Role of Some Food by Product Extracts Compared to Silymarin as Protective Agents against Acute Liver Injury in Paracetamol Overdose-Exposed Rats

Wafaa Gaballah, Asmaa Faramawy, Samah El-Hashash
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Abstract

In paracetamol (PCM) overdose-exposed rats, the hepato-protective properties of ethanolic extracts from grape seeds and peanut skins (GSEE and PSEE, respectively) were compared to silymarin in this study. The total amount of phenolic and flavonoids as well as the ability to scavenge radical DPPH of GSEE and PSEE were measured. Twenty adult male albino rats were split evenly into five groups for the in vivo evaluation; including the control group (GI), while PCM treated group (GII) got paracetamol once orally for 14 days at a dosage of 640 mg/kg/day, with no protective treatment. Silymarin (50 mg /kg /day), and 200 mg /kg /day of either GSEE or PSEE were given concurrently with PCM to GIII, GIV and GV, respectively. PCM overdose led to a significant elevation in the activities of transaminases and alkaline phosphatase (84.00±10.64, 396.00±49.44, and 579.67±72.00 U/L versus 44.00±5.72, 178.00±22.09, and 322.0±40.58 U/L in control group), along with an obvious decline in serum proteins. In the liver, the lipid profile was disrupted associated with a marked elevation in oxidative and inflammation markers, which was further confirmed by histological examination. These disorders were alleviated by the administration of food waste extracts. Even while PSEE showed a little increase in total phenolic, flavonoids and DPPH radical scavenging ability (604.45, 542.05, and 618.59 versus 583.70 mg gallic acid equivalent, 503.80 mg catechin equivalent, and 550.44 mg Trolox equivalent, respectively/g GSEE), GSEE was the nearest treatment when compared to silymarin. This study suggests GSEE and PSEE as alternative therapies for paracetamol-induced hepatotoxicity.
与水飞蓟素相比,一些食品副产品提取物对扑热息痛过量暴露大鼠急性肝损伤的保护作用
本研究比较了葡萄籽乙醇提取物(GSEE)和花生皮乙醇提取物(PSEE)与水飞蓟素对扑热息痛(PCM)过量暴露大鼠的肝脏保护特性。研究测定了 GSEE 和 PSEE 的酚类和类黄酮总量以及清除自由基 DPPH 的能力。将 20 只成年雄性白化大鼠平均分成 5 组进行体内评估,其中包括对照组(GI),而 PCM 处理组(GII)则口服扑热息痛一次,连续 14 天,剂量为 640 毫克/千克/天,不进行任何保护性处理。GIII、GIV 和 GV 在服用 PCM 的同时,分别服用水飞蓟素(50 毫克/千克/天)和 200 毫克/千克/天的 GSEE 或 PSEE。PCM 过量会导致转氨酶和碱性磷酸酶活性显著升高(84.00±10.64、396.00±49.44 和 579.67±72.00 U/L 与对照组的 44.00±5.72、178.00±22.09 和 322.0±40.58 U/L 相比),同时血清蛋白明显下降。在肝脏中,脂质分布紊乱,氧化和炎症标志物明显升高,组织学检查进一步证实了这一点。施用厨余提取物后,这些病症都得到了缓解。尽管 PSEE 的总酚、类黄酮和 DPPH 自由基清除能力略有提高(604.45、542.05 和 618.59 与 583.70 毫克没食子酸当量、503.80 毫克儿茶素当量和 550.44 毫克三氧化碳当量/克 GSEE 相比),但与水飞蓟素相比,GSEE 是最接近的处理方法。本研究建议将 GSEE 和 PSEE 作为扑热息痛引起的肝毒性的替代疗法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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