Investigating retinal toxicity of a lutein-based dye in a model of isolated and perfused bovine retina

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Investigating retinal toxicity of a lutein-based dye in a model of isolated and perfused bovine retina. / Mueller, Sebastian; Krupp, Carlo; Schnichels, Sven; Hofmann, Johanna; Spitzer, Martin; Bartz-Schmidt, Karl Ulrich; Szurman, Peter; Januschowski, Kai.

in: GRAEF ARCH CLIN EXP, Jahrgang 257, Nr. 5, 05.2019, S. 961-966.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Mueller, S, Krupp, C, Schnichels, S, Hofmann, J, Spitzer, M, Bartz-Schmidt, KU, Szurman, P & Januschowski, K 2019, 'Investigating retinal toxicity of a lutein-based dye in a model of isolated and perfused bovine retina', GRAEF ARCH CLIN EXP, Jg. 257, Nr. 5, S. 961-966. https://doi.org/10.1007/s00417-019-04260-y

APA

Mueller, S., Krupp, C., Schnichels, S., Hofmann, J., Spitzer, M., Bartz-Schmidt, K. U., Szurman, P., & Januschowski, K. (2019). Investigating retinal toxicity of a lutein-based dye in a model of isolated and perfused bovine retina. GRAEF ARCH CLIN EXP, 257(5), 961-966. https://doi.org/10.1007/s00417-019-04260-y

Vancouver

Bibtex

@article{5d9884fdea714e849491a70efac9d668,
title = "Investigating retinal toxicity of a lutein-based dye in a model of isolated and perfused bovine retina",
abstract = "PURPOSE: Retidyne{\texttrademark} is a new lutein-based dye for internal limiting membrane staining. It uses the intrinsic staining characteristics of lutein which is already known to act as an antioxidant and blue-light filter in the human retina. We investigated retinal tolerance to different staining times measured by the electroretinogram (ERG) of an isolated and perfused retina whole mount.METHODS: For functionality, testing bovine retinas were prepared and perfused with an oxygen saturated standard solution and the ERG was recorded until stable b-wave amplitudes were reached. Then the perfusion was stopped and Retidyne{\texttrademark} was applied directly onto the retinal surface for exposure times of 60 or 120 s. After restarting the perfusion with standard solution, the ERG amplitudes were monitored for 75 min. To investigate the effects on photoreceptor function alone, 1 mM asparate was added to block b-waves.RESULTS: For an exposure time of 60 s amplitudes of a- and b-waves remained stable throughout the experiment. Exposure times of 120 s caused an initial drop of amplitudes that reached statistical significance only for a-waves (a, - 21%, p = 0.047; b, - 14%, p = 0.052). This effect was only seen during the first minutes of the washout and the ERG recovered completely.CONCLUSIONS: In the model of isolated and perfused bovine retina, Retidyne{\texttrademark} showed a good safety profile for common intraoperatively used staining times. An initial toxic effect regarding the transient drop of amplitudes cannot be ruled out but the effect might also be explained by the partial blockage of the flashlight due to a more intense staining effect at the beginning of the washout.",
keywords = "Animals, Cattle, Coloring Agents/toxicity, Disease Models, Animal, Electroretinography, Lutein/toxicity, Perfusion, Retinal Diseases/chemically induced, Retinal Ganglion Cells/drug effects",
author = "Sebastian Mueller and Carlo Krupp and Sven Schnichels and Johanna Hofmann and Martin Spitzer and Bartz-Schmidt, {Karl Ulrich} and Peter Szurman and Kai Januschowski",
year = "2019",
month = may,
doi = "10.1007/s00417-019-04260-y",
language = "English",
volume = "257",
pages = "961--966",
journal = "GRAEF ARCH CLIN EXP",
issn = "0721-832X",
publisher = "Springer",
number = "5",

}

RIS

TY - JOUR

T1 - Investigating retinal toxicity of a lutein-based dye in a model of isolated and perfused bovine retina

