PAIN AND ANALGESIA

PAIN AND ANALGESIA


PAIN AND ANALGESIA

I. PAIN:

  • Defined as an “Unpleasant sensory & emotional experience associated with actual or potential tissue damage”.

TYPES OF PAIN:

1. Nociceptive pain:

  • Musculoskeletal pain.
  • Due to injury/inflammatory/degenerative disorders.
  • E.g. Bone fracture/Arthritis/Burn.

2. Neuropathic pain:

  • Due to dysfunction/nerve damage.
  • Eg. Intervertebral disc prolapse.

3. Mixed pain:

  • Includes components of both nociceptive & neuropathic pain.

4. Idiopathic/unspecified pain:

  • Purely psychological in nature; Hence, “Psychogenic pain”.

RECEPTORS & INNERVATION:

1. Receptors:

  • Referred as “Nociceptors”.
  • Are mostly “Free nerve endings”.

– Found maximum in skin.

– Also in periosteum, arterial walls, joint surface, falx cerebri & tentorium.

– Pain receptors absent in Brain.

2. Innervation:

  • Impulse from nociceptors transmitted via two fiber types – 

– Aδ & C fibers.

  • Based on type of fibers, pain classified into,

– Fast & slow pain.

2a. Fast pain/Epicritic pain/First pain:

  • Carried by thin myelinated Aδ (Type-III) fibers.
  • Conduction velocity – 12-30 m/s.

Neurotransmitter:

  • Glutamate.
  • Secreted by Aδ fibers.

Receptor:

  • Sensitive to mechanical/thermal stimuli of noxious strength.

Pain type:

  • Produce sharp & well-localized pain.

2b. Slow pain/Protopathic pain/Second pain:

  • Carried by unmyelinated C (Type IV) fibers.
  • Conduction velocity – 0.5 m/s.

Neurotransmitter:

  • Mainly substance P & some glutamate.
  • Released by C fibers.

Receptor:

  • Sensitive to noxious mechanical or thermal stimuli.
  • Also sensitive to chemicals.
  • Histamine, serotonin, bradykinin, K+ ions, H+ ions, prostaglandins, substance P & acetylcholine.
  • Serotonin – Most potent allogenic substance.

Pain type:

  • Produce dull-aching & poorly localized pain.

HYPERALGESIA & ALLODYNIA:

  • Pain accomponied by hyperalgesia & allodynia.
  • Hyperalgesia – Exaggerated response to noxious (painful) stimulus.
  • Allodynia – Pain sensation in response to non-noxious (non-painful) stimuli.

Mechanism:

Noxious stimulus.

↓

Stimulates nociceptors.

↓

Produces tissue injury.

↓

Releases pain-producing substances.

  • Eg: K+ ions, Histamine, Serotonin, Prostaglandins, Bradykinin, Acetylcholine & Substance P.

↓

Increases sensitivity of silent nociceptors.

↓

Hence, increased nociceptors response to noxious stimulus, during tissue injury.

PRIMARY & SECONDARY HYPERALGESIA:

Primary hyperalgesia –

  • Due to nociceptors sensitization.
  • Repetitive stimuli –> Cause tissue damage.
  • This increases nociceptors sensitivity (hypersensitivity) –> Producing hyperalgesia.

Secondary hyperalgesia –

  • Due to spinothalamic tract sensitization.
  • Caused by long-term potentiation.
  • Mainly on continuous primary nociceptor C fibers discharge.

– Hence, “Central sensitization/Winding up”.

Summary:

  • Primary hyperalgesia – Exaggerated response in nociceptors itself.
  • Secondary hyperalgesia – Exaggerated response in spinothalamic tract (nociceptor neurons).

VISCERAL PAIN:

  • A viscus does not have any other sensation (e.g. touch, temperature etc) except pain.
  • Poorly localized – Due to sparse distribution of nociceptors.

Stimulus:

  • Any stimulus exciting pain nerve endings in diffuse visceral areas.
Seen in, 
  • Ischemia of visceral tissue

– Eg. MI.

  • Smooth muscle spasm of hollow viscus.

– Eg. Gallbladder/bile duct/ureter.

  • Excessive distension of a hollow viscus.
  • Stretching of connective tissue surrounding viscus.

– Eg. Mesentery stretching in violent intestinal contraction.

  • Inflammation.

– Eg. appendicitis.

  • Chemical stimuli.

– Eg. gastric acid leak through perforated ulcer-causing chemical peritonitis).

Nerve involved:

  • Visceral pain carried by – Type C afferents.

– In sympathetic system – From thoracic & abdominal viscera.

– In parasympathetic system – From pelvic viscera.

VARIATIONS IN PAIN SENSITIVITY AMONG STRUCTURES:

Important pain producing viscera:

  • Heart.
  • Esophagus.
  • Gallbladder.
  • Stomach.
  • Intestine.
  • Appendix
  • Ureter.
  • Kidney.
  • Urinary bladder.

Completely insensitive viscera:

  • Liver parenchyma.
  • Lung alveoli.
  • Yet, Liver capsule, bronchi & parietal lung pleura are pain sensitive.

Intracranial structures sensitive to pain:

  • Scalp.
  • Aponeurotica.
  • Duramater around venous sinuses & vessels.
  • Falx & Tentorium cerebri.
  • Cranial venous sinuses & some arteries.

Intracranial structures insensitive to pain:

  • Brain parenchyma.
  • Ventricular ependyma.
  • Dura materr over convexity of skull.
  • Pia mater.
  • Pial veins.
  • Arachnoid mater.
  • Choroid plexus.

Exam Important

PAIN AND ANALGESIA

  • Idiopathic/unspecified pain – Purely psychological in nature; Hence, “Psychogenic pain”.
  • Brain is the most conspicuous part of body which has no pain receptors at all.
  • Pain receptors (Nociceptors) – Free nerve endings.
  • Pain receptors absent in Brain.
  • Fast pain/Epicritic pain/First pain – Carried by thin myelinated Aδ (Type-III) fibers with conduction velocity – 12-30 m/s.
  • Slow pain/Protopathic pain/Second pain – Carried by unmyelinated C (Type IV) fibers.

– Neurotransmitter released by C fibers – Mainly substance P.

  • Slow pain receptor sensitive to chemicals – Histamine, serotonin, substance P & acetylcholine.

– Serotonin – Most potent allogenic substance.

  • Hyperalgesia – Exaggerated response to noxious (painful) stimulus.
  • Allodynia – Pain sensation in response to non-noxious (non-painful) stimuli.

– Repetitive stimuli → Cause tissue damage.

– Thus increasing nociceptors sensitivity → Producing primary hyperalgesia.

  • A viscus does not have any other sensation (e.g. touch, temperature etc) except pain.
  • Visceral pain is poorly localized due to sparse distribution of nociceptors.
  • Stimuli for visceral pain –

– Excessive distension of a hollow viscus.

– Stretching of connective tissue surrounding viscus.

– Eg. Mesentery stretching in violent intestinal contraction.

  • Visceral pain sensation carried by – Type C afferents.

– In sympathetic system – From thoracic & abdominal viscera.

– In parasympathetic system – From pelvic viscera.

– Important pain producing viscera – Heart & Stomach

– Completely insensitive viscera – Liver parenchyma.

– Intracranial structures sensitive to pain – Duramater around venous sinuses & vessels, 

– Intracranial structures insensitive to pain – Brain parenchyma, pia meter & pial veins.

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