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  2. Periaqueductal gray - Wikipedia

    en.wikipedia.org/wiki/Periaqueductal_gray

    [1] [2] PAG is also the primary control center for descending pain modulation. It has enkephalin-producing cells that suppress pain. The periaqueductal gray is the gray matter located around the cerebral aqueduct within the tegmentum of the midbrain. It projects to the nucleus raphe magnus, and also contains

  3. Diffuse noxious inhibitory control - Wikipedia

    en.wikipedia.org/wiki/Diffuse_noxious_inhibitory...

    Noxious stimuli activate the endings of nociceptive C and A delta nerve fibers, which carry the signal to neurons in the dorsal horn of spinal cord. DNIC refers to the mechanism by which dorsal horn wide dynamic range neurons responsive to stimulation from one location of the body may be inhibited by noxious stimuli (such as heat, high pressure or electric stimulation) applied to another ...

  4. Nociceptor - Wikipedia

    en.wikipedia.org/wiki/Nociceptor

    ' pain receptor ') is a sensory neuron that responds to damaging or potentially damaging stimuli by sending "possible threat" signals [1] [2] [3] to the spinal cord and the brain. The brain creates the sensation of pain to direct attention to the body part, so the threat can be mitigated; this process is called nociception .

  5. Gate control theory - Wikipedia

    en.wikipedia.org/wiki/Gate_control_theory

    The gate control theory of pain asserts that non-painful input closes the nerve "gates" to painful input, which prevents pain sensation from traveling to the central nervous system. In the top panel, the nonnociceptive, large-diameter sensory fiber (orange) is more active than the nociceptive small-diameter fiber (blue), therefore the net input ...

  6. Dorsolateral pontine reticular formation - Wikipedia

    en.wikipedia.org/wiki/Dorsolateral_pontine...

    It thus complements the classical serotonergic-opioid peptide descending pain-inhibiting system: whereas the serotonergic-opioid peptide pathway ultimately pre-synaptically inhibits first-order nociceptive group C neurons, the DLPRF inhibits - by way of presumably GABAergic inhibitory interneurons - the second-order neurons of the ascending ...

  7. Nociception - Wikipedia

    en.wikipedia.org/wiki/Nociception

    Nociceptive pain consists of an adaptive alarm system. [6] Nociceptors have a certain threshold; that is, they require a minimum intensity of stimulation before they trigger a signal. Once this threshold is reached, a signal is passed along the axon of the neuron into the spinal cord.

  8. Spinoreticular tract - Wikipedia

    en.wikipedia.org/wiki/Spinoreticular_tract

    Most (85%) second-order axons arising from sensory C first-order fibers ascend in the spinoreticular tract - it is consequently responsible for transmitting "slow", dull, poorly-localised pain. By projecting to the reticular activating system (RAS) , the tract also mediates arousal/alertness (including wakefulness) in response to noxious ...

  9. Dorsal longitudinal fasciculus - Wikipedia

    en.wikipedia.org/wiki/Dorsal_longitudinal_fasciculus

    Descending projections of the DLF are functionally involved in mediating chewing, swallowing, [3] [2] salivation and gastrointestinal secretory function, [2] and shivering. [3] Medial zone of hypothalamus → periaqueductal gray (synapse) → solitary nucleus, dorsal nucleus of vagus nerve. [3] Hypothalamus → reticular formation (synapse) → [3]

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