Receptor for protons: First observations on Acid Sensing Ion Channels

Neuropharmacology

Volumn 94, Issue , 2015, Pages 4-8

  Krishtal, Oleg ^a  

^a BOGOMOLETZ INSTITUTE OF PHYSIOLOGY   (Ukraine)

Author keywords

Acid Sensing Ionic Channel; Nociception; Patch clamp; Purinoreceptors; Receptor

Indexed keywords

ACID SENSING ION CHANNEL; PROTON; RECEPTOR;

CENTRAL NERVOUS SYSTEM; CHANNEL GATING; MAMMAL; NERVOUS TISSUE; NOCICEPTION; NONHUMAN; PAIN; PAIN RECEPTOR; PATHOPHYSIOLOGY; PERIPHERAL NERVOUS SYSTEM; PH; PRIORITY JOURNAL; PROTON TRANSPORT; REVIEW; SIGNAL TRANSDUCTION; ANIMAL; GENETICS; METABOLISM; NERVE CELL; PHYSIOLOGY;

ACID SENSING ION CHANNELS; ANIMALS; NEURONS; PROTONS;

EID: 84965087529     PISSN: 00283908     EISSN: 18737064     Source Type: Journal    
DOI: 10.1016/j.neuropharm.2014.12.014     Document Type: Review

References (27)

1. Askwith, C.C., Cheng, C., Ikuma, M., et al. Neuropeptide FF and FMRFamide potentiate acid-evoked currents from sensory neurons and proton-gated DEG/ENaC channels. Neuron 26 (2000), 133–141.
2. Bohlen, Ch. J., Chesler, A.T., Sharif-Naeini, R., et al. A heteromeric Texas coral snake toxin targets acid-sensing ion channels to produce pain. Nature 479 (2011), 410–414.
3. Boyd, I.A., Davey, M.K., Composition of Peripheral Nerves. 1968, Livingstone, Edinburgh.
4. Chen, X., Kalbacher, H., Gründer, S., The tarantula toxin psalmotoxin 1 inhibits acid-sensing ion channel (ASIC) 1a by increasing its apparent H+ affinity. J. Gen. Physiol. 126:1 (2005), 71–79.
5. Davies, N.W., Lux, H.D., Morad, M., Site and mechanism of activation of proton-induced sodium current in chick dorsal root ganglion neurones. J. Physiol. 400 (1988), 159–187.
6. De Preter, K., Vandesompele, J., Heimann, P., et al. Human fetal neuroblast and neuroblastoma transcriptome analysis confirms neuroblast origin and highlights neuroblastoma candidate genes. Genome Biol., 7(9), 2006, R84.
7. Du, J., Reznikov, L.R., Price, M.P., et al. Protons are a neurotransmitter that regulates synaptic plasticity in the lateral amygdala. PNAS 111:24 (2014), 8961–8966.
8. Jahr, C.E., Jessell, T.M., ATP excites a subpopulation of rat dorsal horn neurones. Nature 304:5928 (1983), 730–733.
9. Konnerth, A., Lux, H.D., Morad, M., Proton-induced transformation of calcium channel in chick dorsal root ganglion cells. J. Physiol. 386 (1987), 603–633 Erratum in J Physiol (Lond) 1988 Jan;395:following 753.
10. Korkushko, A.O., Kryshtal’, O.A., Blocking of proton-activated sodium permeability of the membranes of trigeminal ganglion neurons in the rat by organic cations. Neirofiziologiia 16:4 (1984), 557–561 (Article in Russian).
11. Kostyuk, P.G., Krishtal, O.A., Effects of calcium and calcium-chelating agents on the inward and outward current in the membrane of mollusc neurones. J. Physiol. 270:3 (1977), 569–580.
12. Kostyuk, P.G., Krishtal, O.A., Calcium inward current and related charge movements in the membrane of snail neurones. J. Physiol. 310 (1981), 403–421.
13. Kostyuk, P.G., Krishtal, O.A., Pidoplichko, V.I., Effect of internal fluoride and phosphate on membrane currents during intracellular dialysis of nerve cells. Nature 257:5528 (1975), 691–693.
14. Kovalchuk, Yu.N., Krishtal, O.A., Nowycky, M.C., The proton-activated inward current of rat sensory neurons includes a calcium component. Neurosci. Lett. 115:2–3 (1990), 237–242.
15. Kreple, C.J., Lu, Y., Taugher, R.J., et al. Acid-sensing ion channels contribute to synaptic transmission and inhibit cocaine-evoked plasticity. Nat. Neurosci. 17:8 (2014), 1083–1091.
16. Krishtal, O.A., Pidoplichko, V.I., A receptor for protons in the nerve cell membrane. Neuroscience 5:12 (1980), 2325–2327.
17. Kryshtal, O.A., Pidoplichko, V.I., Intracellular perfusion of the giant neurons of snails. Neirofiziologiia 7:3 (1975), 327–329.
18. Krishtal, O.A., Pidoplichko, V.I., Receptor for protons in the membrane of sensory neurons. Brain Res. 214:1 (1981), 150–154.
19. Krishtal, O.A., Pidoplichko, V.I., A “receptor” for protons in small neurons of trigeminal ganglia: possible role in nociception. Neurosci. Lett. 24:3 (1981), 243–246.
20. Krishtal, O.A., Pidoplichko, O.A., Marchenko, S.M., et al. Receptor for ATP in the membrane of mammalian sensory neurones. Neurosci. Lett. 35:1 (1983), 41–45.
21. Krishtal, O.A., Osipchuk, Y.V., Shelest, T.N., et al. Rapid extracellular pH transients related to synaptic transmission in rat hippocampal slices. Brain Res. 436:2 (1987), 352–356.
22. Lee, K.S., Akaike, N., Brown, A.M., Properties of internally perfused, voltage-clamped, isolated nerve cell bodies. J. Gen. Physiol. 71:5 (1978 May), 489–507.
23. Lindahl, O., Pain – a general chemical explanation. Bonica, J.J., (eds.) Pain, Advances in Neurology, vol. 4, 1974, Raven Press, New York, 45–47.
24. Vrublevskiĭ, S.V., Kryshtal’, O.A., Osipchuk, Iu.V., et al. Proton-activated sodium conduction in the brain neurons of the rat. Dokl. Akad. Nauk. SSSR 284:4 (1985), 990–993 (Article in Russian).
25. Waldmann, R., Champigny, G., Bassilana, F., et al. A proton-gated cation channel involved in acid-sensing. Nature 386:6621 (1997), 173–177.
26. Yermolaieva, O., Leonard, A.S., Schnizler, M.K., et al. Extracellular acidosis increases neuronal cell calcium by activating acid-sensing ion channel 1a. Proc. Natl. Acad. Sci. U. S. A. 101:17 (2004), 6752–6757.
27. Yu, Y., Chen, Z., Li, W.G., et al. A nonproton ligand sensor in the acid-sensing ion channel. Neuron 68:1 (2010), 61–72.