Inhibition of Hyperalgesia by Ablation of Lamina I Spinal Neurons Expressing the Substance P Receptor
Patrick W. Mantyh(University of Minnesota), Scott D. Rogers(University of Minnesota), Prisca Honoré(University of Minnesota), Brian Allen(University of Minnesota), Joseph R. Ghilardi(University of Minnesota), Jun Li(University of Minnesota), Randy S. Daughters(University of Minnesota), Douglas A. Lappi(University of Minnesota), Ronald G. Wiley(University of Minnesota), Donald A. Simone(University of Minnesota)
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Abstract
Substance P is released in the spinal cord in response to painful stimuli, but its role in nociceptive signaling remains unclear. When a conjugate of substance P and the ribosome-inactivating protein saporin was infused into the spinal cord, it was internalized and cytotoxic to lamina I spinal cord neurons that express the substance P receptor. This treatment left responses to mild noxious stimuli unchanged, but markedly attenuated responses to highly noxious stimuli and mechanical and thermal hyperalgesia. Thus, lamina I spinal cord neurons that express the substance P receptor play a pivotal role in the transmission of highly noxious stimuli and the maintenance of hyperalgesia.
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