Hypoalgesia

Not to be confused with Hyperalgesia.
Look up hypoalgesia in Wiktionary, the free dictionary.

Hypoalgesia or hypalgesia denotes a decreased sensitivity to painful stimuli.

Hypoalgesia occurs when nociceptive (painful) stimuli are interrupted or decreased somewhere along the path between the input (nociceptors), and the places where they are processed and recognized as pain in the conscious mind. Hypoalgesic effects can be mild, such as massaging a stubbed toe to make it hurt less or taking aspirin to decrease a headache, or they can be severe, like being under strong anesthesia. Hypoalgesia can be caused by exogenous chemicals such as opioids, as well as by chemicals produced by the body in phenomena such as fear- and exercise- induced hypoalgesia. Hypoalgesia can also be associated with diseases, such as CIPA or in less severe cases with diabetes or other diseases associated with hypertension.

Chemical causes

Analgesics

Main article: Analgesics

Analgesics are a class of biochemicals that cause hypoalgesia. Analgesics can act on both the peripheral and central nervous systems to decrease pain. Certain analgesics also work to decrease the source of the pain by working to decrease swelling and inflammation, as in the case of NSAIDs.[1]

Opioids

Main article: Opioids

Opioids refers to a specific group of analgesics - including morphine, codeine, and opium - that act on opioid receptors, which are located mainly in the central nervous system.

Endogenous opioids are types of opioids produced by the body specifically to modulate pain. They include endorphins, enkephalins, dynorphins and endomorphins. These peptides are especially important for modulating pain in response to the environment. These can be released in response to a number of things, including increased blood pressure, pain and danger. It has been found that endogenous opioids are at least partially responsible for phenomena like “Runner's high”, hypoalgesia in the fight-or-flight response, and even for the analgesic effects of acupuncture therapy.[2] In all these cases, there is a certain level of signal processing that occurs in the CNS which leads to the release of these chemicals.

Exercise-induced hypoalgesia

There has been a great deal of research examining the link between exercise and hypoalgesia. Many studies have shown the direct link between the two by subjecting patients to exercise and rating their pain responses, but despite the great deal of research, the mechanism of action is still poorly understood. It has been shown that the triggering mechanism for the hypoalgesic effects is caused by the increase in blood pressure that accompanies a good workout. The body senses the increased blood pressure, and it is hypothesized that in response, endogenous opioids are released.[3] This hypothesis is well supported in human research, and it has been verified that it plays a part, but animal research implies that other mechanisms are also involved.[4]

Fear-induced hypoalgesia

Fear induced hypoalgesia is another example of a mechanism controlled by opioids. It is postulated that fear is a defense mechanism that has evolved over time to provide protection. In the case of hypoalgesia, a decreased response to pain would be very beneficial in a situation where an organism’s life was at stake, since feeling pain would be a hindrance rather than a help. It has been well documented that fear does cause a decrease in pain response,[5] however much like the exercise induced hypoalgesia, the exact mechanisms of action are not well understood. Studies have shown that opioids are definitely involved in the process, yet opiates alone do not completely explain the analgesic response.[6][7] What the other mechanisms of action are is still unknown.

Diseases

It has been demonstrated that many diseases can cause hypoalgesia. Some diseases, like CIPA, are hereditary disorders where genes essential for the correct functioning of nociceptors no longer work. There are many diseases like this, and they all fall under the category of hereditary sensory autonomic neuropathies. Alternatively, some diseases affect other functions in your body, which can activate the pathways that cause hypoalgesia. This effect happens in people with diabetes and other diseases associated with hypertension.

Hereditary neuropathies

Hereditary sensory and autonomic neuropathies (HSAN), e.g. CIPA, are hereditary disorders that are characterized by malfunctioning or nonfunctioning pain receptors.[8] Most of these diseases are also associated with decreased temperature sensation as well. In some cases these diseases are also associated with other symptoms like mental retardation and diminished production of sweat and tears. Diseases like this can be very dangerous for the patients, because they are not able to judge what hurts, and therefore when they should stop doing something. A child with the disease might bite their finger clean off before they realized that what they were doing might harm them, or they might leave their hand on a hot stove without ever realizing it was on. These examples support the theory that pain is essential for life, more specifically, survival.

Hypoalgesia and hypertension

Some studies have shown that hypertension in patients can cause hypoalgesia.[9][10] Diseases like diabetes, which are associated with hypertension are also associated with hypoalgesia, however this is due to diabetic neuropathy. Just like in Exercise-Induced Hypoalgesia, the increased blood pressure of hypertension works as a signal to the body to release opioids and activate other pain modulation pathways. Also, although the area is not widely studied, there is evidence that this is not the only cause. Diseases may lead to activation of any of these mechanisms, just like diabetes causing hypertension. A full study of the pathways regulating pain is needed.

See also

References

  1. ↑ Vane, J. (2003). "The mechanism of action of anti-inflammatory drugs." Int J Clin Pract Suppl(135): 2.
  2. ↑ Yang, J., Y. Yang, et al. (2007). "Effect of oxytocin on acupuncture analgesia in the rat." Neuropeptides 41(5): 285-92.
  3. ↑ Koltyn, K. F. and M. Umeda (2006). "Exercise, hypoalgesia and blood pressure." Sports Med 36(3): 207-14.
  4. ↑ Koltyn, K. F. (2000). "Analgesia following exercise: a review." Sports Med 29(2): 85-98.
  5. ↑ Rhudy, J. L., J. S. Grimes, et al. (2004). "Fear-induced hypoalgesia in humans: effects on low intensity thermal stimulation and finger temperature." J Pain 5(8): 458-68.
  6. ↑ J.M. Lichtman and M.S. Fanselow, Cats produce analgesia in rats on the tail-flick test: naltrexone sensitivity is determined by the nociceptive test stimulus. Brain Res 533 (1990), pp. 91–94.
  7. ↑ H.S. Hagen and K.F. Green, Effects of time of testing, stress level and number of conditioning days on naloxone sensitivity of conditioned stress-induced analgesia in rats. Behav Neurosci 102 (1988), pp. 906–914.
  8. ↑ Schalka, M. M., M. S. Correa, et al. (2006). "Congenital insensitivity-to-pain with anhidrosis (CIPA): a case report with 4-year follow-up." Oral Surg Oral Med Oral Pathol Oral Radiol Endod 101(6): 769-73.
  9. ↑ Zamir, N., Shuber, E., 1980. Altered pain perception in hypertensive humans. Brain Research 201, 471–474.
  10. ↑ Edwards, L., C. Ring, et al. (2007). "Nociceptive flexion reflex thresholds and pain during rest and computer game play in patients with hypertension and individuals at risk for hypertension." Biol Psychol 76(1-2): 72-82.
This article is issued from Wikipedia - version of the 7/8/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.