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Science Chic wrote: I used to study the capsaicin receptor (now called TrpV1) when I worked in the Anesthesiology Dept at UCSF. My hubby liked to joke that I used him as my experimental guinea pig for pain research! It's a fascinating topic, and I hardly got to delve into it at all. The capsaicin receptor, at that time at least (I haven't kept up on the research and this may have changed with new discoveries) was unique in that it was activated not only by the chemical capsaicin (the hot ingredient in chili peppers), but also by thermal heat, and with continued application of capsaicin it would switch from being nociceptive to analgesic - ie, no activation with stimulation, like an anesthetic (eg your tongue goes numb if you keep eating hot peppers). There was much hope in the early days to determine the mechanics of this polar opposite function and apply it in a clinical application of topical analgesics. I don't know if that's ever come to pass, but would be totally cool. The study of anesthetics itself is pretty neat; the brain is an amazing organ! A lack of sensing pain can occur anywhere along the pathway - at the pain receptor, along the nerve fiber, or in the brain.
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lol lol Leave it to you to find a unique angle, TPP.TPP wrote: Getting older, just means more pain.
PAIN is a 4-letter word.
Better living though chemicals!!!!
Nuff said.
Wait! wife & pain are both 4-letter words..... Hmmmmmmmm Connection?
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Very likely - physically, continued stimulation of the nerve will cause a depletion of calcium ions which will impair the neuron's ability to generate an action potential and signal the brain. Why is it important that the neuron be "desensitized" or shut down? Continued stimulation would probably lead to apoptosis - programmed cell death - which would result in losing that nerve and ability to respond to capsaicin, forever. Back when we were foraging for food, and learning what would kill us and what wouldn't, these kinds of taste receptors could mean the difference between life and death.Rockdoc Franz wrote: Reading this has me wondering if the polar opposite of prolonged exposure to capsaicin is once again a shut-down function to protect the body in some way?? That is rather interesting. Peppers are a distasteful experience for me, so I've no experience with what you describe. It is most interesting indeed. Why would the body switch sensations? Interesting question.
(Rather interesting, too, is the paragraph on TRPV1 in the central nervous system and its role in depression).In humans, drugs acting at TRPV1 receptors could be used to treat neuropathic pain associated with multiple sclerosis, chemotherapy, or amputation, as well as pain associated with the inflammatory response of damaged tissue, such as in osteoarthritis.[10]
The major roadblock for the usefulness of these drugs is their effect on body temperature (hyperthermia). The role of TRPV1 in the regulation of body temperature has emerged in last few years. Based on a number of TRPV-selective antagonists' causing an increase in body temperature (hyperthermia), it was proposed that TRPV1 is tonically active in vivo and regulates body temperature[11] by telling the body to "cool itself down". Without these signals, the body overheats.
Capsaicin is being explored as a possible prophylaxis for Type 1 diabetes by researchers in Toronto, Canada.
The American Association for Cancer Research reports studies suggesting capsaicin is able to kill prostate cancer cells by causing them to undergo apoptosis.[37][38] There have been several clinical studies conducted in Japan and China that showed natural capsaicin directly inhibits the growth of leukemic cells.[39] Another study carried out at the University of Nottingham suggests capsaicin is able to trigger apoptosis in human lung cancer cells as well.[40]
Capsaicin is also the key ingredient in the experimental drug Adlea, which is in Phase 2 trials as a long-acting analgesic to treat post-surgical and osteoarthritis pain for weeks to months after a single injection to the site of pain.[41] More over, it reduces pain resulted rheumatoid arthritis[42] as well as joint or muscle pain from fibromyalgia or other causes.
Capsaicin may help treat ear infections such as otitis.[43] There is some evidence that capsaicin may help treat heartburn and circulatory problems such as heart disease from atherosclerosis or plaque that block the arteries to the heart. Capsaicin may also help in reducing risks of arrhythmia. Capsaicin is also a great natural expectorant and can be used to clear the lungs of mucus.
In 2006, it was discovered that tarantula venom activates the same pathway of pain as is activated by capsaicin, the first demonstrated case of such a shared pathway in both plant and animal anti-mammal defense.[23]
So is love, food, mate (no gender implied), and drug!TPP wrote: Thank You! I try.
And we all know that men die before women...
So Pain, wife & dead are all 4 letter words... See there is a connection....
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:thumbsup:Science Chic wrote:
So is love, food, mate (no gender implied), and drug!TPP wrote: Thank You! I try.
And we all know that men die before women...
So Pain, wife & dead are all 4 letter words... See there is a connection....
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Negative or harsh words such as 'pain' and 'sting' used to describe sensations prior to potentially painful procedures have been shown to increase pain. We aimed to determine whether the reporting of pain and its severity is affected by the way it is assessed during anaesthesia follow-up after caesarean section. Following caesarean section, 232 women were randomised prior to post-anaesthesia review. Group N participants were asked questions containing the negative word 'pain, "Do you have any pain?" and then asked to rate it on a 0 to 10 point Verbal Numerical Rating Scale. Group P participants were asked questions using more positive words, "How are you feeling?" and "Are you comfortable?".
The assessment of pain after caesarean section, using more positive words, decreases its incidence but does not affect its severity when measured by pain scores. Words that focus the patient on pain during its assessment may lead some to interpret sensations as pain which they might not do otherwise. These findings may have important implications when assessing and researching postoperative pain.
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rofllol rofllol :bashTPP wrote: Thank You! I try.
And we all know that men die before women...
So Pain, wife & dead are all 4 letter words... See there is a connection....
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The protein that they discuss below is involved in strengthening neurons' "memories", but like everything, not enough, or too much of it, can be adverse to our health or quality of life.Unlike the text of a book or the bytes of a hard disk, the information stored in our brain is constantly on the verge of being erased.
You slam your hand in a door, and the experience becomes etched into your brain. Your body remembers it too. For days afterwards, the neurons in your spine carry pain signals more easily from your hand to your brain. As a result, your hand feels more sensitive, and even the lightest touch will trigger an unpleasant reaction. It’s as if your spine carries a memory for pain.
This is more than a metaphor. Two groups of scientists have found that one special molecule underlies both processes. It helps to store memories in our brains, and it sensitises neurons in our spines after a painful experience. It’s a protein called PKMzeta. It’s the engine of memory. http://topicfire.com/share/A-memory-for ... 27503.html
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