VISCERAL SENSATION Flashcards
List all types of pain and explain for each type of pain
- Fast pain
> Pain that is felt less than 0.1s after the pain stimulus is applied
> Also known as first pain - Slow pain
> Pain that is occur after fast pain
> Also known as second pain
> Dull diffuse intense unpleasant feeling
> Example: feeling sore at the whole thumb area after it is pricked by a needle - Cutaneous/ superficial pain
> Pain that occur at the skin - Deep pain
> Pain coming from the deep tissues such as bones, ligaments, tendons, skeletal muscle - Visceral pain
> Pain coming from the visceral organ
> Visceral is the internal organ of the body such as stomach and heart - Acute pain
> Sudden onset, usually the result of a clearly defined cause such as an injury or infection and usually resolves with the healing of its underlying cause - Chronic pain
> Persists for weeks or months and is usually associated with an underlying condition, such as inflammation like arthritis or neuropathic pain
State the definition of pain
Pain is an unpleasant sensory and emotional experience that associated with actual or potential damage of tissue. It has protective purpose or function to the body where pain will warn the body about the actual or potential injury
What is referred pain?
> Referred pain is pain that actually coming from/ originates from the visceral organ is referred to an area of the body surface.
Pain that is not felt in the organ but felt in the somatic structure (other organ)
Give 3 examples of referred pain
- Cardiac pain is referred to the left shoulder, inner aspect of left arm, tip of fingers
- Diaphragmatic pain is referred to the shoulder area
- Ovarian pain is referred to the lower abdominal area
What is the difference of A(delta) and C fibers?
A(delta) fibers are myelinated and has small diameter. Due to the presence of myelin, the conduction velocity is rapid. A(delta) fibers respond to mechanical and also thermal stimuli. It is an initial reflex response to acute pain and the NT is glutamate
While, C fibers are unmyelinated and has small diameter. Due to the absent of myelin, the conduction velocity is slow. It is the smallest type of primary afferent fiber. Polymodal respond to chemical, mechanical as well as thermal stimuli. Since the conduction velocity is slow, activition of C fibers causes slow, burning pain. The NTs are glutamate and substance P
Explain the neospinothalamic tract
> Neospinothalamic tract for fast pain
The A(delta) fibers will be terminate in the lamina I in the dorsal horn.
The glutamate which is the NT are release
This causes the second order neurone to be excited
The second order neurone cross over immediately to the opposite side of the cord and travel upwards to the brain in anterolateral pathway.
The fibers pass onto the ventrobasal complex of the thalamus along with the dorsal column-medial lemniscal tract for tectile sensation
This is to help with localisation of the fast pain
Explain the paleospinothalamic tract.
> Paleospinothalamic tract for slow pain
The type C fibers carrying the slow pain are terminate in the lamina II and III of dorsal horn.
Glutamate and substance P are release as their NTs
Most of the signals pass through one or more additional short fiber neurons within the dorsal horn before they enter the lamina V of the dorsal horn.
They cross over immediately to the opposite side of the cord and travel upwards to the brain in anterolateral pathway
What can influence the pain modulation?
> By neuron within spinal cord
By neuron or substances within the area of somatosensory region
via descending pathway
at the site of receptors
What is gate control theory?
> Gate control theory states that:
Ascending nociceptive signals can be suppressed by the activity of inhibitory interneurons that function as gates to decrease the transmission by the second order neurons
As for example:
Rubbing the area that hurts stimulates mechanoreceptor
These mechanoreceptors will send signal along the A(beta) fibers that stimulate inhibitory interneurons that in turn inhibit the signalling in the second order neuron.
Inbiting the second order neuron will stop the pain signal from being send to the brain for interpretation.
What is the function of inhibitory interneuron?
To reduce the transmission of second order neuron so that pain sensation can be reduced
Why rubbing the pain area can make you feel better?
> During unmodulated pain, stimulation of pain receptors activates C fiber.
This causes the excitation of second order neuron.
The excitation of second order neuron leads to inhibition of inhibitory interneuron.
Hence, the nociceptive receptor will send the information to the thalamus then to the brain for interpretation.
The brain will interpret and send information on the action to the damaged tissues to feel pain
However, when we rub on the pain area, it will activate mechanoreceptor which also going to activate A(beta) fiber.
Since the A(beta) fiber is activated, it will stimulate the inhibitory interneurone.
The activation of inhibitory interneurone causes the activation of second order to be reduced
Reduced second order neuron leads to decreasing flow of nociceptive signals
Hence, the pain sensation is reduced and feels better.
State 2 NTs acting at inhibitory interneurones
Glycine, gamma- aminobutyric acid (GABA)
What does it mean convergence theory?
> The first order neuron supplying both the visceral afferent as well as the somatic sensory nerve of the same dermatome converge onto the same second order neuron in the dorsal horn
Somatic pain is really common
The visceral pain is interpreted as somatic pain originating from the nerve by the brain
What does it mean facilitation theory?
> The visceral irritation is inadequate for producing pain by itself
However, there are collateral connections from visceral afferents to the dorsal horn neurons receiving pain impulses from the somatic structure
Increased in the visceral afferents lead to an increase in the excitation of neurons from somatic structure
Where can we find convergence theory and facilitation theory?
During referred pain
Pain can be modulated by…..
Analgesics and anesthetics