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
2014年
5期
348-351
,共4页
巴婧翀%王玥%王声远%焦冬%吴永会
巴婧翀%王玥%王聲遠%焦鼕%吳永會
파청충%왕모%왕성원%초동%오영회
镍%粉尘%细胞毒性%丙二醛%过氧化酶
鎳%粉塵%細胞毒性%丙二醛%過氧化酶
얼%분진%세포독성%병이철%과양화매
Nickel%Dust%Cytotoxicity%Malondialdehyde%Catalase
目的 研究镍冶炼烟尘对NIH/3T3细胞的毒性作用和氧化损伤作用.方法 使用采自我国某镍冶炼厂的镍冶炼烟尘,用PBS配制浓度为0、6.25、12.50、25.00、50.00和100.00μg/ml的镍冶炼烟尘悬液,对NIH/3T3细胞染毒6h,进行CCK-8、中性红摄取(neutral red uptake,NRU)和乳酸脱氢酶(LDH)泄漏实验观察镍冶炼烟尘的细胞毒性;检测过氧化氢酶(CAT)活力、超氧化物歧化酶(SOD)抑制百分率及丙二醛(MDA)含量,评价细胞氧化损伤程度.结果 染毒组NIH/3T3细胞相对存活率随着镍冶炼烟尘浓度的增加而降低,CCK-8实验100 μg/ml染毒剂量组细胞生长抑制率达到86%,与对照组的差异有统计学意义(P<0.05);LDH活力随染毒浓度的增加而增加,12.50、25.00、50.00、100.00 μg/ml染毒剂量组LDH活力明显高于对照组,差异有统计学意义(P<0.05);与对照组比较,25.00、50.00和100.00μg/ml染毒剂量组细胞CAT活力明显降低,差异有统计学意义(P<0.05);与对照组比较,随着染毒剂量增加,SOD抑制百分率明显上升,MDA含量增加,差异均有统计学意义(P<0.05).结论 NIH/3T3细胞暴露于镍冶炼烟尘6h后能够造成抗氧化系统损伤,导致细胞死亡.
目的 研究鎳冶煉煙塵對NIH/3T3細胞的毒性作用和氧化損傷作用.方法 使用採自我國某鎳冶煉廠的鎳冶煉煙塵,用PBS配製濃度為0、6.25、12.50、25.00、50.00和100.00μg/ml的鎳冶煉煙塵懸液,對NIH/3T3細胞染毒6h,進行CCK-8、中性紅攝取(neutral red uptake,NRU)和乳痠脫氫酶(LDH)洩漏實驗觀察鎳冶煉煙塵的細胞毒性;檢測過氧化氫酶(CAT)活力、超氧化物歧化酶(SOD)抑製百分率及丙二醛(MDA)含量,評價細胞氧化損傷程度.結果 染毒組NIH/3T3細胞相對存活率隨著鎳冶煉煙塵濃度的增加而降低,CCK-8實驗100 μg/ml染毒劑量組細胞生長抑製率達到86%,與對照組的差異有統計學意義(P<0.05);LDH活力隨染毒濃度的增加而增加,12.50、25.00、50.00、100.00 μg/ml染毒劑量組LDH活力明顯高于對照組,差異有統計學意義(P<0.05);與對照組比較,25.00、50.00和100.00μg/ml染毒劑量組細胞CAT活力明顯降低,差異有統計學意義(P<0.05);與對照組比較,隨著染毒劑量增加,SOD抑製百分率明顯上升,MDA含量增加,差異均有統計學意義(P<0.05).結論 NIH/3T3細胞暴露于鎳冶煉煙塵6h後能夠造成抗氧化繫統損傷,導緻細胞死亡.
목적 연구얼야련연진대NIH/3T3세포적독성작용화양화손상작용.방법 사용채자아국모얼야련엄적얼야련연진,용PBS배제농도위0、6.25、12.50、25.00、50.00화100.00μg/ml적얼야련연진현액,대NIH/3T3세포염독6h,진행CCK-8、중성홍섭취(neutral red uptake,NRU)화유산탈경매(LDH)설루실험관찰얼야련연진적세포독성;검측과양화경매(CAT)활력、초양화물기화매(SOD)억제백분솔급병이철(MDA)함량,평개세포양화손상정도.결과 염독조NIH/3T3세포상대존활솔수착얼야련연진농도적증가이강저,CCK-8실험100 μg/ml염독제량조세포생장억제솔체도86%,여대조조적차이유통계학의의(P<0.05);LDH활력수염독농도적증가이증가,12.50、25.00、50.00、100.00 μg/ml염독제량조LDH활력명현고우대조조,차이유통계학의의(P<0.05);여대조조비교,25.00、50.00화100.00μg/ml염독제량조세포CAT활력명현강저,차이유통계학의의(P<0.05);여대조조비교,수착염독제량증가,SOD억제백분솔명현상승,MDA함량증가,차이균유통계학의의(P<0.05).결론 NIH/3T3세포폭로우얼야련연진6h후능구조성항양화계통손상,도치세포사망.
Objective To investigate the cytotoxicity and oxidative damage on NIH/3T3 cells induced by nickel smelting fume.Methods NIH/3T3 cells were treated with nickel smelting fume collected from a nickel smelting factory in China with doses of 0,6.25,12.50,25.00,50.00,and 100.00 μg/ml for 6 h.Dose-dependent cytotoxicity in cells were assessed by Cell Counting Kit-8 (CCK-8),natural red uptake assay,and lactate dehydrogenase (LDH) leakage assay,and the level of oxidative damage was assessed based on the activity of catalase (CAT),percentage inhibition of superoxide dismutase (SOD),and content of malonaldehyde (MDA).Results The relative survival of NIH/3T3 cells decreased with the increase in the dose of nickel smelting fume.In the CCK-8 assay,the group with 100 μg/ml nickel smelting fume showed a cell growth inhibition rate of 86%,with a significant difference compared with the control group (P<0.05).LDH activity increased with increasing dose of nickel smelting fume:the groups of 12.50,25,50,and 100 μg/ml nickel smelting fume all showed increased LDH activities as compared with the control group (P<0.05).The activities of CAT were significantly reduced in groups of 25,50,and 100 μg/ml nickel smelting fume as compared with that of the control group (P<0.05).As the dose of nickel smelting fume increased,the percentage inhibition of SOD and the content of MDA increased,with significant differences compared with the control group (P<0.05).Conclusion Oxidative damage may be induced in NIH/3T3 cells after 6 h of exposure to nickel smelting fume,which leads to cell death.