Abstract:Penoxsulam is a new sulfonamide herbicide used on rice crops for annual grasses, broadleaf weeds, and sedges control, either grown through transplanting or direct dry or direct seeding methods of planting. In this study, Allium cepa ana-telophase and comet assay were used to examine the cyto-genotoxic effects of herbicide penoxsulam on A. cepa roots. A. cepa bulbs were exposed to ½xEC50 (12.5 µg/L), EC50 (25 µg/L) and 2xEC50 (50 µg/L) concentrations of penoxsulam for 24, 48, 72 and 96 h. Distilled water and 10… Show more
“…Genotoxicity of the used herbicide is higher than normal with use of the highest concentration (1.6 ppm) for each application period. These outcomes agree with former studies (Ping et al, 2012;Karaismailoğlu et al, 2013;Karaismailoğlu, 2014bKaraismailoğlu, , 2015Bonciu et al, 2018;Liman and Özkan, 2019;Rosculete et al,2019;Aydın and Liman, 2020).…”
Section: Discussionsupporting
confidence: 93%
“…In this work, sublethal impact has found in 1.6 ppm concentration when compared to the control in 12, 24 and 36 h treatments, and sublethal impact valuation are defined as 35.50%, 34.96% and 46.16%, respectively. The obtained outcomes are suitable with the results of the earlier works (Liman et al, 2011;Dragoeva et al, 2012;Karaismailoglu, 2015;Liman and Özkan, 2019).…”
In this work, the cytotoxic and genotoxic influences of oxyfluorfen herbicide were surveyed by examining of mitotic index, mitotic stages, chromosomal anomalies, micronucleus percentage, and comet assay parameters on the somatic cells of Allium cepa. The roots were treated with 0.2, 0.4, 0.8 and 1.6 ppm herbicide concentrations with 12, 24 and 36 h. application periods. Mitotic index was noticeably diminished by oxyfluorfen in each application group when matched with their control, except for 0.2 ppm. The percentages of mitotic stages were altered. Oxyfluorfen enhanced drastically the aberrant cell ratio at all application groups and application periods in contrast to their control, excluding 0.2 ppm. Mitotic anomalies were noted as disturbed prophase, stickiness, C-mitosis, chromatid bridges and laggards. The micronucleus was detected at interphase and its percentage was determined in the applied concentrations. Also, the comet assay was employed to examine the single strand breakages. Almost all of the used concentrations of oxyfluorfen increased DNA losses. A positive relationship was discovered between micronucleus occurrence and DNA loss.
“…Genotoxicity of the used herbicide is higher than normal with use of the highest concentration (1.6 ppm) for each application period. These outcomes agree with former studies (Ping et al, 2012;Karaismailoğlu et al, 2013;Karaismailoğlu, 2014bKaraismailoğlu, , 2015Bonciu et al, 2018;Liman and Özkan, 2019;Rosculete et al,2019;Aydın and Liman, 2020).…”
Section: Discussionsupporting
confidence: 93%
“…In this work, sublethal impact has found in 1.6 ppm concentration when compared to the control in 12, 24 and 36 h treatments, and sublethal impact valuation are defined as 35.50%, 34.96% and 46.16%, respectively. The obtained outcomes are suitable with the results of the earlier works (Liman et al, 2011;Dragoeva et al, 2012;Karaismailoglu, 2015;Liman and Özkan, 2019).…”
In this work, the cytotoxic and genotoxic influences of oxyfluorfen herbicide were surveyed by examining of mitotic index, mitotic stages, chromosomal anomalies, micronucleus percentage, and comet assay parameters on the somatic cells of Allium cepa. The roots were treated with 0.2, 0.4, 0.8 and 1.6 ppm herbicide concentrations with 12, 24 and 36 h. application periods. Mitotic index was noticeably diminished by oxyfluorfen in each application group when matched with their control, except for 0.2 ppm. The percentages of mitotic stages were altered. Oxyfluorfen enhanced drastically the aberrant cell ratio at all application groups and application periods in contrast to their control, excluding 0.2 ppm. Mitotic anomalies were noted as disturbed prophase, stickiness, C-mitosis, chromatid bridges and laggards. The micronucleus was detected at interphase and its percentage was determined in the applied concentrations. Also, the comet assay was employed to examine the single strand breakages. Almost all of the used concentrations of oxyfluorfen increased DNA losses. A positive relationship was discovered between micronucleus occurrence and DNA loss.
