中国畜牧兽医 ›› 2022, Vol. 49 ›› Issue (4): 1532-1544.doi: 10.16431/j.cnki.1671-7236.2022.04.036

• 基础兽医 • 上一篇    下一篇

辣蓼黄酮提取物的急性毒性和亚慢性毒性研究

张文, 覃志彪, 成静, 于美玲, 韦英益, 黎江, 胡庭俊   

  1. 广西大学动物科学技术学院, 南宁 530005
  • 收稿日期:2021-09-13 出版日期:2022-04-05 发布日期:2022-03-25
  • 通讯作者: 黎江, 胡庭俊 E-mail:354550865@qq.com;tingjunhu@126.com
  • 基金资助:
    国家自然科学基金项目(32072907);广西创新驱动发展专项资金项目-渔用中草药免疫增强剂的研发与应用课(桂科AA17204081-2);国家现代农业产业技术体广西创新团队建设专项资金(nycytxgxcxtd-14-02)

Study on Acute and Subchronic Toxicity of Polygonum hydropiper L. Extract

ZHANG Wen, QIN Zhibiao, CHENG Jing, YU Meiling, WEI Yingyi, LI Jiang, HU Tingjun   

  1. College of Animal Science and Technology, Guangxi University, Nanning 530005, China
  • Received:2021-09-13 Online:2022-04-05 Published:2022-03-25

摘要: 【目的】 明确辣蓼黄酮提取物的毒理作用,评价其安全性。【方法】 在急性毒性试验预试验中,选取20只健康SPF级昆明系小鼠,随机分为6组,对照组(0 g/kg BW)和辣蓼黄酮提取物1~5组(灌胃给予辣蓼黄酮提取物20、10、5、2.5和1.25 g/kg BW),连续观察7 d,记录小鼠中毒和死亡情况。在急性毒性试验的最大给药量试验中,对20只小鼠分3次在24 h内按照30 g/kg BW灌胃给药,观察其生理状态,中毒情况及有无死亡情况,于试验第8天剖检观察其脏器有无异常情况。在亚慢性毒性试验中,取80只健康SPF级SD大鼠,随机分为4组,对照组(0 g/kg BW)和辣蓼黄酮高、中、低剂量组(分别灌胃给予辣蓼黄酮提取物20、10和5 g/kg BW),每组20只大鼠(雌、雄各半),喂养30 d,记录其体重、摄食量和饮水量。停药第7天,采血进行血常规和血液生化指标检查,计算其脏器指数,并进行组织病理学检查。【结果】 急性毒性试验各剂量组小鼠均未出现死亡情况,无法得出辣蓼黄酮提取物的半数致死量(LD50),小鼠对辣蓼黄酮提取物的最大耐受量为30 g/kg BW,说明辣蓼黄酮提取物安全无急性毒性。亚慢性毒性试验中,各给药组大鼠体重、饮水量、采食量及脏器系数与对照组虽有差异,但在正常范围内。给药30 d血常规指标中,与对照组相比,高剂量组大鼠白细胞及淋巴细胞显著下降(P<0.05),中性粒细胞显著上升(P<0.05);中剂量组大鼠白细胞显著或极显著下降(P<0.05;P<0.01);其余各组之间无显著差异(P>0.05)。血液生化指标中,与对照组相比,高剂量组大鼠甘油三酯(TG)水平显著上升(P<0.05),尿素氮(BUN)、肌酐(CREA)、总胆红素(TBIL)水平显著下降(P<0.05);中剂量组大鼠BUN水平显著下降(P<0.05),CREA水平显著上升(P<0.05),低剂量组大鼠谷丙转氨酶(ALT)、TG水平显著上升(P<0.05),BUN水平显著下降(P<0.05),其余各组间均无显著差异(P>0.05)。剖检和病理学检查未见明显异常变化,说明辣蓼黄酮提取物安全无亚慢性毒性。【结论】 5 g/kg BW及以下的辣蓼黄酮提取物无毒副作用,安全性好。

关键词: 辣蓼黄酮提取物; 急性毒性试验; 亚慢性毒性试验

Abstract: 【Objective】 The aim of this study was to determine the toxicity and safety of Polygonum hydropiper L. extract.【Method】 In the acute toxicity test,20 healthy SPF Kunming mice were randomly divided into 6 groups:Control group 0 g/kg BW and five treatment groups with Polygonum hydropiper L. extract at doses of 20,10,5,2.5 and 1.25 g/kg BW.The toxicity and death of the animals were observed for 7 days.In the maximum dose test of acute toxicity test,20 mice were given the drug by equal volume for 3 times within 24 h,and their physiological status,poisoning and death were observed.On the 8th day post treatment,their organs were observed for abnormalities.In the 30-day feeding experiment,80 healthy SPF SD rats were randomly divided into 4 groups:Control group 0 g/kg BW and Polygonum hydropiper L. high,medium and low dose groups (20,10 and 5 g/kg BW) with 20 mice each group (half female and half male).The rats were treated for 30 days.Their weight,food intake and water intake were recorded daily.On the 7th day after drug withdrawal,blood samples were collected for routine blood test and blood biochemistry test,organ index was calculated,and histopathological examination was performed.【Result】 The results showed that no death occurred in all groups in acute toxicity test,and the LD50 of Polygonum hydropiper L. extract was not obtained.The maximum tolerance of Polygonum hydropiper L. extract in mice was 30 g/kg BW,indicating that the Polygonum hydropiper L. extract was safe and had no acute toxicity.In the subchronic toxicity test,although the body weight,water intake,feed intake and organ index of rats in each administration group were different from those of the control group,they were within the normal range.The white blood cell and lymphocyte indexes of the rats in high dose group decreased significantly (P<0.05),and the neutrophils increased significantly (P<0.05).The white blood cell index of the rats in the middle dose group decreased significantly (P<0.05;P<0.01),there was no significant difference among the other groups (P>0.05).Among the blood biochemical indexes,compared with control group,the TG level of rats in high dose group increased significantly (P<0.05),and the levels of BUN,CREA and TBIL decreased significantly (P<0.05).The BUN level of rats in middle dose group decreased significantly (P<0.05).CREA levels increased significantly (P<0.05),ALT and TG levels in low dose group increased significantly (P<0.05),BUN levels decreased significantly (P<0.05),and there was no significant difference between the other groups (P>0.05).Necropsy and pathological examination showed no obvious abnormal changes,indicating that the extract of Polygonum hydropiper L. was safe and had no subchronic toxicity.【Conclusion】 In brief, Polygonum hydropiper L. spp. extract of 5 g/kg BW and below was safe and nontoxic.

Key words: Polygonum hydropiper L. extract; acute toxicity test; sub-chronic toxicity test

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