医药导报
醫藥導報
의약도보
HERALD OF MEDICINE
2014年
8期
981-984
,共4页
崔楠楠%孟祥龙%马俊楠%李坤%张朔生
崔楠楠%孟祥龍%馬俊楠%李坤%張朔生
최남남%맹상룡%마준남%리곤%장삭생
商陆皂苷甲%毒性,急性%利尿作用
商陸皂苷甲%毒性,急性%利尿作用
상륙조감갑%독성,급성%이뇨작용
Esculentoside A%Toxicity,acute%Diuresis effect
目的了解商陆皂苷甲对小鼠急性毒性特点,观察其对大鼠的利尿作用。方法向小鼠腹腔注射不同浓度的商陆皂苷甲,观察给药后小鼠毒性反应,测定急性毒性的相关参数。向水负荷状态大鼠腹腔注射不同剂量商陆皂苷甲,测定给药后连续6 h总尿量。结果 Bliss法计算商陆皂苷甲LD50为26.19 mg·kg-1,95%可信区间为23.11~29.85 mg·kg-1。随着商陆皂苷甲浓度的增加,小鼠的毒性反应表现越明显,且小鼠的死亡数随之增加,空白对照组小鼠无异常反应。高剂量组大鼠尿量与阴性对照组差异有统计学意义,而中、低剂量组差异无统计学意义。结论商陆皂苷甲单次腹腔注射对小鼠有一定的毒性且商陆皂苷甲高剂量对大鼠有利尿作用。
目的瞭解商陸皂苷甲對小鼠急性毒性特點,觀察其對大鼠的利尿作用。方法嚮小鼠腹腔註射不同濃度的商陸皂苷甲,觀察給藥後小鼠毒性反應,測定急性毒性的相關參數。嚮水負荷狀態大鼠腹腔註射不同劑量商陸皂苷甲,測定給藥後連續6 h總尿量。結果 Bliss法計算商陸皂苷甲LD50為26.19 mg·kg-1,95%可信區間為23.11~29.85 mg·kg-1。隨著商陸皂苷甲濃度的增加,小鼠的毒性反應錶現越明顯,且小鼠的死亡數隨之增加,空白對照組小鼠無異常反應。高劑量組大鼠尿量與陰性對照組差異有統計學意義,而中、低劑量組差異無統計學意義。結論商陸皂苷甲單次腹腔註射對小鼠有一定的毒性且商陸皂苷甲高劑量對大鼠有利尿作用。
목적료해상륙조감갑대소서급성독성특점,관찰기대대서적이뇨작용。방법향소서복강주사불동농도적상륙조감갑,관찰급약후소서독성반응,측정급성독성적상관삼수。향수부하상태대서복강주사불동제량상륙조감갑,측정급약후련속6 h총뇨량。결과 Bliss법계산상륙조감갑LD50위26.19 mg·kg-1,95%가신구간위23.11~29.85 mg·kg-1。수착상륙조감갑농도적증가,소서적독성반응표현월명현,차소서적사망수수지증가,공백대조조소서무이상반응。고제량조대서뇨량여음성대조조차이유통계학의의,이중、저제량조차이무통계학의의。결론상륙조감갑단차복강주사대소서유일정적독성차상륙조감갑고제량대대서유이뇨작용。
Objective To understand the intensity and characteristics of acute toxicity of esculentoside A on mice and measure relevant parameters and observe its diuresis effect on rat. Methods After intraperitoneal injection of different concentrations of esculentoside A to mice, toxic reactions were observed. Rats with water load were intraperitoneally injected with different doses of esculentoside A. Total urine volume in six consecutive hours after the injection was determined. Results The LD50 of esculentoside A calculated by Bliss method was 26. 19 mg · kg-1 , and the 95% confidence interval was 23. 11-29. 85 mg·kg-1 . The mortality and acute toxicity of esculentoside A appeared to be dose-dependent while the blank control group had no abnormal reaction. The urine volume was significantly different between high dose group and the negative control group. No significant difference in urine volume was found between middle and the negative control group, and between low dose group and the negative control group. Conclusion Esculentoside A is poisonous to mice when single dose was intraperitoneally injected, and high dose of esculentoside A has diuresis effect on rat.