玉米(Zea mays)皮水提物对Wistar白化大鼠的安全性评价

Olanrewaju Samson Odelola, Victor Olusegun Oyetayo, Ayodele Oluwayemisi Ogundare, Babatunde Ogunlade
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摘要

目的:研究玉米皮水提物(HA)对Wistar白化大鼠可能的毒性作用。 研究设计:实验设计 研究地点和时间:本研究于2020年1月至2020年4月在尼日利亚阿库雷联邦科技大学进行。 方法:采用冷提取工艺制备。本研究采用48只Wistar白化大鼠。分别按2000、4000、8000mg /kg体重单剂量灌胃给药,进行急性毒性研究。观察大鼠14天是否有死亡或中毒迹象。在亚急性研究中,每天口服200、400和800 mg/kg体重的剂量,持续28天。实验结束后进行生化、血液学参数及组织病理学检查。 结果:急性毒性试验结果显示,HA的中位致死剂量(LD50)大于8000mg /kg。8000mg/kg亚急性组和急性组雄性和雌性大鼠体重均显著增加(P≤0.05)。在急性和亚急性毒性研究中,给药大鼠的生化和血液学参数与对照组有轻微差异。800 mg/mL和400 mg/mL分别使雌性大鼠的堆积细胞体积(PCV)和雄性大鼠的淋巴细胞显著增加。200 mg/mL处理的雄性大鼠总蛋白、葡萄糖和尿素水平降低,200 mg/mL和400 mg/mL处理的雌性大鼠尿素水平也显著降低。但组织学资料显示无显著差异。 结论:该提取物对大鼠无毒性作用,具有潜在的治疗价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Assessment of the Safety of Aqueous Extract of Maize (Zea mays) Husks in Wistar Albino Rats
Aims: The possible toxic impact of aqueous extract of maize husks (HA) on Wistar albino rats was investigated. Study Design: Experimental design. Place and Duration of Study: This study was conducted at the Federal University of Technology, Akure, Nigeria between January 2020 and April 2020. Methodology: The extract was prepared adopting the cold extraction procedure. Forty-eight (48) Wistar albino rats were used for this study. Acute toxicity study was carried out by administering HA at a single dose of 2000, 4000 and 8000 mg/kg body weight to the rats by oral gavage. The rats were observed for 14 days for any mortality or signs of toxicity. For sub-acute study, doses of 200, 400 and 800 mg/kg body weight were orally administered daily for 28 days. Biochemical and haematological parameters as well as histopathological studies were carried out after the experiments. Results: Acute toxicity results indicated that the median lethal dose (LD50) of HA was greater than 8000 mg/kg. There was remarkable body weight gain (P ≤ 0.05) in both male and female rats in all the sub-acute groups and acute group treated with 8000mg/kg. In the acute and sub-acute toxicity study, slight difference was recorded between the biochemical and haematological parameters of the treated rats dosed with the extract and the control. There was a significant increase in Packed Cell Volume (PCV) of female rats and lymphocytes of male rats treated with 800 mg/mL and 400 mg/mL respectively. The total protein, glucose and urea level of male rats treated with 200 mg/mL reduced while urea level of females treated with 200 mg/mL and 400 mg/mL also reduced remarkably. However, histological data showed no significant difference. Conclusion: In general, the extract was found to show no toxic effect on the rats and hence it is safe for potential therapeutic use.
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