“…However, the application of blueberry extracts either alone or in combination with penoxsulam enhanced the mitotic index in a concentration-dependent manner emphasizing the protective role of blueberry extract. Similar inhibitory effects of penoxsulam on root growth and mitotic activity were reported by Özkan and Liman 63 . Panneerselvam et al .…”
The present study aimed at exploring to explore the penoxsulam toxicity and protective effects of blueberry extract in roots of Allium cepa L. The effective concentration (EC50) of penoxsulam was determined at 20 µg/L by the root growth inhibition test as the concentration reducing the root length by 50%. The bulbs of A. cepa L. were treated with tap water, blueberry extracts (25 and 50 mg/L), penoxsulam (20 µg/L) and combination of blueberry extracts (25 and 50 mg/L) with penoxsulam (20 µg/L) for 96 h. The results revealed that penoxsulam exposure inhibited cell division, rooting percentage, growth rate, root length and weight gain in the roots of A. cepa L. In addition, it induced chromosomal anomalies such as sticky chromosome, fragment, unequal distribution of chromatin, bridge, vagrant chromosome and c-mitosis and DNA strand breaks. Further, penoxsulam treatment enhanced malondialdehyde content and SOD, CAT and GR antioxidant enzyme activities. Molecular docking results supported the up-regulation of antioxidant enzyme SOD, CAT and GR. Against all these toxicity, blueberry extracts reduced penoxsulam toxicity in a concentration-dependent manner. The highest amount of recovery for cytological, morphological and oxidative stress parameters was observed when using blueberry extract at a concentration of 50 mg/L. In addition, blueberry extracts application showed a positive correlation with weight gain, root length, mitotic index and rooting percentage whereas a negative correlation with micronucleus formation, DNA damage, chromosomal aberrations, antioxidant enzymes activities and lipid peroxidation indicating its protecting effects. As a result, it has been seen that the blueberry extract can tolerate all these toxic effects of penoxsulam depending on the concentration, and it has been understood that it is a good protective natural product against such chemical exposures.
“…In literature, there are records on the cytotoxicity and genotoxicity of sulfonamides. Özkan and Liman reported that the penoxsulam, is a sulfonamide herbicide, showed a cytotoxic effect by reducing MI, a genotoxic effect because it increased CA, which are stickiness, anaphase bridge, disturbed anaphasetelophase, chromosomal laggards, and polyploidy [7]. Badr (1982) analysed the cytogenetic effects of 3 sulphonamides, which were sulphadiazine, sulphadimidine, and sulphaphenazole and showed the mitotic and chromosomal abnormalities [21].…”
“…The sulfasalazine (azulfidine), sulfamethoxazole (gantanol), sulfapiridine, sulfacetamide, and sulfadiazine, which are derivatives of sulfonamide and have a commercial market share, are important drug examples [6]. In addition, sulfonamide derivative are important compounds used as plant growth regulator [7]. The Allium test was first conducted by Levan (1938) to determine the effect of colchicine.…”
The continuous production and release into the environment of chemicals has revealed the need to determine their cytotoxicity and genotoxicity. Sulfonamide-aldehyde (SA) derivatives, whose biological activity properties vary in a wide spectrum, are frequently used in agriculture, medicine, pharmacy and many other fields. These compounds have an important cycle in the ecological system due to their use and diversity. In the present study, the potential cytotoxic and genotoxic effects of sulfonamide-aldehyde derivative were investigated using Allium test system with the concentrations of 6.25, 12.5, 25, 50, and 100 µM. In A. cepa cells, the increasing concentrations of SA caused cytotoxic effects by inducing nuclear lesions and inhibition of mitotic index. In addition, the increasing concentrations of SA caused genotoxic effects by inducing micronucleus and chromosome aberrations, which the most common ones are C-mitosis, sticky metaphase, and anaphase bridge. The results indicate that the concentration of 25 µM is EC50 in micronucleus, nuclear lesions, and chromosome aberrations; and 50 µM is EC50 in mitotic index (p < 0.05).
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.