June 2023
Volume 64, Issue 8
Open Access
ARVO Annual Meeting Abstract  |   June 2023
Inhibition of early choroidal neovascularization by transcorneal electrical stimulation for a week in rats
Author Affiliations & Notes
  • Yukari Nakano
    Artificial Vision Institute, R&D Div., NIDEK CO., LTD., Gamagori, Aichi, Japan
  • Junichiro Shikata
    Artificial Vision Institute, R&D Div., NIDEK CO., LTD., Gamagori, Aichi, Japan
  • Hiroki Sato
    Artificial Vision Institute, R&D Div., NIDEK CO., LTD., Gamagori, Aichi, Japan
  • Nobuharu Asai
    Bioengineering Institute, R&D Div., NIDEK CO., LTD., Gamagori, Aichi, Japan
  • Yasuo Terasawa
    Artificial Vision Institute, R&D Div., NIDEK CO., LTD., Gamagori, Aichi, Japan
  • Footnotes
    Commercial Relationships   Yukari Nakano NIDEK CO., LTD., Code E (Employment); Junichiro Shikata NIDEK CO., LTD., Code E (Employment); Hiroki Sato NIDEK CO., LTD., Code E (Employment); Nobuharu Asai NIDEK CO., LTD., Code E (Employment); Yasuo Terasawa NIDEK CO., LTD., Code E (Employment)
  • Footnotes
    Support  None
Investigative Ophthalmology & Visual Science June 2023, Vol.64, 2111. doi:
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    • Get Citation

      Yukari Nakano, Junichiro Shikata, Hiroki Sato, Nobuharu Asai, Yasuo Terasawa; Inhibition of early choroidal neovascularization by transcorneal electrical stimulation for a week in rats. Invest. Ophthalmol. Vis. Sci. 2023;64(8):2111.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose : Chronic electrical stimulation might inhibit the growth of angiogenesis [Y. Inoue et al., 2018]. To investigate the inhibitory effect of transcorneal electrical stimulation (TES) on the progression of early choroidal neovascularization (CNV), we measured and compared CNV volumes, with and without TES in rat CNV models and evaluated this hypothesis.

Methods : CNVs were induced using a photocoagulation laser device in both eyes of 15 Brown Norway rats. A 4 mA, 60 kHz sinusoidal current was applied to the cornea through a conductive gel (2% agarose) for 30 min/day for 7 days in one eye on the day after beginning laser irradiation. Eight days after laser irradiation, fluorescein angiography (FA) was performed to observe the CNV status. Then, the CNV was observed after the choroid-sclera specimen was stained with GSL I-B4 isolectin (DL-1207, Vector Laboratories). The volume of the CNV was calculated by combining images taken with a confocal laser microscope (C2, Nikon) at a 1 um pitch along the Z-axis from the CNV apex to the sclera side. All the experiments were conducted in accordance with the approval of the institutional Animal Care and Use Committee of Nidek Co., Ltd.

Results : CNV lesions were observed at the laser-irradiated location from the hyperfluorescence in the second half of FA (Fig. 1). CNVs showed strong red fluorescence when viewed under a confocal laser microscope with a 561 nm light source (Fig. 1). The CNV volumes are shown in Figure 2. The CNV volume of electrically stimulated eyes (827,513 ± 341,693 μm3, CNV; n = 40, Mean ± SD) was significantly smaller (p 0.05, independent t-test) compared to the CNV volume of control eyes without electrical stimulation (1,108,831 ± 349,279 μm3, CNV; n = 32). No rat suffered corneal opacity or other injuries due to TES.

Conclusions : The results of this study suggest that TES can inhibit the progression of early CNV. We will investigate more effective stimulation conditions in the future studies.

This abstract was presented at the 2023 ARVO Annual Meeting, held in New Orleans, LA, April 23-27, 2023.

 

Fig. 1. The hyperfluorescent portions of FA and the corresponding confocal laser microscopy images after eight days of laser irradiation; the hyperfluorescent portions of FA and the corresponding confocal laser microscopy images are shown in A, B, C, D (Stimulated), and E, F, G, H (Unstimulated).

Fig. 1. The hyperfluorescent portions of FA and the corresponding confocal laser microscopy images after eight days of laser irradiation; the hyperfluorescent portions of FA and the corresponding confocal laser microscopy images are shown in A, B, C, D (Stimulated), and E, F, G, H (Unstimulated).

 

Fig. 2. Comparison of CNV volumes. (Stimulated; 40 CNVs in 10 eyes, Unstimulated; 32 CNVs in 8 eyes, p < 0.05, independent t-test)

Fig. 2. Comparison of CNV volumes. (Stimulated; 40 CNVs in 10 eyes, Unstimulated; 32 CNVs in 8 eyes, p < 0.05, independent t-test)

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