2022
DOI: 10.1007/s12264-022-00837-6
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Mitochondrial Reactive Oxygen Species Elicit Acute and Chronic Itch via Transient Receptor Potential Canonical 3 Activation in Mice

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Cited by 8 publications
(8 citation statements)
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“…Using a mouse cheek model of dry skin-induced chronic itch, Oh's team demonstrated that TRPC3 but not TRPA1 and TRPV1 contributes to dry skin-induced itch. They also showed increased mROS levels in the dry skin [11]. Therefore, TRPC3 may serve as a new therapeutic target for itch.…”
mentioning
confidence: 93%
“…Using a mouse cheek model of dry skin-induced chronic itch, Oh's team demonstrated that TRPC3 but not TRPA1 and TRPV1 contributes to dry skin-induced itch. They also showed increased mROS levels in the dry skin [11]. Therefore, TRPC3 may serve as a new therapeutic target for itch.…”
mentioning
confidence: 93%
“…For the TRPC channels, TRPC1, TRPC4, and TRPC5 are activated directly by inositol-1,4,5-trisphosphate, and TRPC3, TRPC6, and TRPC7 are activated by diacylglycerol (DAG), independent of the storage reduction of intracellular calcium [ 16 ]. The TRPC channels have been reported to play important roles in both the nociceptor signaling and the sensitization of the nociceptors by the inflammatory mediators [ 25 ]. This previous study [ 25 ] revealed a major contribution of TRPC to the neuronal calcium homeostasis in the somatosensory pathways.…”
Section: Introductionmentioning
confidence: 99%
“…The TRPC channels have been reported to play important roles in both the nociceptor signaling and the sensitization of the nociceptors by the inflammatory mediators [ 25 ]. This previous study [ 25 ] revealed a major contribution of TRPC to the neuronal calcium homeostasis in the somatosensory pathways. These channels are non selectively permeable to cations, with variable selectivity for calcium over sodium among the different members.…”
Section: Introductionmentioning
confidence: 99%
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“…Interestingly, chronic pruritus is a common feature of many of these diseases. Recently, it has also been shown that mitochondrial reactive oxygen species (mROS) may play a role in pain processing and that mitochondrial dysfunction can contribute to painful peripheral neuropathies [6] .…”
mentioning
confidence: 99%