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中华口腔医学研究杂志(电子版) ›› 2017, Vol. 11 ›› Issue (04) : 204 -210. doi: 10.3877/cma.j.issn.1674-1366.2017.04.003

所属专题: 文献

基础研究

大鼠氟斑牙(含氟牙膏型)动物模型的建立及实验检测
杨凯1, 张绍伟2,(), 叶小明1   
  1. 1. 518002 深圳市宝安区中心医院口腔科
    2. 563000 遵义医学院附属口腔医院口腔预防及儿童牙科
  • 收稿日期:2016-12-25 出版日期:2017-08-01
  • 通信作者: 张绍伟

Fluoride toothpaste type dental fluorosis animal model and experimental detection

Kai Yang1, Shaowei Zhang2,(), Xiaoming Ye1   

  1. 1. Baoan District Central Hospital Stomatology, Shenzhen 518002, China
    2. Zunyi Medical College Affiliated Stomatological Hospital of Oral Preventive and Pediatric Dentistry, Zunyi 563000, China
  • Received:2016-12-25 Published:2017-08-01
  • Corresponding author: Shaowei Zhang
  • About author:
    Corresponding author: Zhang Shaowei, Email:
引用本文:

杨凯, 张绍伟, 叶小明. 大鼠氟斑牙(含氟牙膏型)动物模型的建立及实验检测[J]. 中华口腔医学研究杂志(电子版), 2017, 11(04): 204-210.

Kai Yang, Shaowei Zhang, Xiaoming Ye. Fluoride toothpaste type dental fluorosis animal model and experimental detection[J]. Chinese Journal of Stomatological Research(Electronic Edition), 2017, 11(04): 204-210.

目的

从公共卫生的角度探讨含氟牙膏引起氟中毒的危险性。

方法

选用3周龄清洁型SD大鼠42只,按雌雄各半体重均衡原则随机分为7组(A组,阴性对照组;B组,阳性对照组;C组,50%含氟牙膏浓度灌胃组;D组,100%含氟牙膏浓度灌胃组;E组,30 mg/L NaF溶液组;F组,30 mg/L NaF溶液组+50%含氟牙膏浓度灌胃组;G组,30 mg/L NaF溶液组+100%含氟牙膏浓度灌胃组),每组6只。实验每周记录大鼠一般情况、体重;第0和112天分别测量采集尿液及血清,检测标本氟含量并记录分析;第0、28、56、84和112天分别记录各组下颌中切牙氟斑牙发生情况,根据氟斑牙分级计分统计。在第112天麻醉下处死各组大鼠,留取下颌中切牙,经苏木精-伊红染色切片观察牙齿结构改变。

结果

(1)大鼠体内尿氟和血氟含量会随着氟摄入量增高会有不断上升趋势,但当进入高氟摄入量时,上升幅度变缓,有1个平台期。(2)大鼠下切牙氟斑牙变化情况:在第28天,B组下切牙釉质表面可见棕白相间的细横纹,横纹逐渐向切方不断生长,但未发现釉质明显实质性缺损;第56天时,G组可见棕白相间横纹,釉质透明度下降,B组见少许白垩色斑块出现;第84天时,B组及G组个别大鼠出现粉笔样颜色改变,釉质透明度浑浊,E、F组个别大鼠出现棕白相间横纹,A、C呈棕色或棕黄色,表面光滑,半透明状,D组有1只大鼠釉质半透明改变,少许混浊;第112天时,B组及G组大鼠出现粉笔样颜色改变,釉质透明度浑浊,E、F组大鼠出现棕白相间横纹,横纹间见0.5~ 1 mm宽的透明区,A、C、D组与第84天的情况无明显差异。(3)大鼠下切牙病理切片情况:B、F、G组与A组比较,生长线均有明显的加深、加重,结构排列不均一。E组与A组比较,生长线有加深、加重,结构排列不均,但无B、F、G组明显;C、D组与A组比较,生长线及结构排列没有明显异常。

结论

高氟地区学龄前儿童使用含氟牙膏,可能会促进氟斑牙的产生;适氟地区的学龄前儿童使用含氟牙膏,须掌握使用方法,否则可能与儿童在其他日常生活中摄入的氟一起导致体内氟含量超标,促进氟斑牙的产生。

Objective

To test the safety of the use of fluoride toothpaste and the establishment of fluoride toothpaste type dental fluorosis animal model on the basis of public health on the point of view of fluoride toothpaste discussed by fluorosis risk.

Methods

Choose 3 weeks clean type 42 only SD rats, according to male and female half weight equilibrium principle randomly divided into seven groups with six rats each. Grouping was as follows: group A: negative control; group B: positive control; group C: 50% fluoride toothpaste concentration irrigation stomach group; group D: 100% fluoride toothpaste concentration irrigation stomach group; group E: 30 mg/L NaF solution group; group F: 30 mg/L NaF solution group + 50% fluoride toothpaste concentration irrigation stomach group; group G: 30 mg/L NaF solution group + 100% fluoride toothpaste concentration irrigation stomach group. The general situation and weight of the experimental rats were recorded every week. The urine and serum were collected at 0 day and 112 days. The specimen fluorine content and record analysis were investigated. The mandibular incisor of dental fluorosis conditions were recorded at 0 day, 28 days, 56 days, 84 days and 112 days respectively and according to the dental fluorosis grading scoring statistics. Harvested the rats at the 112th day under anesthesia. Mandible incisors of each rat were stained with the hematoxylin-eosin (HE) to observe the change of teeth structure.

