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多加热食用油促进成年雄性大鼠肝肾功能早衰:橄榄苦苷的潜在再生能力。

Multiple-heated cooking oil promotes early hepatic and renal senescence in adult male rats: the potential regenerative capacity of oleuropein.

机构信息

Pharmacology Department, Zagazig University, Zagazig, Egypt.

Medicines Information Center, Zagazig University Hospitals, Zagazig, Egypt.

出版信息

Toxicol Mech Methods. 2024 Oct;34(8):936-953. doi: 10.1080/15376516.2024.2365431. Epub 2024 Jul 8.

Abstract

For economic purposes, cooking oil is repeatedly heated in food preparation, which imposes serious health threats. This study investigated the detrimental effects of multiple-heated cooking oil (MHO) on hepatic and renal tissues with particular focusing on cellular senescence (CS), and the potential regenerative capacity of oleuropein (OLE). Adult male rats were fed MHO-enriched diet for 8 weeks and OLE (50 mg/kg, PO) was administered daily for the last four weeks. Liver and kidney functions and oxidative stress markers were measured. Cell cycle markers p53, p21, cyclin D, and proliferating cell nuclear antigen (PCNA) were evaluated in hepatic and renal tissues. Tumor necrosis factor-α (TNF-α) and Bax were assessed by immunohistochemistry. General histology and collagen deposition were also examined. MHO disturbed hepatic and renal structures and functions. MHO-fed rats showed increased oxidative stress, TNF-α, Bax, and fibrosis in liver and kidney tissues. MHO also enhanced the renal and hepatic expression of p53, p21, cyclin D and PCNA. On the contrary, OLE mitigated MHO-induced oxidative stress, inflammatory burden, apoptotic and fibrotic changes. OLE also suppressed CS and preserved kidney and liver functions. Collectively, OLE displays marked regenerative capacity against MHO-induced hepatic and renal CS, its potent antioxidant and anti-inflammatory effects.

摘要

出于经济目的,食用油在食品制备过程中会被反复加热,这给健康带来了严重威胁。本研究主要探讨了多次加热食用油(MHO)对肝脏和肾脏组织的有害影响,特别关注细胞衰老(CS),以及橄榄苦苷(OLE)的潜在再生能力。成年雄性大鼠喂食富含 MHO 的饮食 8 周,并在最后 4 周每天给予 OLE(50mg/kg,PO)。测量肝脏和肾脏功能以及氧化应激标志物。评估肝肾功能衰竭患者肝脏和肾脏组织中的细胞周期标志物 p53、p21、细胞周期蛋白 D 和增殖细胞核抗原(PCNA)。通过免疫组织化学评估肿瘤坏死因子-α(TNF-α)和 Bax。还检查了一般组织学和胶原蛋白沉积。MHO 扰乱了肝脏和肾脏的结构和功能。MHO 喂养的大鼠表现出肝脏和肾脏组织中氧化应激、TNF-α、Bax 和纤维化增加。MHO 还增强了肾脏和肝脏中 p53、p21、细胞周期蛋白 D 和 PCNA 的表达。相反,OLE 减轻了 MHO 诱导的氧化应激、炎症负担、细胞凋亡和纤维化变化。OLE 还抑制了 CS 并维持了肾脏和肝脏功能。总的来说,OLE 对 MHO 诱导的肝脏和肾脏 CS 具有显著的再生能力,具有强大的抗氧化和抗炎作用。

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