Influence of K ⁺ Channel Openers on Interferon-γ Dependent Immune Response in Experimental Allergic Neuritis (Ean)

References

• McKinnon D, Ceredig R. Changes in expression of potassium channels during mouse T cell development. J Exp Med 1986; 164: 1846–61
   PubMed Web of Science ®Google Scholar
• Lewis RS, Cahalan MD. Subset-specific expression of potassium channels in developing murine T lymphocytes. Science 1988; 239: 771–5
   PubMed Web of Science ®Google Scholar
• DeCoursey TE, Chandy KG, Gupta S, Cahalan MD. Voltage-dependent ion channels in T lymphocytes. J Neu-roimmunol 1985; 10: 71–95
   PubMed Web of Science ®Google Scholar
• Schlichter L, Sidell N, Hagiwara S. K channels are expressed early in human T-cell development. Proc Natl Acad SciUSA 1986; 83: 5625–9
   PubMedGoogle Scholar
• Sutro JB, Vayuvegula B, Gupta S, Cahalan MD. Voltage-sensitive ion channels in human B lymphocytes. Adv Exp Med Biol 1989; 254: 113–22
   Google Scholar
• Amigorena S, Choquet D, Teillaud J-L, Korn H, Fridman WH. Ion channel blockers inhibit B cell activation at a precise stage of the Gl phase of the cell cycle. Possible involvement of K+ channels. J Immunol 1990; 144: 2038–45
   PubMedGoogle Scholar
• Fukushima Y, Hagiwara S, Saxton RE. Variation of calcium current during the cell growth cycle in mouse hybridoma lines secreting immunoglobulins. J Physiol 1984; 355: 313–21
   Google Scholar
• Attali B, Romey G, Houore E, Schmid-Alliana A, Matte M-G, Lesage F, Ricard P, Barhanin J, Lazdunski M. Cloning, functional expression, and regulation of two K + channels in human T lymphocytes. J Biol Chem 1992; 267: 8650–7
   PubMedGoogle Scholar
• Freedman B, Price MA, Deutsch CJ. Evidence for voltage modulation of IL-2 prodcution in mitogen-stimulated human peripheral blood lymphocytes. J Immunol 1992; 149: 3784–94
   Google Scholar
• Dos Reis GA., Nobrega AF, Persechini PM. Stage-specific distinctions in potassium channel blocker control of T-lymphocyte activation. Int J Immunopharmacol 1988; 10: 217–26
   PubMedGoogle Scholar
• Lin CS, Boltz RC, Blake JT, Nguyen M, Talento A, Fischer PA, Springer MS, Sigal NH, Slaughter RS, Garcia ML, Kaczorowski GJ, Koo GC. Voltage-gated potassium channels regulate calcium-dependent pathways involved in human T lymphocyte activation. J Exp Med 1993; 177: 637–45
   PubMed Web of Science ®Google Scholar
• Sharma B. Inhibition of the generation of cytotoxic lymphocytes by potassium ion channel blockers. Immunology 1988; 65: 101–5
   Google Scholar
• Sidell N, Schlichter LC, Wright SC, Hagiwars S, Golub SH. Potassium channels in human NK cells are involved in discrete stages of the killing process. J Immunol 1986; 137: 1650–8
   PubMed Web of Science ®Google Scholar
• Mix E, Olsson T, Solders G, Link H. Effect of ion channel blockers on immune response and course of experimental allergic neuritis. Brain 1989; 112: 1405–18
   PubMed Web of Science ®Google Scholar
• Edwards G, Weston AH. Structure-activity relationships of K+ channel openers. Trends Pharmacol Sci 1990; 11: 417–22
   PubMed Web of Science ®Google Scholar
• Edwards G, Weston AH. The pharmacology of ATP-sensitive potassium channels. Ann Rev Pharmacol Toxicol 1993; 33: 597–637
   PubMed Web of Science ®Google Scholar
• Cook NS. The pharmacology of potassium channels and their therapeutic potential. Trends Pharmacol Sci 1988; 9: 21–8
   PubMed Web of Science ®Google Scholar
• Robertson DW, Steinberg MI. Potassium channel modulators: scientific applications and therapeutic promise. J Med Chem 1990; 33: 1529–41
   PubMed Web of Science ®Google Scholar
• Steinberg MI, Wiest SA, Zimmermann KM, Ertel PJ, Bemis K, Robertson DW. Chiral recognition of pinacidil and its 3-pyridil isomer by canine cardiac and smooth muscle: antagonism by sulfonylureas. J Pharmacol Exp Ther 1991; 256: 222–9
   PubMedGoogle Scholar
• Perreault T, De Marte J. Maturational changes in endothelium-derived relaxations in newborn piglet pulmonary circulation. Am J Physiol 1993; 264: H302–H309
   PubMed Web of Science ®Google Scholar
• Schmid-Antomarchi H, Amoroso S, Fosset M, Lazdunski M. K+ channel openers activate brain sulfonylurea-sensitive K+ channels and block neurosecretion. Proc Natl Acad Sci USA 1990; 87: 3489–92
   PubMed Web of Science ®Google Scholar
• Murphy KPSJ, Greefield SA. Neuronal selectivity of ATP-sensitive potassium channels in guinea-pig substantia nigra revealed by responses to anoxia. J Physiol 1992; 453: 167–83
   Google Scholar
• Garrino MG, Plant TD, Henquin JC. Effects of putative activators of K + channels in mouse pancreatic P-cells. Br J Pharmacol 1989; 98: 957–65
   PubMed Web of Science ®Google Scholar
