淡水渔业
淡水漁業
담수어업
FRESHWATER FISHERIES
2014年
5期
54-57
,共4页
熊斌%王杨科%解雷%路宏朝%王琦
熊斌%王楊科%解雷%路宏朝%王琦
웅빈%왕양과%해뢰%로굉조%왕기
鲫(Carassius auratus)%染毒%镉%维生素C%微核率
鯽(Carassius auratus)%染毒%鎘%維生素C%微覈率
즉(Carassius auratus)%염독%력%유생소C%미핵솔
Carassius auratus%contamination%vitamin C%micronucleus
为探究维生素C对镉导致鲫( Carassius auratus)红细胞微核的干预作用,用0.5 mg/L的镉溶液单一染毒作对照组,设置0.5 mg/L的镉溶液分别添加1、2、3 g/L的维生素C( VC)三组作为实验组。在染毒后的第5、10、15、20天分别取鲫尾部血液制作血涂片,镜检并统计红细胞微核率。结果显示:0.5 mg/L的镉溶液单一染毒对照组,镉诱发鲫红细胞产生微核率与时间呈现线性关系,回归函数为: y=0.1587 x+2.5167( R2=0.9357);实验组随着VC浓度增加和处理时间的延长,微核率降低,其中以0.5 mg/L Cd2++3 g/L VC组处理20 d的微核率最低,微核率为仅为0.26‰,与处理20 d的对照组相比,微核抑制率达到95.62%。 T检验分析表明, VC对镉导致鲫鱼红细胞微核干预作用极显著( t>t0.01),干预作用在试验中呈现出随VC浓度增加干预作用增强的趋势。实验表明, VC对镉导致鲫红细胞微核率升高的现象有明显的干预作用。
為探究維生素C對鎘導緻鯽( Carassius auratus)紅細胞微覈的榦預作用,用0.5 mg/L的鎘溶液單一染毒作對照組,設置0.5 mg/L的鎘溶液分彆添加1、2、3 g/L的維生素C( VC)三組作為實驗組。在染毒後的第5、10、15、20天分彆取鯽尾部血液製作血塗片,鏡檢併統計紅細胞微覈率。結果顯示:0.5 mg/L的鎘溶液單一染毒對照組,鎘誘髮鯽紅細胞產生微覈率與時間呈現線性關繫,迴歸函數為: y=0.1587 x+2.5167( R2=0.9357);實驗組隨著VC濃度增加和處理時間的延長,微覈率降低,其中以0.5 mg/L Cd2++3 g/L VC組處理20 d的微覈率最低,微覈率為僅為0.26‰,與處理20 d的對照組相比,微覈抑製率達到95.62%。 T檢驗分析錶明, VC對鎘導緻鯽魚紅細胞微覈榦預作用極顯著( t>t0.01),榦預作用在試驗中呈現齣隨VC濃度增加榦預作用增彊的趨勢。實驗錶明, VC對鎘導緻鯽紅細胞微覈率升高的現象有明顯的榦預作用。
위탐구유생소C대력도치즉( Carassius auratus)홍세포미핵적간예작용,용0.5 mg/L적력용액단일염독작대조조,설치0.5 mg/L적력용액분별첨가1、2、3 g/L적유생소C( VC)삼조작위실험조。재염독후적제5、10、15、20천분별취즉미부혈액제작혈도편,경검병통계홍세포미핵솔。결과현시:0.5 mg/L적력용액단일염독대조조,력유발즉홍세포산생미핵솔여시간정현선성관계,회귀함수위: y=0.1587 x+2.5167( R2=0.9357);실험조수착VC농도증가화처리시간적연장,미핵솔강저,기중이0.5 mg/L Cd2++3 g/L VC조처리20 d적미핵솔최저,미핵솔위부위0.26‰,여처리20 d적대조조상비,미핵억제솔체도95.62%。 T검험분석표명, VC대력도치즉어홍세포미핵간예작용겁현저( t>t0.01),간예작용재시험중정현출수VC농도증가간예작용증강적추세。실험표명, VC대력도치즉홍세포미핵솔승고적현상유명현적간예작용。
To investigate the effect of vitamin C intervention on cadmium induced erythrocyte micronucleus of Carassius au-ratus, with the 0.5 mg/L cadmium solution as the control group , the 0.5 mg/L cadmium solution separately added 1 g, 2 g, 3 g/L of vitamin C(VC) were as experimental group.Firstly, C.auratus were separately exposure 5, 10, 15, 20 d. Then, blood smears were taken from crucian carp tail blood , microscopic examination , and the erythrocyte micronucleus rate was measured .The results showed that the erythrocyte micronucleus rate induced by cadmium increased linearly with time in the control group, y=0.158 7 X+2.516 7 (R2 =0.935 7).However, in the experimental group, the erythro-cyte micronucleus rate decreased with vitamin C concentration increasing and treatment time .The micronucleus rate was lowest for the experimental group with 3 g/L vitamin C and treating 20 d, and only 0.26%; contrast to the control group treating 20 d, control rate of micronucleus was 95.62%.The T-test results showed that the effect of vitamin C intervention on cadmium induced erythrocyte micronucleus rate was significant ( t>t0.01 ) , the effect increased with vitamin C concen-tration increasing .