Topic 8: Modulation of Nociception

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58 Terms

1
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What are the two primary types of modulation of nociception in the CNS?

Segmental modulation (spinal gating) and suprasegmental modulation (descending).

2
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Where does segmental modulation of nociception occur?

In the dorsal horn of the spinal cord.

3
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Where does suprasegmental modulation of nociception originate?

From brain structures (cortex, brainstem) descending to the spinal cord dorsal horn.

4
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What is meant by "spinal gating" in nociceptive modulation?

Local interneurons in the dorsal horn inhibit or amplify pain signals before they reach the brain.

5
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What is the main principle of suprasegmental (descending) pain modulation?

Descending fibers from the brainstem or cortex can inhibit or facilitate nociceptive transmission in the spinal cord.

6
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Is there always a direct relationship between tissue injury and pain perception?

No—there is no simple relationship; pain perception can be influenced by CNS modulation and psychological factors.

7
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Give an example of how pain and tissue injury do not always correlate.

Traumatic injuries in athletes or combat may be described as relatively painless at first.

8
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Name three psychological factors that can alter pain perception.

Arousal, attention, and expectation.

9
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What determines whether pain is transmitted or inhibited in the CNS?

The balance of inhibitory and facilitatory influences on somatosensory neural circuits.

10
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At what CNS levels does integration of pain modulation occur?

At the spinal cord, brainstem, and multiple cortical regions.

11
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Why are derangements in central pain modulation systems important clinically?

They are often critical in the generation and maintenance of chronic pain.

12
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What is the first site of central modulation of nociception?

The dorsal horn of the spinal cord.

13
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According to the Gate Control Theory, what determines whether pain signals are transmitted?

The balance of activity between nociceptive and non-nociceptive afferent fibers.

14
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Which fibers "open the gate" to pain transmission?

Small-diameter nociceptive fibers (A-delta and C fibers).

15
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Which fibers "close the gate" to pain transmission?

Large-diameter non-nociceptive fibers (A-β mechanoreceptors).

16
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What common everyday action demonstrates the gate control theory?

Rubbing a painful area reduces pain by activating A-β mechanoreceptors.

17
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Which laminae of the dorsal horn contain interneurons involved in nociceptive modulation?

Laminae I, II, and V.

18
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What neurotransmitters do inhibitory interneurons in the dorsal horn release?

Glycine and dynorphin (an opioid peptide).

19
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Which second-order neurons in the dorsal horn receive modulatory input from interneurons?

Wide Dynamic Range (WDR) and Nociceptive-Specific (NS) neurons.

20
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How do A-β mechanoreceptors affect WDR and NS neurons of the spinothalamic tract (STT)?

They exert an inhibitory influence, reducing nociceptive activity.

21
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Which clinical therapy is based on the principle of activating A-β mechanoreceptors to inhibit pain?

Transcutaneous Electrical Nerve Stimulation (TENS).

22
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What is the role of low-threshold mechanical stimulation in pain modulation?

It can override or desensitize nociceptive signals within the STT.

23
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In a normal joint, which type of afferent input dominates?

Large-diameter mechanoreceptive afferents (proprioception).

24
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In a normal joint, what is the level of nociceptive input?

Low nociceptive input.

25
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What happens to mechanoreceptive input in a subluxated joint?

Mechanoreceptive input decreases.

26
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What happens to nociceptive input in a subluxated joint?

Nociceptive input increases.

27
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After a chiropractic adjustment, what happens to mechanoreceptive input?

Mechanoreceptive input increases again.

28
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After a chiropractic adjustment, what happens to nociceptive input compared to the subluxated state?

Nociceptive input decreases.

29
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What overall effect does a chiropractic adjustment have on afferent input balance?

It restores mechanoreceptive dominance and reduces nociceptive drive.

30
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Which neurophysiological principle helps explain how increased mechanoreceptor activity reduces pain perception?

The Gate Control Theory of pain modulation.

