FORM & FUNCTION (Synaptic Transmission) Flashcards

1
Q

Sensory input: mechanosensitive channels example

A

-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

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2
Q

Receptor potential magnitude correlates with:

A

-stimulus strength
-when receptor potential threshold, VG Na+ channels open=initiating an AP

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3
Q

If receptor potential surpasses the threshold value:

A

-triggers multiple Aps
-higher receptor potential intensity leads to more FREQUENT APs

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4
Q

AP frequency is limited by:

A

-duration of the absolute refractory period

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5
Q

Synaptic transmission at neural junction:

A

-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

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6
Q

NT vesicles moving and release of NTs:

A
  1. Minor increase in Ca2+ promotes vesicles to move to Active Zone via actin
  2. Several proteins participate in attaching vesicle to the active zone
  3. Docking: complex of SNARE proteins docks vesicle to membrane
  4. Fusion between vesicle and membrane requires an increase in Ca2+ in cytoplasm
  5. Ca2+ binds with synaptotagmin and interacts with SNARE complex and cause fusion
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7
Q

Proteins involved in NT vesicles release:

A

-synaptotagmin
-v-SNARES: on the vesicle surface
-t-SNARES: on membrane
*SNARE is a neurotoxin target

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8
Q

Chemical synapses:

A

-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

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9
Q

Mechanisms of NTs removal:

A
  1. Enzymatic breakdown of enzymes
  2. Reuptake
  3. Diffusion
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10
Q

Enzymatic breakdown of enzymes:

A

-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

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11
Q

Reuptake of NT:

A

-NT taken up by specific transporters on the presynaptic neuron (ex. serotonin, NE) or on astrocytes (ex. glutamate)

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12
Q

Diffusion:

A

-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

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13
Q

Substance P:

A

-neuropeptide involved in pain
-can use it as a potential biomarker of pain assessment in dogs

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14
Q

Response initiation on postsynaptic neuron:

A

-NTs influence cellular activated based on receptor type, altering MP directly or indirectly through a secondary messenger system

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15
Q

Receptor diversity:

A

-a single NT can elicit varied responses by bind to different receptor subtypes

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16
Q

Receptor types:

A

-ionotropic receptors (fast)
-metabotropic receptors (slow)

17
Q

Ionotropic receptors:

A

-fast
-directly coupled to ion channels, causing IMMEDIATE MP changes upon biding
Ex. Na and Cl

18
Q

Metabotropic receptors:

A

-influences ion channels INDIRECTLY through intracellular signaling pathways
-more steps=slower
Ex. GPCR

19
Q

PNS NTs:

A

-Ach: parasympathetic
-NE and E (sympathetic)

20
Q

CNS NTs:

A

-glutamate and aspartate (excitatory: cause depolarization)
-glycine and GABA (inhibitory: hyperpolarization)

21
Q

Ach receptors:

A

-nicotinic cholinergic receptor (ionotrop)ic): skeletal muscle
-muscarinic cholinergic receptor (metabotropic): autonomic NS

22
Q

E/NE receptors:

A

-metabotropic: autonomic NS
>alpha-adrenergic receptor
>beta-adrenergic receptor

23
Q

Regeneration in peripheral nerves:

A
  1. Nerve fiber and its myeline sheath distal to the injury degenerates
  2. Schwaan cells proliferate to form a column to guide axon regeneration (0.5-3mm/day)
  3. Functional connections with muscles established after several months
24
Q

CNS vs. PNS synaptic types:

A

-CNS: complex (axodendritic, axosomatic and axoaxonic synapse)
-PNS: direct: simple synapses (NM or neuroglandular)

25
Q

CNS vs. PNS myelination:

A

-CNS: one oligodendrocyte insulates many axons
-PNS: one Schwann cell insulates one axon

26
Q

CNS vs PNS regeneration capacity:

A

-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)