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      Multiplexed Representation of Itch and Pain and Their Interaction in the Primary Somatosensory Cortex

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          Abstract

          Itch and pain are distinct sensations that share anatomically similar pathways: from the periphery to the brain. Over the last decades, several itch-specific neural pathways and molecular markers have been identified at the peripheral and spinal cord levels. Although the perception of sensation is ultimately generated at the brain level, how the brain separately processes the signals is unclear. The primary somatosensory cortex (S1) plays a crucial role in the perception of somatosensory information, including touch, itch, and pain. In this study, we investigated how S1 neurons represent itch and pain differently. First, we established a spontaneous itch and pain mouse model. Spontaneous itch or pain was induced by intradermal treatment with 5-HT or capsaicin on the lateral neck and confirmed by a selective increase in scratching or wiping-like behavior, respectively. Next, in vivo two-photon calcium imaging was performed in awake mice after four different treatments, including 5-HT, capsaicin, and each vehicle. By comparing the calcium activity acquired during different sessions, we distinguished the cells responsive to itch or pain sensations. Of the total responsive cells, 11% were both responsive, and their activity in the pain session was slightly higher than that in the itch session. Itch- and pain-preferred cells accounted for 28.4% and 60.6%, respectively, and the preferred cells showed the lowest activity in their counter sessions. Therefore, our results suggest that S1 uses a multiplexed coding strategy to encode itch and pain, and S1 neurons represent the interaction between itch and pain.

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          Most cited references34

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          New insights into the classification and nomenclature of cortical GABAergic interneurons.

          A systematic classification and accepted nomenclature of neuron types is much needed but is currently lacking. This article describes a possible taxonomical solution for classifying GABAergic interneurons of the cerebral cortex based on a novel, web-based interactive system that allows experts to classify neurons with pre-determined criteria. Using Bayesian analysis and clustering algorithms on the resulting data, we investigated the suitability of several anatomical terms and neuron names for cortical GABAergic interneurons. Moreover, we show that supervised classification models could automatically categorize interneurons in agreement with experts' assignments. These results demonstrate a practical and objective approach to the naming, characterization and classification of neurons based on community consensus.
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            Regulation of Pain and Itch by TRP Channels

            Nociception is an important physiological process that detects harmful signals and results in pain perception. In this review, we discuss important experimental evidence involving some TRP ion channels as molecular sensors of chemical, thermal, and mechanical noxious stimuli to evoke the pain and itch sensations. Among them are the TRPA1 channel, members of the vanilloid subfamily (TRPV1, TRPV3, and TRPV4), and finally members of the melastatin group (TRPM2, TRPM3, and TRPM8). Given that pain and itch are pro-survival, evolutionarily-honed protective mechanisms, care has to be exercised when developing inhibitory/modulatory compounds targeting specific pain/itch-TRPs so that physiological protective mechanisms are not disabled to a degree that stimulus-mediated injury can occur. Such events have impeded the development of safe and effective TRPV1-modulating compounds and have diverted substantial resources. A beneficial outcome can be readily accomplished via simple dosing strategies, and also by incorporating medicinal chemistry design features during compound design and synthesis. Beyond clinical use, where compounds that target more than one channel might have a place and possibly have advantageous features, highly specific and high-potency compounds will be helpful in mechanistic discovery at the structure-function level.
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              TRPV1-expressing primary afferents generate behavioral responses to pruritogens via multiple mechanisms.

              The mechanisms that generate itch are poorly understood at both the molecular and cellular levels despite its clinical importance. To explore the peripheral neuronal mechanisms underlying itch, we assessed the behavioral responses (scratching) produced by s.c. injection of various pruritogens in PLCbeta3- or TRPV1-deficient mice. We provide evidence that at least 3 different molecular pathways contribute to the transduction of itch responses to different pruritogens: 1) histamine requires the function of both PLCbeta3 and the TRPV1 channel; 2) serotonin, or a selective agonist, alpha-methyl-serotonin (alpha-Me-5-HT), requires the presence of PLCbeta3 but not TRPV1, and 3) endothelin-1 (ET-1) does not require either PLCbeta3 or TRPV1. To determine whether the activity of these molecules is represented in a particular subpopulation of sensory neurons, we examined the behavioral consequences of selectively eliminating 2 nonoverlapping subsets of nociceptors. The genetic ablation of MrgprD(+) neurons that represent approximately 90% of cutaneous nonpeptidergic neurons did not affect the scratching responses to a number of pruritogens. In contrast, chemical ablation of the central branch of TRPV1(+) nociceptors led to a significant behavioral deficit for pruritogens, including alpha-Me-5-HT and ET-1, that is, the TRPV1-expressing nociceptor was required, whether or not TRPV1 itself was essential. Thus, TRPV1 neurons are equipped with multiple signaling mechanisms that respond to different pruritogens. Some of these require TRPV1 function; others use alternate signal transduction pathways.
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                Author and article information

                Journal
                Exp Neurobiol
                Exp Neurobiol
                Experimental Neurobiology
                The Korean Society for Brain and Neural Sciences
                1226-2560
                2093-8144
                31 October 2022
                31 October 2022
                31 October 2022
                : 31
                : 5
                : 324-331
                Affiliations
                [1 ]Department of Science in Korean Medicine, Graduate School, Kyung Hee University, Seoul 02447, Korea
                [2 ]Department of Physiology, Seoul National University College of Medicine, Seoul 03080, Korea
                [3 ]Neuroscience Research Institute, Seoul National University College of Medicine, Seoul 03080, Korea
                [4 ]Department of Physiology, College of Korean Medicine, Kyung Hee University, Seoul 02447, Korea
                [5 ]Department of Biomedical Sciences, Seoul National University College of Medicine, Seoul 03080, Korea
                Author notes
                [* ]To whom correspondence should be addressed. Sang Jeong Kim, TEL: 82-2-740-8229, FAX: 82-2-763-9667, e-mail: sangjkim@ 123456snu.ac.kr
                Sun Kwang Kim, TEL: 82-2-961-0323, FAX: 82-2-961-0333, e-mail: skkim77@ 123456khu.ac.kr
                Article
                en-31-5-324
                10.5607/en22029
                9659493
                36351842
                b44a0711-660d-4dbb-a131-516217da4fc7
                Copyright © Experimental Neurobiology 2021

                This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License ( http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 13 September 2022
                : 21 October 2022
                : 24 October 2022
                Categories
                Short Communication

                Neurosciences
                itch,pain,primary somatosensory cortex,two-photon imaging
                Neurosciences
                itch, pain, primary somatosensory cortex, two-photon imaging

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