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评估马拉硫磷对洋葱根系细胞生理活性、DNA 损伤和抗氧化酶的毒性作用。

Assessment of malathion toxicity on cytophysiological activity, DNA damage and antioxidant enzymes in root of Allium cepa model.

机构信息

Laboratory of Cytogenetics, Department of Botany, Banaras Hindu University, Varanasi, 221005, India.

出版信息

Sci Rep. 2020 Jan 21;10(1):886. doi: 10.1038/s41598-020-57840-y.

Abstract

The current study was emphasized to assess the effect of malathion on root system (cell division and kinetics of the root elongation) and stress related parameters in Allium cepa L. The roots were exposed to different concentrations (0.05, 0.13, 0.26, 0.39 and 0.52 g/L) of malathion for different treatment periods (4, 8 and 18 h). The results revealed that malathion application affected the growth rate and cell division in root tips. The root elongation kinetics were impaired at 0.13 to 0.52 g/L concentrations. Reduction in tissue water content (TWC) indicated the limited osmotic adjustment due to membrane damage. Further, a decrease in sucrose content was observed in contrast to the accumulation of proline (upto 0.39 g/L). Moreover, malathion exposure elevated the levels of lipid peroxidation followed by changes in antioxidant enzymes status. The activities of ascorbate peroxidase (APX) and glutathione reductase (GR) were down-regulated whereas the activities of catalase (CAT), glutathione-S-transferase (GST) and superoxide dismutase (SOD) were up-regulated except in 0.52 g/L malathion. The molecular docking study of malathion with CAT, GST, SOD, APX and GR also supported of above results for their activity. All these physiological responses varied with increasing malathion concentration and duration of treatment. The single cell gel electrophoresis results showed that all concentrations of malathion induced DNA damage in root cells. The findings depicted that malathion application induces cytotoxic and phytotoxic effects mediated through oxidative stress and subsequent injuries.

摘要

本研究旨在评估马拉硫磷对洋葱根系(细胞分裂和根伸长动力学)和应激相关参数的影响。将根系暴露于不同浓度(0.05、0.13、0.26、0.39 和 0.52 g/L)的马拉硫磷中不同的处理时间(4、8 和 18 h)。结果表明,马拉硫磷的应用影响根尖的生长速度和细胞分裂。根伸长动力学在 0.13 至 0.52 g/L 浓度下受到损害。组织含水量(TWC)的减少表明由于膜损伤导致的渗透调节有限。此外,与脯氨酸(高达 0.39 g/L)积累相反,观察到蔗糖含量减少。此外,马拉硫磷暴露会升高脂质过氧化水平,随后改变抗氧化酶的状态。抗坏血酸过氧化物酶(APX)和谷胱甘肽还原酶(GR)的活性下调,而 CAT、谷胱甘肽-S-转移酶(GST)和超氧化物歧化酶(SOD)的活性上调,除 0.52 g/L 马拉硫磷外。马拉硫磷与 CAT、GST、SOD、APX 和 GR 的分子对接研究也支持了它们的活性的上述结果。所有这些生理反应随马拉硫磷浓度和处理时间的增加而变化。单细胞凝胶电泳结果表明,马拉硫磷的所有浓度都诱导了根细胞的 DNA 损伤。研究结果表明,马拉硫磷的应用通过氧化应激和随后的损伤引起细胞毒性和植物毒性作用。

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