20 KiB
Pain
- Submodality of the sense of touch, warns of injury and things that should be avoided
- More subjective than the other senses. The same stimulus can produce different responses in different individuals, or in the same individual in different circumstances
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Congenital insensitivity to pain
from: http://ghr.nlm.nih.gov/condition/congenital-insensitivity-to-pain
20 cases have been reported in the scientific literature
Mutations in the SCN9A gene cause congenital insensitivity to pain. The SCN9A gene provides instructions for making one part (the alpha subunit) of a sodium channel called NaV1.7.
NaV1.7 sodium channels are found in nerve cells called nociceptors that transmit pain signals to the spinal cord and brain. The NaV1.7 channel is also found in olfactory sensory neurons, which are nerve cells in the nasal cavity that transmit smell-related signals to the brain.
The SCN9A gene mutations that cause congenital insensitivity to pain result in the production of nonfunctional alpha subunits that cannot be incorporated into NaV1.7 channels. As a result, the channels cannot be formed.
autosomal recessive pattern
Pain perception involves activation of specialized neurons (not just mechanoreceptors)
- Nociceptor doesn’t fire until pain is felt. Other thermoreceptors fire at all temps and at about the same frequency
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Scheme for transcutaneous nerve recording
How do we detect pain?
- A family of ion channel receptors have been found that open in response to heat as well as capsaicin called TRP (transient receptor potential) channels
- Structurally resemble voltage-gated K⁺ channels, having 6 transmembrane domains that make a pore
- When open allows Ca²⁺ and Na⁺ across membrane to generate a receptor potential
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Heat gated ion channels
- Capsaicin receptors are nonselective cation channels opened by heat, low pH, and capsaicin (the hot in hot peppers)
- Mice without TRPV1 (VR1) have impaired sensitivity to pain. Can drink capsaicin as if it were water
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transient receptor potential cation channel subfamily V member 1 (TrpV1), also known as the capsaicin receptor or the vanilloid receptor 1 (VR1)
function of TRPV1 is detection and regulation of body temperature. In addition, TRPV1 provides a sensation of scalding heat and pain (nociception).
43ºC threshold (110ºF)
There is recent evidence for endovanilloids that are released by other cells that can stimulate TRPV1 and contribute to nociception
receptors for transduction of mechanical and chemical forms of nociceptive stimulation are not well understood, candidate include
- TRP family (TRPV2 and TRPA1)
- ASIC acid sensing family (ASIC3 cardiac pain)
- TRPV3 TRPV4 warm temperatures
- TRPM8 cold temperatures
repeated applications of capsaicin desensitize pain fibers, preventing neuromodulatiors like sub P, VIP, and somatostatin from being released by PNS and CNS nerve terminals
NAV 1.7 and NAV 1.8 are sodium channels especially important for transmission of nociceptive information
Nociceptors
- Transfer information about pain
- Three major classes of nociceptors: Aδ mechanosensitive nociceptors, Aδ thermal nociceptors, and polymodal nociceptors
- Aδ mechanosensitive nociceptors-activated by intense pressure, are lightly myelinated and have speeds of 5-30 m/s
- Aδ thermal nociceptors are activated by very hot or very cold temperatures. Are lightly myelinated
- Polymodal nociceptors (C fibers) respond to temperature, pressure, or chemicals, are unmyelinated and conduct at speeds of 1 m/s
- Aδ and C fibers have cold temperature gated ion channels. When they fire they are perceived as pain
- Pain receptor receptive fields are generally pretty large, presumably because the detection of pain is more important than its exact location
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Two categories of pain perception
- first pain (sharp), Aδ fibers
- second pain (dull, longer lasting) C-fibers
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Hyperalgesia
- Enhanced sensitivity and response to stimulation of the area around the damaged tissue. Stimuli that would not ordinarily be perceived as pain now is. For example after a sunburn a normal shower now feels painful
- Due to the release of stuff from the damaged cells, such as prostaglandins, bradykinin, histamine, serotonin, ATP, can increase the sensitivity of nociceptors by interacting with the channel (directly or indirectly) and making it open easier, or by interacting with other receptors on nociceptive fibers to potentiate activity of TRP channels
- Aspirin and ibuprofen inhibit cyclooxygenases (COX-2 inhibitors), necessary for prostaglandin synthesis
- Shows that pain and injury are inter-related
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- allodynia (hyper sensitization), clinically relevant pain from normally unpainful stimuli. Contrast with nociceptive pain (actual response to real tissue injury associated with inflammation like aches, sprains, arthritis, cancer pain, headache). Clinical issue is shifting noxious stimuli in pain sensation-stimulus intensity activation curve to the left into innocuous stimuli
- injury to a nerve is called neuropathic pain (phantom limb pain falls into this category), nerves in limbs, spinal cord, or brain can all call neuropathic pain. Also shingles, MS, spinal cord injury, cancer pain. Often severe burning sensation pain and chronic.
