红花HSYA减轻肝缺血再灌注损伤的氧化应激、炎症和细胞凋亡。

IF 1.3 4区 医学 Q4 PHARMACOLOGY & PHARMACY
Jianhua Liao, Chunyan Meng, Jun Cheng, Baoqing Liu, Yuzhi Shao
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引用次数: 0

摘要

肝缺血再灌注损伤(IRI)是肝移植和手术中常见的并发症,以氧化应激、炎症和细胞凋亡为特征,可导致肝细胞损伤和肝功能受损。红花以其抗氧化和抗炎特性而闻名,但其缓解肝脏IRI的潜力尚未得到充分探索。本研究旨在探讨红花成分对肝脏IRI中氧化应激和细胞凋亡的影响。采用微流控肝细胞缺血再灌注模型,筛选红花成分对氧化应激和细胞凋亡的保护作用。通过测量细胞活力、ROS水平、凋亡、DNA损伤(8-oxo-dG)、脂质过氧化(MDA)和炎症细胞因子(TNF-α、IL-1β、IL-6)的产生来评估HSYA和其他化合物的作用。HSYA表现出优异的保护作用,显著减少ROS、细胞凋亡、DNA损伤和脂质过氧化。它还能降低促炎细胞因子水平,强调其抗氧化和抗炎特性。这些发现表明,HSYA可有效减轻肝脏IRI中的氧化应激、炎症和细胞凋亡,使其成为治疗性肝脏保护的有希望的候选药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
HSYA from safflower mitigates oxidative stress, inflammation, and apoptosis in liver ischemia-reperfusion injury.

Liver ischemia-reperfusion injury (IRI) is a common complication during liver transplantation and surgery, characterised by oxidative stress, inflammation, and apoptosis, which contribute to hepatocyte damage and impaired liver function. Safflower, known for its antioxidant and anti-inflammatory properties, has not been fully explored for its potential to alleviate liver IRI.This study aims to investigate the effects of safflower components on oxidative stress and cell apoptosis in liver IRI. A microfluidic liver cell ischemia-reperfusion model was employed to screen safflower components for their protective effects against oxidative stress and apoptosis. The effects of HSYA and other compounds were assessed by measuring cell viability, ROS levels, apoptosis, DNA damage (8-oxo-dG), lipid peroxidation (MDA), and inflammatory cytokine production (TNF-α, IL-1β, IL-6). HSYA exhibited superior protective effects, significantly reducing ROS, apoptosis, DNA damage, and lipid peroxidation. It also decreased pro-inflammatory cytokine levels, underscoring its antioxidant and anti-inflammatory properties.These findings suggest that HSYA effectively mitigates oxidative stress, inflammation, and apoptosis in liver IRI, positioning it as a promising candidate for therapeutic liver protection.

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来源期刊
Xenobiotica
Xenobiotica 医学-毒理学
CiteScore
3.80
自引率
5.60%
发文量
96
审稿时长
2 months
期刊介绍: Xenobiotica covers seven main areas, including:General Xenobiochemistry, including in vitro studies concerned with the metabolism, disposition and excretion of drugs, and other xenobiotics, as well as the structure, function and regulation of associated enzymesClinical Pharmacokinetics and Metabolism, covering the pharmacokinetics and absorption, distribution, metabolism and excretion of drugs and other xenobiotics in manAnimal Pharmacokinetics and Metabolism, covering the pharmacokinetics, and absorption, distribution, metabolism and excretion of drugs and other xenobiotics in animalsPharmacogenetics, defined as the identification and functional characterisation of polymorphic genes that encode xenobiotic metabolising enzymes and transporters that may result in altered enzymatic, cellular and clinical responses to xenobioticsMolecular Toxicology, concerning the mechanisms of toxicity and the study of toxicology of xenobiotics at the molecular levelXenobiotic Transporters, concerned with all aspects of the carrier proteins involved in the movement of xenobiotics into and out of cells, and their impact on pharmacokinetic behaviour in animals and manTopics in Xenobiochemistry, in the form of reviews and commentaries are primarily intended to be a critical analysis of the issue, wherein the author offers opinions on the relevance of data or of a particular experimental approach or methodology
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