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The functions of TRPA1 and TRPV1: moving away from sensory nerves

期刊

BRITISH JOURNAL OF PHARMACOLOGY
卷 166, 期 2, 页码 510-521

出版社

WILEY-BLACKWELL
DOI: 10.1111/j.1476-5381.2012.01851.x

关键词

TRPV1; TRPA1; capsaicin; non-neuronal; expression; functionality

资金

  1. Arthritis Research UK [19296]
  2. Capacity Building Award in Integrative Mammalian Biology
  3. BBSRC
  4. BPS
  5. HEFCE
  6. KTN
  7. MRC
  8. SFC
  9. Biotechnology and Biological Sciences Research Council [BB/E527098/1] Funding Source: researchfish
  10. Versus Arthritis [19296] Funding Source: researchfish
  11. BBSRC [BB/E527098/1] Funding Source: UKRI

向作者/读者索取更多资源

The transient receptor potential vanilloid 1 and ankyrin 1 (TRPV1 and TRPA1, respectively) channels are members of the TRP superfamily of structurally related, non-selective cation channels. It is rapidly becoming clear that the functions of TRPV1 and TRPA1 interlink with each other to a considerable extent. This is especially clear in relation to pain and neurogenic inflammation where TRPV1 is coexpressed on the vast majority of TRPA1-expressing sensory nerves and both integrate a variety of noxious stimuli. The more recent discovery that both TRPV1 and TRPA1 are expressed on a multitude of non-neuronal sites has led to a plethora of research into possible functions of these receptors. Non-neuronal cells on which TRPV1 and TRPA1 are expressed vary from vascular smooth muscle to keratinocytes and endothelium. This review will discuss the expression, functionality and roles of these non-neuronal TRP channels away from sensory nerves to demonstrate the diverse nature of TRPV1 and TRPA1 in addition to a direct role in pain and neurogenic inflammation.

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