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Multiple mechanisms of hERG liability: K+ current inhibition, disruption of protein trafficking, and apoptosis induced by amoxapine

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The antidepressant amoxapine has been linked to cases of QT prolongation, acute heart failure, and sudden death. Inhibition of cardiac hERG (Kv11.1) potassium channels causes prolonged repolarization and is implicated in apoptosis. Apoptosis in association with amoxapine has not yet been reported. This study was designed to investigate amoxapine effects on hERG currents, hERG protein trafficking, and hERG-associated apoptosis in order to elucidate molecular mechanisms underlying cardiac side effects of the drug. hERG channels were expressed in Xenopus laevis oocytes and HEK 293 cells, and potassium currents were recorded using patch clamp and two-electrode voltage clamp electrophysiology. Protein trafficking was evaluated in HEK 293 cells by Western blot analysis, and cell viability was assessed in HEK cells by immunocytochemistry and colorimetric MTT assay. Amoxapine caused acute hERG blockade in oocytes (IC50 = 21.6 µM) and in HEK 293 cells (IC50 = 5.1 µM). Mutation of residues Y652 and F656 attenuated hERG blockade, suggesting drug binding to a receptor inside the channel pore. Channels were mainly blocked in open and inactivated states, and voltage dependence was observed with reduced inhibition at positive potentials. Amoxapine block was reverse frequency-dependent and caused accelerated and leftward-shifted inactivation. Furthermore, amoxapine application resulted in chronic reduction of hERG trafficking into the cell surface membrane (IC50 = 15.3 µM). Finally, the antidepressant drug triggered apoptosis in cells expressing hERG channels. We provide evidence for triple mechanisms of hERG liability associated with amoxapine: (1) direct hERG current inhibition, (2) disruption of hERG protein trafficking, and (3) induction of apoptosis. Further experiments are required to validate a specific pro-apoptotic effect mediated through blockade of hERG channels.

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References

  • Becchetti A, Arcangeli A (2008) A comment on ion channels as pharmacological targets in oncology. J Gen Physiol 132:313–314

    Article  PubMed  Google Scholar 

  • Coccaro EF, Siever LJ (1983) Second generation antidepressants: a comparative review. J Clin Pharmacol 25:241–260

    Google Scholar 

  • Delgado C, Manzanares J, Tamargo J, Valenzuela C (1986) Electrophysiological effects of amoxapine in untreated and in amoxapine-pretreated rat atria. Br J Pharmacol 87:317–325

    PubMed  CAS  Google Scholar 

  • Dennis AT, Wang L, Wan X, Ficker E (2007) hERG channel trafficking: novel targets in drug-induced long QT syndrome. Biochem Soc Trans 35:1060–1063

    Article  PubMed  CAS  Google Scholar 

  • Dorian P, Newman D (2000) Rate dependence of the effect of antiarrhythmic drugs delaying cardiac repolarization: an overview. Europace 2:277–285

    Article  PubMed  CAS  Google Scholar 

  • Duncan RS, McPate MJ, Ridley JM, Gao Z, James AF, Leishman DJ, Leaney JL, Witchel HJ, Hancox JC (2007) Inhibition of the HERG potassium channel by the tricyclic antidepressant doxepin. Biochem Pharmacol 74:425–437

    Article  PubMed  CAS  Google Scholar 

  • Ficker E, Dennis AT, Wang L, Brown AM (2003) Role of cytosolic chaperones Hsp70 and Hsp90 in maturation of the cardiac potassium channel HERG. Circ Res 92:e87–e100

    Article  PubMed  CAS  Google Scholar 

  • Ficker E, Kuryshev YA, Dennis AT, Obejero-Paz C, Wang L, Hawryluk P, Wible BA, Brown AM (2004) Mechanisms of arsenic-induced prolongation of cardiac repolarization. Mol Pharmacol 66:33–44

    Article  PubMed  CAS  Google Scholar 

  • Gonzalez-Juanatey JR, Iglesias MJ, Alcaide C, Pineiro R, Lago F (2003) Doxazosin induces apoptosis in cardiomyocytes cultured in vitro by a mechanism that is independent of α1-adrenergic blockade. Circulation 107:127–131

    Article  PubMed  CAS  Google Scholar 

  • Guo J, Massaeli H, Li W, Xu J, Luo T, Shaw J, Kirshenbaum LA, Zhang S (2007) Identification of I Kr and its trafficking disruption induced by probucol in cultured neonatal rat cardiomyocytes. J Pharmacol Exp Ther 321:911–920

    Article  PubMed  CAS  Google Scholar 

  • Guo J, Massaeli H, Xu J, Jia Z, Wigle JT, Mesaeli N, Zhang S (2009) Extracellular K+ concentration controls cell surface density of I Kr in rabbit hearts and of the HERG channel in human cell lines. J Clin Invest 119:2745–2757

