天津农学院学报
天津農學院學報
천진농학원학보
JOURNAL OF TIANJIN AGRICULTURAL COLLEGE
2014年
1期
19-22
,共4页
陈思怀%刘杰%杨凡%肖武林%石志敏
陳思懷%劉傑%楊凡%肖武林%石誌敏
진사부%류걸%양범%초무림%석지민
全氟十二烷酸%雌激素%促卵泡刺激素%卵巢基因表达
全氟十二烷痠%雌激素%促卵泡刺激素%卵巢基因錶達
전불십이완산%자격소%촉란포자격소%란소기인표체
perfluorododecanonic acid%estradiol%follicle-stimulating hormone%ovary gene expression
全氟烷酸类化合物(PFAAs)是一类新型的持久性有机污染物,该类化合物的环境和健康风险已经引起了人们的广泛关注。由于长链PFAAs的生殖毒性效应尚缺乏系统的研究,本文采用含全氟十二烷酸(PFDoA)0.1 mg/kg的饲料饲喂大鼠180 d,应用放射免疫分析法和实时荧光定量PCR方法检测了大鼠血清中生殖激素的水平以及卵巢中相关受体的表达。结果显示,PFDoA暴露导致血清雌二醇水平出现减少的趋势,PFDoA显著增加了血清促卵泡刺激素水平,但并不影响血清促黄体生成素水平;PFDoA处理导致卵巢雌激素受体α的mRNA水平降低了25%,卵巢促卵泡刺激素受体的表达增加了36%,但PFDoA并不影响卵巢中促黄体生成素受体的表达。以上结果暗示慢性PFDoA暴露有影响雌激素以及促卵泡刺激素的信号在卵巢中传导的趋势。
全氟烷痠類化閤物(PFAAs)是一類新型的持久性有機汙染物,該類化閤物的環境和健康風險已經引起瞭人們的廣汎關註。由于長鏈PFAAs的生殖毒性效應尚缺乏繫統的研究,本文採用含全氟十二烷痠(PFDoA)0.1 mg/kg的飼料飼餵大鼠180 d,應用放射免疫分析法和實時熒光定量PCR方法檢測瞭大鼠血清中生殖激素的水平以及卵巢中相關受體的錶達。結果顯示,PFDoA暴露導緻血清雌二醇水平齣現減少的趨勢,PFDoA顯著增加瞭血清促卵泡刺激素水平,但併不影響血清促黃體生成素水平;PFDoA處理導緻卵巢雌激素受體α的mRNA水平降低瞭25%,卵巢促卵泡刺激素受體的錶達增加瞭36%,但PFDoA併不影響卵巢中促黃體生成素受體的錶達。以上結果暗示慢性PFDoA暴露有影響雌激素以及促卵泡刺激素的信號在卵巢中傳導的趨勢。
전불완산류화합물(PFAAs)시일류신형적지구성유궤오염물,해류화합물적배경화건강풍험이경인기료인문적엄범관주。유우장련PFAAs적생식독성효응상결핍계통적연구,본문채용함전불십이완산(PFDoA)0.1 mg/kg적사료사위대서180 d,응용방사면역분석법화실시형광정량PCR방법검측료대서혈청중생식격소적수평이급란소중상관수체적표체。결과현시,PFDoA폭로도치혈청자이순수평출현감소적추세,PFDoA현저증가료혈청촉란포자격소수평,단병불영향혈청촉황체생성소수평;PFDoA처리도치란소자격소수체α적mRNA수평강저료25%,란소촉란포자격소수체적표체증가료36%,단PFDoA병불영향란소중촉황체생성소수체적표체。이상결과암시만성PFDoA폭로유영향자격소이급촉란포자격소적신호재란소중전도적추세。
Perfluoroalkyl acids are a class of emerging persistent organic pollutants, the concerns on PFAAs potential risk in environment and health has been generated in environmental scientists and related agencies. In order to study the reproductive toxicology of PFAAs with long carbon chains, after 0.1 mg/kg of perfluorododecanonic acid (PFDoA) in food was used to feed female rats for 180 days, radioimmunoassay and real-time PCR were applied to detect the serum reproductive hormones and the expression of the related ovary receptors. The results show that PFDoA exhibited inhibitory trend on serum estradiol (E2) and markedly increased serum follicle-stimulating hormone level. No change in serum luteinizing hormone was observed between control and PFDoA exposure group. Following PFDoA exposure, mRNA level of ovary E2 receptor was dropped by 25% while ovary FSH receptor expression was increased by 36%. PFDoA exposure did not affect ovary LH receptor expression. These results suggest that chronic PFDoA exposure mainly impacts ovary E2and FSH signal transduction.