Polydatin作为缓解铅中毒的潜在候选药物:从铅诱导的Wistar大鼠的生化和氧化损伤中获得的见解

IF 1.8 Q3 PHARMACOLOGY & PHARMACY
Salisu M. Highab, Jamilu Ya’u, Muhammad G. Magaji, Dalhatu M. Shehu
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引用次数: 0

摘要

铅是最常见的重金属元素之一,具有很高的生物毒性。多靛素(PD),又称 piceid(3, 4′, 5-三羟基二苯乙烯-3-β-D-葡萄糖苷),是一种从蓼科植物蓼(Polygonum cuspidatum Sieb. et Zucc.)中分离出来的单晶化合物,也存在于水果和许多日常饮食中。这项研究的目的是将多靛红作为缓解铅中毒的潜在候选物质:从铅诱导的 Wistar 大鼠的生化和氧化损伤中获得启示。研究采用了 42 只 90 天大的 Wistar 大鼠(150-200 克),将其随机分为六(6)组,并根据 OECD 407 准则进行亚慢性毒性研究。对照组 DW(1 毫升/千克);PbAc(120 毫克/千克);PbAc(120 毫克/千克)+ PD(250 毫克/千克);PbAc(120 毫克/千克)+ PD(500 毫克/千克);PbAc(120 毫克/千克)+ PD(1000 毫克/千克);PbAc(120 毫克/千克)+ DMSA(10 毫克/千克),每天口服,共 16 周。治疗结束时,对血液、血浆和器官样本进行血铅含量(BLLs)、生化指标、氧化应激标记物和组织病理学评估。除总胆红素和直接胆红素明显升高(p < 0.05)外,PD 和 DMSA 能明显降低 PbAc 诱导的大鼠肝脏毒性指标(p < 0.05)。PD 和 DMSA 通过降低血清中铅酸诱导毒性大鼠的肾脏指数和脂质概况的水平,明显(p < 0.05)恢复了这些指数和概况的水平,并且所有参数的影响都与剂量有关。此外,PD 和 DMSA 还能缓解 PbAc 诱导的大鼠 MDA、GSH 水平以及 CAT 和 SOD 的抑制作用。多效萘能改善铅诱导大鼠的生化和氧化损伤,从而缓解铅中毒。总的研究结果表明,多靛红能减轻铅中毒,这可能是因为它能通过稳定铅诱导的 Wistar 大鼠体内 GSH、MDA 水平以及 SOD、CAT 的活性来改善生化和氧化损伤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Polydatin as a potential candidate that alleviates lead poisoning: insights from biochemical and oxidative damage in lead-induced Wistar rats

Lead is one of the most common heavy metal elements and has high biological toxicity. Polydatin (PD), also known as piceid (3, 4′, 5-trihydroxystilbene-3-β-D-glucoside), is a monocrystalline compound isolated from Polygonum cuspidatum Sieb. et Zucc. (Polygonaceae), but is also found in fruits and many daily diets. Aim of this research is polydatin as a potential candidate that alleviates lead poisoning: insights from biochemical and oxidative damage in lead-Induced Wistar rats. The study employed 42 Wistar rats of 90 days of age (150–200 g) which were randomly divided into six (6) groups and used for sub-chronic toxicity study according to OECD 407 guideline were lead acetate (PbAc) was administered for 90 days and followed by treatment with PD for 30 days. Control DW (1 mL/kg); PbAc (120 mg/kg); PbAc (120 mg/kg) + PD (250 mg/kg); PbAc (120 mg/kg) + PD (500 mg/kg); PbAc (120 mg/kg) + PD (1000 mg/kg); and PbAc (120 mg/kg) + DMSA (10 mg/kg) daily for 16 weeks per oral. At the end of treatment period, blood, plasma and organs samples were evaluated for blood lead levels (BLLs), biochemical parameters, oxidative stress markers and histopathology. PD and DMSA significantly (p < 0.05) reduced liver indices of PbAc-induced toxicity in rats with the exceptions of total and direct bilirubin which were significantly (p < 0.05) elevated. PD and DMSA significantly (p < 0.05) restored levels of renal indices and lipid profiles in PbAc-induced toxicity in rats by reducing the levels in serum and the effects were dose depended in all parameters. Furthermore, PD and DMSA also alleviate PbAc-induced MDA, GSH levels and inhibition of CAT and SOD in rats. PD alleviates lead poisoning through its ability to improve biochemical and oxidative damage in lead-induced rats. The overall findings shows that polydatin alleviates lead poisoning which might be due its ability to improve biochemical and oxidative damage through stabilizing the levels GSH, MDA and activities of SOD, CAT in lead-induced toxicity in Wistar rats.

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来源期刊
Advances in Traditional Medicine
Advances in Traditional Medicine PHARMACOLOGY & PHARMACY-
CiteScore
4.30
自引率
0.00%
发文量
50
期刊介绍: Advances in Traditional Medicine (ADTM) is an international and peer-reviewed journal and publishes a variety of articles including original researches, reviews, short communications, and case-reports. ADTM aims to bridging the gap between Traditional knowledge and medical advances. The journal focuses on publishing valid, relevant, and rigorous experimental research and clinical applications of Traditidnal Medicine as well as medical classics. At the same time, the journal is devoted to communication among basic researcher and medical clinician interested in the advancement of Traditional Medicine. Topics covered by the journal are: Medical Classics & History; Biomedical Research; Pharmacology & Toxicology of Natural Products; Acupuncture & Moxibustion; Sasang Constitutional Medicine; Diagnostics and Instrumental Development; Clinical Research. ADTM is published four times yearly. The publication date of this journal is 30th March, June, September, and December.
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