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β-Adrenoceptors and potassium channels

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References

  • Ahlquist RP (1948) A study of the adrenotropic receptors. Am J Physiol 153:586–600

    CAS  Google Scholar 

  • Arch JRS (2004) Do low-affinity states of β-adrenoceptors have roles in physiology and medicine? Br J Pharmacol 143:517–518

    Article  PubMed  CAS  Google Scholar 

  • Bieger D, Parai K, Ford AC, Tabrizchi R (2006) β-Adrenoceptor mediated responses in rat pulmonary artery: evidence for a role of TASK-1 related K channels. Naunyn-Schmiedeberg’s Arch Pharmacol (this issue)

  • Brown AM, Birnbaumer L (1988) Direct G protein gating of ion channels. Am J Physiol 254:H401–H410

    PubMed  CAS  Google Scholar 

  • Duffy SM, Cruse G, Lawley WJ, Bradding P (2005) β2-Adrenoceptor regulation of the K+ channel iKCa1 in human mast cells. FASEB J 19:1006–1008

    PubMed  CAS  Google Scholar 

  • Duprat F, Lesage F, Fink M, Reyes R, Heurteaux C, Lazdunski M (1997) TASK, a human background K+ channel to sense external pH variations near physiological pH. EMBO J 16:5464–5471

    Article  PubMed  CAS  Google Scholar 

  • Emorine L, Marullo S, Briend-Sutren MM, Patey G, Tate K, Delavier-Klutchko C et al (1989) Molecular characterization of the human β3-adrenergic receptor. Science 245:1118–1121

    Article  PubMed  CAS  Google Scholar 

  • Ferro A, Coash M, Yamamoto T, Rob J, Ji Y, Queen L (2004) Nitric oxide-dependent β2-adrenergic dilatation of rat aorta is mediated through activation of both protein kinase A and Akt. Br J Pharmacol 43:397–403

    Article  CAS  Google Scholar 

  • Foerster K, Kaeferstein T, Groner F, Engelhardt S, Matthes J, Koch W, Lohse MJ, Herzig S (2004) Channel function and regulation in β1- and β2-adrenoceptor transgenic mice. Naunyn-Schmiedeberg’s Arch Pharmacol 369:490–495

    Article  PubMed  CAS  Google Scholar 

  • Frazier EP, Matthy MJ, Peters SLM, Michel MC (2005) Does cyclic AMP mediate rat urinary bladder relaxation by isoproterenol? J Pharmacol Exp Ther 313:260–267

    Article  PubMed  CAS  Google Scholar 

  • Fujii K, Onaka U, Goto K, Abe I, Fujishima M (1999) Impaired isoproterenol-induced hyperpolarization in isolated mesenteric arteries of aged rats. Hypertension 34:222–228

    PubMed  CAS  Google Scholar 

  • Galitzky J, Langin D, Montastruc J-L, Lafontan M, Berlan M (1998) On the presence of a putative fourth β-adrenoceptor in human adipose tissue. TIPS 19:164–166

    PubMed  CAS  Google Scholar 

  • Gardener MJ, Johnson IT, Burnham MP, Edwards G, Heagerty AM, Weston AH (2004) Functional evidence of a role for two-pore domain potassium channels in rat. Br J Pharmacol 142:192–202

    Article  PubMed  CAS  Google Scholar 

  • Granneman JG (2001) The putative β4-adrenergic receptor is a novel state of the β1-adrenergic receptor. Am J Physiol 43:E199–E202

    Google Scholar 

  • Gurney AM, Osipenko ON, Macmillan D, McFarlane KM, Tate RJ, Kempsill FEJ (2003) Two-pore domain K channel, TASK1, in pulmonary artery smooth muscle cells. Circ Res 93:957–964

    Article  PubMed  CAS  Google Scholar 

  • Joseph SS, Lynham JA, Colledge WH, Kaumann AJ (2004a) Binding of (-)-[3H]-CGP12177 at two sites in recombinant β1-adrenoceptors and interaction with β-blockers. Naunyn-Schmiedeberg’s Arch Pharmacol 369:525–532

