Maternal curcumin supplementation ameliorates placental function and fetal growth in mice with intrauterine growth retardation

被引:26
|
作者
Qi, Lina [1 ]
Jiang, Jingle [1 ]
Zhang, Jingfei [1 ]
Zhang, Lili [1 ]
Wang, Tian [1 ]
机构
[1] Nanjing Agr Univ, Coll Anim Sci & Technol, Natl Expt Teaching Demonstrat Ctr Anim Sci, Nanjing 210095, Peoples R China
基金
中国国家自然科学基金;
关键词
intra-uterine growth retardation; placenta; curcumin; LOW-PROTEIN DIET; OXIDATIVE STRESS; RESTRICTION LEADS; GENE-EXPRESSION; INFLAMMATION; APOPTOSIS; RAT; RECEPTOR; MODEL; NRF2;
D O I
10.1093/biolre/ioaa005
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Intrauterine growth retardation (IUGR) is a serious reproductive problem in humans. The objective of this study was to investigate the effects of daily maternal curcumin supplementation during pregnancy on placental function and fetal growth in a mouse model of IUGR fed the low-protein (LP) diet. Pregnant mice were divided into four groups: (1) normal protein (19% protein) diet (NP); (2) LP (8% protein) diet; (3) LP diet + 100 mg/kg curcumin (LPL); (4) LP diet +400 mg/kg curcumin (LPH). The results showed that the LP group decreased fetal weight, placental weight, placental efficiency, serum progesterone level, placental glutathione peroxidase activity activity, blood sinusoids area, and antioxidant gene expression of placenta. In addition, in comparison with the NP group, LP diet increased serum corticosterone level, placental malondialdehyde content, and apoptotic index. Daily curcumin administration decreased the placental apoptosis, while it increased placental efficiency, placental redox balance, blood sinusoids area, and antioxidant-related protein expression in fetal liver. The antioxidant gene expression of placenta and fetal liver was normalized to the NP level after curcumin administration. In conclusion, daily curcumin supplementation could improve maternal placental function and fetal growth in mice with IUGR. Summary Sentence Daily curcumin supplementation could improve maternal placental function and fetal growth in mice with IUGR.
引用
收藏
页码:1090 / 1101
页数:12
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