| Literature DB >> 31324538 |
Haili Pan1, Mahar Fatima2, Alan Li2, Hankyu Lee2, Wei Cai3, Lorraine Horwitz2, Chia Chun Hor2, Nizam Zaher2, Mitchell Cin2, Hannah Slade2, Tianwen Huang4, X Z Shawn Xu3, Bo Duan5.
Abstract
Lightly stroking the lips or gently poking some skin regions can evoke mechanical itch in healthy human subjects. Sensitization of mechanical itch and persistent spontaneous itch are intractable symptoms in chronic itch patients. However, the underlying neural circuits are not well defined. We identified a subpopulation of excitatory interneurons expressing Urocortin 3::Cre (Ucn3+) in the dorsal spinal cord as a central node in the pathway that transmits acute mechanical itch and mechanical itch sensitization as well as persistent spontaneous itch under chronic itch conditions. This population receives peripheral inputs from Toll-like receptor 5-positive (TLR5+) Aβ low-threshold mechanoreceptors and is directly innervated by inhibitory interneurons expressing neuropeptide Y::Cre (NPY+) in the dorsal spinal cord. Reduced synaptic inhibition and increased intrinsic excitability of Ucn3+ neurons lead to chronic itch sensitization. Our study sheds new light on the neural basis of chronic itch and unveils novel avenues for developing mechanism-specific therapeutic advancements.Entities:
Year: 2019 PMID: 31324538 PMCID: PMC6763390 DOI: 10.1016/j.neuron.2019.06.016
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173