• Schwanstecher C, Dickel C, Ebers I, Lins S, Ziinkler BJ, Panten U. Diazoxide-sensitivity of the adenosine 5′-triphosphate-dependent K+ channel in mouse pancreatic, β-cells. Br J Pharmacol 1992; 107: 87–94
   PubMedGoogle Scholar
• Weston AH, Edwards G. Recent progress in potassium channel opener pharmacology. Biochem Pharmacol 1992; 43: 47–54
   PubMed Web of Science ®Google Scholar
• Ho K, Nichols CG, Lederer WJ, Lytton J, Vassilev PM, Kanazirska MV, Hebert SC. Cloning and expression of an inwardly rectifying ATP-regulated potassium channel. Nature 1993; 362: 31–7
   PubMed Web of Science ®Google Scholar
• Kubo Y, Baldwin TJ, Jan YN, Jan LY. Primary structure and functional expression of a mouse inward rectifier potassium channel. Nature 1993; 362: 127–33
   PubMed Web of Science ®Google Scholar
• Hughes RAC. Guillain-Barre Syndrome. Chapter 3: Experimental Allergic Neuritis. Springer, London Berlin Heidelberg New York Paris Tokyo, Hong Kong 1990; 49–81
   Google Scholar
• Hartung H-P, Stoll G, Toyka KV. Immune reactions in the peripheral nervous system. Peripheral Neuropathy, PJ Dyck, PK Thomas, JW Griffin, PA Low, JF. Poduslo. Saunders, Philadelphia London Toronto Montreal Sydney, Tokyo 1993; 418–44
   Google Scholar
• Hartung H-P, Schafer B, van der Meide PH, Fierz W, Heininger K, Toyka KV. The role of interferon-gamma in the pathogenesis of experimental autoimmune disease of the peripheral nervous system. Ann Neurol;, 27: 247–57
   Google Scholar
• Olsson T. Cytokines in neuroinflammatory disease: role of myelin autoreactive T cell production of interferon-gamma. J Neuroimmunol 1992; 40: 211–8
   PubMed Web of Science ®Google Scholar
• Schmidt B, Stoll G, van der Meide P, Jung S, Hartung H-P. Transient cellular expression of -/-interferon in myelin-induced and T-cell line-mediated experimental autoimmune neuritis. Brain 1992; 115: 1633–46
   PubMedGoogle Scholar
• Strigard K, Holmdahl R, van der Meide PH, Klareskog L, Olsson T. In vivo treatment of rats with monoclonal antibodies against gamma interferon:' effects on experimental allergic neuritis. Acta Neurol Scand 1989; 80: 201–7
   PubMed Web of Science ®Google Scholar
• Kadlubowski M, Hughes RAC, Gregson NA. Experimental allergic neuritis in Lewis rat: characterzation of the activity of peripheral myelin and its major basic protein P2. Brain Res 1980; 184: 439–54
   PubMed Web of Science ®Google Scholar
• Olsson T, Wang W-Z, Hbjeberg B, Kostulas V, Jiang Y-P, Andersson G, Ekre H-P, Link H., Autoreactive T. lymphocytes in multiple sclerosis determined by antigen induced secretion of interferon-gamma. J Clin Invest 1990; 86: 981–5
   PubMed Web of Science ®Google Scholar
• van der Meide PH., Dubbeld M, Vijverberg K, Kos T, Schellekens H. The purification and characterization of rat gamma interferon by use of two monoclonal antibodies. J Gen Virol 1986; 67: 1054–71
   Google Scholar
• Kaplow LS. Substitute for benzidine in myeloperoxidase stains. Amer J Clin Pathol 1974; 63: 451
   Web of Science ®Google Scholar
• Waugh CJ, Dockrell MEC, Haynes WG, Olvermann HJ, Williams BC, Webb DJ. The potassium channel opener BRL 38227 inhibits binding of (125I)-labelled endothelin-I to rat cardiac membranes. Biochem Biophys Res Comm 1992; 185: 630–635
   PubMedGoogle Scholar
• Tsien RY, Pozzan T, Rink TJ. T-cell mitogens cause early changes in cytoplasmic-free Ca2+ and membrane potential in lymphocytes. Nature 1982; 295: 68–71
   PubMed Web of Science ®Google Scholar
• Lee SC, Sabath DE, Deutsch C, Prytowsky MB. Increased voltage-gated potassium conductance during interleukin-2 stimulated proliferation of a mouse helper T lymphocyte clone. J Cell Biol 1986; 102: 1200–8
   Google Scholar
• Bray KM, Newgreen DT, Small RC, Southerton JS, Taylor SG, Weir SW, Weston AH. Evidence that the mechanism of the inhibitory action of pinacidil in rat and guinea-pig smooth muscle differs from that of glyceryl trinitrate. Br J Phamacol 1987; 91: 421–9
   Google Scholar
• Sanguinetti MC, Scott AL, Zingaro GJ, Siegl KS. BRL 34915 (cromakalim) activates ATP-active K* current in cardiac muscle. Proc Natl Acad Sci USA 1988; 85: 8360–4
   Google Scholar
• Reichelt W, Stolzenburg J-U, Eberhardt W, Reichenbach A., Arendt T, Bruckner M, Rothe T. Influence of high potassium concentrations on proliferation and differentiation of glial cells in vitro. 8th Gen Meeting Eur Soc Neurochem (Abstr), Leipzig. 1990; 160
   Google Scholar
• Pieper GM, Gross GJ. EMD 52692 (bimakalim), a new potassium channel opener, attenuates luminol-enhanced chemoluminescence and superoxide anion radical formation by zymosan-activated polymorphonuclear leukocytes. Immunopharmacology 1992; 23: 191–97
   PubMedGoogle Scholar
• Zhu J, Mix E, Olsson T, Link H. Influence of ion channel modulators on in vitro interferon-J induced MHC class I and II expression on macrophages
   Google Scholar