PEPTIDE COMPONENTS OF LYCOSA SPIDER VENOM MODULATE P2X RECEPTROR ACTIVITY OF RAT DRG NEURONS
G.A.Savchenko1, A.A.Vassilevski2, K.A.Pluzhnikov2, Y.V.Korolkova2, M.V.Mamenko1, T.M.Volkova1, O.P.Maximyuk1,3, Ya.A.Boychuk1, E.V.Grishin2, O.O.Krishtal1,3
- O.O. Bogomoletz Institute of Physiology, National Academy Sciences of Ukraine, Kyiv, Ukraine
- Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, Russia
- International Center of Molecular Physiology National Academy Sciences of Ukraine, Kyiv, Ukraine
Abstract
Almost each natural venom comprises a considerable combinatorial library of bioactive substances that have been optimized during evolution. Particular attention is devotedcurrently on a search for new modulators of ion channels from the venoms of arthropods. We have studied the effect of peptidous compounds of the Lycosa spider venom on the activity of P2X receptors in DRG neurons of rats. As a result, at least 7 proteins modulating various P2X receptor-operated ionic currents in the sensory neurons of rats have been found.
Keywords:
bioactive substances, P2X receptors, DRG neurons
References
- Bleehen T., Keele C. A. Observations on the algogenic actions of adenosine compounds on the human blister base preparation . Pain. 1977. 3, N 4. P. 367-377.
- Burnstock G. Purinergic signalling: past, present and future . Braz. J. Med. Biol. Res. 2008.
- Chen X., Kalbacher H., Grunder S. Interaction of acid-sensing ion channel (ASIC) 1 with the tarantula toxin psalmotoxin 1 is state dependent . J. Gen. Physiol. 2006. 127, N 3. P. 267-276.
- Collier H. O., James G. W., Schneider C. Antagonism by aspirin and fenamates of bronchoconstriction and nociception induced by adenosine-5'-triphosphate . Nature. 1966. 212, N 5060. P. 411-412.
- De Roo M., Rodeau J. L., Schlichter R. Dehydro-epiandrosterone potentiates native ionotropic ATP receptors containing the P2X2 subunit in rat sensory neurones . J. Physiol. 2003. 552, N Pt 1. P. 59-71.
- Escoubas P., De Weille, Jr., Lecoq A. et al. Isolation of a tarantula toxin specific for a class of proton-gated Na+ channels . J. Biol. Chem. 2000. 275, N 33. P. 25116-25121.
- Fisyunov A., Pluzhnikov K., Molyavka A. et al. Novel spider toxin slows down the activation kinetics of P-type Ca2+ channels in Purkinje neurons of rat . Toxicology. 2005. 207, N 1. P. 129-136.
- Hamill O. P., Marty A., Neher E. et al. Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches . Pflug. Arch. 1981. 391, N 2. P. 85-100.
- Jarvis M. F., Wismer C. T., Schweitzer E. et al. Modulation of BzATP and formalin induced nociception: attenuation by the P2X receptor antagonist, TNP-ATP and enhancement by the P2X(3) allosteric modulator, cibacron blue . Brit. J. Pharmacol. 2001. 132, N 1. P. 259-269.
- Lalo U. V., Pankratov Y. V., Arndts D. et al. Omega-conotoxin GVIA potently inhibits the currents mediated by P2X receptors in rat DRG neurons . Brain Res. Bull. 2001. 54, N 5. P. 507-512.
- Pankratov YuV, Lalo U. V., Dashkin A. N. et al. Heterogeneity of the functional expression of P2X3 and P2X2. 3 receptors in the primary nociceptive neurons of rat . Neurochem. Res. 2001. 26, N 8-9. P. 993-1000.
- Pignataro G., Simon R. P., Xiong Z. G. Prolonged activation of ASIC1a and the time window for neuroprotection in cerebral ischaemia . Brain. 2007. 130, N Pt 1. P. 151-158.
- Staats P. S., Yearwood T., Charapata S. G. et al. Intrathecal ziconotide in the treatment of refractory pain in patients with cancer or AIDS: a randomized controlled trial . JAMA. 2004. 291, N 1. P. 63-70.
- Xiong Z. G., Zhu X. M., Chu X. P. et al. Neuroprotection in ischemia: blocking calcium-permeable acid-sensing ion channels . Cell. 2004. 118, N 6. P. 687-698.
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