Results

(1) The concentration of fluorine in rats urine as well as blood fluorine concentration were increased continually as fluorine intake increased. The blood fluorine concentration in rats reached a stationary platform phase when high concentration fluorine was provided. (2) The rats dental fluorosis teeth had various changes as follows: in 28 days, group B enamel surface had visible brown and white horizontal grain from gingival region to incisal margin but did not identify any enamel substantial defect; in 56 days, group G visible brown and white horizontal grain appeared and the reduced transparency in enamel could be seen as well as group B showed a little cretaceous splash piece in the enamel; in 84 days, some of the rats in group B and group G rats appeared chalk like color changes and enamel transparency turbidity. Some of the rats in group E, F showed brown and white horizontal grain in the enamel. Group A, C showed brown, smooth and translucent enamel surface, Only one rat in group D has one rat enamel translucent change with a little cloudy appearance; in 112 days, the chalk sample color changes were seen in the group B and G rats with enamel transparency turbidity. The brown and white horizontal grain appeared in group E, F rats with the 0.5~ 1 mm wide transparent area between the the grains. In overall, rats in group A, C, D had no significant difference compared with the baseline until 84 days. (3) The histopathological observation in rats teeth slice: comparing with group A, the growth lines in group B, group F and group G were obviously deepened, aggravating and more uneven structure arrangement. Group E also showed deepened and aggravating growth lines, but not obvious structure arrangement comparing with group A; However, the growth lines and structure arrangement in group C and D group had no significant changes.

Conclusions

Preschool children′s use of fluoride toothpaste could promote the generation of dental fluorosis in the high fluoride area. On the other hand, preschool childrens in Optimal fluorine area should strictly follow the guideline of usage of fluoride toothpaste to prevent generation of dental fluorosis together with daily life of the other intake of fluorine.

图1 SD大鼠下切牙氟斑牙分级
表1 实验SD大鼠体内尿氟和血氟含量监测结果(±s,mg/L)
图2 不同实验组SD大鼠尿氟含量的变化
图3 不同实验组SD大鼠血氟含量的变化
图4 实验各组SD大鼠下切牙病理切片图(苏木精-伊红 × 400)
图5 实验第112天各组SD大鼠下切牙唇侧氟斑牙肉眼观
表2 实验各组SD大鼠氟斑牙分级情况表
[1]
孔利佳.实验动物学[M].武汉:湖北人民出版社,2006:281-282.
[2]
中华人民共和国卫生部、卫生部卫生监督司. WS/T 89-1996尿中氟化物的测定 离子选择电极法[S].北京:中国标准出版社,1997.
[3]
中华人民共和国卫生部、卫生部疾病控制司. WS/T 212-2001血清中氟化物的测定 离子选择电极法[S].北京:中国标准出版社,2004.
[4]
Clark DC. Trends in prevalence of dental fluorosis in North America[J]. Community Dent Oral Epidemiol,1994,22(3):148-152.
[5]
Zohouri FV, Swinbank CM, Maguire A,et al. Is the fluoride/creatinine ratio of a spot urine sample indicative of 24-h urinary fluoride?[J]. Community Dent Oral Epidemiol,2006,34(2):130-138.
[6]
de Almeida BS, da Silva Cardoso VE, Buzalaf MA,et al. Fluoride ingestion from toothpaste and diet in 1- to 3-year-old Brazilian children[J]. Community Dent Oral Epidemiol,2007,35(1):53-63.
[7]
王国英,冯希平.学龄前儿童使用含氟牙膏安全性的研究进展[J].广东牙病防治,2009,17(2):93-94.
[8]
Cochran JA, Ketley CE, Duckworth RM,et al. Development of a standardized method for comparing fluoride ingested from toothpaste by 1.5-3.5-year-old children in seven European countries. Part 2:Ingestion results[J]. Community Dent Oral Epidemiol,2004,32(Suppl 1):47-53.
[9]
Browne D, Whelton H, O′Mullane D. Fluoride metabolism and fluorosis[J]. J Dent,2005,33(3):177-186.
[10]
Davies RM, Ellwood RP, Davies GM. The rational use of fluoride toothpaste[J]. Int J Dent Hyg,2003,1(1):3-8.
[11]
Pendrys DG. Risk of enamel fluorosis in nonfluoridated and optimally fluoridated populations:considerations for the dental professional[J]. J Am Dent Assoc,2000,131(6):746-755.
[12]
Tavener JA, Davies GM, Davies RM,et al. The prevalence and severity of fluorosis in children who received toothpaste containing either 440 or 1,450 ppm F from the age of 12 months in deprived and less deprived communities[J]. Caries Res,2006,40(1):66-72.
[13]
Do LG, Spencer AJ. Risk-benefit balance in the use of fluoride among young children[J]. J Dent Res,2007,86(8):723-728.
[14]
中华人民共和国国家质量监督检验检疫总局、中国国家标准化管理委员会. GB 8372-2008中华人民共和国牙膏标准[S].北京:中国标准出版社,2008.
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