    Article  PubMed  CAS  Google Scholar 

  • Hondeghem LM, Snyders DJ (1990) Class III antiarrhythmic drugs have a lot of potential but a long way to go. Reduced effectiveness and dangers of reverse use dependence. Circulation 81:686–690

    PubMed  CAS  Google Scholar 

  • Jo SH, Hong HK, Chong SH, Won KH, Jung SJ, Choe H (2008) Clomipramine block of the hERG K+ channel: accessibility to F656 and Y652. Eur J Pharmacol 592:19–25

    Article  PubMed  CAS  Google Scholar 

  • Kiehn J, Thomas D, Karle CA, Schöls W, Kübler W (1999) Inhibitory effects of the class III antiarrhythmic drug amiodarone on cloned HERG potassium channels. Naunyn Schmiedebergs Arch Pharmacol 359:212–219

    Article  PubMed  CAS  Google Scholar 

  • Kiesecker C, Alter M, Kathöfer S, Zitron E, Scholz EP, Thomas D, Kreuzer J, Katus HA, Bauer A, Karle CA (2006) Atypical tetracyclic antidepressant maprotiline is an antagonist of cardiac hERG potassium channels. Naunyn Schmiedebergs Arch Pharmacol 373:212–220

    Article  PubMed  CAS  Google Scholar 

  • Kinugawa T, Kotake H, Mashiba H (1988) Inhibitory actions of amoxapine, a tricyclic antidepressant agent, on electrophysiological properties of mammalian isolated cardiac preparations. Br J Pharmacol 94:1250–1256

    PubMed  CAS  Google Scholar 

  • Kudo K, Inoue H, Ishida T, Tsuji A, Ikeda N (2007) A fatal case of amoxapine poisoning under the influence of chronic use of psychotropic drugs. Leg Med 9:63–67

    Article  CAS  Google Scholar 

  • Mahapatra RK, Paul SK, Mahapatra D, Winter S (1986) Cardiovascular effects of polycyclic antidepressants. Angiology 37:709–717

    Article  PubMed  CAS  Google Scholar 

  • Milnes JT, Crociani O, Arcangeli A, Hancox JC, Witchel HJ (2003) Blockade of HERG potassium currents by fluvoxamine: incomplete attenuation by S6 mutations at F656 or Y652. Br J Pharmacol 139:887–898

    Article  PubMed  CAS  Google Scholar 

  • Mitcheson JS (2003) Drug binding to HERG channels: evidence for an “non-aromatic” binding site for fluvoxamine. Br J Pharmacol 139:883–884

    Article  PubMed  CAS  Google Scholar 

  • Mitcheson JS, Chen J, Lin M, Culberson C, Sanguinetti MC (2000) A structural basis for drug-induced long QT syndrome. Proc Natl Acad Sci USA 97:12329–12333

    Article  PubMed  CAS  Google Scholar 

  • Mosmann T (1983) Rapid colorimetric assay for cellular growth and survival: application to cytotoxic and survival assays. J Immunol Methods 65:55–63

    Article  PubMed  CAS  Google Scholar 

  • Munger MA, Effron BA (1988) Amoxapine cardiotoxicity. Ann Emerg Med 17:274278

    Article  Google Scholar 

  • Napolitano C, Priori S, Schwartz P (1994) Torsade de pointes: mechanism and management. Drugs 47:51–65

    Article  PubMed  CAS  Google Scholar 

  • Ortiz A, Josef NC (1983) Premature atrial contractions and amoxapine therapy: a case report. J Clin Psychopharmacol 3:246–249

    Article  PubMed  CAS  Google Scholar 

  • Paul AA, Witchel HJ, Hancox JC (2002) Inhibition of the current of heterologously expressed HERG potassium channels by flecainide and comparison with quinidine, propafenone and lignocaine. Br J Pharmacol 136:717–729

    Article  PubMed  CAS  Google Scholar 

  • Rajamani S, Eckhardt LL, Valdivia CR, Klemens CA, Gillman BM, Anderson CL, Holzem KM, Delisle BP, Anson BD, Makielski JC, January CT (2006) Drug-induced long QT syndrome: hERG K+ channel block and disruption of protein trafficking by fluoxetine and norfluoxetine. Br J Pharmacol 149:481–489

    Article  PubMed  CAS  Google Scholar 

  • Redfern WS, Carlsson L, Davis AS, Lynch WG, MacKenzie I, Palethorpe S, Siegl PK, Strang I, Sullivan AT, Wallis R, Camm AJ, Hammond TG (2003) Relationships between preclinical cardiac electrophysiology, clinical QT interval prolongation and torsade de pointes for a broad range of drugs: evidence for a provisional safety margin in drug development. Cardiovasc Res 58:32–45