- phantom limb pain, often severe grip sensation (nails digging into hand)
Nice talk on pain from Allan Basbaum UCSF. Argues against the existence of a 'pain' pathway. Can't just cut nerve to abolish pain-- maybe for acute pain but not chronic pain. peripheral sensitization.
tissue injury --> arachidonic acid, cyclooxgenase--> prostaglandins --> C fiber threshold lowered --> allodynia
central sensitization (pain memories)-- is a CNS disease, not a symptom of other diseases it is argued (A. Basbaum)
Sensory discriminative (SI and SII) and affective motivational (limbic system activated, including cortical areas anterior cingulate gyrus, insular cortex (between parietal and temporal lobes ventral to S1)) dimensions of the pain experience. (MC Bushnell, Basbaum lecture). Anterior cingulate gyrus positively correlates with unpleasant experience
More fMRI brain activation (amplitude and size of actiation) in parts of brain with same painful stimulus for females vs males. Pain threshold almost the same (45degs hot) between the sexes but is a little bit lower for women. But pain tolerance is much higher in women. (Casey et al, Basbaum lecture). Who can tolerate delivering a baby.
Expectancy can alter pain (sawamoto 2000 interesting fMRI study, after Basbaum lecture 51:07). Imaging the brain of an empathetic spouse (female) reveals activity patterns characteristic of a spouse that is in pain (no citation someone from germany, Basbaum lecture 52:27)
Inflammatory response to tissue damage
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Another type of peripheral sensitization can occur due to substances released within damaged tissues can modulate the response of nociceptive fibers. A host of molecules that can augment the activity of free nerve endings like…
Most interact directly with the receptors or ion channels of the nociceptive fibers. e.g. TRPV1 capacin receptor can be potentiated form the channels direct interactions with extracellular protons that are released by immune cells or through indirect interaction with other enzyme receptors like TrkA for NGF or bradykinin receptors.
Prostaglandins reduce the threshold depolarization needed for AP generation by phosphorylation of special TTX resistant Na+ channels expressed in nociceptor afferents and also incr levels of cAMP.
Cells that contribute to this inflammatory soup include mast cells, patelets, basophils, macrophages, neutrophils, endothelial cells, keratinocytes, and fibroblasts. Cells are responsible for releasing protons (lowering the pH), arachidonic acid, bradykinini, histamine, serotonini, prostaglandins, neucleotides, NGF, cytkines (interleukin 1beta, and TNF-alpha). COX2 inhibitors, NSAIDs -- or nonsteroidal anti-inflammatory drugs block Cox-1 and Cox-2 enzymes so that prostaglandins can't be made.
a peptide that causes blood vessels to dilate (enlarge), and therefore causes blood pressure to fall
- nociceptive
- of or related to pain arising from stimulation of nerve fibers
Pain pathways
- Spinothalamic tract
- Cell bodies found in the most lateral parts of the dorsal root ganglia, but not discretely localized.
- Innervate neurons in the dorsal horn of the spinal cord. Some of these neurons project within the spinal cord. These are important for reflex behaviors.
- Others project axons cross the midline in the same segment and then go up to the brain.
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Major pathways for pain (and temperature) sensation of the body
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nociceptive projections into dorsal horn branch into ascending and descending collaterals forming the dorsolateral tract of Lissauer (named after 19th c. German neurologist).
C fibers (slow pain) terminate in layer 1 (Rexed’s laminae, named after anatomist who first described spinal gray matter layers in 1950s) of dorsal horn.
Adelta (fast pain) terminate in layer 5 of dorsal horn where Abeta mechanosensory terminals innervate.
Pathways for pain (and temperature) sensation of the face
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Nociceptive component in the ventral posterior nuclei in the thalamus
- Pain and temp go to VPM and VPL nuclei just like the mechanosensory axons
- VPM from the face, VPL from the body
- Presumably responsible for our ability to locate a pain with respect to body position
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Cerebral cortex
- VPM and VPL neurons project to primary somatosensory cortex. These thalamic neurons have small receptive fields and are likely used to locate where the pain is, but are not responsible for dull aches that are associated with chronic pain as ablation does not reduce pain
- There are also direct projections to the reticular formation (in medulla), and the midline thalamic nuclei. These neurons project to areas of the limbic system and are responsible for the emotional aspects of pain
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Anterolateral system sends information to different parts of the brainstem/forebrain
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sensory discrimative: location, intensity, and quality of noxious stimulation
affective-motivational: unpleasant feeling, fear, anxiety, autonomic activation for fight-flight
Spinothalamic tract
- Also called anterolateral column part of the ventral column
- Note where axons cross over the midline
- Touch and pain are on opposite sides below medulla
- Touch and pain are on the same side above medulla
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The anterolateral and dorsal column-medial leminiscal systems cross the midline at different sites
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nociceptive and mechanosensory pathways
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Pain vs touch
- 2nd order mechanosensory axons cross at the level of the medulla but 2nd order pain axons cross at about the segment their cell bodies are in
- If there is a damage on one side of the spinal cord, below the injury site, there would be no sense of touch on the same side and no sense of pain on the contralateral side
Referred pain
- Few if any neurons in dorsal horn are specialized solely for the transmission of visceral pain
- It is conveyed to brain via dorsal horn neurons that also get inputs from skin
- Therefore a person may feel pain at a site completely different than its source
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anginal pain which is pain arising from heart muscle that is not being adequately perfused with blood. Referred to the upper chest wall, with radiation into the left arm and hand.
