FENTANYL GENOTOXICITY EVALUATION VIA COMET ASSAY

DNA is our main genetic structure that can be affected by various molecules we come into contact with. Therefore, there is a high probability of DNA damage. Genotoxicity tests involve systematic methods designed to assess the safety of drugs and chemicals. Comet assay evaluates the possible genotoxicity resulting from DNA single-strand breaks.Fentanyl is a powerful painkiller from the group called opioid analgesics administered intravenously. In this research, we evaluated the possible DNA damage in human lymphocytes after fentanyl exposure via single-cell gel electrophoresis (Comet Assay). DNA damage in healthy human peripheral lymphocytes treated with fentanyl was investigated via comet assay. Lymphocytes were treated with 5, 10, 20, and 40 µg/mL doses of fentanyl for 1 hour. After the incubation period, the cells' DNA tail length, tail intensity, and tail moment values were evaluated by comparing them with the spontaneous control and positive control data. EtBr stained slides were visualized under the fluorescent microscope. Fentanyl induced the comet parameters such as tail length, tail intensity, and tail moment but dose-dependent increase was not obtained after fentanyl administration. Fentanyl showed the highest tail length and tail moment value at the dose of 10 µg/mL. The highest tail intensity value was obtained at the dose of 40 µg/mL fentanyl administration.This study aimed to reveal previously undiscovered genotoxicity of fentanyl on healthy human lymphocytes in vitro via comet assay. Fentanyl exposure induces DNA damage in healthy human lymphocytes, as shown via comet parameters (tail length, tail intensity, and tail moment). Genotoxic effect does not display a consistent dose-dependent increase.

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Publication Details

Journal
DergiPark (Istanbul University)
Published
2024-12-29
DOI
https://doi.org/10.18036/estubtdc.1609497
Primary Topic
Carcinogens and Genotoxicity Assessment
Type
article
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article

FENTANYL GENOTOXICITY EVALUATION VIA COMET ASSAY

Öge Artagan, Bahar Köklü
DergiPark (Istanbul University)
Carcinogens and Genotoxicity Assessment
article

FENTANYL GENOTOXICITY EVALUATION VIA COMET ASSAY

Öge Artagan, Bahar Köklü
article en

Abstract

DNA is our main genetic structure that can be affected by various molecules we come into contact with. Therefore, there is a high probability of DNA damage. Genotoxicity tests involve systematic methods designed to assess the safety of drugs and chemicals. Comet assay evaluates the possible genotoxicity resulting from DNA single-strand breaks.Fentanyl is a powerful painkiller from the group called opioid analgesics administered intravenously. In this research, we evaluated the possible DNA damage in human lymphocytes after fentanyl exposure via single-cell gel electrophoresis (Comet Assay). DNA damage in healthy human peripheral lymphocytes treated with fentanyl was investigated via comet assay. Lymphocytes were treated with 5, 10, 20, and 40 µg/mL doses of fentanyl for 1 hour. After the incubation period, the cells' DNA tail length, tail intensity, and tail moment values were evaluated by comparing them with the spontaneous control and positive control data. EtBr stained slides were visualized under the fluorescent microscope. Fentanyl induced the comet parameters such as tail length, tail intensity, and tail moment but dose-dependent increase was not obtained after fentanyl administration. Fentanyl showed the highest tail length and tail moment value at the dose of 10 µg/mL. The highest tail intensity value was obtained at the dose of 40 µg/mL fentanyl administration.This study aimed to reveal previously undiscovered genotoxicity of fentanyl on healthy human lymphocytes in vitro via comet assay. Fentanyl exposure induces DNA damage in healthy human lymphocytes, as shown via comet parameters (tail length, tail intensity, and tail moment). Genotoxic effect does not display a consistent dose-dependent increase.

DergiPark (Istanbul University)
Eskisehir Technical University (TR), Muğla University (TR)
Openalex Percentile: Top 65%
Carcinogens and Genotoxicity Assessment
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