利用小鼠进行致死剂量口服绿门冬叶片提取物的阿库特毒性测试

Ni Kadek Eka Widiadnyani, L. M. Sudimartini
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引用次数: 0

摘要

研究结果表明,使用绿麦饭石叶提取物(Phylanthus niruri Linn)必须了解其安全性的剂量限制。本研究旨在确定急性致死剂量(LD50)的毒性,并检查小鼠重要器官的宏观病理变化。研究人员将 30 只雄性小鼠和 30 只雌性小鼠分成 5 组,每组 6 个重复。 对照组(K)的实验小鼠服用 0.9% 氯化钠,而服用剂量为 50、300、2000 和 5000mg/KgBW 的麦尼朗提取物的实验小鼠作为治疗组。小鼠口服一次该制剂,然后在给药后的 30 分钟内进行观察,在最初的 24 小时内每 4 小时定期观察一次,然后每天观察一次小鼠的临床症状、死亡率和体重。 在研究结束时(第 14 天),将实验小鼠处死,进行大体病理学评估。连续 14 天口服剂量达 5000 毫克的麦尼朗提取物不会导致小鼠死亡,也不会出现中毒症状和正常生长。对所有器官的大小、颜色和一致性进行大体病理学检查后发现,所有器官都处于正常状态。绿膜兰叶提取物制剂的剂量大于 5000 毫克/千克体重实际上是无毒的,不会导致器官异常。有必要通过更长的研究时间、更高的剂量和更多样的剂量范围,对毒性、生物相容性、影响以及亚慢性毒性对组织病理学结构变化的潜在影响进行研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
THE AKUT TOXICITY TESTING LETHAL DOSE ORAL GREEN MENIRAN LEAF EXTRACT BY USING MICE
The use of a dose limit of green meniran leaf extract (Phylanthus niruri Linn) must be known for its safety which is supported by research results. The aims of this research to determine the acute lethal dose (LD50) toxicity and to examine the macropathological changes in the vital organs of mice. A total of 30 male mice and 30 female mice were divided into five groups and six replicates.  Experimental mice in the control group (K) were given 0.9% NaCl, while those given meniran extract at doses of 50, 300, 2000 and 5000mg/KgBW were grouped as treatments. The preparation was given orally once and then the observations were made in the first 30 minutes after giving the preparation and periodically every 4 hours for the first 24 hours and once a day then the mice were observed for clinical symptoms, mortality and body weight.  At the end of the study (day 14), the experimental mice were sacrificed for macropathological evaluation.  giving meniran extract orally up to a dose of 5000 for 14 days did not cause death or showed toxic symptoms and normal growth. On macropathological examination of size, color and consistency, all organs were in normal condition. Green meniran leaf extract preparations > 5000 mg/kgBW are practically non-toxic and didn’t cause organ abnormalities. It is necessary to do research on toxicity, biocompatibility, effects, and potential for subchronic toxicity to changes in histopathological structure with a longer study duration, higher doses and more varied dosage ranges.
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