从莪术、鹅掌楸和巴戟天中提取的鸡尾酒提取物的急性和亚慢性毒理学研究

IF 3.4 Q2 TOXICOLOGY
Journal of Toxicology Pub Date : 2024-03-27 eCollection Date: 2024-01-01 DOI:10.1155/2024/9445226
Idah Rosidah, Tiya Novlita Renggani, Nisrina Firdausi, Sri Ningsih, Prasetyawan Yunianto, Devi Permatasari, Olivia Bunga Pongtuluran, Hismiaty Bahua, Julham Efendi, Siska Andrina Kusumastuti, Nuralih, Sjaikhurrizal El Muttaqien, Nizar, Susi Kusumaningrum, Kurnia Agustini
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引用次数: 0

摘要

Curcuma xanthorrhiza Roxb、Phyllanthus niruri L.和 Morinda citrifolia L.是印度尼西亚的药草,根据经验被用作维持健康的传统疗法。这三种植物的鸡尾酒提取物(CECPM)已被开发出来,并在大鼠体内显示出免疫刺激活性。本研究旨在评估 CECPM 在体内的急性和亚慢性毒性。急性毒性试验通过给雌性小鼠口服不同剂量的 CECPM(313、625、1250、2500 或 5000 毫克/千克体重)一次,然后在 14 天后每天评估毒性症状。慢性毒性试验是通过连续 90 天给雌性和雄性大鼠口服不同剂量的 CECPM(600、800 和 1000 毫克/千克体重)来进行的。在给药后 90 天和 28 天对毒性症状进行评估。急性口服毒性实验表明,实验期间没有发现中毒综合征和死亡现象。CECPM 的致死剂量水平(LD50)大于 5000 克/千克,属于基本无毒。同时,在亚慢性毒性研究中,给药后 90 天和停药 28 天的一些参数,如体重、相对器官重量、进食量、血液和生化指标,以及五个主要组织(心、肝、肾、脾和肺)的组织病理学检查均未发现异常。在本研究中,大鼠摄入 1000 毫克/千克体重的 CECPM 未达到无观测不良效应水平(NOAEL)。因此,可以得出结论,在急性和亚慢性毒理学研究中,口服 CECPM 相对无毒。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Acute and Subchronic Toxicological Study of the Cocktail Extract from Curcuma xanthorrhiza Roxb, Phyllanthus niruri L. and Morinda citrifolia L.

Curcuma xanthorrhiza Roxb, Phyllanthus niruri L., and Morinda citrifolia L. are Indonesian medicinal herbs used empirically as traditional therapeutics for maintaining health. The cocktail extract of these three plants (CECPM) had been developed and demonstrated immunostimulant activity in rats. This study aimed to evaluate the acute and subchronic toxicity of CECPM in vivo. The acute toxicity assay was conducted by orally administering a range dose of CECPM (313, 625, 1250, 2500, or 5000 mg/kg body weight (bw) on female mice once and then evaluating the toxic symptom every day for 14 days later. The chronic toxicity test was carried out by giving various doses of CECPM (600, 800, and 1000 mg/kg·bw) to female and male rats orally continuously for 90 consecutive days. The signs of toxicities were evaluated at the 90- and 28 days postadministration. The acute oral toxicity assays showed that there was no toxic syndrome and mortality found during the period of the experiment. The lethal dose level (LD50) of CECPM was more than 5000 g/kg, which was categorized as practically non-toxic. Meanwhile, in the sub-chronic toxicity study, some parameters tested at 90 days postadministration and after 28 days of withdrawal, such as the body weight, relative organ weight, food intake, hematological and biochemical blood parameters, and also histopathological examination of five primary tissues (heart, liver, kidney, spleen, and lung) revealed no abnormalities. There was no-observed adverse effect level (NOAEL) for the present study of CECPM 1000 mg/kg·bw of the rat. Therefore, it is concluded that the orally administered CECPM was relatively nontoxic during acute and subchronic toxicology studies.

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来源期刊
Journal of Toxicology
Journal of Toxicology TOXICOLOGY-
CiteScore
5.50
自引率
3.40%
发文量
0
审稿时长
10 weeks
期刊介绍: Journal of Toxicology is a peer-reviewed, Open Access journal that publishes original research articles, review articles, and clinical studies in all areas of toxicological sciences. The journal will consider articles looking at the structure, function, and mechanism of agents that are toxic to humans and/or animals, as well as toxicological medicine, risk assessment, safety evaluation, and environmental health.
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