中华劳动卫生职业病杂志
中華勞動衛生職業病雜誌
중화노동위생직업병잡지
CHINESE JOURNAL OF INDUSTRIAL HYGIENE AND OCCUPATIONAL DISEASES
2010年
6期
410-413
,共4页
徐幽琼%郑能雄%许旭艳%赵小贞%任南%林炜%汪家梨
徐幽瓊%鄭能雄%許旭豔%趙小貞%任南%林煒%汪傢梨
서유경%정능웅%허욱염%조소정%임남%림위%왕가리
电磁场%海马%脱噬作用
電磁場%海馬%脫噬作用
전자장%해마%탈서작용
Electromagnetic fields%Hippocampus%Apoptosis
目的 研究短期及亚慢性暴露高频电磁场(HF-EMF,30MHz,电场强度0~1600V/m)对雌性大鼠海马细胞凋亡及超微结构的影响,探讨HF-EMF对雌性大鼠海马细胞损伤的作用.方法 选用清洁级Wistar雌性大鼠120只,按体重随机分为10组,大鼠置于HF-EMF辐射源,频率30MHz,各组辐射剂量平均电场强度为0、25、100、400、1600 V/m,短期实验是连续辐射8 h/d,连续3 d后取海马;亚慢性实验是8 h,d,每周连续5 d,停2 d,共暴露56 d后取海马,HE染色法光学显微镜下观察海马细胞病理改变,脱氧核苷酸转移酶介导的dUTP缺口末端标记法(TUNEL)系统检测海马细胞凋亡情况,电子显微镜下观察细胞的超微结构.结果 (1)短期实验:各组大鼠海马细胞病理改变不明显,细胞凋亡率的差异无统计学意义(P>0.05).(2)亚慢性实验:与对照组(0.052%±0.016%)比较,400、1600 V/m组DG区颗粒细胞凋亡率(分别为0.165%±0.049%、0.189%±0.049%)明显增加,差异有统计学意义(P<0.01);光学显微镜下可见,400、1600 V/m组大鼠海马细胞核固缩明显增多,电子显微镜下可见,100 V/m以上剂量组的神经元细胞超微结构有轻微改变,1600 V/m组大鼠海马神经元细胞超微结构改变较明显.结论 短期暴露HF-EMF(30 MHz,25~1600 V/m)对雌性大鼠海马细胞形态学影响不明显;亚慢性高剂量暴露HF-EMF(400~1600 V/m)对大鼠海马细胞形态学影响较明显,低剂量暴露(25~100 V/m)对大鼠海马细胞形态学影响不明显.
目的 研究短期及亞慢性暴露高頻電磁場(HF-EMF,30MHz,電場彊度0~1600V/m)對雌性大鼠海馬細胞凋亡及超微結構的影響,探討HF-EMF對雌性大鼠海馬細胞損傷的作用.方法 選用清潔級Wistar雌性大鼠120隻,按體重隨機分為10組,大鼠置于HF-EMF輻射源,頻率30MHz,各組輻射劑量平均電場彊度為0、25、100、400、1600 V/m,短期實驗是連續輻射8 h/d,連續3 d後取海馬;亞慢性實驗是8 h,d,每週連續5 d,停2 d,共暴露56 d後取海馬,HE染色法光學顯微鏡下觀察海馬細胞病理改變,脫氧覈苷痠轉移酶介導的dUTP缺口末耑標記法(TUNEL)繫統檢測海馬細胞凋亡情況,電子顯微鏡下觀察細胞的超微結構.結果 (1)短期實驗:各組大鼠海馬細胞病理改變不明顯,細胞凋亡率的差異無統計學意義(P>0.05).(2)亞慢性實驗:與對照組(0.052%±0.016%)比較,400、1600 V/m組DG區顆粒細胞凋亡率(分彆為0.165%±0.049%、0.189%±0.049%)明顯增加,差異有統計學意義(P<0.01);光學顯微鏡下可見,400、1600 V/m組大鼠海馬細胞覈固縮明顯增多,電子顯微鏡下可見,100 V/m以上劑量組的神經元細胞超微結構有輕微改變,1600 V/m組大鼠海馬神經元細胞超微結構改變較明顯.結論 短期暴露HF-EMF(30 MHz,25~1600 V/m)對雌性大鼠海馬細胞形態學影響不明顯;亞慢性高劑量暴露HF-EMF(400~1600 V/m)對大鼠海馬細胞形態學影響較明顯,低劑量暴露(25~100 V/m)對大鼠海馬細胞形態學影響不明顯.
