NVV:4

Інститут фізіології ім. О. О. Богомольця
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  • 1. Duzhyy DE, Viatchenko-Karpinski VY, Khomula EV, Voitenko NV, Belan PV (2015). Upregulation of T-type Ca2+ channels in long-term diabetes determines increased excitability of a specific type of capsaicin-insensitive DRG neurons. // Molecular Pain. 20;11(1):29
  • 2. Kopach O., Krotov V., Belan P., Voitenko N. (2015) Inflammatory-induced changes in synaptic drive and postsynaptic AMPARs in lamina II dorsal horn neurons are cell-type-specific. // Pain, 156(3):428-38
  • 3. Khomula E, Borisyuk A, Viatchenko-Karpinski V, Briede A, Belan P, Voitenko N. (2014) Nociceptive neurons differentially express fast and slow T-type Ca²⁺ currents in different types of diabetic neuropathy. // Neural Plasticity. Epub 2014 Feb 18.
  • 4. Khomula E, Viatchenko-Karpinski V, Borisyuk A, Duzhyy D, Belan P, Voitenko N. (2013) Specific functioning of Cav3.2 T-type calcium and TRPV1 channels under different types of STZ-diabetic neuropathy. // Biochimica et Biophysica Acta, 1832(5), Pages 636–649
  • 5. Kopach O, Viatchenko-Karpinski V, Atianjoh F, Belan P, Tao Y, and Voitenko N. (2013) PKCα is required for inflammation-induced trafficking of extrasynaptic AMPA receptors in tonically firing lamina II dorsal horn neurons during the maintenance of persistent inflammatory pain. // The Journal of Pain, 14(2):182-92.
  • 6. Kopach O and Voitenko N. (2012) Extrasynaptic AMPA receptors in the dorsal horn: evidence and functional significance. // Brain Research Bulletin, 93:47-56.
  • 7. Kopach O, Viatchenko-Karpinski V, Belan P, and Voitenko N. (2012) Development of inflammation-induced hyperalgesia and allodynia is associated with the upregulation of extrasynaptic AMPA receptors in tonically firing lamina II dorsal horn neurons. // Frontiers in Physiology. 3:391 doi: 10.3389/fphys.2012.00391. eCollection 2012.
  • 8. Kopach O, Kao S, Petralia R, Belan P, Tao Y, Voitenko N. (2011) Inflammation alters trafficking of extrasynaptic AMPA receptors in tonically firing lamina II neurons of the rat spinal dorsal horn. // Pain, 152(4):912-23.
  • 9. Grishin E, Savchenko G, Vassilevski A, Korolkova Y, Boychuk Y, Viatchenko-Karpinski V, Nadezhdin K, Arseniev A, Pluzhnikov K, Voitenko N, Krishtal O. (2010) Novel peptide from spider venom affects P2X3 receptors in sensory neurons ameliorating inflammatory hyperalgesia. // Annals of Neurology, 67(5):680-3
  • 10. Park J, Voitenko N, Petralia R, Guan X, Xu J, Steinberg J, Takamiya K, Sotnik A, Kopach O, Huganir R, Tao Y. (2009) Persistent inflammation induces GluR2 internalization via NMDA receptor-triggered PKC activation in dorsal horn neurons. // Journal of Neuroscience. 29(10):3206-19
  • 11. Shutov L, Kruglikov I, Gryshchenko O, Khomula E, Viatchenko-Karpinski V, Belan P, and Voitenko N. (2006) The Effect of Nimodipine on Calcium Homeostasis and Pain Sensitivity in Diabetic Rats. // Cellular and Molecular Neurobiology, 26 (7-8), 1541-57.
  • 12. Fedirko N, Kruglikov I, Kopach O, Vats J, Kostyuk P, Voitenko N. (2006) Changes in functioning of rat submandibular salivary gland under streptozotocin-induced diabetes are associated with alterations of Ca2+ signaling and Ca2+ transporting pumps // Biochimica et Biophysica Acta 1762, 294–303.
  • 13. Youn D, Voitenko N, Gerber G, Park Y, Galik J, Randic M. (2005) Altered long-term synaptic plasticity and kainate-induced Ca2+ transients in the substantia gelatinosa neurons in GLU(K6)-deficient mice. // Molecular Brain Research 142(1), 9-18
  • 14. Kruglikov I, Gryshchenko O, Shutov L, Kostyuk E and Voitenko N. (2004) Diabetes-induced abnormalities in ER calcium mobilization in primary and secondary nociceptive neurons. // Pfluger Archive, 448 (4), 395-401
  • 15. Voitenko N, Gerber G, Youn D, Randic M. (2004) Peripheral inflammation-induced increase of AMPA-mediated currents and Ca2+ transients in the rat substantia gelatinosa neurons // Cell Calcium, 35 (5),461-469
  • 16. Kostyuk E, Voitenko N, Kruglikov I, Shmigol A, Shishkin V, Efimov A and Kostyuk P (2001) Diabetes-induced changes in calcium homeostasis and the effects of calcium channel blockers in rat and mice nociceptive neurons. // Diabetologia 44 (10), 1302-1309
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