    Article  PubMed  CAS  Google Scholar 

  • Robertson GA (2009) Endocytic control of ion channel density as a target for cardiovascular disease. J Clin Invest 119:2531–2534

    Article  PubMed  CAS  Google Scholar 

  • Roden D (2008) Repolarization reserve: a moving target. Circulation 118:981–982

    Article  PubMed  Google Scholar 

  • Sanguinetti MC, Jiang C, Curran ME, Keating MT (1995) A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the I kr potassium channel. Cell 81:299–307

    Article  PubMed  CAS  Google Scholar 

  • Satoh MS, Lindahl T (1992) Role of poly(ADP-ribose) formation in DNA repair. Nature 356:356–358

    Article  PubMed  CAS  Google Scholar 

  • Scherer D, von Löwenstern K, Zitron E, Scholz EP, Bloehs R, Kathöfer S, Thomas D, Bauer A, Katus HA, Karle CA (2008) Inhibition of cardiac hERG potassium channels by tetracyclic antidepressant mianserin. Naunyn Schmiedebergs Arch Pharmacol 378:73–83

    Article  PubMed  CAS  Google Scholar 

  • Schumacher SM, McEwen DP, Zhang L, Arendt KL, Van Genderen KM, Martens JR (2009) Antiarrhythmic drug-induced internalization of the atrial-specific K+ channel Kv1.5. Circ Res 104:1390–1398

    Article  PubMed  CAS  Google Scholar 

  • Smith GAM, Tsui HW, Newell EW, Jiang X, Zhu XP, Tsui FWL, Schlichter LC (2002) Functional up-regulation of HERG K+ channels in neoplastic hematopoietic cells. J Biol Chem 277:18528–18534

    Article  PubMed  CAS  Google Scholar 

  • Sorensen MR (1988) Acute myocardial failure following amoxapine intoxication. J Clin Psychopharmacol 8:75

    Article  PubMed  CAS  Google Scholar 

  • Spector PS, Curran ME, Keating MT, Sanguinetti MC (1996) Class III antiarrhythmic drugs block HERG, a human cardiac delayed rectifier K+ channel. Open-channel block by methanesulfonanilides. Circulation 78:499–503

    CAS  Google Scholar 

  • Staudacher I, Schweizer PA, Katus HA, Thomas D (2010) hERG: protein trafficking and potential for therapy and drug side effects. Curr Opin Drug Discov Dev 13:23–30

    CAS  Google Scholar 

  • Takemasa H, Nagatomo T, Abe H, Kawakami K, Igarashi T, Tsuguri T, Kabashima N, Tamura M, Okazaki M, Delisle BP, January CT, Otsuji Y (2007) Coexistence of hERG current block and disruption of protein trafficking in ketoconazole-induced long QT syndrome. Br J Pharmacol 153:439–447

    Article  PubMed  CAS  Google Scholar 

  • Teschemacher AG, Seward EP, Hanox JC, Witchel HJ (2003) Inhibition of the current of heterologously expressed HERG potassium channels by imipramine and amitriptyline. Br J Pharmacol 128:479–485

    Article  Google Scholar 

  • The ALLHAT Officers and Coordinators for the ALLHAT Collaborative Research Group (2000) Major cardiovascular events in hypertensive patients randomized to doxazosin vs chlorthalidone: the Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial (ALLHAT). JAMA 283:1967–1975

    Article  Google Scholar 

  • Thomas D, Zhang W, Karle CA, Kathöfer S, Schöls W, Kübler W, Kiehn J (1999) Deletion of protein kinase a phosphorylation sites in the HERG potassium channel inhibits activation shift by protein kinase A. J Biol Chem 274:27457–27462

    Article  PubMed  CAS  Google Scholar 

  • Thomas D, Wendt-Nordahl G, Röckl K, Ficker E, Brown AM, Kiehn J (2001) High affinity blockade of HERG human cardiac potassion channels by the novel antiarrhythmic drug BRL-32872. J Pharmacol Exp Ther 297:735–761

    Google Scholar 

  • Thomas D, Gut B, Wendt-Nordahl G, Kiehn J (2002) The antidepressant drug fluoxetine is an inhibitor of HERG potassium channels. J Pharmacol Exp Ther 300:543–548

    Article  PubMed  CAS  Google Scholar 

  • Thomas D, Kiehn J, Katus HA, Karle CA (2003a) Defective protein trafficking in hERG-associated hereditary long QT syndrome (LQT2): molecular mechanisms and restoration of intracellular protein processing. Cardiovasc Res 60:235–241

    Article  PubMed  CAS  Google Scholar 

  • Thomas D, Wu K, Kathöfer S, Katus HA, Schoels W, Kiehn J, Karle CA (2003b) The antipsychotic drug chlorpromazine inhibits hERG potassium channels. Br J Pharmacol 139:567–574

