中华放射医学与防护杂志
中華放射醫學與防護雜誌
중화방사의학여방호잡지
Chinese Journal of Radiological Medicine and Protection
2014年
2期
95-98
,共4页
李丽丽%王芹%郝建秀%姜立平%徐文清%姜恩海%邢志伟%李进
李麗麗%王芹%郝建秀%薑立平%徐文清%薑恩海%邢誌偉%李進
리려려%왕근%학건수%강립평%서문청%강은해%형지위%리진
抗放利%染色体畸变%微核%单细胞凝胶电泳%辐射防护
抗放利%染色體畸變%微覈%單細胞凝膠電泳%輻射防護
항방리%염색체기변%미핵%단세포응효전영%복사방호
2,2-dimethylthiazolidine%Chromosome aberration%Micronucleus%Single cell gel electrophoresis%Radioprotection
目的 探讨2,2-二甲基四氢噻唑盐酸盐(抗放利)对辐射诱导人外周血淋巴细胞遗传损伤的防护作用.方法 采集健康人外周血,分为健康对照组、单纯照射组和抗放利防护组.照射剂量为2 Gy.抗放利防护组分0.2、0.5、1、2 mmol/L 4个浓度组,于照前30 min给药.通过染色体畸变分析、微核及单细胞凝胶电泳检测,观察抗放利对辐射致人外周血淋巴细胞遗传损伤的防护作用.结果 各浓度抗放利防护组与单纯照射组比较,染色体畸变率(t=5.34 ~25.48,P<0.05)、微核细胞率(t=5.18~29.44,P<0.05)与微核率(=4.67~12.04,P<0.05)、彗星细胞尾长(t=16.18~ 19.64,P<0.05)、尾矩(t=11.79 ~ 13.01,P<0.05)和Olive尾矩(t=12.44~14.88,P<0.05)、尾部DNA含量(t=12.05 ~ 17.30,P<0.05)均明显降低.两个高浓度防护组(1、2 mmol/L)分别与两个低浓度防护组(0.2、0.5 mmol/L)比较,Olive尾矩明显降低(t=5.67 ~ 16.56,P<0.05).2 mmol/L防护组与其余各防护组相比,微核率和微核细胞率明显降低(=4.23~5.57,P <0.05).结论 抗放利对辐射诱导人外周血淋巴细胞遗传损伤具有防护作用.
目的 探討2,2-二甲基四氫噻唑鹽痠鹽(抗放利)對輻射誘導人外週血淋巴細胞遺傳損傷的防護作用.方法 採集健康人外週血,分為健康對照組、單純照射組和抗放利防護組.照射劑量為2 Gy.抗放利防護組分0.2、0.5、1、2 mmol/L 4箇濃度組,于照前30 min給藥.通過染色體畸變分析、微覈及單細胞凝膠電泳檢測,觀察抗放利對輻射緻人外週血淋巴細胞遺傳損傷的防護作用.結果 各濃度抗放利防護組與單純照射組比較,染色體畸變率(t=5.34 ~25.48,P<0.05)、微覈細胞率(t=5.18~29.44,P<0.05)與微覈率(=4.67~12.04,P<0.05)、彗星細胞尾長(t=16.18~ 19.64,P<0.05)、尾矩(t=11.79 ~ 13.01,P<0.05)和Olive尾矩(t=12.44~14.88,P<0.05)、尾部DNA含量(t=12.05 ~ 17.30,P<0.05)均明顯降低.兩箇高濃度防護組(1、2 mmol/L)分彆與兩箇低濃度防護組(0.2、0.5 mmol/L)比較,Olive尾矩明顯降低(t=5.67 ~ 16.56,P<0.05).2 mmol/L防護組與其餘各防護組相比,微覈率和微覈細胞率明顯降低(=4.23~5.57,P <0.05).結論 抗放利對輻射誘導人外週血淋巴細胞遺傳損傷具有防護作用.
목적 탐토2,2-이갑기사경새서염산염(항방리)대복사유도인외주혈림파세포유전손상적방호작용.방법 채집건강인외주혈,분위건강대조조、단순조사조화항방리방호조.조사제량위2 Gy.항방리방호조분0.2、0.5、1、2 mmol/L 4개농도조,우조전30 min급약.통과염색체기변분석、미핵급단세포응효전영검측,관찰항방리대복사치인외주혈림파세포유전손상적방호작용.결과 각농도항방리방호조여단순조사조비교,염색체기변솔(t=5.34 ~25.48,P<0.05)、미핵세포솔(t=5.18~29.44,P<0.05)여미핵솔(=4.67~12.04,P<0.05)、혜성세포미장(t=16.18~ 19.64,P<0.05)、미구(t=11.79 ~ 13.01,P<0.05)화Olive미구(t=12.44~14.88,P<0.05)、미부DNA함량(t=12.05 ~ 17.30,P<0.05)균명현강저.량개고농도방호조(1、2 mmol/L)분별여량개저농도방호조(0.2、0.5 mmol/L)비교,Olive미구명현강저(t=5.67 ~ 16.56,P<0.05).2 mmol/L방호조여기여각방호조상비,미핵솔화미핵세포솔명현강저(=4.23~5.57,P <0.05).결론 항방리대복사유도인외주혈림파세포유전손상구유방호작용.
Objective To investigate the protective effect of 2,2-dimethylthiazolidine (KFL) on human peripheral blood lymphocytes in radiation-induced genetic damage.Methods Peripheral blood samples were collected from healthy volunteers and divided into normal control group,irradiation group and KFL protective groups with four different concentrations (0.2,0.5,1,2 mmol/L).KFL was administrated 30 min before 2 Gy irradiation.Chromosome aberration analysis,micronucleus test and single cell gel electrophoresis were used to observe the protective effects of KFL on the radiation-induced genetic damage in human peripheral blood lymphocytes.Results Compared with the irradiation group,the four KFL protection groups showed significant reduction in the chromosomal aberration frequencies (t =5.34-25.48,P <0.05),the micronucleus cell frequencies (t =5.18-29.44,P < 0.05),the micronucleus frequencies (t =4.67-12.04,P < 0.05),the tailleghth (t =16.18-19.64,P < 0.05),the tailmoment (t =11.79-13.01,P < 0.05),the olivetailmoment (t =12.44-14.88,P < 0.05) and the tail DNA% of comet cells (t =12.05-17.30,P < 0.05).The olivetailmoment of the two high concentrations in protective groups(1,2 mmol/L) were significantly decreased compared with the other two KFL groups (0.2,0.5 mmol/L),respectively (t =5.67-16.56,P < 0.05).Compared with other KFL groups,the micronucleus frequencies and micronucleus cell frequencies of the 2 mmol/L KFL group was significantly decreased (t =4.23-5.57,P < 0.05).Conclusions KFL may have protective effect on human peripheral blood lymphocytes in the genetic damage induced by radiation.