鹿血磷脂(DBP)对玉米赤霉烯酮诱导的猪肥大细胞氧化损伤的保护作用和机制。

Neuro endocrinology letters Pub Date : 2024-08-12
Yile Sun, Hongmei Gao, Yiwei Wang, Guoshi Liu, Bingyuan Wang, Huansheng Han
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引用次数: 0

摘要

背景:猪的 Sertoli 细胞(SCs)比其他物种更容易受到环境的伤害。我们观察到,玉米赤霉烯酮(ZEA)是一种普遍存在的食品污染物,会导致 Sertoli 细胞氧化损伤并抑制其增殖。因此,我们选择了一种天然抗氧化剂,即鹿血磷脂(DBP),来测试其对 SCs 的潜在保护作用:收集猪睾丸新鲜样本,分离、培养和鉴定原代猪 SCs。方法:采集猪睾丸新鲜样本,分离、培养并鉴定原代猪 SCs,检测不同浓度 ZEA 24 小时诱导 SCs 中的 ROS 水平,并建立氧化损伤模型。在损伤后 24 小时向 SCs 中添加 DBP 后,用 ELISA 试剂盒检测氧化和抗氧化指标。最后,通过RNA-seq解释了DBP的保护机制:结果表明,DBP能有效防止ZEA诱导的生殖毒性。DBP的保护作用主要由其强大的抗氧化能力介导。DBP 提高了内源性抗氧化酶(包括 CAT 和 GSH-PX)的活性,降低了细胞内 ROS 水平和 MDA。此外,DBP 还能促进 SCs 增殖。转录组测序结合 DEGs、GO 和 KEGG 分析表明,DBP 处理富集了各种具有潜在生物学意义的信号通路,包括 MAPK 和 PI3K-Akt 信号通路。这两条通路还能促进细胞增殖。EdU 检测进一步证实了 DBP 对 SCs 增殖的有利影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Protective effects and mechanisms of deer blood phospholipids (DBP) on zearalenone-induced oxidative damage in swine Sertoli cells.

Background: The swine Sertoli cells (SCs) are more vulnerable to the environmental insults than other species. We observed that zearalenone (ZEA), a prevalent food contaminant, caused SCs oxidative damage and inhibits their proliferation. Therefore, a naturally occurring antioxidant, i.e., the deer blood phospholipids (DBP) has been selected to test its potentially protective effects on SCs.

Methods: Collect fresh samples of swine testicles, isolated, cultured and identified primary swine SCs. The ROS levels in SCs 24 h induced by different concentrations of ZEA were detected, and the oxidative damage model was established. After DBP was added to the SCs 24 h after the damage, the oxidative and antioxidant indexes were detected by ELISA kit. Finally, the protective mechanism of DBP was explained by RNA-seq.

Results: The results showed that DBP effectively protected against the reproductive toxicity induced by ZEA. The protective effects of DBP were mainly mediated by its potent antioxidative capacity. DBP upregulated the activities of the endogenous antioxidant enzymes including CAT and GSH-PX and reduced intracellular ROS level and MDA. In addition, DBP also promoted the SCs proliferation. The transcriptome sequencing combined with DEGs, GO and KEGG analyses suggested that DBP treatment enriched various signaling pathways of potentially biological significance including MAPK and PI3K-Akt signaling pathways. Both pathways also promote the cell proliferation. EdU assay further confirmed the beneficial effects of DBP on SCs proliferation.

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