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未分化人神经母细胞瘤 SH-SY5Y 细胞提取物对乙基对氧磷的解毒作用。

Detoxification of paraoxon-ethyl by extracts in undifferentiated human neuroblastoma SH-SY5Y cells.

机构信息

Chulabhorn International College of Medicine, Thammasat University, Pathumthani, Thailand.

出版信息

Pharm Biol. 2024 Dec;62(1):882-891. doi: 10.1080/13880209.2024.2430262. Epub 2024 Nov 25.

Abstract

CONTEXT

(Craib) A. Schmitz. (Fabaceae) is a Thai traditional medicine used to remove food and alcohol toxins from the body.

OBJECTIVE

This study investigates the molecular mechanism of extracts against paraoxon-ethyl-induced apoptosis in SH-SY5Y cells.

MATERIALS AND METHODS

The ethanol and water extracts of leaves and stems of were prepared at various concentrations (0-100 μg/mL) and co-treated to the cells with 0.375 mM paraoxon-ethyl for 24 and 48 h. Cell viability was performed using the PrestoBlue assay. ROS and caspase activity were detected using 2',7'-dichlorodihydrofluorecein diacetate and caspase-Glo® 3/7, 8, and 9 assay kits. Apoptotic and ER stress-related gene expression were determined by real-time PCR, and nuclear and mitochondrial morphology were observed using Hoechst 33342 and MitoTracker® Deep Red FM staining.

RESULTS

The most effective concentrations of each extract against paraoxon-ethyl-induced cell death were 25 μg/mL of leaf ethanol, 12.5 μg/mL of stem ethanol, 100 μg/mL of leaf water, and 25 μg/mL of stem water extracts. The leaf ethanol extract was the most effective at detoxifying, while stem extracts were highly toxic in high doses. The detoxifying extracts against paraoxon-ethyl-induced oxidative stress decreased , and gene expression and minimized caspase 9 and caspase 3, protecting cells from apoptosis. The extracts could also restore mitochondrial membrane potential and reduce the swollen globule mitochondrial shape.

DISCUSSION AND CONCLUSION

These findings could potentially protect neuron cells from neurodegenerative issues due to oxidative damage, apoptosis, and other potential consequences.

摘要

背景

(Craib)A. Schmitz(豆科)是一种泰国传统药物,用于清除体内的食物和酒精毒素。

目的

本研究旨在探讨叶和茎的乙醇和水提取物对抗 0.375mM 对氧磷乙基诱导的 SH-SY5Y 细胞凋亡的分子机制。

材料和方法

制备不同浓度(0-100μg/mL)的叶和茎的乙醇和水提取物,并与 0.375mM 对氧磷乙基共同处理细胞 24 和 48h。采用 PrestoBlue 法检测细胞活力。用 2',7'-二氯二氢荧光素二乙酸酯和 caspase-Glo®3/7、8 和 9 检测试剂盒检测 ROS 和 caspase 活性。通过实时 PCR 测定凋亡和 ER 应激相关基因的表达,并通过 Hoechst 33342 和 MitoTracker®Deep Red FM 染色观察核和线粒体形态。

结果

每种提取物对抗对氧磷乙基诱导的细胞死亡的最有效浓度分别为叶乙醇提取物 25μg/mL、茎乙醇提取物 12.5μg/mL、叶水提取物 100μg/mL 和茎水提取物 25μg/mL。叶乙醇提取物在解毒方面最有效,而茎提取物在高剂量下毒性很高。解毒提取物对抗对氧磷乙基诱导的氧化应激降低了 和 基因表达,并最小化了 caspase 9 和 caspase 3,保护细胞免受凋亡。提取物还可以恢复线粒体膜电位,减少肿胀的球状线粒体形状。

讨论和结论

这些发现可能有助于保护神经元细胞免受氧化损伤、凋亡和其他潜在后果引起的神经退行性问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe05/11600548/e426089f52f0/IPHB_A_2430262_F0001_C.jpg

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