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Electrophysiologic evaluation of the visual pathway at different depths of sevoflurane anesthesia in diabetic rats
Our study investigated the changes produced by diabetes on the visual pathway in a Wistar rat model. The impact of diabetes at 10 weeks after intraperitoneal streptozotocin (STZ) injection was evaluated through electrophysiological methods like visual evoked potentials (VEP) and electroretinogram (E...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Romanian Society of Ophthalmology
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5959023/ https://www.ncbi.nlm.nih.gov/pubmed/29796432 |
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author | Iliescu, Daniela Adriana Ciubotaru, Alexandra Ghiţă, Mihai Aurelian Păun, Adrian Marius Ion, Tudor Zăgrean, Leon |
author_facet | Iliescu, Daniela Adriana Ciubotaru, Alexandra Ghiţă, Mihai Aurelian Păun, Adrian Marius Ion, Tudor Zăgrean, Leon |
author_sort | Iliescu, Daniela Adriana |
collection | PubMed |
description | Our study investigated the changes produced by diabetes on the visual pathway in a Wistar rat model. The impact of diabetes at 10 weeks after intraperitoneal streptozotocin (STZ) injection was evaluated through electrophysiological methods like visual evoked potentials (VEP) and electroretinogram (ERG). VEP and ERG were recorded simultaneously under different sevoflurane anesthetic depths. In all tested concentrations, sevoflurane affected the amplitude and latency of VEP and ERG component elements. With increasing anesthetic depths, sevoflurane increased the latencies of VEP N1, P1 and N2 peaks and ERG a- and b- waves in both control and diabetic animals. On the other hand, the amplitude of VEP showed enhancement in higher concentrations of sevoflurane, contrariwise to the drop of amplitude seen in the ERG. Diabetes additionally increased the latencies of VEP peaks and decreased the N1-P1 amplitude of the VEP when compared to control at the same anesthetic depth. The a- and b- waves were also delayed by diabetes at 10 weeks post-STZ diabetic induction, with the exception of highly profound anesthetic depth in which the result for the b wave were conflicting. We found a reduction in amplitude of the a-b wave in diabetic animals, when ERG was recorded under 6% and 8% sevoflurane concentration. In conclusion, neurophysiological studies like VEP and ERG are useful in the assessment of retinal and optic nerve dysfunctions produced by diabetes, yet considering the alterations that occur during anesthesia if this is used. |
format | Online Article Text |
id | pubmed-5959023 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Romanian Society of Ophthalmology |
record_format | MEDLINE/PubMed |
spelling | pubmed-59590232018-05-24 Electrophysiologic evaluation of the visual pathway at different depths of sevoflurane anesthesia in diabetic rats Iliescu, Daniela Adriana Ciubotaru, Alexandra Ghiţă, Mihai Aurelian Păun, Adrian Marius Ion, Tudor Zăgrean, Leon Rom J Ophthalmol General Articles Our study investigated the changes produced by diabetes on the visual pathway in a Wistar rat model. The impact of diabetes at 10 weeks after intraperitoneal streptozotocin (STZ) injection was evaluated through electrophysiological methods like visual evoked potentials (VEP) and electroretinogram (ERG). VEP and ERG were recorded simultaneously under different sevoflurane anesthetic depths. In all tested concentrations, sevoflurane affected the amplitude and latency of VEP and ERG component elements. With increasing anesthetic depths, sevoflurane increased the latencies of VEP N1, P1 and N2 peaks and ERG a- and b- waves in both control and diabetic animals. On the other hand, the amplitude of VEP showed enhancement in higher concentrations of sevoflurane, contrariwise to the drop of amplitude seen in the ERG. Diabetes additionally increased the latencies of VEP peaks and decreased the N1-P1 amplitude of the VEP when compared to control at the same anesthetic depth. The a- and b- waves were also delayed by diabetes at 10 weeks post-STZ diabetic induction, with the exception of highly profound anesthetic depth in which the result for the b wave were conflicting. We found a reduction in amplitude of the a-b wave in diabetic animals, when ERG was recorded under 6% and 8% sevoflurane concentration. In conclusion, neurophysiological studies like VEP and ERG are useful in the assessment of retinal and optic nerve dysfunctions produced by diabetes, yet considering the alterations that occur during anesthesia if this is used. Romanian Society of Ophthalmology 2018 /pmc/articles/PMC5959023/ /pubmed/29796432 Text en ©Romanian Society of Ophthalmology http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | General Articles Iliescu, Daniela Adriana Ciubotaru, Alexandra Ghiţă, Mihai Aurelian Păun, Adrian Marius Ion, Tudor Zăgrean, Leon Electrophysiologic evaluation of the visual pathway at different depths of sevoflurane anesthesia in diabetic rats |
title | Electrophysiologic evaluation of the visual pathway at different depths of sevoflurane anesthesia in diabetic rats
|
title_full | Electrophysiologic evaluation of the visual pathway at different depths of sevoflurane anesthesia in diabetic rats
|
title_fullStr | Electrophysiologic evaluation of the visual pathway at different depths of sevoflurane anesthesia in diabetic rats
|
title_full_unstemmed | Electrophysiologic evaluation of the visual pathway at different depths of sevoflurane anesthesia in diabetic rats
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title_short | Electrophysiologic evaluation of the visual pathway at different depths of sevoflurane anesthesia in diabetic rats
|
title_sort | electrophysiologic evaluation of the visual pathway at different depths of sevoflurane anesthesia in diabetic rats |
topic | General Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5959023/ https://www.ncbi.nlm.nih.gov/pubmed/29796432 |
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