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- PrajapatiJagat NarayanJNCenter for Neuroscience, Indian Institute of Science, Bengaluru 560012, India., ShahDevanshi PiyushDPCenter for Neuroscience, Indian Institute of Science, Bengaluru 560012, India., and Arnab Barik.
- Center for Neuroscience, Indian Institute of Science, Bengaluru 560012, India.
- Neuroscience. 2025 Jan 6; 568: 9510795-107.
AbstractPain and itch are unpleasant and distinct sensations that give rise to behaviors such as reflexive withdrawal and scratching in humans and mice. Interestingly, it has been observed that pain modulates itch through the neural circuits housed in the brain and spinal cord. However, we have yet to fully understand the identities and mechanisms by which specific neural circuits mediate pain-induced modulation of itch. Independent studies indicate that brainstem nuclei such as the lateral parabrachial nucleus (LPBN), and rostral ventromedial medulla (RVM) are important for suppressing itch by noxious somatosensory stimuli. Here, using mouse and viral genetics, rabies tracing, chemogenetics, and calcium imaging, we show that the synaptic connections between LPBN and RVM play an instrumental role in the interactions between pain and itch. Notably, we found that the LPBN neurons that express the gene encoding the substance P receptor, Tacr1 (LPBNTacr1), synapse onto Tacr1-expressing RVM neurons (RVMTacr1). The RVMTacr1 neurons were found to be nociceptive, sufficient for inhibiting itch, and necessary for pain-induced itch suppression. Moreover, through brain-wide anterograde and retrograde viral tracing studies, we found that the RVMTacr1 neurons are bidirectionally connected with LPBN, periaqueductal gray (PAG), and lateral hypothalamic area (LHA). Thus, together, our data indicate that the RVMTacr1 neurons integrate nociceptive information to mediate itch-induced scratching and can mediate the physiological effects of itch through their downstream targets.Copyright © 2025 International Brain Research Organization (IBRO). Published by Elsevier Inc. All rights reserved.
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