哈尔滨医科大学学报
哈爾濱醫科大學學報
합이빈의과대학학보
JOURNAL OF HARBIN MEDICAL UNIVERSITY
2014年
1期
32-35
,共4页
苑洪菲%王晓蓉%于波%张树林%施宏宇%陈必良
苑洪菲%王曉蓉%于波%張樹林%施宏宇%陳必良
원홍비%왕효용%우파%장수림%시굉우%진필량
内分泌干扰%环境雌激素%胚胎发育%植入前暴露%生后性发育%性激素水平
內分泌榦擾%環境雌激素%胚胎髮育%植入前暴露%生後性髮育%性激素水平
내분비간우%배경자격소%배태발육%식입전폭로%생후성발육%성격소수평
endocrine disruptors%environmental estrogens%embryo development%preimplant-ation exposures%postnatal sexual development%sex hormone level
目的:研究在小鼠妊娠早期(前植入)体内暴露雌激素样甲氧滴滴涕( MXC)或雌二醇的长期效应。方法妊娠1~3天孕鼠给予皮下注射1μg的雌二醇和5.0 mg的MXC(出现阴道栓为第0天)。妊娠对照组小鼠仅用载体芝麻油处理。检测胎仔数,出生后的生存率,出生时的性别比率和两种性别子代的肛门与生殖器间距离( AGD),同时检测雌性子代阴道开放时间。采用放射免疫法检测雄性子代血清黄体生成素( LH)、卵泡刺激素( FSH)和睾丸酮( T)含量。结果由于MXC暴露的子代可记录高的死亡率。暴露雌二醇或MXC不能改变出生时的性别比率,但是胎仔数减少。出生后21天雄性仔鼠AGD比对照组短,此变化在MXC处理组最为明显。在MXC暴露后雌性子代的AGD没有受到影响,但是雌二醇处理组雌性小鼠的AGD比对照组更长。植入前暴露雌二醇或MXC使更多的雌性小鼠在断奶时明显出现早熟阴道开放。 MXC处理组的雄性小鼠可降低血LH和FSH但是不改变睾丸酮水平。结论在前植入阶段暴露MXC或雌二醇造成在两性子代断乳后长期的性发育改变。 MXC处理也阻滞两性子代的发育和体重。
目的:研究在小鼠妊娠早期(前植入)體內暴露雌激素樣甲氧滴滴涕( MXC)或雌二醇的長期效應。方法妊娠1~3天孕鼠給予皮下註射1μg的雌二醇和5.0 mg的MXC(齣現陰道栓為第0天)。妊娠對照組小鼠僅用載體芝痳油處理。檢測胎仔數,齣生後的生存率,齣生時的性彆比率和兩種性彆子代的肛門與生殖器間距離( AGD),同時檢測雌性子代陰道開放時間。採用放射免疫法檢測雄性子代血清黃體生成素( LH)、卵泡刺激素( FSH)和睪汍酮( T)含量。結果由于MXC暴露的子代可記錄高的死亡率。暴露雌二醇或MXC不能改變齣生時的性彆比率,但是胎仔數減少。齣生後21天雄性仔鼠AGD比對照組短,此變化在MXC處理組最為明顯。在MXC暴露後雌性子代的AGD沒有受到影響,但是雌二醇處理組雌性小鼠的AGD比對照組更長。植入前暴露雌二醇或MXC使更多的雌性小鼠在斷奶時明顯齣現早熟陰道開放。 MXC處理組的雄性小鼠可降低血LH和FSH但是不改變睪汍酮水平。結論在前植入階段暴露MXC或雌二醇造成在兩性子代斷乳後長期的性髮育改變。 MXC處理也阻滯兩性子代的髮育和體重。
목적:연구재소서임신조기(전식입)체내폭로자격소양갑양적적체( MXC)혹자이순적장기효응。방법임신1~3천잉서급여피하주사1μg적자이순화5.0 mg적MXC(출현음도전위제0천)。임신대조조소서부용재체지마유처리。검측태자수,출생후적생존솔,출생시적성별비솔화량충성별자대적항문여생식기간거리( AGD),동시검측자성자대음도개방시간。채용방사면역법검측웅성자대혈청황체생성소( LH)、란포자격소( FSH)화고환동( T)함량。결과유우MXC폭로적자대가기록고적사망솔。폭로자이순혹MXC불능개변출생시적성별비솔,단시태자수감소。출생후21천웅성자서AGD비대조조단,차변화재MXC처리조최위명현。재MXC폭로후자성자대적AGD몰유수도영향,단시자이순처리조자성소서적AGD비대조조경장。식입전폭로자이순혹MXC사경다적자성소서재단내시명현출현조숙음도개방。 MXC처리조적웅성소서가강저혈LH화FSH단시불개변고환동수평。결론재전식입계단폭로MXC혹자이순조성재량성자대단유후장기적성발육개변。 MXC처리야조체량성자대적발육화체중。
Objective To study the long-term effects of in vivo exposures to proestrogen meth-oxychlor ( MXC) or estradiol during early pregnancy ( preimplantation ) in mice.Methods Pregnant dams received either subcutaneous injections of 1μg of estradiol ( E2 ) and 5.0 mg of MXC on Days 1~3 of pregnancy ( vaginal plug=Day 0 ) .Pregnant control mice were treated with the vehicle only.Litter size, postnatal survival, sex ratio at birth, and anogenital distance ( AGD) in offspring of both sexes were examined , as well as vaginal opening in female off-spring .The concentrations of LH , FSH and testosterone ( T) in sera of the pregnant mice were determined using radioimmunoassay .Results High mortality rate was recorded in MXC-exposed offspring due to infanticide .Exposures to either E 2 or MXC did not change sex ratio at birth, but the litter size was smaller in the former group .On postnatal Day 21, male pups ex-posed to either E 2 or MXC at preimplantation stage exhibited shorter AGD than the controls , with the change most pronounced after MXC treatments .AGD in female offspring was unaffect-ed after MXC exposures, but E2 treatments produced longer AGD in the females than that recor-ded in the controls.Preimplantation exposures to E 2 or MXC also accelerated sexual maturation as significantly more females exhibited precocious vaginal opening at weaning .In males, MXC exposure during early pregnancy decreased serum LH and FSH , but not testosterone levels . Conclusion Exposures to MXC or E 2 at preimplantation stages cause long term alteration of sexual development during weaning in offspring of both sexes .Also, MXC treatments retarded both growth and weight of both sexes of offspring .