Physiology of Pain Lecture (Dr. Karius) TEST 3 Flashcards
Pain: The Introduction
Pain is DIFFERENT from all Other Senses because:
1) The Sensation is ELICITED by MULTIPLE STIMULI
2) It “PRE-EMPTS) all OTHER SIGNALS
3) These differences result in MULTIPLE ALTERATIONS in the Physiological Functioning of the Pain Pathways
Pain can also be CHARACTERIZED as:
1) FAST PAIN
- Generally associated with the Immediate Injury (Sharp Pain)
2) SLOW PAIN:
- Often Characterized as DULL or ACHY
- Often occurs AFTER the Injury
Pain can be CHARACTERIZED by LOCATION:
1) Deep Pain
2) Muscle Pain
3) Visceral Pain
4) Somatic/ Cutaneous Pain
* **The Characteristics of these forms of Pain VARY due to Physiological and Anatomical Considerations
Sensory Receptors: General Information
- Many are BARE NERVE ENDINGS with Specialized Ion Channels that OPEN in response to SPECIFIC STIMULI (Ex Thermoreceptors)
- Some Sensory Receptors show QUITE EXTENSIVE Morphological Specialization
Review of Nociceptive System
Sensing NOXIOUS Stimuli: The Nociceptors
- Bare Nerve Endings
- Two Types of Fibers:
1) A GAMMA FIBERS: Small, Sparsely MYELINATED. Fast, SHARP PAIN
2) C FIBERS: UNMYELINATED Fibers associated with DULL PAIN (SLOW PAIN)
Sensing Noxious Stimuli: The Nociceptors
ISSUE:
- Must be able to Detect a Wide Variety of Damaging Stimuli
TYPE of NOCICEPTORS:
1) Sensitive to BOTH THERMAL and MECHANICAL Stimuli (Majority)
2) Sensitive ONLY to THERMAL Stimuli
3) Sensitive ONLY to MECHANICAL
4) SILENT/ SLEEPING
Many Mixed Modality Nociceptors also express a MECHXNOSENSITIVE Na+ Channel (SCN9A or Na1.7)
- Mutations in this Channel lead to an ABSENCE of PAIN SENSATION!!!!!!!!!!!!!
- Another Class of MUTATION produces a PAROXYSMAL PAIN SYNDROME!!!!!
Sensing Noxious Stimuli: The Nociceptors
Description
1) Unlike other receptors, NOCICEPTORS Express a Number of LIGAND-GATED Receptors (In Addition to the Stimulus- Gated Channels) which ALTER the Sensitivity of the NOCICEPTORS to Input
2) These Include Receptors for:
a) Substance P
b) The KININS (Ex Bradykinin)
c) ATP
d) H+
2a) Interestingly, this Collection of Chemicals also EXISTS in the Spinal Cord, where they also Influence NOCICEPTIVE Inputs at those Synapses!!!
2b) When these Chemicals bind to their Receptors, they Change the SENSITIVITY of the Nociceptors (Usually Increasing) and Activate the SILENT NOCICEPTORS!!!!!
2c) Activated Nociceptors, the DAMAGED TISSUE, and Recruited WBC RELEASE THESE INTO THE PERIPHERY AS WELL AS IN THE SPINAL CORD!!!!!
Sensing Noxious Stimuli: Pathways to the Brain
There are Multiple Pathways to the Brain:
1) Dorsal Columns: PROPRIOCEPTIVE and Discriminative (FINE TOUCH)
2) Spinothalamic Tract: FAST PAIN
3) Spinoreticulothalamic System: SLOW PAIN
4) Spinocerebellar Tract
Sensing Noxious Stimuli: The Spinal Cord
A) Neurotransmitter Released:
1) EAA (From A Delta): Acting Primarily on Non-NMDA Receptors
* FAST PAIN*
2) From C Fibers:
- Substance P
- EAA
*** B) Nocicpetors that travel with the SPINORETICULOTHALAMIC Pathway (Slow Pain) Synapse on an INTERNEURON in the Spinal Cord before CROSSING and ASCENDING to the RETICULAR FORMATION
C) This Synapse is the Site of Much MODULATION of Spinal Cord Function:
- Local (GATE THEORY)
- Descending (OPIOD PATHWAYS)
Sensing Noxious Stimuli: Visceral Pain
- The Visceral AFFERENT travel with AUTONOMIC NERVES rather than with either of the Two Spinal Pathways described already
Central Processing of Noxious Stimuli: The Brain
Introduction
- Unlike other senses, NOCICEPTIVE INPUT is DISTRIBUTED WIDELY in the Cortex!!!!
