP changes upon biding
Ex. Na and Cl
Metabotropic receptors:
-influences ion channels INDIRECTLY through intracellular signaling pathways
-more steps=slower
Ex. GPCR
PNS NTs:
-Ach: parasympathetic
-NE and E (sympathetic)
CNS NTs:
-glutamate and aspartate (excitatory: cause depolarization)
-glycine and GABA (inhibitory: hyperpolarization)
Ach receptors:
-nicotinic cholinergic receptor (ionotrop)ic): skeletal muscle
-muscarinic cholinergic receptor (metabotropic): autonomic NS
E/NE receptors:
-metabotropic: autonomic NS
>alpha-adrenergic receptor
>beta-adrenergic receptor
Regeneration in peripheral nerves:
- Nerve fiber and its myeline sheath distal to the injury degenerates
- Schwaan cells proliferate to form a column to guide axon regeneration (0.5-3mm/day)
- Functional connections with muscles established after several months
CNS vs. PNS synaptic types:
-CNS: complex (axodendritic, axosomatic and axoaxonic synapse)
-PNS: direct: simple synapses (NM or neuroglandular)
CNS vs. PNS myelination:
-CNS: one oligodendrocyte insulates many axons
-PNS: one Schwann cell insulates one axon
CNS vs PNS regeneration capacity:
-CNS: limited due to complex microenvironment
-PNS: possible when damage is moderate (Schwaan cells play a pivotal role in guiding and supporting axonal regrowth and target innervation)