목적 연구단기급아만성폭로고빈전자장(HF-EMF,30MHz,전장강도0~1600V/m)대자성대서해마세포조망급초미결구적영향,탐토HF-EMF대자성대서해마세포손상적작용.방법 선용청길급Wistar자성대서120지,안체중수궤분위10조,대서치우HF-EMF복사원,빈솔30MHz,각조복사제량평균전장강도위0、25、100、400、1600 V/m,단기실험시련속복사8 h/d,련속3 d후취해마;아만성실험시8 h,d,매주련속5 d,정2 d,공폭로56 d후취해마,HE염색법광학현미경하관찰해마세포병리개변,탈양핵감산전이매개도적dUTP결구말단표기법(TUNEL)계통검측해마세포조망정황,전자현미경하관찰세포적초미결구.결과 (1)단기실험:각조대서해마세포병리개변불명현,세포조망솔적차이무통계학의의(P>0.05).(2)아만성실험:여대조조(0.052%±0.016%)비교,400、1600 V/m조DG구과립세포조망솔(분별위0.165%±0.049%、0.189%±0.049%)명현증가,차이유통계학의의(P<0.01);광학현미경하가견,400、1600 V/m조대서해마세포핵고축명현증다,전자현미경하가견,100 V/m이상제량조적신경원세포초미결구유경미개변,1600 V/m조대서해마신경원세포초미결구개변교명현.결론 단기폭로HF-EMF(30 MHz,25~1600 V/m)대자성대서해마세포형태학영향불명현;아만성고제량폭로HF-EMF(400~1600 V/m)대대서해마세포형태학영향교명현,저제량폭로(25~100 V/m)대대서해마세포형태학영향불명현.
Objective To analyze the effects of high-frequency electromagnetic field (HF-EMF, 30 MHz,0~1600 V/m) on the apoptosis and ultramicrostructure of the hippocamp and demonstrate the cytotoxici-ty of hippocamp. Methods 120 Wistar female adult rats were randomly divided into ten groups based on body weight with different levels of 30 MHz electromagnetic field (0, 25, 100, 400, 1600 V/m) for eight hours daily. Five group rats were irradiated for three days. The other five group rats were irradiated for fifty-six days. Weekly the rats were continuously exposed five days. The apoptotic rate of the hippocamp was detected with TUNEL System. Meanwhile, the ultramicrostructure was observed with the transmission electron microscope. Results (1)There was no significant difference on the apoptotic rate and pathological change of the hip-pocamp cell between the exposure and the control groups through short term experiment (P>0.05). (2) The apoptotic rate of the granulocyte on the DG campus of the hippocamp in the 400 V/m group and the 1600 V/m group (0.165%±0.049%, 0.189%±0.049% respectively) were increased significantly(P<0.01) through inferior chronic experiment compared with the control group (0.052%±0.016%). Along with the increase of radiation dose, the ultramicrostructure of the neuron cell appeared more abnormal cells. Especially there were marked change on the neuron in the 1600 V/m group. Conclusions There is no association between cell apoptotic rate of the hippocamp and short period exposure to HF-KMF(30 MHz,25~1600 V/m). However inferior chron-ic exposures to HF-EMF might induce the cytotoxicity, especially in the high dose exposure (1600 V/m) under our experiment.