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Difference between revisions of "Linley 2012 Proc Natl Acad Sci U S A"

From Bioblast
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excitability. This signaling cascade requires activation of phospholipase
excitability. This signaling cascade requires activation of phospholipase
C but is largely uncoupled from the inositol 1,4,5-trisphosphate
C but is largely uncoupled from the inositol 1,4,5-trisphosphate
sensitive Ca2+ stores. In rats SP causes sensitization of TRPV1
sensitive Ca<sup>2+</sup> stores. In rats SP causes sensitization of TRPV1
and produces thermal hyperalgesia. However, the lack of coupling
and produces thermal hyperalgesia. However, the lack of coupling
between SP signaling and inositol 1,4,5-trisphosphate sensitive Ca2+
between SP signaling and inositol 1,4,5-trisphosphate sensitive Ca<sup>2+</sup>
stores, together with the augmenting effect onMchannels, renders
stores, together with the augmenting effect onMchannels, renders
the SP pathway ineffective to excite nociceptors acutely and produce
the SP pathway ineffective to excite nociceptors acutely and produce

Revision as of 20:42, 27 June 2012

Publications in the MiPMap
Linley JE, Ooi L, Pettinger L, Kirton H, Boyle JP, Chris Peers C, Gampera N (2012) Reactive oxygen species are second messengers of neurokinin signaling in peripheral sensory neurons. Proc Natl Acad Sci U S A doi/10.1073/pnas.1201544109.

Β» doi/10.1073/pnas.1201544109

Linley JE, Ooi L, Pettinger L, Kirton H, Boyle JP, Peers C, Gampera N (2012) Proc Natl Acad Sci U S A

Abstract: Substance P (SP) is a prominent neuromodulator, which is produced and released by peripheral damage-sensing (nociceptive) neurons; these neurons also express SP receptors. However, the mechanisms of peripheral SP signaling are poorly understood. We report a signaling pathway of SP in nociceptive neurons: Acting predominantly through NK1 receptors and Gi/o proteins, SP stimulates increased release of reactive oxygen species from the mitochondrial electron transport chain. Reactive oxygen species, functioning as second messengers, induce oxidative modification and augment M-type potassium channels, thereby suppressing excitability. This signaling cascade requires activation of phospholipase C but is largely uncoupled from the inositol 1,4,5-trisphosphate sensitive Ca2+ stores. In rats SP causes sensitization of TRPV1 and produces thermal hyperalgesia. However, the lack of coupling between SP signaling and inositol 1,4,5-trisphosphate sensitive Ca2+ stores, together with the augmenting effect onMchannels, renders the SP pathway ineffective to excite nociceptors acutely and produce spontaneous pain. Our study describes a mechanism for neurokinin signaling in sensory neurons and provides evidence that spontaneous pain and hyperalgesia can have distinct underlying mechanisms within a single nociceptive neuron. β€’ Keywords: dorsal root ganglia

β€’ O2k-Network Lab: UK Leeds Peers C


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Stress:RONS; Oxidative Stress"RONS; Oxidative Stress" is not in the list (Cell death, Cryopreservation, Ischemia-reperfusion, Permeability transition, Oxidative stress;RONS, Temperature, Hypoxia, Mitochondrial disease) of allowed values for the "Stress" property.  Organism: Rat  Tissue;cell: Neurons; Brain"Neurons; Brain" is not in the list (Heart, Skeletal muscle, Nervous system, Liver, Kidney, Lung;gill, Islet cell;pancreas;thymus, Endothelial;epithelial;mesothelial cell, Blood cells, Fat, ...) of allowed values for the "Tissue and cell" property.  Preparation: Intact Cell; Cultured; Primary"Intact Cell; Cultured; Primary" is not in the list (Intact organism, Intact organ, Permeabilized cells, Permeabilized tissue, Homogenate, Isolated mitochondria, SMP, Chloroplasts, Enzyme, Oxidase;biochemical oxidation, ...) of allowed values for the "Preparation" property. 

Regulation: Respiration; OXPHOS; ETS Capacity"Respiration; OXPHOS; ETS Capacity" is not in the list (Aerobic glycolysis, ADP, ATP, ATP production, AMP, Calcium, Coupling efficiency;uncoupling, Cyt c, Flux control, Inhibitor, ...) of allowed values for the "Respiration and regulation" property. 


HRR: Oxygraph-2k