Central Mechanisms of Pain Flashcards

1
Q

What is the gate control theory of pain modulation?

A

Non-painful stimuli can produce analgesia

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2
Q

What type of input do projection neurons (2nd order) receive?

A

Inhibitory from dorsal horn interneurons

Excitatory from axon terminals of both nociceptors and non-nociceptor mechanoreceptors

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3
Q

What type of input do dorsal horn interneurons receive?

A

Excitatory from mechanoreceptors

Inhibitory from nociceptors

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4
Q

How does the inhibitor interneuron act as a gate keeper?

A

Nociceptors inhibit the interneuron, allowing pain to be transmitted

Mechanoreceptors excite the interneuron, thereby inhibiting the projection neuron, suppressing AP firing

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5
Q

What are the three classes of endogenous opioid peptide in the nervous system?

A

Enkephalins

Dynorphins

Endorphins

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6
Q

What are the three classes of opioid receptors in the nervous system?

A

mu

delta

kappa

All metabotropic (G-protein coupled)

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7
Q

What are the major opioid and receptor in the dorsal horn of the spinal cord?

A

Enkephalin

mu receptor

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8
Q

How do opioid receptors cause postsynaptic inhibition?

A

Opening of K channels, hyperpolarizing the projection neurons

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9
Q

What are the three ways opioid receptors cause presynaptic inhibition?

A

Opening of K channels in the presynaptic terminal, hyperpolarization

Inhibition of VG calcium channels, reducing transmitter release

Inhibit Adenylyl cyclase, reducing mobilization of vesicles from the reserve pool

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10
Q

What is the role of opioids in the PAG?

A

Excite neurons in the PAG by disinhibition (inhibit GABA interneurons)

PAG controls pain transmission in the dorsal horn of the spinal cord

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11
Q

What are two ways opioid drugs produce analgesia?

A

Excitation of PAG projection neurons

Inhibition of neurotransmisstion from nociceptors to dorsal horn projection neurons

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12
Q

What is the role of the PAG system?

A

Receives pain sensory input, activating the descending pain control system to produce analgesia

Can also be affected by stress and emotion

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13
Q

What is wind-up?

A

Increase in pain sensitivity due to repeated firing of C-fiber nociceptors

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14
Q

How does wind-up occur?

A

Projection neurons contain AMPA and NMDA glutamate receptors and receptors for substance P and CGRP (NK1)

NK1 receptors are metabotropic, and close K channels, decreases K conductance

This produces EPSPs that easily undergo temporal summation

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15
Q

What is a longer lasting consequence to repeated C-fiber firing?

A

Products of repeated phospholipase C and adenylyl cyclase activation lead to a persistent increase in the ability of C-fibers to trigger firing of the second order neuron

I.e. long-term potentiation of the pain pathway

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16
Q

What can result from inflammation and nerve injury?

A

Reduced effectiveness of Cl-mediated synaptic inhibition in the dorsal horn (GABAa and glycine receptors)

I.e. reduced gate control process

Contributes to allodynia and hyperalgesia

17
Q

How does allodynia occur from the loss of the gate control process?

A

Without the inhibitory gate control mechanisms, mechanoreceptors can excite second order pain projection neurons

This leads to the upward flow of sensory information in the pain pathways that results from non-painful stimulation

18
Q

How does the activation of microglia due to inflammatory peripheral injury cause a loss of the gate control process?

A

Mircorglia activated by ATP release from nocicpetors, in turn, release brain-derived neurotrophic factor (BDNF)

BDNF inhibits the expression of K-Cl cotransporters (KCC)

The loss of KCC transporter results in the loss of the chloride equilibrium potential, and therefore the loss of gate control

19
Q

What are three classes of non-opiate analgesic drugs?

A

Antidepressants - act on descending pain control system

NMDA receptor antagonists - inhibits processes of wind-up and LTP

Anticonvulsants - reduce abnormal excitability in the pain system