美洲Ximenia americana Linn (Olacaceae)茎皮甲醇提取物对Wistar大鼠急性和亚慢性毒性评价

Isaac A. Agyigra, Jane I. Ejiofor, Mohammed G. Magaji
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引用次数: 7

摘要

美洲西门尼亚在非洲民族医学中用于治疗痉挛性肠病,其茎皮特别用于溃疡。本研究评价了甲醇茎皮提取物的毒性。提取物剂量选择自急性毒性试验估计口服中位致死剂量(LD50)。将10只雄性Wistar大鼠分为4组,按体重按周称重和每日口服生理盐水和提取液剂量(250、500、1000 mg/kg),连续28 d进行安乐死。各组分别取普通和抗凝血(EDTA)样瓶进行生化和血液学分析。分离重要器官,称重,用缓冲福尔马林固定,进行组织分析。评价所得资料的均数±标准误差和统计学显著性(p≤0.05)。高达5000mg /kg的提取物不会造成死亡或行为毒性症状,因此,口服LD50估计大于5000mg /kg。在1000 mg/kg剂量下,肾脏血管充血,多形核细胞浸润,肺部多形核浸润区巩固,脾脏生发中心变形,器官大小、体重或解剖结构均无变化。肝酶和尿素水平没有显著改变,但总蛋白仅在1000 mg/kg时呈剂量依赖性显著增加;500和1000 mg/kg时,白蛋白水平显著降低。观察到的肌酸酐的剂量依赖性降低并不显著。总钙离子和氯离子浓度仅在250 mg/kg时显著增加。综上所述,小鼠急性口服西menia americana甲醇茎皮提取物相对无毒,但大鼠在使用数周后肾脏、肺和脾脏的解剖变化很小。
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 toxicity evaluation of methanol stem-bark extract of Ximenia americana Linn (Olacaceae) in Wistar rats

Ximenia americana is used in African ethno-medicine for spasmodic bowel diseases with stem bark particularly used for ulcers. This study evaluated the toxicity-profile of methanol stem-bark extract. Extract doses were selected from estimated oral median lethal dose (LD50) of acute toxicity test. Ten male Wistar rats in 4-groups, weekly weighed and daily treated orally per body-weight for 28 days with normal-saline and extract-doses (250, 500, 1000 mg/kg) respectively were euthanized. Blood for biochemical and haematological analyses were collected into plain and anticoagulated (EDTA) sample-bottles respectively from each group. Vital-organs were isolated, weighed and fixed in buffered-formalin fixatives for histo-analyses. Mean ± standard-error of mean and statistical-significance at (p  0.05) of obtained-data were evaluated. The extract at up to 5000 mg/kg caused no mortality or behavioural toxic-signs and thus, oral LD50 was estimated to be greater than 5000 mg/kg. No changes in organ-sizes, body-weights or anatomy of brain, heart, liver and stomach occurred, but at 1000 mg/kg, kidney showed vascular-congestion with polymorphonuclear cells, lungs had consolidated areas of polymorphs infiltration, while spleen had distorted germinal-centres. Liver enzymes and urea levels were not altered significantly, but a dose dependent significant increase in total-protein only at 1000 mg/kg; and significant reduction in albumin level at 500 and 1000 mg/kg were observed. The observed dose-dependent reduction in creatinine was not significant. Total-calcium and chloride ion concentrations increased significantly only at 250 mg/kg. In conclusion, acute oral administration of methanol stem-bark extract of Ximenia americana was relatively non-toxic in mice, but minimal anatomical changes in kidney, lungs and spleen occurred when used for few weeks in rats.

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