pruritus Flashcards

1
Q

define pruritus

A

unpleasant sensation that elicits the desire or reflex to scratch, rub, lick, chew

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2
Q

how does pruritus commonly manifest in dogs

A
  • scratch
  • rub
  • nibble
  • lick
  • temperament changes
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3
Q

how does pruritus often manifest in cats

A
  • often secretive and not noticed by owner
  • overgrooming (sometimes bilateral symmetrical alopecia not caused by endocriopathy)
  • hair plucking (resulting in hair balls, tufts of hair around house and hair in feces)
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4
Q

what are the 3 classifications of pruritus

A
  • pruriceptive pruritus
  • neuropathic pruritus
  • psychogenic (stress)
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4
Q

how does pruritus often manifest in horses

A
  • rubbing
  • stamping
  • biting
  • scratching
  • bucking/kicking
  • temperament changes
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5
Q

what is pruriceptive pruritus

A

due to stimulation of peripheral receptors in skin (in presence of a healthy nervous system) usually due to a skin disease

originates from the skin

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6
Q

what is neuropathic pruritus

A

generated in the CNS in response to:
- anatomical lesion of PNS or CNS
- circulating pruritogens
- pharmacological mediators

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6
Q

what receptors are responsible for sensation of itch

A

nociceptors

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7
Q

what nerve fibres conduct itch

A
  • unmyelinated slow-conducting C fibres
  • A-delta fibres
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8
Q

what other itch receptors are in the skin

A
  • fine network of free nerve endings at dermo-epidermal junction and within epidermis contain itch-associated receptors
  • epidermis with free C-neuron receptors act as main itch receptor in skin
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9
Q

what is the main itch receptor type

A

free C-neuron receptors within the epidermis

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10
Q

what chemical mediators are involved in cutaneous itch

A

a lot of different mediators
- various proteases/leukotrienes/neurotropins
- peptides
- prostaglandins
- cytokines
- histamine

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11
Q

where do chemical mediators involved in itch originate

A
  • keratinocytes (leukotrine, cannabinoids, thymic stromal lymphopoietin)
  • mast cells (histamine, LTB-4, IL-2, NGF)
  • Skin leucocytes (T-cells produce IL-31 and eosinophils which produce NGF)
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12
Q

how do chemical mediators act to cause itch

A
  • direct stimulation of intraepidermal nerve fibres
  • stimulate mast cells
  • stimulate other mediators/transduction cascades
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13
Q

why is IL-31 important

A
  • produced by activated T-cells in allergic skin disease
  • binds to receptors on surface neurons in skin and activates JAK enzymes to stimulate pruritic nerve impulse to brain
  • important focus of therapy for allergic skin disease in dogs (apoquel and cytopoint)
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14
Q

describe the neural pathway for itch

A
  1. sensory afferent from skin (mainly via C-neurons which are slow conducting)
  2. dorsal nerve root to spinal cord
  3. dorsal horn and synapse with spinal interneurons (some inhibitory, some activatory)
  4. cross and ascend in lateral spinothalamic tract
  5. thalamus to internal capsule
  6. sensory cortex (left hemisphere dominance)

itch perception can be altered by emotiuonal factors and competing cutaneous sensations

15
Q

sensory fibres from thehead carry itch sensations via which cranial nerves

A
  • trigeminal (V)
  • facial (VII)
  • Glossopharyngeal (IX)
  • Vagus (X)
16
Q

discuss neuronal regulatory mechanisms

A

multiple factors on/in skin can also suppress/exacerbate pruritus
- physical factors (painful heat/cold supresses while moderate cold exacerbates)
- mechanical factors (rubbing/scratching causes pain) induces brief suppression of itch
- distraction

NB a truly pruritic animal (one that is severely itchy) cannot be distracted and will itch even while eating

17
Q

how does scratching work to inhibit itchy sensations

A

scratch
1. fast conducting A-beta neurons stimulated
2. activation of inhibitory neuronal circuits
3. results in widespread surround inhibition of sensation

18
Q

how does distraction work to prohibit sensations of itch

A
  1. increased activity in descending pathways from reticular formation
  2. activation of inhibitory circuits in dorsal horns of spinal cord
  3. closes gated mechanism
  4. diminishes afferent itch messages
19
Q

discuss how sensitisation in chronic pruritus works

A

not well studied in animals but in man:
peripheral sensitisation: scratching leads to increased local inflammation, leading to production of pruritogens by inflammatory cells leading to increased C-fibre responsiveness
central sensitisation: chronic inflammation of skin leads to altered perception of gentle mechanical/other stimuli which is the perceived as pruritus (allokinesis)

20
Q

list and discuss some therapeutic interventions for pruritus

A
  • reduction of skin inflammation (steroids/ciclosporin)
  • blocking of peripheral inflammatory mediators (cytopoint and antihistamines)
  • moisturiser (dry skin is itchy)
  • topical cooling preparations (calamine and menthol)
21
Q

why are some treatments for pruritus preferred over others

A

pathogenesis of pruritus involves a variety of cells/mediators/neurological pathways which can vary between species and individuals
- a single drug is unlikely to uniformly be effective in all cases
- narrowly targeted treatments generally give less side effects than those with a broader action (steroids) but will be effective in a lower % of patients
- treatments that affect a target that is only present for a short time are less likely to be effective than those in which the target is long term