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暴露于苯并[a]芘和光下的卵形鲷(Epinephelus coioides)肝细胞培养物会导致抗氧化酶测量的氧化损伤。

Exposure of liver cell culture from the orange-spotted grouper, Epinephelus coioides, to benzo[a]pyrene and light results in oxidative damage as measured by antioxidant enzymes.

机构信息

Department of Marine Biology, Faculty of Marine Sciences, Khorramshahr University of Marine Science and Technology, Khorramshahr, Iran.

Department of Marine Biology, Faculty of Marine Sciences, Khorramshahr University of Marine Science and Technology, Khorramshahr, Iran.

出版信息

Chemosphere. 2019 Jul;226:534-544. doi: 10.1016/j.chemosphere.2019.03.181. Epub 2019 Mar 29.

Abstract

Among the various toxicants discharged into aquatic environments, benzo (a) pyrene (BaP) has been shown to effect on the antioxidant system of fish and the evaluation of its impact on biota is of considerable concern. The aim of the present study was to use the primary hepatocyte culture obtained from the orange-spotted grouper, Epinephelus coioides, to evaluate the adverse effects of benzo (a) pyrene (BaP) on cell viability and liver antioxidant system. BaP was selected for its high ability to produce reactive oxygen species (ROS) and oxidative stress. The liver was minced by a scalpel and digested in the PBS solution with 0.1% collagenase IV at room temperature for 20 min. Then, the cell suspension was transferred to a plate contained an equal amount of Leibovitz's L-15 medium with 20% fetal bovine serum (FBS), 100 IU mL of penicillin and 100 μg mL streptomycin. 5 mL of cell suspension were plated into sterile 25 cm tissue culture flasks at the density of 1.5 × 10 cell/ml L-15 and incubated at 30 °C for two weeks. The medium was renewed after 24-48 h. The number of the liver cells was adjusted to 4 × 10 after two weeks. 10 mol l was verified by MTT assay as the IC50 of BaP. Then, hepatocytes were exposed to three concentrations of BaP (10, 2 × 10, 3 × 10 mol L) and incubated for 24 h. Samples were collected after 6, 12 and 24 h and the amounts of SOD, CAT, GPx, LPO, LDH, AST, ALT, ALP and total protein were analyzed. The results showed that, 10 mol L of BaP was not significantly toxic to cultivated hepatocytes, however, the sensitivity of cells to BaP increased in a dose-related pattern. The activity of the antioxidant enzymes (SOD, CAT and GPx) and liver enzymes (ALT, AST, ALP, LDH) significantly increased, though the amount of LPO, total antioxidant power and total protein decreased dose-dependently in BaP-exposed cells. In conclusion, according to the finding of the present study, BaP has a high potential to induce the oxidative stress in primary liver cell culture of E. coioides.

摘要

在排入水生环境的各种毒物中,苯并(a)芘(BaP)已被证明会影响鱼类的抗氧化系统,因此评估其对生物群的影响受到了相当大的关注。本研究的目的是使用从橙斑石斑鱼(Epinephelus coioides)获得的原代肝细胞培养物来评估苯并(a)芘(BaP)对细胞活力和肝脏抗氧化系统的不良影响。选择 BaP 是因为它具有产生活性氧 (ROS) 和氧化应激的高能力。用手术刀将肝脏切碎,然后在含有 0.1%胶原酶 IV 的 PBS 溶液中于室温下消化 20 分钟。然后,将细胞悬液转移到含有等量 Leibovitz 的 L-15 培养基的平板中,其中含有 20%胎牛血清 (FBS)、100 IU mL 青霉素和 100μg mL 链霉素。将 5mL 细胞悬液以 1.5×10 个细胞/ml L-15 的密度接种到无菌 25cm 组织培养瓶中,在 30°C 下孵育两周。24-48 小时后更换培养基。两周后将肝细胞数量调整至 4×10。通过 MTT 测定证实 10mol L 是 BaP 的 IC50。然后,将肝细胞暴露于三种浓度的 BaP(10、2×10、3×10mol L)并孵育 24 小时。在 6、12 和 24 小时后收集样品,并分析 SOD、CAT、GPx、LPO、LDH、AST、ALT、ALP 和总蛋白的含量。结果表明,10mol L 的 BaP 对培养的肝细胞没有明显毒性,然而,细胞对 BaP 的敏感性呈剂量相关模式增加。抗氧化酶(SOD、CAT 和 GPx)和肝酶(ALT、AST、ALP、LDH)的活性显著增加,而 BaP 暴露细胞中的 LPO、总抗氧化能力和总蛋白的量则呈剂量依赖性下降。总之,根据本研究的结果,BaP 具有诱导 E. coioides 原代肝培养物氧化应激的高潜力。

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