安徽农业科学
安徽農業科學
안휘농업과학
JOURNAL OF ANHUI AGRICULTURAL SCIENCES
2010年
4期
2115-2117
,共3页
宁红梅%葛亚明%安志兴%银梅%刘俊伟%陈永耀%崔艳红%钟华
寧紅梅%葛亞明%安誌興%銀梅%劉俊偉%陳永耀%崔豔紅%鐘華
저홍매%갈아명%안지흥%은매%류준위%진영요%최염홍%종화
高氟低碘%老年大鼠%肝脏%DNA损伤%单细胞凝胶电泳
高氟低碘%老年大鼠%肝髒%DNA損傷%單細胞凝膠電泳
고불저전%노년대서%간장%DNA손상%단세포응효전영
High-F and low-I%Aged rats%Liver%DNA damage%Single cell gel electrophoresis
[目的]研究高氟低碘对大鼠肝脏细胞DNA损伤的影响.[方法]离乳Wistar大鼠21只,随机分为4组:①CK(5只),饲喂大鼠标准饲料,饮自来水;②高氟组(5只),饲喂大鼠正常饲料,饮100 mg/L氟化钠(NaF)去离子水;③低碘组(5只),饲喂低碘饲料(定做),饮去离子水;④高氟低碘组(6只),饲喂低碘饲料,饮100 mg/L氟化钠(NaF)去离子水.在大鼠20月龄时,处死取肝脏组织,检查其DNA的损伤情况.[结果]与①CK相比,②、③和④的老年大鼠肝细胞拖尾率显著增高(P<0.01);②、③和④的老年大鼠肝细胞的拖尾长度亦显著增长(P<0.01);肝细胞DNA损伤分级结果显示,②(高氟组)老年大鼠肝细胞DNA损伤主要是Ⅱ级、Ⅲ级.③(低碘组)肝细胞DNA几乎全部损伤,主要是Ⅲ级损伤.④(高氟低碘组)的细胞损伤以Ⅲ级损伤为主.[结论]高氟、低碘、高氟低碘都影响了大鼠肝脏细胞DNA 的损伤.
[目的]研究高氟低碘對大鼠肝髒細胞DNA損傷的影響.[方法]離乳Wistar大鼠21隻,隨機分為4組:①CK(5隻),飼餵大鼠標準飼料,飲自來水;②高氟組(5隻),飼餵大鼠正常飼料,飲100 mg/L氟化鈉(NaF)去離子水;③低碘組(5隻),飼餵低碘飼料(定做),飲去離子水;④高氟低碘組(6隻),飼餵低碘飼料,飲100 mg/L氟化鈉(NaF)去離子水.在大鼠20月齡時,處死取肝髒組織,檢查其DNA的損傷情況.[結果]與①CK相比,②、③和④的老年大鼠肝細胞拖尾率顯著增高(P<0.01);②、③和④的老年大鼠肝細胞的拖尾長度亦顯著增長(P<0.01);肝細胞DNA損傷分級結果顯示,②(高氟組)老年大鼠肝細胞DNA損傷主要是Ⅱ級、Ⅲ級.③(低碘組)肝細胞DNA幾乎全部損傷,主要是Ⅲ級損傷.④(高氟低碘組)的細胞損傷以Ⅲ級損傷為主.[結論]高氟、低碘、高氟低碘都影響瞭大鼠肝髒細胞DNA 的損傷.
[목적]연구고불저전대대서간장세포DNA손상적영향.[방법]리유Wistar대서21지,수궤분위4조:①CK(5지),사위대서표준사료,음자래수;②고불조(5지),사위대서정상사료,음100 mg/L불화납(NaF)거리자수;③저전조(5지),사위저전사료(정주),음거리자수;④고불저전조(6지),사위저전사료,음100 mg/L불화납(NaF)거리자수.재대서20월령시,처사취간장조직,검사기DNA적손상정황.[결과]여①CK상비,②、③화④적노년대서간세포타미솔현저증고(P<0.01);②、③화④적노년대서간세포적타미장도역현저증장(P<0.01);간세포DNA손상분급결과현시,②(고불조)노년대서간세포DNA손상주요시Ⅱ급、Ⅲ급.③(저전조)간세포DNA궤호전부손상,주요시Ⅲ급손상.④(고불저전조)적세포손상이Ⅲ급손상위주.[결론]고불、저전、고불저전도영향료대서간장세포DNA 적손상.
[Objective] The research aimed to study the effects of high-fluoirde and low-iodine on DNA damage of liver cells in rats. [Method] 21 weaned Wistar rats were randomly divided into 4 groups, including ① CK (feeding 5 rats with standard diet and tap water), ② high-F group (feeding 5 rats with normal diet and 100 mg/L NaF deionized water), ③ low-I group (feeding 5 rats with low-I diet and deionized water) and ④ high-F and low-I group (feeding 6 rats with low-I diet and 100 mg/L NaF deionized water). On the 20th month, rats were killed and their liver tissues were taken to detect the situations of DNA damage. [Result] Compared with CK, the tailing rate of liver cells in aged rats in groups ②, ③ and ④ was significantly increased (P<0.01) and the tail length of liver cells in aged rats in groups ②, ③ and ④ was longer(P<0.01). The classification results of DNA damage in liver cells indicated that DNA damage in liver cells in aged rats in group ② were mainly Ⅱ-class and Ⅲ -class. DNA in liver cells in group ③ were almost damaged, being mainly Ⅲ-class. The cell damage in group ④ was Ⅲ -class. [Conclusion] High-F, low-I, high-F and low-I all affected DNA damage in liver cells in rats.