中国畜牧兽医 ›› 2025, Vol. 52 ›› Issue (6): 2915-2924.doi: 10.16431/j.cnki.1671-7236.2025.06.043

• 基础兽医 • 上一篇    下一篇

辣蓼散的急性毒性和亚慢性毒性研究

周博武1,2, 赵雯1, 张业怀2, 顾祖华2, 杨楷2, 熊飙2, 居融程2, 邓根福3, 黄文飞3, 胡庭俊1, 俸祥仁2   

  1. 1. 广西大学动物科学技术学院, 南宁 530004;
    2. 广西农业职业技术大学, 南宁 530007;
    3. 恭城瑶族自治县动物疫病预防控制中心, 桂林 542500
  • 收稿日期:2024-09-24 发布日期:2025-05-27
  • 通讯作者: 胡庭俊, 俸祥仁 E-mail:tingjunhu@126.com;450768007@qq.com
  • 作者简介:周博武,E-mail:952452838@qq.com。
  • 基金资助:
    广西农业职业技术大学科学研究与技术开发项目(XKJ2329、XKJ2335);广西农业科技自筹经费项目(Z2023091);来宾市科学研究与技术开发项目(来科攻240109)

Study on the Acute Toxicity and Sub-chronic Toxicity of Polygonum hydropiper Powder

ZHOU Bowu1,2, ZHAO Wen1, ZHANG Yehuai2, GU Zuhua2, YANG Kai2, XIONG Biao2, JU Rongcheng2, DENG Genfu3, HUANG Wenfei3, HU Tingjun1, FENG Xiangren2   

  1. 1. College of Animal Science and Technology, Guangxi University, Nanning 530004, China;
    2. Guangxi Vocational University of Agriculture, Nanning 530007, China;
    3. Gongcheng Yao Autonomous County Animal Disease Prevention and Control Center, Guilin 542500, China
  • Received:2024-09-24 Published:2025-05-27

摘要: 【目的】全面评估辣蓼散的安全性,为其在临床中的安全应用提供科学依据。【方法】设计急性毒性试验与亚慢性毒性试验。在急性毒性试验中,先选取20只昆明系小鼠进行预试验,随机分为5组,每组4只,雌雄各半,设置5个不同剂量组(1.875、3.75、7.5、15和30 g/kg BW),经口灌胃一次性给药后连续观察7 d并记录小鼠的行为变化、体重增减及脏器异常情况;若预试验无小鼠死亡,正式试验时每组增至10只,分组、给药方式及观察指标与预试验相同;若正式试验仍无小鼠死亡则进行最大耐受试验,另选20只小鼠以最大耐受剂量30 g/kg BW给药后观察7 d。在亚慢性毒性试验中,将80只SD大鼠随机分为4组,辣蓼散高(20 g/kg BW)、中(10 g/kg BW)、低(5 g/kg BW)剂量组及空白对照组(给予等体积纯化水),每组20只,连续给药30 d,观察大鼠行为表现、中毒及死亡状况,记录体重、摄食量与饮水量,检测血液生理生化指标,采集脏器称重并计算脏器系数,制作病理切片。【结果】在小鼠急性毒性试验中,预试验、正式试验和最大耐受试验中均未出现中毒症状或死亡现象,剖检脏器无异常变化,半数致死量(LD50)>30 g/kg BW。在大鼠亚慢性毒性试验中,各剂量组大鼠无中毒症状和死亡现象,体重增长趋势与对照组相似,雄性大鼠体重增长高于雌性;高剂量组雌性大鼠胸腺指数显著低于对照组(P<0.05),其余脏器系数与对照组均无显著差异(P>0.05);血液生理生化指标除中性粒细胞百分比(Neu)、丙氨酸氨基转移酶(ALT)、天门冬氨酸氨基转移酶(AST)有一定变化外,其余指标均无显著差异(P>0.05),且均在正常范围内,各脏器组织病理切片也未见明显病理变化。【结论】辣蓼散在本研究设定的剂量范围内对昆明系小鼠和SD大鼠均无毒副作用,安全性良好。在小鼠急性毒性试验中,辣蓼散的LD50>30 g/kg BW;在大鼠亚慢性毒性试验中,高剂量辣蓼散(20 g/kg BW)连续给药30 d,未观察到明显毒性反应。

关键词: 辣蓼散; 急性毒性; 亚慢性毒性; 小鼠; 大鼠; 安全性

Abstract: 【Objective】 This study was conducted to comprehensively evaluate the safety of Polygonum hydropiper powder and provide a scientific basis for its safe application in clinical practice.【Method】 Acute toxicity tests and sub-chronic toxicity tests were designed for the study.In the acute toxicity test,20 Kunming mice were firstly selected for the preliminary test and randomly divided into 5 groups,with 4 mice in each group and an equal number of males and females.Five different dose groups (1.875,3.75,7.5,15 and 30 g/kg BW) were set.After a single oral gavage administration,the mice were continuously observed for 7 days,and their behavioral changes,weight gain or loss,and abnormal conditions of organs were recorded.If no mice died in the preliminary test,the number of mice in each group was increased to 10 in the formal test,with the same grouping,administration method and observation indicators.If no mice died still in the formal test,the maximum tolerance test was carried out.Another 20 mice were given the maximum tolerated dose of 30 g/kg BW and then observed for 7 days.In the sub-chronic toxicity test,80 SD rats were randomly divided into 4 groups,namely the high-dose (20 g/kg BW),medium-dose (10 g/kg BW) and low-dose (5 g/kg BW) groups of Polygonum hydropiper powder and the blank control group (given an equal volume of purified water),with 20 rats in each group.The drug was continuously administered for 30 days.The behavioral manifestations,poisoning and death status of the rats were observed,their body weights,food intakes and water intakes were recorded,the blood physiological and biochemical indexes were detected,the organs were collected and weighed and the organ coefficients were calculated,and pathological sections were made.【Result】 In the acute toxicity test of mice,no poisoning symptoms or death occurred in the preliminary test,formal test and maximum tolerated dose test.There were no abnormal changes in the internal organs during autopsy,and the median lethal dose (LD50) was greater than 30 g/kg BW.In the sub-chronic toxicity test of rats,there were no poisoning symptoms or death in each dose group.The trend of body weight gain was similar to that of control group,and the body weight gain of male rats was higher than that of female rats.The thymus index of female rats in the high-dose group was significantly lower than that of control group (P<0.05),while there were no significant differences in the other organ coefficients compared with control group (P>0.05).Except for certain changes in the percentage of neutrophils (Neu),alanine aminotransferase (ALT) and aspartate aminotransferase (AST) among the blood physiological and biochemical indexes,there were no significant differences in the other indexes (P>0.05),and all indexes were within the normal range.There were also no obvious pathological changes in the pathological sections of various internal organs.【Conclusion】 Within the dose range set in this study,Polygonum hydropiper powder had no toxic or side effects on Kunming mice and SD rats and had good safety.In the acute toxicity test of mice,the LD50 of Polygonum hydropiper powder was greater than 30 g/kg BW.In the sub-chronic toxicity test of rats,the high-dose of Polygonum hydropiper powder was administered at 20 g/kg BW for 30 consecutive days,and no obvious toxic reactions were observed.

Key words: Polygonum hydropiper powder; acute toxicity; sub-chronic toxicity; mice; rats; safety

中图分类号: