Study of Acute Toxicity of an Herbal Extract of Astragalus vulpinus

M. Sergalieva, A. A. Tsibizova, O. Bashkina, M. Samotrueva
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Abstract

This paper studies the acute toxicity of an herbal extract of Astragalus vulpinus Willd. growing in the Astrakhan Oblast. Experiments were carried out on white nonlinear rats. The animals were divided into several groups (n = 6): the control group receiving intragastric distilled water and the experimental groups receiving intragastric extract of the Astragalus vulpinus extract once at doses of 100, 500, 1000, 2000, and 4000 mg/kg. On the first day after extract administration, the animals were under continuous observation. During the entire observation period for 14 days, the animals were monitored in terms of their general condition, body weight, food refusal, and coat appearance, as well as their response to sound, light, and tactile stimuli. The response to sound was evaluated by a sudden sharp knock on the cage and identification of the animal’s flinching. The response to light was assessed by shining light into the eye with a penlight to control eye lid closure. Tactile stimuli were evaluated by compressing the basal part of the tail. After removing the animals from the experiment, macroscopic examination of internal organs (brain, liver, spleen, heart, stomach) and hematological analysis of blood smears were performed. During the research, the LD50 of the Astragalus vulpinus herbal extract under study was established. When the extract was administered at a dose of 4000 mg/kg, animal mortality was recorded (3 individuals died by the third day). In the remaining animals, a decrease in weight and leukocyte count was observed along with changes in the gastric mucosa. In terms of acute toxicity, the extract under study was found to belong to low-toxic substances with an LD50 of 4000 mg/kg. However, its administration at a dose of 4000 mg/kg led to changes in leukocyte count and gastric mucosa. Therefore, the chronic toxicity of Astragalus vulpinus herbal extracts requires additional research.
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黄芪提取物的急性毒性研究
本文研究了黄芪提取物的急性毒性。生长在阿斯特拉罕州。实验采用白色非线性大鼠。将实验动物分为几组(n = 6):对照组灌胃蒸馏水,试验组灌胃黄芪提取物1次,剂量分别为100、500、1000、2000、4000 mg/kg。给药后第1天连续观察。在整个14 d的观察期内,监测动物的一般状况、体重、拒食、被毛外观以及对声、光、触觉刺激的反应。对声音的反应是通过对笼子的突然猛烈敲击和动物畏缩的识别来评估的。对光线的反应是通过用笔灯照射眼睛来控制眼睑闭合来评估的。通过压缩尾部基部来评估触觉刺激。将动物从实验中取出后,进行内脏器官(脑、肝、脾、心、胃)的宏观检查和血液涂片的血液学分析。在研究过程中,确定了所研究的黄芪提取物的LD50。以4000mg /kg剂量给药时,记录动物死亡率(3只死亡)。在其余的动物中,观察到体重和白细胞计数的减少以及胃粘膜的变化。在急性毒性方面,所研究的提取物属于低毒物质,LD50为4000 mg/kg。然而,4000mg /kg的剂量可导致白细胞计数和胃粘膜的变化。因此,黄芪提取物的慢性毒性有待进一步研究。
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