Korean J Physiol Pharmacol.  2017 Mar;21(2):225-232. 10.4196/kjpp.2017.21.2.225.

Nortriptyline, a tricyclic antidepressant, inhibits voltage-dependent K+ channels in coronary arterial smooth muscle cells

Affiliations
  • 1Department of Physiology, Kangwon National University School of Medicine, Chuncheon 24341, Korea. parkws@kangwon.ac.kr
  • 2Department of Molecular and Cellular Biochemistry, Kangwon National University School of Medicine, Chuncheon 24341, Korea.
  • 3Department of Medical Environmental Biology and Tropical Medicine, Kangwon National University School of Medicine, Chuncheon 24341, Korea.
  • 4Department of Internal Medicine, Kangwon National University School of Medicine, Chuncheon 24341, Korea.
  • 5Department of Pulmonary, Critical Care and Sleep Medicine, University of Southern California, Keck School of Medicine, Los Angeles, CA90033, USA.
  • 6Department of Microbiology, Inje University College of Medicine, Busan 48516, Korea.
  • 7Department of Physiology, Konkuk University School of Medicine, Chungju 27478, Korea.

Abstract

We demonstrated the effect of nortriptyline, a tricyclic antidepressant drug and serotonin reuptake inhibitor, on voltage-dependent K⁺ (Kv) channels in freshly isolated rabbit coronary arterial smooth muscle cells using a whole-cell patch clamp technique. Nortriptyline inhibited Kv currents in a concentration-dependent manner, with an apparent ICâ‚…â‚€ value of 2.86±0.52 µM and a Hill coefficient of 0.77±0.1. Although application of nortriptyline did not change the activation curve, nortriptyline shifted the inactivation current toward a more negative potential. Application of train pulses (1 or 2 Hz) did not change the nortriptyline-induced Kv channel inhibition, suggesting that the effects of nortiprtyline were not use-dependent. Preincubation with the Kv1.5 and Kv2.1/2.2 inhibitors, DPO-1 and guangxitoxin did not affect nortriptyline inhibition of Kv channels. From these results, we concluded that nortriptyline inhibited Kv channels in a concentration-dependent and state-independent manner independently of serotonin reuptake.

Keyword

Coronary artery; Nortriptyline; Voltage-dependent K⁺ channel

MeSH Terms

Coronary Vessels
Muscle, Smooth*
Myocytes, Smooth Muscle*
Nortriptyline*
Serotonin
Nortriptyline
Serotonin

Figure

  • Fig. 1 Effects of nortriptyline on voltage-dependent K+ (Kv) channel currents.Representative Kv currents were elicited by 600-ms depolarizing step pulses from −60 to +60 mV in steps of 10-mV at a holding potential of −60 mV in the control condition (A) and in the presence of 10 µM nortriptyline (B). (C) The current-voltage (I~V) relationship at steady-state Kv current under control conditions (○) and in the presence of 10 µM nortriptyline (●). n=7. *p<0.05. (D) Voltage-dependence of Kv current inhibition by nortriptyline. Normalized inhibition shown as relative current from panel in (C) are plotted as a function of membrane potential.

  • Fig. 2 Concentration-dependent inhibition of Kv channels by nortriptyline.(A) Superimposed currents were elicited by 600-ms depolarizing pulse of +60 from a holding potential of −60 mV in the presence of 0, 0.1, 0.3, 1, 3, 10, 30, and 100 mM nortriptyline. (B) Concentration-dependent curve for nortriptyline-induced inhibition of the Kv current measured at steady-state. n=8.

  • Fig. 3 Influence of nortriptyline on steady-state activation and steady-state inactivation curves.(A) Activation currents in the absence (○) and presence of 10 µM nortriptyline (●). Tail currents were elicited by short depolarizing pulses (20~50 ms) from −80 to +60 mV in steps of 10 mV at a holding potential of −80 mV. Subsequent pulses returned to −40 mV. The current was normalized from the peak value of the tail current. n=10. (B) Inactivation currents in the absence (○) and presence of nortriptyline (●). The currents were elicited by a two-pulse protocol with a test step to +40 mV after 7-s conditioning pre-pulses between −80 and −30 mV. The elicited currents were normalized to the current of the peak test pulse. n=9. *p<0.05.

  • Fig. 4 The effects of pre-treatment with Kv1.5 and/or Kv2.1/2.2 inhibitors on the nortriptyline-induced inhibition of Kv current.Current traces were obtained by one-step depolarizing pulses to +60 mV at a holding potential of −60 mV. (A) Superimposed currents under control, in the presence of DPO-1, and in the presence of DPO-1+nortriptyline. (B) Summary of the results shown in panel (A). n=5. *p<0.05. (C) Superimposed currents under control, in the presence of guangxitoxin, and in the presence of guangxitoxin+nortriptyline. (D) Summary of the results shown in panel (C). n=5. *p<0.05. (E) Superimposed currents under control, in the presence of DPO-1+guangxitoxin, and in the presence of DPO-1+guangxitoxin+nortriptyline. (F) Summary of the results shown in panel (E). n=6. *p<0.05.

  • Fig. 5 Frequency-dependent inhibition of Kv currents by nortriptyline.Twenty depolarizing pulses from −60 mV to +60 mV in duration of 150-ms were applied in the absence (○) and presence of nortriptyline (●), at frequencies of 1 Hz (A) and 2 Hz (B). Each peak current was normalized by the peak current at first pulse and plotted against the pulse number. n=5.


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