Phoenix dactylifera 果实中的水溶性酚类化合物作为潜在的顺铂诱导毒性再保护剂:处理前和处理后策略

IF 2.1 4区 医学 Q3 CHEMISTRY, MULTIDISCIPLINARY
Drug and Chemical Toxicology Pub Date : 2024-11-01 Epub Date: 2024-03-26 DOI:10.1080/01480545.2024.2329762
Omowumi Oyeronke Adewale, Roseline Fadera Oyelola, Oluwatosin Adefunke Adetuyi, Oluwaseun Abraham Adebisi, Damilare Adedayo Adekomi, Johnson Olaleye Oladele
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引用次数: 0

摘要

顺铂是一种有效的铂类化疗药物,可用于治疗多种实体组织癌症,肾毒性是顺铂的主要副作用。研究表明,某些水溶性酚类物质具有保护肾脏的作用。因此,本研究调查了用 Phoenix dactylifera(PdP)中的水溶性酚类化合物对大鼠进行前后处理对顺铂引起的肾毒性的作用。在连续 7 天腹腔注射单次治疗剂量的顺铂(5 毫克/千克体重)之前或之后,用 200 毫克/千克体重的 PdP 对大鼠进行口服预处理或后处理。PdP 对顺铂诱导的肾毒性的保护作用是基于对各种生化和氧化还原生物标志物的评估,以及对肾组织的组织病理学检查。根据色谱、光谱和体外抗氧化模型确定了钯的成分、结构特征和抗氧化影响。顺铂单次暴露导致测试的肾功能生物标志物(尿酸、肌酐和尿素水平)大幅增加,同时丙二醛增加,表明脂质过氧化,而顺铂单次暴露则显著下降(p
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Water-soluble phenolics from Phoenix dactylifera fruits as potential reno-protective agent against cisplatin-induced toxicity: pre- and post-treatment strategies.

Nephrotoxicity is the major side effect of cisplatin, an effective platinum-based chemotherapeutic drug that is applicable in the treatment of several solid-tissue cancers. Studies have indicated that certain water-soluble phenolics offer renal protection. Thus, this study investigates the role of pre and post-treatment of rats with water-soluble phenolics from Phoenix dactylifera (PdP) against nephrotoxicity induced by cisplatin. Rats were either orally pretreated or post-treated with 200 mg/kg body weight of PdP before or after exposure to a single therapeutic dose of cisplatin (5 mg/kg body weight) for 7 successive days intraperitoneally. The protective effects of PdP against Cisplatin-induced nephrotoxicity was based on the evaluation of various biochemical and redox biomarkers, together with histopathological examination of kidney tissues. The composition, structural features, and antioxidative influence of PdP were determined based on chromatographic, spectroscopic, and in vitro antioxidative models. Cisplatin single exposure led to a substantial increase in the tested renal function biomarkers (uric acid, creatinine, and urea levels), associated with an increase in malondialdehyde indicating lipid peroxidation and a significant decline (p < 0.05) in reduced glutathione (GSH) levels in the renal tissue when compared with the control group. A marked decline exists in the kidney antioxidant enzymes (catalase, SOD, and GPx). Nevertheless, treatment with PdP significantly suppressed the heightened renal function markers, lipid peroxidation, and oxidative stress. Spectroscopic analysis revealed significant medicinal phenolics, and in vitro tests demonstrated antioxidative properties. Taken together, results from this study indicate that pre- and/or post-treatment strategies of PdP could serve therapeutic purposes in cisplatin-induced renal damage.

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来源期刊
Drug and Chemical Toxicology
Drug and Chemical Toxicology 医学-毒理学
CiteScore
6.00
自引率
3.80%
发文量
99
审稿时长
3 months
期刊介绍: Drug and Chemical Toxicology publishes full-length research papers, review articles and short communications that encompass a broad spectrum of toxicological data surrounding risk assessment and harmful exposure. Manuscripts are considered according to their relevance to the journal. Topics include both descriptive and mechanics research that illustrates the risk assessment implications of exposure to toxic agents. Examples of suitable topics include toxicological studies, which are structural examinations on the effects of dose, metabolism, and statistical or mechanism-based approaches to risk assessment. New findings and methods, along with safety evaluations, are also acceptable. Special issues may be reserved to publish symposium summaries, reviews in toxicology, and overviews of the practical interpretation and application of toxicological data.
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