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Published on: March 17, 2015
Nociception and TRP Channels
Mitsuko Numazaki1, Makoto Tominaga
1Department of Anesthesiology, University of Tsukuba School of Medicine, Tsukuba 305-0006, Japan.
Abstract:
Noxious thermal, mechanical, or chemical stimuli evoke pain through excitation of the peripheral terminals called nociceptor, and many kinds of ionotropic and metabotropic receptors are involved in this process. Capsaicin receptor TRPV1 is a nociceptor-specific ion channel that serves as the molecular target of capsaicin. TRPV1 can be activated not only by capsaicin but also by noxious heat (with a thermal threshold >43 degrees C) or protons (acidification), all of which are known to cause pain in vivo. Studies using TRPV1-deficient mice have shown that TRPV1 is essential for selective modalities of pain sensation and for thermal hyperalgesia. One mechanism underlying inflammatory pain which is initiated by tissue damage/inflammation and characterized by hypersensitivity is sensitization of TRPV1. In addition to TRPV1, there are five thermosensitive ion channels in mammals, all of which belong to the TRP (transient receptor potential) super family. These include TRPV2, TRPV3, TRPV4, TRPM8 and TRPA1. These channels exhibit distinct thermal activation thresholds (> 52 degrees C for TRPV2, > approximately 34-38 degrees C for TRPV3, > approximately 27-35 degrees C for TRPV4, < approximately 25-28 degrees C for TRPM8 and < 17 degrees C for TRPA1) and are expressed in primary sensory neurons as well as other tissues. Some of the thermosensitive TRP channels are likely to be involved in thermal nociception, since their activation thresholds are within the noxious range of temperatures.
Insights
The capsaicin receptor TRPV1 is crucial for pain sensation and thermal hyperalgesia. Other thermosensitive transient receptor potential (TRP) channels also play roles in detecting noxious temperatures.
Area of Science:
- Neuroscience
- Molecular Biology
- Pain Research
Background:
- Pain perception involves nociceptors and various receptors, including the capsaicin receptor TRPV1.
- TRPV1 is activated by heat (>43°C), acid, and capsaicin, and is essential for certain pain sensations and thermal hyperalgesia.
- Inflammatory pain involves TRPV1 sensitization, leading to hypersensitivity.
Purpose of the Study:
- To investigate the role of TRPV1 and other thermosensitive TRP channels in pain sensation.
- To understand the mechanisms of thermal nociception and inflammatory pain.
Main Methods:
- Studies utilizing TRPV1-deficient mice to assess pain modalities and thermal hyperalgesia.
- Analysis of the expression and thermal activation thresholds of various thermosensitive TRP channels (TRPV2-4, TRPM8, TRPA1).
Main Results:
- TRPV1 is essential for specific pain sensations and thermal hyperalgesia.
- TRPV1 sensitization contributes to inflammatory pain.
- Five other thermosensitive TRP channels (TRPV2-4, TRPM8, TRPA1) exist with distinct temperature activation thresholds.
- These channels are expressed in sensory neurons and other tissues.
Conclusions:
- TRPV1 is a key player in detecting noxious stimuli and mediating thermal hyperalgesia.
- Other thermosensitive TRP channels likely contribute to thermal nociception due to their activation thresholds within the noxious temperature range.
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