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

Biol Reprod. 2020 Apr 24;102(5):1090-1101. doi: 10.1093/biolre/ioaa005.

Abstract

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.

Keywords: curcumin; intra-uterine growth retardation; placenta.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / pharmacology
  • Apoptosis / drug effects
  • Curcumin / administration & dosage
  • Curcumin / pharmacology*
  • Diet, Protein-Restricted / adverse effects
  • Dietary Supplements
  • Female
  • Fetal Development / drug effects*
  • Fetal Growth Retardation / chemically induced
  • Fetal Growth Retardation / drug therapy*
  • Fetus / drug effects
  • Fetus / metabolism
  • Gene Expression Regulation, Developmental / drug effects
  • Liver / metabolism
  • Mice
  • Mice, Inbred ICR
  • Oxidative Stress
  • Placenta / drug effects*
  • Pregnancy
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • RNA, Messenger
  • Curcumin