    Article  PubMed  CAS  Google Scholar 

  • Thomas D, Karle CA, Kiehn J (2006) The cardiac hERG/IKr potassium channel as pharmacological target: structure, function, regulation, and clinical applications. Curr Pharm Des 12:2271–2283

    Article  PubMed  CAS  Google Scholar 

  • Thomas D, Bloehs R, Koschny R, Ficker E, Sykora J, Kiehn J, Schlömer K, Gierten J, Kathöfer S, Zitron E, Scholz EP, Kiesecker C, Katus HA, Karle CA (2008) Doxazosin induces apoptosis of cells expressing hERG potassium channels. Eur J Pharmacol 579:98–103

    Article  PubMed  CAS  Google Scholar 

  • Van der Heyden MAG, Smits ME, Vos MA (2008) Drugs and trafficking of ion channels: a new pro-arrhythmic threat on the horizon? Br J Pharmacol 153:406–409

    Article  PubMed  CAS  Google Scholar 

  • Viskin S (1999) Long QT syndromes and torsade de pointes. Lancet 354:1625–1633

    Article  PubMed  CAS  Google Scholar 

  • Walker BD, Singleton CB, Bursill JA, Wyse KR, Valenzuela SM, Qiu MR, Breit SN, Campbell TJ (1999) Inhibition of human ether-a-go-go-related gene (HERG) potassium channels by cisapride: affinity for open and inactivated states. Br J Pharmacol 128:444–450

    Article  PubMed  CAS  Google Scholar 

  • Wang H, Zhang Y, Cao L, Han H, Wang J, Yang B, Nattel S, Wang Z (2002) HERG K+ channel, a regulator of tumor cell apoptosis and proliferation. Cancer Res 62:4843–4848

    PubMed  CAS  Google Scholar 

  • Wang L, Wible BA, Wan X, Ficker E (2007) Cardiac glycosides as novel inhibitors of human ether-a-go-go-related gene channel trafficking. J Pharmacol Exp Ther 320:525–534

    Article  PubMed  CAS  Google Scholar 

  • Warmke JW, Ganetzky B (1994) A family of potassium channel genes related to eag in Drosophila and mammals. Proc Natl Acad Sci USA 91:3438–34342

    Article  PubMed  CAS  Google Scholar 

  • Wedin GP, Oderda GM, Klein-Schwartz W, Gorman RL (1986) Relative toxicity of cyclic antidepressants. Ann Emerg Med 15:797–804

    Article  PubMed  CAS  Google Scholar 

  • Witchel HJ, Pabbathi VK, Hofmann G, Paul AA, Hancox JC (2002) Inhibitory actions of the selective serotonin re-uptake inhibitor citalopram on HERG and ventricular L-type calcium currents. FEBS Lett 512:59–66

    Article  PubMed  CAS  Google Scholar 

  • Witchel HJ, Hancox JC, Nutt DJ (2003) Psychotropic drugs, cardiac arrhythmia, and sudden death. J Clin Psychopharmacol 23:58–77

    Article  PubMed  CAS  Google Scholar 

  • Witchel HJ, Dempsey CE, Sessions RB, Perry M, Milnes JT, Hancox JC, Mitcheson JS (2004) The low-potency, voltage-dependent HERG blocker propafenone—molecular determinants and drug trapping. Mol Pharmacol 66:1201–1212

    Article  PubMed  CAS  Google Scholar 

  • Yeoung KS, Meanwell NA (2008) Inhibition of hERG channel trafficking: an under-explored mechanism for drug-induced QT prolongation. ChemMedChem 3:1501–1502

    Article  Google Scholar 

  • Zitron E, Kiesecker C, Scholz E, Lück S, Bloehs R, Kathöfer S, Thomas D, Kiehn J, Kreye VA, Katus HA, Schoels W, Karle CA (2004) Inhibition of cardiac HERG potassium channels by the atypical antidepressant trazodone. Naunyn Schmiedebergs Arch Pharmacol 370:146–156

    Article  PubMed  CAS  Google Scholar 

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Acknowledgments

This work was supported in part by grants from the University of Heidelberg (FRONTIERS program to D.T.), from the ADUMED-Foundation (to D.T.), from the National Institutes of Health (HL71789 to E.F.), from the Max Planck Society (Tandem project to P.A.S.), and from the Deutsche Forschungsgemeinschaft (project KA 1714/1-1 to C.A.K.)

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Obers, S., Staudacher, I., Ficker, E. et al. Multiple mechanisms of hERG liability: K+ current inhibition, disruption of protein trafficking, and apoptosis induced by amoxapine. Naunyn-Schmied Arch Pharmacol 381, 385–400 (2010). https://doi.org/10.1007/s00210-010-0496-7

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