31
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Why does rubbing or massaging a painful area often reduce pain?

It activates mechanoreceptors (A-β fibers), which inhibit nociceptive signaling via Gate Control Theory.

32
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How does a chiropractic adjustment influence afferent input to the spinal cord?

It increases mechanoreceptive input and decreases nociceptive input from the joint.

33
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What is the clinical significance of increased mechanoreceptive afferentation after adjustment?

It can improve proprioception, normalize joint function, and reduce pain perception.

34
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What happens when mechanoreceptive input decreases and nociceptive input dominates?

The CNS receives more pain-related signals, which can contribute to chronic pain and dysfunctional motor control.

35
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Which type of afferent fibers are associated with nociception?

Small-diameter fibers (A-delta and C fibers).

36
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Which type of afferent fibers are associated with mechanoreception?

Large-diameter A-β fibers.

37
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Why might a subluxated joint lead to altered motor patterns or reflexes?

Increased nociceptive input and decreased mechanoreceptive input disrupt CNS integration of sensory information.

38
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What neurophysiological model explains how chiropractic adjustments reduce pain?

The Gate Control Theory combined with restoration of normal joint afferentation.

39
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What midbrain structure is the principal site for endogenous pain control?

The periaqueductal gray (PAG).

40
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Which inputs can activate PAG opioid neurons?

Mesolimbic structures, the hypothalamus, and the paleospinothalamic tract (PSTT).

41
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How does the PAG exert descending pain modulation?

By disinhibition of bulbospinal projections from the raphe nuclei and reticular nuclei.

42
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Which brainstem nuclei relay descending signals from the PAG?

The nucleus raphe magnus (NRM) and the reticular magnocellular nuclei (RMC: NRGC & NpGL).

43
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What nuclei form the reticular magnocellular group (RMC)?

Nucleus reticularis gigantocellularis (NRGC) and nucleus paragigantocellularis lateralis (NpGL).

44
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What nuclei form the nucleus raphe magnus (NRM)?

Nucleus raphe alatus and nucleus raphe lateralis.

45
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Which tract carries descending projections from NRM and RMC to the spinal cord?

The dorsolateral funiculus (DLF).

46
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Which spinal cord laminae receive input from descending projections?

Laminae I, II, and V of the dorsal horn.

47
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What neurotransmitters are released by inhibitory interneurons in the dorsal horn?

Glycine, enkephalin, and dynorphin.

48
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What is the net effect of suprasegmental modulation from PAG → NRM/RMC → spinal cord?

Inhibition of nociceptive transmission and reduced pain perception.

49
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What type of afferent input do chiropractic adjustments increase?

Mechanoreceptive input from joint and muscle receptors.

50
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How does increased mechanoreceptive input affect nociception?

It activates descending inhibitory pathways and reduces nociceptive signaling.

51
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Which neurotransmitters are released by descending brainstem pathways to modulate pain in the dorsal horn?

Norepinephrine (NE) and serotonin (5-HT).

52
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Which neurotransmitters are released by inhibitory interneurons in the dorsal horn to suppress pain transmission?

Enkephalin (ENK) and dynorphin.

53
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What excitatory neurotransmitters are released by primary nociceptive afferents in the dorsal horn?

Glutamate and substance P.

54
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Where do descending fibers from the brainstem travel in the spinal cord?

The dorsolateral funiculus (DLF).

55
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Which spinal cord laminae are the main targets of descending inhibitory fibers?

Laminae I, II, and V of the dorsal horn.

56
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How do enkephalin-containing interneurons inhibit pain transmission?

By presynaptic inhibition of neurotransmitter release and postsynaptic inhibition of projection neurons.

57
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Which midbrain structure is the principal site of endogenous pain control that initiates descending modulation?

The periaqueductal gray (PAG).

58
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Overall, how do chiropractic adjustments reduce pain perception?

By increasing mechanoreceptor input, activating descending anti-nociceptive pathways, and suppressing nociceptive transmission in the dorsal horn.