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蒙药荜茇提取物荜茇宁的致畸试验研究

包勒朝鲁 乌兰图雅 那生桑

癌变·畸变·突变2012,Vol.24Issue(6):462-464,473,4.
癌变·畸变·突变2012,Vol.24Issue(6):462-464,473,4.DOI:10.3969/j.issn.1004-616x.2012.06.015

蒙药荜茇提取物荜茇宁的致畸试验研究

Teratogenicity of the natural effective component piperlonguminine of Piper longum L.

包勒朝鲁 1乌兰图雅 2那生桑1

作者信息

  • 1. 内蒙古医学院蒙药研究所,内蒙古 呼和浩特 010110
  • 2. 内蒙古自治区国际蒙医医院,内蒙古 呼和浩特 010010
  • 折叠

摘要

Abstract

OBJECTIVE: To study the teratogenicity of the natural effective component piperlonguminine Piper longum L. on normal Wistar pregnant rats. METHODS: Rats were randomly divided into 5 group. Stomach of the Wistar rat was irrigated with different doses of piperlonguminine suspension, high dosage 500 mg/kg, medium dosage 100 mg/kg, low dosage 20 mg/kg on the 6th to the 15th day during the gestation period. Stomach of the negative group was irrigated with the same volume CMC-Na solution. For the positive group, intraperitoneal cyclophosphamide 10 mg/kg was administered on the 11th day of gestation. Weights on the 0, 3rd , 7th , 10th , 13th , 16th , 20th days were recorded. All were killed on the 20th day of gestation. The situation of the pregnancy, appearance of internal organs and bone morphology were examined. RESULTS: Compared to each dose group and negative group, the appearance and weight gain of pregnant rats, the appearance of the fetus, growth indicators and the degree of ossification of the occipital bone, parietal bone, sternum, ribs and other bones ; and the appearance of the liver, kidney, testis or uterus and other organs revealed no significant difference (P>0.05). During the experiment, 2 fetuses were absorbed in the high dose group, but was insignificant when compared with the negative group(P>0.05). CONCLUSION: The lipid-lowering active ingredients of Mongolian drug piperlonguminine, under our experimental dose range, did not demonstrated obvious toxicity in pregnant mice and fetuses .

关键词

蒙药/荜茇/荜茇宁/致畸试验

Key words

mongolian drug/Piper longum L./ piperlonguminine/teratogenicity

分类

医药卫生

引用本文复制引用

包勒朝鲁,乌兰图雅,那生桑..蒙药荜茇提取物荜茇宁的致畸试验研究[J].癌变·畸变·突变,2012,24(6):462-464,473,4.

基金项目

国家自然科学基金资助项目(30160103) (30160103)

癌变·畸变·突变

OACSCDCSTPCD

1004-616X

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