    Article  PubMed  CAS  Google Scholar 

  • Joseph SS, Colledge WH, Kaumann AJ (2004b) Aspartate138 is required for the high-affinity ligand binding site but not for the low-affinity binding site of the β1-adrenoceptor. Naunyn-Schmiedeberg’s Arch Pharmacol 370:223–226

    Article  PubMed  CAS  Google Scholar 

  • Kaumann AJ (1997) Four beta-adrenoceptor subtypes in the mammalian heart. TIPS 18:70–76

    PubMed  CAS  Google Scholar 

  • Kaumann AJ, Engelhardt S, Hein L, Molenaar P, Lohse M (2001) Abolition of (-)-CGP 12177-evoked cardiostimulation in double β12-adrenoceptor knockout mice. Obligatory role of β1-adrenoceptors for putative β4-adrenoceptor pharmacology. Naunyn-Schmiedeberg’s Arch Pharmacol 363:87–93

    Article  PubMed  CAS  Google Scholar 

  • Lands AM, Arnold A, McAuliff JP, Luduena FP, Brown TG (1967) Differentiation of receptor systems activated by sympathomimetic amines. Nature 214:597–598

    Article  PubMed  CAS  Google Scholar 

  • Lin C, Nagai M, Ishigaki D, Hayasaka K, Endoh M, Ishii K (2005) Cross-talk between β1-adrenoceptors and ETA receptors in modulation of the slow component of delayed rectifier K+ currents. Naunyn Schmiedebergs Arch Pharmacol 371:133–140

    Article  PubMed  CAS  Google Scholar 

  • Ming Z, Parent R, Lavallée M (1997) β2-Adrenergic dilation of resistance coronary vessels involves KATP channels and nitric oxide in conscious dogs. Circulation 95:1568–1576

    PubMed  CAS  Google Scholar 

  • Molenaar P, Sarsero D, Kaumann AJ (1997) Proposal for the interaction of non-conventional partial agonists and catecholamines with the putative beta-4-adrenoceptor in mammalian heart. Clin Exp Pharmacol Physiol 24(9–10):647–656

    Article  PubMed  CAS  Google Scholar 

  • Nakashima M, Vanhoutte PM (1995) Isoproterenol causes hyperpolarization through opening of ATP-sensitive potassium channels in vascular smooth muscle of the canine saphenous vein. J Pharmacol Exp Ther 272:379–384

    PubMed  CAS  Google Scholar 

  • Patel AJ, Honoré E (2001) Properties and modulation of mammalian 2P domain K+ channels. Trends Neurosci 24:339–346

    Article  PubMed  CAS  Google Scholar 

  • Petkov GV, Nelson MT (2005) Differential regulation of Ca2+-activated K+ channels by β-adrenoceptors in guinea pig urinary bladder smooth muscle. Am J Physiol Cell Physiol 288:C1255–C1263

    Article  PubMed  CAS  Google Scholar 

  • Sarsero D, Russell FD, Lynham JA, Rabnott G, Yang I, Fong KM, Li L, Kaumann AJ & Molenaar P (2003) (-)-CGP 12177 increases contractile force and hastens relaxation of human myocardial preparations through a propranolol-resistant state of the β1-adrenoceptor. Naunyn-Schmiedeberg’s Arch Pharmacol 367:10–21

    Article  PubMed  CAS  Google Scholar 

  • Uchida H, Shishido K, Nomiya M, Yamaguchi O (2005) Involvement of cyclic AMP-dependent and -independent mechanisms in the relaxation of rat detrusor muscle via β-adrenoceptors. Eur J Pharmacol 518:195–202

    Article  PubMed  CAS  Google Scholar 

  • Zheng M, Zhu W, Han Q, Xiao R-P (2005) Emerging concepts and therapeutic implications of β-adrenergic receptor subtype signalling. Pharmacol Ther 108:257–268

    Article  PubMed  CAS  Google Scholar 

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Correspondence to Albert Ferro.

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Ferro, A. β-Adrenoceptors and potassium channels. Naunyn-Schmied Arch Pharmacol 373, 183–185 (2006). https://doi.org/10.1007/s00210-006-0065-2

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