哈尔滨商业大学学报(自然科学版)
哈爾濱商業大學學報(自然科學版)
합이빈상업대학학보(자연과학판)
JOURNAL OF HARBIN UNIVERSITY OF COMMERCE(NATURAL SCIENCES EDITION)
2014年
3期
271-274
,共4页
农药残留%卵巢颗粒细胞%ERK1/2%p-ERK1/2%五味子
農藥殘留%卵巢顆粒細胞%ERK1/2%p-ERK1/2%五味子
농약잔류%란소과립세포%ERK1/2%p-ERK1/2%오미자
pesticide residues%ovarian granulose cell%ERK1/2%p-ERK1/2%schisandra
探讨五味子中残留农药对卵巢颗粒细胞的毒性作用.MTT 法测定农药提取物作用于卵巢颗粒细胞24、48、72 h后的细胞增殖情况;Western blot法检测农药提取物对卵巢颗粒细胞MAPK信号通路的ERK1/2及p-ERK1/2蛋白表达水平的影响.MTT结果显示农药提取物能够显著促进卵巢颗粒细胞增殖,48 h增殖率最高(P<0.01),Western blot 结果显示提取物能够促进ERK1/2、p-ERK1/2蛋白表达,与阴性对照组相比差异极显著( P<0.01).因此农药提取物作用于体外培养的卵巢颗粒细胞能够显著促进细胞增殖,通过促进MAPK信号通路的ERK1/2、p-ERK1/2蛋白表达,对颗粒细胞产生毒性作用.
探討五味子中殘留農藥對卵巢顆粒細胞的毒性作用.MTT 法測定農藥提取物作用于卵巢顆粒細胞24、48、72 h後的細胞增殖情況;Western blot法檢測農藥提取物對卵巢顆粒細胞MAPK信號通路的ERK1/2及p-ERK1/2蛋白錶達水平的影響.MTT結果顯示農藥提取物能夠顯著促進卵巢顆粒細胞增殖,48 h增殖率最高(P<0.01),Western blot 結果顯示提取物能夠促進ERK1/2、p-ERK1/2蛋白錶達,與陰性對照組相比差異極顯著( P<0.01).因此農藥提取物作用于體外培養的卵巢顆粒細胞能夠顯著促進細胞增殖,通過促進MAPK信號通路的ERK1/2、p-ERK1/2蛋白錶達,對顆粒細胞產生毒性作用.
탐토오미자중잔류농약대란소과립세포적독성작용.MTT 법측정농약제취물작용우란소과립세포24、48、72 h후적세포증식정황;Western blot법검측농약제취물대란소과립세포MAPK신호통로적ERK1/2급p-ERK1/2단백표체수평적영향.MTT결과현시농약제취물능구현저촉진란소과립세포증식,48 h증식솔최고(P<0.01),Western blot 결과현시제취물능구촉진ERK1/2、p-ERK1/2단백표체,여음성대조조상비차이겁현저( P<0.01).인차농약제취물작용우체외배양적란소과립세포능구현저촉진세포증식,통과촉진MAPK신호통로적ERK1/2、p-ERK1/2단백표체,대과립세포산생독성작용.
The research method of the pesticide residues toxic effect from schisandra on the o-varian granulose cell was explored .MTT assay was used to determine pesticide extract on o-varian granulosa cells after 24, 48,72 h cell proliferation,and Western blot was used to de-tect the impact of pesticide extract on the expression levels of ERK 1/2 and p-ERK1/2 pro-tein of MAPK signal pathway of ovarian granulosa cell .MTT results showed that pesticide ex-tract could significantly promote cell proliferation , and the highest growth rate was at 48 h ( P <0.01 ) .Western blot showed that pesticide extract could promote the expression of ERK1/2 and p-ERK1/2 protein , which compared with the negative control group had sig-nificant difference ( P <0 .01 ) .Therefore pesticides extract on ovarian granulosa cells in vitro could significantly promote cell proliferation by promoting the expression of ERK 1/2 , p-ERK1/2 protein of MAPK signal pathway to produce toxic effects for granulosa cells .