Author/Authors :
G. Gregory Neely، نويسنده , , Andreas Hess، نويسنده , , Michael Costigan، نويسنده , , Alex C. Keene، نويسنده , , Spyros Goulas، نويسنده , , Michiel Langeslag، نويسنده , , Robert S. Griffin، نويسنده , , Inna Belfer، نويسنده , , Feng Dai، نويسنده , , Shad B. Smith، نويسنده , , Luda Diatchenko، نويسنده , , Vaijayanti Gupta، نويسنده , , Cui-ping Xia، نويسنده , , Sabina Amann، نويسنده , , Silke Kreitz، نويسنده , , Cornelia Heindl-Erdmann، نويسنده , , Susanne Wolz، نويسنده , , Cindy V. Ly، نويسنده , , Suchir Arora، نويسنده , , Rinku Sarangi، نويسنده , , et al.، نويسنده ,
Abstract :
Worldwide, acute, and chronic pain affects 20% of the adult population and represents an enormous financial and emotional burden. Using genome-wide neuronal-specific RNAi knockdown in Drosophila, we report a global screen for an innate behavior and identify hundreds of genes implicated in heat nociception, including the α2δ family calcium channel subunit straightjacket (stj). Mice mutant for the stj ortholog CACNA2D3 (α2δ3) also exhibit impaired behavioral heat pain sensitivity. In addition, in humans, α2δ3 SNP variants associate with reduced sensitivity to acute noxious heat and chronic back pain. Functional imaging in α2δ3 mutant mice revealed impaired transmission of thermal pain-evoked signals from the thalamus to higher-order pain centers. Intriguingly, in α2δ3 mutant mice, thermal pain and tactile stimulation triggered strong cross-activation, or synesthesia, of brain regions involved in vision, olfaction, and hearing.
