TRPV1 is an element of or mechanism used by the mammalian somatosensory system.
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TRPV1 is an element of or mechanism used by the mammalian somatosensory system.
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TRPV1 receptors are found mainly in the nociceptive neurons of the peripheral nervous system, but they have been described in many other tissues, including the central nervous system.
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TRPV1 is involved in the transmission and modulation of pain, as well as the integration of diverse painful stimuli.
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Desensitization of TRPV1 is thought to underlie the paradoxical analgesic effect of capsaicin.
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TRPV1 receptor is useful to be able to measure how an organism can sense temperature change.
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TRPV1 plays an important role not only in neurones but in immune cells.
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TRPV1 is not the only TRP channel expressed in immune cells.
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TRPV1 can be found in monocytes, macrophages, dendritic cells, T lymphocytes, natural killer cells and neutrophiles.
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TRPV1 is said to be potentially very important in immune cell functioning as it senses higher temperature and lower pH, which can affect the immune cell performance.
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TRPV1 is an important membrane channel in T cells as it regulates the influx of calcium cations.
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TRPV1's involvement is mainly in T cell receptor signalling signalling, T cell activation and TCR-mediated influx of calcium ions, but it is involved in T cell cytokine production as well.
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Indeed, T cells with TRPV1 knockout show impaired calcium uptake after T cell activation via TCR, thus they show dysregulation in signalling pathways such as NF-?B and NFAT.
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TRPV1 activation caused by its agonist capsaicin was shown to induce G0-G1 cell arrest and apoptosis in leukemic cell lines, Adult T-Cell Leukaemia and Multiple Myeloma.
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Interplay between neurons and immune cells is a well-known phenomenon, therefore it is no surprise that TRPV1 plays its role in neuroinflammation, as it is expressed both in neurons and in immune cells.
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TRPV1 is said to contribute to autophagy of microglia via its Ca-signalling, which leads to mitochondria-induced cell death.
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TRPV1 is therefore involved in the neuro-immune axis via its function in microglia as well.
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TRPV1 was shown to have protective effect in neurologic disorders such as Huntington's disease, vascular dementia, and Parkinson's disease.
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TRPV1 antagonists have shown efficacy in reducing nociception from inflammatory and neuropathic pain models in rats.
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TRPV1 is expressed at high levels in the central nervous system and has been proposed as a target for treatment not only of pain but for other conditions such as anxiety.
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Furthermore, TRPV1 appears to mediate long-term synaptic depression in the hippocampus.
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