摘要
【目的】观察宫内发育迟缓(intrauterine growth restriction,IUGR)新生大鼠胰腺中MafA的表达。【方法】清洁级Wister大鼠,雌雄鼠5∶1合笼,孕鼠按受孕顺序随机分为两组(低蛋白组和对照组),低蛋白组自妊娠第1天至分娩给予低蛋白饲料,对照组妊娠全程给予标准饲料。测量IUGR组和对照组新生大鼠空腹血糖及糖负荷后的血糖,摘取胰腺组织,称重,采用HE染色,光镜观察胰腺形态学变化,应用免疫组织化学法检测新生大鼠胰腺组织中MafA的表达。【结果】IUGR组新生大鼠空腹血糖低于对照组,给予糖负荷后,IUGR组血糖下降较慢,至120min仍明显高于对照组(P<0.05);胰重显著低于对照组(P<0.05)。与对照组相比,IUGR组胰腺表现为组织松散,胰岛数量及面积减少,胰腺中MafA的表达明显低于对照组(P<0.05)。【结论】宫内蛋白营养不良可致大鼠发生IUGR,IUGR新生大鼠胰腺中MafA的表达下降,这可能是影响新生大鼠胰腺发育和功能完善的机制之一。
[Objective] To investigate the expression of MafA in pancreas of rats with intrauterine growth retardation (IUGR). [Methods] Female and male Wister rats were copulated by 5 : 1,followed by randomly dividing into two groups:low protein group(LPG)and control group(CG). Rats in LPG were treated with low protein fodder from 1st day after pregnancy until delivery; meanwhile,standard fodder was given to the rats in CG. Fasting blood glucose and blood glucose after glucose load were detected between IUGR and CG. The removed pancreas of the rats measured weight. HE staining was applied to detect the pancreatic morphological changes under light microscope. Eventually, immunohistochemisty staining was performed to detect the expression of MafA in pancreas of rats. [Result] Statistically significant reduction of fasting blood glucose were observed in IUGR compared with CG. Likewise, the pancreatic weight was significantly de pressed in IUGR compared with CG(P〈0.05) ;however, slowly decrease of blood glucose in IUGR was observed after glu eose load given,yet,it was still significantly higher in LPG until 120 rain compared with CG. The most striking finding was that lower expression of MafA was detected in IUGR compared with CG(P〈0.05). [Conclusion] LPG may cause IUGR of rats and the lower expression of MafA in pancreas of newborn rats. It may influences the development of generation and systems of the pancreas of newborn rats.
出处
《中国儿童保健杂志》
CAS
北大核心
2013年第5期487-489,493,共4页
Chinese Journal of Child Health Care
基金
辽宁省教育厅资助(09730A)
关键词
宫内发育迟缓
大鼠
胰腺发育
MAFA
intrauterine growth restriction
rats
development of pancreas
MafA