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بسم الله الرحمن الرحيم
 
PAIN SENSATION   According to The International Association for the Study of Pain (IASP): Definition:   Pain is an  unpleasant sensory and emotional experience associated with actual or potential tissue damage. 1)  warning signal against tissue damage .  Pain is one of the most prominent symptoms of tissue damage.  2)  Initiate protective reflexes  which causes the subject to get rid of the painful stimulus, or at least, to minimize tissue injury or damage  ,[object Object]
 
If persistent, physiological pain may progress to a  pathological condition  itself, often referred to as  maladaptive  pain, in which case pain is dissociated from the original noxious stimulation or the healing process and thus does not represent anymore a symptom of disease but rather abnormal sensory processing due to  damage to tissues  (inflammatory pain) or  the nervous system  (neuropathic pain), or to  abnormal function of the nervous system itself (functional pain) . pain resulting from activation of pain receptors may be referred to as  adaptive  or  physiological  pain, because it minimizes tissue damage and promotes healing.
[object Object],[object Object],1. Nociceptive  is  pain caused by tissue damage  (inflammation) which stimulate pain receptors (nociceptors). 2. Neuropathic:  (pain due to injury of nerve pathway) site of injury:  Central   Central pain (thalamic infarct). Mixed   Plexus avulsion, Post herpetic neuralgia. Peripheral   Neuroma, nerve compression, phantom, neuralgias. character:  burning, tingling, numbness, pressing, squeezing, itching, constant +/- intermittent shooting, lancinating, electric. 3. Psychogenic:  (difficult to differentiate whether secondary to or actual cause of pain),  anxiety, depression (30% of depressives complain of pain on initial presentation). ,[object Object]
Types of Pain Receptors  ,[object Object],Polymodal Pain Receptors (most pain receptors)   ,[object Object],Mechanical  Pain  Receptors  ,[object Object],Thermal Pain Receptors  ,[object Object],Chemical Pain Receptors  ,[object Object],[object Object]
Distribution of Pain Receptors ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object]
Pain Threshold: ,[object Object],[object Object],[object Object],[object Object],[object Object]
Stimulation of Pain Receptors: ,[object Object],PGE 2 IL-1 Both    threshold of pain receptors facilitating their stimulation
[object Object],1- Direct stimulators Substances which when reach specific threshold directly stimulate pain receptors ----> pain, as: - K +  ions.  - H +  ions - Serotonin.  - Histamine - Bradykinin  2- Sensitizers Substances which lower the threshold for stimulation of pain receptors by direct stimulators ----> facilitate pain production. They include: a) Substances released by the injured tissues  as: PGE2 & IL-1 b) Substances released by pain receptors  through antidromic impulses as: substance P N.B.: Substance P also stimulate mast cells to release histamine which is a direct stimulator.
[object Object],Function Molecular receptor Stimulation Acid sensing receptor (H+) Stimulation Purinergic receptor (ATP) Stimulation Transient receptor potential rec. (thermal)  Stimulation & sensitization Bradykinin receptor Stimulation & sensitization Histamine recptor Stimulation & sensitization Serotonin receptor sensitization Prostaglandin receptor sensitization Interleukin-1 receptor sensitization Substance P receptor Inhibition Cannabinoid receptor Inhibition Opioid receptor
 
Pain Tolerance: ,[object Object],[object Object],[object Object],[object Object],Non  Adaptation  of  Pain  Receptors  ,[object Object],[object Object]
THE CHARACTER (QUALITY) of pain 1) Pricking or Cutting Pain  2) Burning Pain  3) Aching Pain  4) Throbbing Pain  5) Colicky Pain  ,[object Object],[object Object],[object Object],[object Object],[object Object]
Visceral Somatic sympathetically innervated organs can be transferred to body surface cutaneous, deep tissues site vague distribution and  Quality deep, ache, dragging, squeezing acute: colic, paroxysmal, +/- N/V, sweating, BP and heart rate changes constant, localised aching, throbbing, gnawing character Acute nociceptive pain:
Slow (delayed) pathophysiological pain Fast (Immediate) physiological pain Shortly after application if tissue damage occurs Longer duration Burning Poorly-localized C-fibers Thalamus Substance-P * Associated with arousal, autonomic & emotional reactions Abolished by local anaethesia & morphine onset:  during application of the stimulus Duration:  short duration. Nature:  pricking Localization:  well-localized Afferent:  A-delta fibers Higher center:  CC Neurotransmitter:  glutamate Significance:  * determine site & severity. * Initiate withdrawal reflexes. Abolished by  deep pressure and not abolished by morphine.
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Pain1

  • 2.  
  • 3.
  • 4.  
  • 5. If persistent, physiological pain may progress to a pathological condition itself, often referred to as maladaptive pain, in which case pain is dissociated from the original noxious stimulation or the healing process and thus does not represent anymore a symptom of disease but rather abnormal sensory processing due to damage to tissues (inflammatory pain) or the nervous system (neuropathic pain), or to abnormal function of the nervous system itself (functional pain) . pain resulting from activation of pain receptors may be referred to as adaptive or physiological pain, because it minimizes tissue damage and promotes healing.
  • 6.
  • 7.
  • 8.
  • 9.
  • 10.
  • 11.
  • 12.
  • 13.
  • 14.  
  • 15.
  • 16.
  • 17. Visceral Somatic sympathetically innervated organs can be transferred to body surface cutaneous, deep tissues site vague distribution and Quality deep, ache, dragging, squeezing acute: colic, paroxysmal, +/- N/V, sweating, BP and heart rate changes constant, localised aching, throbbing, gnawing character Acute nociceptive pain:
  • 18. Slow (delayed) pathophysiological pain Fast (Immediate) physiological pain Shortly after application if tissue damage occurs Longer duration Burning Poorly-localized C-fibers Thalamus Substance-P * Associated with arousal, autonomic & emotional reactions Abolished by local anaethesia & morphine onset: during application of the stimulus Duration: short duration. Nature: pricking Localization: well-localized Afferent: A-delta fibers Higher center: CC Neurotransmitter: glutamate Significance: * determine site & severity. * Initiate withdrawal reflexes. Abolished by deep pressure and not abolished by morphine.