Innervation of same neuron in the dorsal horn of the spinal cord.
Pain perception is subjective
- Rubbing the site of injury can make pain less severe. Soldiers wounded in battle feel less pain than if one gets the same injury at home
- Pain can be subjective. Depends on context.
- There is a descending pain pathway that can impinge on the dorsal horn to quiet neurons
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e.g. prostaglandins lower threshold for phosphorylation of TTX resistant sodium channels.
TrPV1 receptor potentiations.
cox2 inhibit prostaglandin syn
Brain modulation of ascending pain signals
- Stimulation of periaqueductal grey (in midbrain) or rostral medulla reduces pain, producing analgesia
- Stimulation only reduces pain sensation, animal/person still responds to touch, temp etc, just feels less pain
- Cerebral cortex and hypothalamus project to periaqueductal gray which then projects to nuclei in the medulla (Raphe nuclei, reticular formation), which project to the dorsal horn and inhibit ascending pain fibers, forming a descending pathway that modulates pain
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Modulation of ascending pain signal transmission
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enkephalins, endorphins, dynorphins— present in the periacq. gray matter, ventral medulla, and in spinal cord regions in dorsal horn.
Also CB1 and endocannabinoids work similiarly here in the dorsal horn. CB1 on presynaptic terminals of dorsal horn nociceptive terminals can be activated by endocannabinoid release in a retrograde fashion and decrease the release of neurotransmitters such as GABA and glutamate. Interestingly, the analgesic effecs of PAG stimulation is blocked if CB1 antagonists are administered highlighting the importance of endocannabinoids in descending control of pain transmission.
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Modulation of ascending pain signal transmission
- Axons from neurons with mechanoreceptors can synapse onto inhibitory interneurons in spine to dampen pain response
- Descending pathways from the brainstem can dampen pain response
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enkephalins, endorphins, dynorphins— present in the periacquaductal gray matter, ventral medulla, and in spinal cord regions in dorsal horn.
Also CB1 and endocannabinoids work similiarly here in the dorsal horn.
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Descending systems modulate the transmission of ascending pain signals
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Descending systems modulate the transmission of ascending pain signals
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Endogenous opioids dampen pain signal transmission
- Opioid receptors (metabotropic) are expressed in the areas of descending pain pathway (also expressed in other areas, such as muscles of the bowel and anal sphincter)
- Ligands– enkephalins, endorphins, and dynorphin. Found in all descending pain areas
- Opioids decrease the chance that a nociceptor afferent will fire by causing inhibition
- Opiate antagonist naloxone (competitive opioid receptor antagonist) blocks stimulation produced analgesia as well as morphine-induced analgesia. Suggests that they are the same thing
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- endogenous opioids
- all are 5–30 a.a. long peptides
- enkephalins, endorphins, dynorphins
- leucine-enkephalin
- methionine-enkephalin
- alpha-endorphin
- alpha-neoendorphin
- beta-endorphin
- gamma-endorphin
- dynorphin A
- dynorphin B
- oxycontin, percoset
Placebo effect
- Sugar pills can reduce perception of pain
- Effect can be blocked by naloxone, a competitive antagonist of opioid receptors
- Therefore placebo effect is based on a biochemical change in the brain, as are all perceptions
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mind separate from body. No– this highlights something that neuroscientists already widely accept, that you cannot separate the mind from the body, the mind is body and vice versa
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what is or is not reality philosophers
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highlights descending control and higher order processing of pain
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endogenous opioids
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children are not placebo reactors less than 10 yr old. acupuncture works likely as a placebo (needle can be stuck anywhere). Hypnosis can alter perception (reduce activity in anterior cingulate) without sensory discrimination (Rainville Science 1997). But not sensitive to naloxone, so not through opiate system.
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hypnosis (80% of people can be hypnotized)
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35% of people are placebo reactors