云南植物研究
雲南植物研究
운남식물연구
ACTA BOTANICA YUNNANICA
2003年
6期
724-729
,共6页
付祥%谭宁华%姜立花%贾锐锐%嵇长久%LANDRO James%FEKETE Alexander%MUELLER Hartwig%HENKEL Thomas
付祥%譚寧華%薑立花%賈銳銳%嵇長久%LANDRO James%FEKETE Alexander%MUELLER Hartwig%HENKEL Thomas
부상%담저화%강립화%가예예%혜장구%LANDRO James%FEKETE Alexander%MUELLER Hartwig%HENKEL Thomas
抗骨质疏松活性筛选%碳酸酐酶II%天然产物%提取物%分离部位
抗骨質疏鬆活性篩選%碳痠酐酶II%天然產物%提取物%分離部位
항골질소송활성사선%탄산항매II%천연산물%제취물%분리부위
Antiosteoporotic activity screening%Carbonic anhydrase II (CA II)%Natural products%Extracts%Fractions
目的是以碳酸酐酶II(CA II)为靶点筛选其抑制剂,以期寻找抗骨质疏松活性样品.实验是在96孔酶标板上对来源于178个科、608个属、1020种动植物2919个提取物或分离部位样品在CA-II模型上进行了批量筛选.结果表明在10μg/ml浓度下发现了来源于40个科、61个属、72个种的100个样品有活性,其中5个样品的IC50小于2.50μg/ml,22个样品的IC50在2.51~5.00μg/ml范围,73个样品的IC50在5.01~10.00μg/ml范围.通过以上工作我们认为以碳酸酐酶II为分子靶点的体外筛选方法稳定、方便、快速、微量、有效,特别适用于天然产物的抗骨质疏松活性筛选.
目的是以碳痠酐酶II(CA II)為靶點篩選其抑製劑,以期尋找抗骨質疏鬆活性樣品.實驗是在96孔酶標闆上對來源于178箇科、608箇屬、1020種動植物2919箇提取物或分離部位樣品在CA-II模型上進行瞭批量篩選.結果錶明在10μg/ml濃度下髮現瞭來源于40箇科、61箇屬、72箇種的100箇樣品有活性,其中5箇樣品的IC50小于2.50μg/ml,22箇樣品的IC50在2.51~5.00μg/ml範圍,73箇樣品的IC50在5.01~10.00μg/ml範圍.通過以上工作我們認為以碳痠酐酶II為分子靶點的體外篩選方法穩定、方便、快速、微量、有效,特彆適用于天然產物的抗骨質疏鬆活性篩選.
목적시이탄산항매II(CA II)위파점사선기억제제,이기심조항골질소송활성양품.실험시재96공매표판상대래원우178개과、608개속、1020충동식물2919개제취물혹분리부위양품재CA-II모형상진행료비량사선.결과표명재10μg/ml농도하발현료래원우40개과、61개속、72개충적100개양품유활성,기중5개양품적IC50소우2.50μg/ml,22개양품적IC50재2.51~5.00μg/ml범위,73개양품적IC50재5.01~10.00μg/ml범위.통과이상공작아문인위이탄산항매II위분자파점적체외사선방법은정、방편、쾌속、미량、유효,특별괄용우천연산물적항골질소송활성사선.
To discover inhibitors of carbonic anhydrase II (CA II) with antiosteoporotic activity a batch of 2919 extract or fraction samples prepared from plants and animals belonging to 178 families,608 genera and 1020 species were tested on carbonic anhydrase II bioassay (CA-II) in 96-well microtiterplates.Finally 100 samples, which belong to 40 families, 61 genera and 72 species, showed inhibitory activity at 10 μg/ml, in which 5 samples showed IC50 at =<2.50 μg/ml,22 samples showed IC50 at 2.51-5.00 μg/ml and 73 samples showed IC50 at 5.01-10.00 μg/ml.It is indicated that this in-vitro bioassay is convenient,stable,rapid,sensitive and effective in searching for antiosteoporotic activity samples from natural sources.