4.2 Article

Inhibitory Effect of Amitriptyline on the Impulse Activity of Cold Thermoreceptor Terminals of Intact and Tear-Deficient Guinea Pig Corneas

Journal

JOURNAL OF OCULAR PHARMACOLOGY AND THERAPEUTICS
Volume 34, Issue 1-2, Pages 195-203

Publisher

MARY ANN LIEBERT, INC
DOI: 10.1089/jop.2017.0066

Keywords

dry eye; cold thermoreceptors; hyperexcitability; sodium channels; amitriptyline

Funding

  1. Ministerio de Economia y Competitividad, Spain [SAF2014-54518-C3-1R, SAF2014-54518-C3-2-R]
  2. ERDF, European Union [SAF2014-54518-C3-1R, SAF2014-54518-C3-2-R]
  3. JSPS KAKENHI, Japan [25870852, 26460348, 15K08250, 16K19023]
  4. Grants-in-Aid for Scientific Research [25870852, 16K19023, 15K08250] Funding Source: KAKEN

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Purpose: Chronic dryness of the ocular surface evokes sensitization of corneal cold-sensitive neurons through an increase of sodium currents and a decrease of potassium currents, leading to the unpleasant dryness and pain sensations typical of dry eye disease. Here, we explored the effects of amitriptyline, a voltage-gated Na+ channel blocker used for the treatment of depression and chronic pain, on nerve terminal impulse (NTI) activity of cold-sensitive nerve terminals recorded in intact and tear-deficient guinea pig corneas. Methods: Main lachrymal gland was surgically removed in anesthetized guinea pigs to induce chronic tear deficiency. Four to 6 weeks afterward, animals were sacrificed and both corneas placed in a perfusion chamber superfused at 34 degrees C. Thermal stimuli were induced by changing the solution temperature from 34 degrees C to 20 degrees C (cooling ramp) and from 34 degrees C to 50 degrees C (heating ramp). Spontaneous and stimulus-evoked NTIs of cold-sensitive nerve terminals were recorded before, during, and after perfusion with solutions containing amitriptyline at different concentrations (3-30M). Results: Perfusion with amitriptyline inhibited irreversibly and in a concentration-dependent manner the spontaneous NTI activity of cold thermoreceptors of intact corneas. This effect was less evident in tear-deficient corneas. In addition, amitriptyline (10M) attenuated the maximal response to cooling ramps without changing cold threshold in intact but not in tear-deficient corneas. Only cold thermoreceptors with low cooling threshold values were sensitive to amitriptyline. Conclusion: Amitriptyline effectively reduces the activity of cold thermoreceptors, although its efficacy is different in intact and tear-deficient corneas, which might be due to the changes induced by ocular dryness in the expression of the various voltage-gated Na+ channels responsible of the action potential generation and propagation.

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