AU - Mueller, Sebastian

AU - Krupp, Carlo

AU - Schnichels, Sven

AU - Hofmann, Johanna

AU - Spitzer, Martin

AU - Bartz-Schmidt, Karl Ulrich

AU - Szurman, Peter

AU - Januschowski, Kai

PY - 2019/5

Y1 - 2019/5

N2 - PURPOSE: Retidyne™ is a new lutein-based dye for internal limiting membrane staining. It uses the intrinsic staining characteristics of lutein which is already known to act as an antioxidant and blue-light filter in the human retina. We investigated retinal tolerance to different staining times measured by the electroretinogram (ERG) of an isolated and perfused retina whole mount.METHODS: For functionality, testing bovine retinas were prepared and perfused with an oxygen saturated standard solution and the ERG was recorded until stable b-wave amplitudes were reached. Then the perfusion was stopped and Retidyne™ was applied directly onto the retinal surface for exposure times of 60 or 120 s. After restarting the perfusion with standard solution, the ERG amplitudes were monitored for 75 min. To investigate the effects on photoreceptor function alone, 1 mM asparate was added to block b-waves.RESULTS: For an exposure time of 60 s amplitudes of a- and b-waves remained stable throughout the experiment. Exposure times of 120 s caused an initial drop of amplitudes that reached statistical significance only for a-waves (a, - 21%, p = 0.047; b, - 14%, p = 0.052). This effect was only seen during the first minutes of the washout and the ERG recovered completely.CONCLUSIONS: In the model of isolated and perfused bovine retina, Retidyne™ showed a good safety profile for common intraoperatively used staining times. An initial toxic effect regarding the transient drop of amplitudes cannot be ruled out but the effect might also be explained by the partial blockage of the flashlight due to a more intense staining effect at the beginning of the washout.

AB - PURPOSE: Retidyne™ is a new lutein-based dye for internal limiting membrane staining. It uses the intrinsic staining characteristics of lutein which is already known to act as an antioxidant and blue-light filter in the human retina. We investigated retinal tolerance to different staining times measured by the electroretinogram (ERG) of an isolated and perfused retina whole mount.METHODS: For functionality, testing bovine retinas were prepared and perfused with an oxygen saturated standard solution and the ERG was recorded until stable b-wave amplitudes were reached. Then the perfusion was stopped and Retidyne™ was applied directly onto the retinal surface for exposure times of 60 or 120 s. After restarting the perfusion with standard solution, the ERG amplitudes were monitored for 75 min. To investigate the effects on photoreceptor function alone, 1 mM asparate was added to block b-waves.RESULTS: For an exposure time of 60 s amplitudes of a- and b-waves remained stable throughout the experiment. Exposure times of 120 s caused an initial drop of amplitudes that reached statistical significance only for a-waves (a, - 21%, p = 0.047; b, - 14%, p = 0.052). This effect was only seen during the first minutes of the washout and the ERG recovered completely.CONCLUSIONS: In the model of isolated and perfused bovine retina, Retidyne™ showed a good safety profile for common intraoperatively used staining times. An initial toxic effect regarding the transient drop of amplitudes cannot be ruled out but the effect might also be explained by the partial blockage of the flashlight due to a more intense staining effect at the beginning of the washout.

KW - Animals

KW - Cattle

KW - Coloring Agents/toxicity

KW - Disease Models, Animal

KW - Electroretinography

KW - Lutein/toxicity

KW - Perfusion

KW - Retinal Diseases/chemically induced

KW - Retinal Ganglion Cells/drug effects

U2 - 10.1007/s00417-019-04260-y

DO - 10.1007/s00417-019-04260-y

M3 - SCORING: Journal article

C2 - 30788607

VL - 257

SP - 961

EP - 966

JO - GRAEF ARCH CLIN EXP

JF - GRAEF ARCH CLIN EXP

SN - 0721-832X

IS - 5

ER -