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受近端相互作用影响的 d-苎烯通过凋亡和脂肪变性对胚胎斑马鱼(Danio rerio)体内固有有害作用的控制。

Controlled in vivo intrinsic detrimental effect of d-Limonene channelized by influential proximal interaction through apoptosis and steatosis in embryonic zebrafish (Danio rerio).

机构信息

School of Biotechnology, KIIT University, Bhubaneswar, Odisha, India.

Markham College of Commerce, Vinoba Bhave University, Hazaribagh, Jharkhand 825001, India.

出版信息

Sci Total Environ. 2024 Nov 1;949:175243. doi: 10.1016/j.scitotenv.2024.175243. Epub 2024 Aug 2.

Abstract

Bioaccumulation of d-Limonene in environment due to the aggrandised usage of their natural sources like citrus food wastes and industrial day to day life products has raised concern to their biotoxicity to environment biotic health. Moreover, their after-usage discharge to aquatic system has enhanced the distress of posing threat and needs attention. This study entails mechanistic and molecular evaluation of in-vivo biotoxicity of d-Limonene in zebrafish embryo models. Experimental analysis excavated the controlled concentration-dependent morphological, physiological and cellular in-vivo impact of d-Limonene in zebrafish embryos through significant changes in oxidative stress, steatosis and apoptosis regulated via 6-fold and 5-fold mRNA expression change in p53 and Sod1 genes. Computational evaluation deduced the cellular mechanism of d-limonene biotoxicity as irregularities in oxidative stress, apoptosis and steatosis due of their intrinsic interaction with metabolic proteins like Zhe1a (-4.8 Kcal/mol), Sod1(-5.3 Kcal/mol), p53, caspase3 and apoa1 leading to influential change in structural and functional integrity of the metabolic proteins. The study unravelled the measured in-vivo biotoxicity of d-Limonene at cellular and molecular level to advocate the controlled usage of d-Limonene related natural and industrial product for a sustainable environmental health.

摘要

由于柑橘类食物废物和工业日常产品等天然资源的使用增加,d-柠檬烯在环境中的生物蓄积引起了人们对其生物毒性对环境生物健康的关注。此外,它们使用后的排放到水生系统中增加了威胁的紧迫性,需要引起重视。本研究涉及在斑马鱼胚胎模型中对 d-柠檬烯的体内生物毒性进行机制和分子评估。通过 p53 和 Sod1 基因的 mRNA 表达变化倍数分别为 6 倍和 5 倍,实验分析揭示了 d-柠檬烯在斑马鱼胚胎中对氧化应激、脂肪变性和细胞凋亡的浓度依赖性形态、生理和细胞体内影响的控制浓度依赖性。计算评估推断了 d-柠檬烯生物毒性的细胞机制,由于其与代谢蛋白如 Zhe1a(-4.8 Kcal/mol)、Sod1(-5.3 Kcal/mol)、p53、caspase3 和 apoa1 的内在相互作用,导致代谢蛋白的结构和功能完整性发生了有影响的变化,从而导致氧化应激、细胞凋亡和脂肪变性的不规律。该研究揭示了 d-柠檬烯在细胞和分子水平上的体内生物毒性,以提倡在可持续的环境健康方面对与 d-柠檬烯相关的天然和工业产品进行控制使用。

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