- S1 and S2 receive INPPUT from the NOCICEPTORS and play a role in LOCALIZING the PAIN!!!
Central Processing of Noxious Stimuli: The Brain
INSULAR CORTEX
The INSULAR CORTEX is particularly important in the INTERPRETATION of NOCICEPTIVE INPUTS:
1) Processes Information about the INTERNAL STATE of the Body
2) Contributes to the AUTONOMIC RESPONSE to the Pain
3) INTEGRATES AL SIGNALS RELATED TO THE PAIN (Asymbolia)!!!!!!!!!!!!!!!!!!
Central Processing of Noxious Stimuli: the Brian
Description
- Lesions in any one are DOES NOT ABOLISH the ability to Experience Pain, although the Experience is CHANGED
- Many Nociceptive Inputs go to the AMYGDALA. This is particularly important for activating/ producing the Emotional Components inherent in the SENSATION of Pain
Central Processing of Noxious Stimuli: Visceral Pain
- Visceral Nociceptors, traveling with the Autonomic Nerves, have additional Synapses WITHIN the HYPOTHALAMUS and the MEDULLA
- These additional Synapses form the basis of the Physiological Changes associated with VISCERAL PAIN, including DIAPHORESIS and ALTERED Blood Pressure
The Gate Theory of Pain
- Based in part on the Observation that other SOMATIC INPUT can alleviate Pain (Rubbing the Area)
* The First Synapse onto Interneuron: Is the site where the Substance P and EAA are being released because it is a C Fiber!!!**
STEP 1:
- Activate A Beta Fibers (Bright Green) by the Normal Stimuli. The A Beta Fiber has a Branch the travels via the DORSAL COLUMNS, BUT it also Branches WITHIN the Spinal Cord
STEP 2:
- The A Beta Fiber (Green) releases EAA and ACTIVATES an INHIBITORY INTERNEURON (Yellow) in the Spinal Cord
STEP 3:
- The INHIBITORY Interneuron releases GLYCINE to INHIBIT the activity of the SECOND ORDER NEURON in the Pain Pathway
END RESULT:
- Rubbing the area of Skin ACTIVATED the A Beta Fiber will REDUCE the Sensation of Pain!!!!!!
Descending Mechanisms of Painful Inputs
Basic Idea: Use Presynaptic INHIBITION to reduce Activation of the Second-order Nociceptive Neuron in the SPINAL CORD
STEP 1:
- Neurons in the PERIAQUEDUCTAL GRAY are activated by Numerous Inputs, Including OPIATE (Mu Receptors), EAA, and CANNIBINOIDS (CB1 Receptor)
STEP 2:
- Axons from the PAG Neurons travels to the MIDLINE RAPHE NUCLEI (Serotonin) and release ENKEPHALINS (Mu Receptors), which activate the RAPHE NEURONS
STEP 3:
- Axons from the Raphe Neurons travel to the Spinal Cord and release SEROTONIN, which Activate INHIBITORY INTERNEURONS, causing them to release OPIATES
STEP 4:
- The Opiates released by the Interneuron (Yellow) activate MU RECEPTORS on the Presynaptic Terminal of the C Fiber
STEP 5:
- This produces PRE-SYNAPTIC Inhibition that reduces the release of Substance P from the NOCICEPTOR (Blue) and REDUCES PAIN TRANSMISSION
Qualities of Pain from Different Locations
Case 1
Medical Student Seuss was taking his FOM Final when, while turning pages of the Exam, he suffered a Paper Cut. There was a SHAPR PAIN when he FIRST sustained the Injury, but with time it has “Settled” to a DULL, ACHY PAIN
- The skin is Innervated by BOTH A Delta and C Fibers, leading to Fast, Sharp Pain at the time of Injury. However, the C Fibers (Group IV Fibers) were also activated, leading to the sensation of a DULL, ACHY Pain
MUSCLE PAIN:
- Cause: Usually Injury or Ischemia during Contraction
- Both Group III and IV Fibers Present
- Get BOTH FAST and SLOW Pain associated with Muscle