Suppr超能文献

在妊娠早期至中期营养限制的母羊的子叶中,生长信号和营养转运蛋白的上调。

Upregulation of growth signaling and nutrient transporters in cotyledons of early to mid-gestational nutrient restricted ewes.

机构信息

Center for the Study of Fetal Programming, University of Wyoming, Laramie, WY 82071, USA.

出版信息

Placenta. 2011 Mar;32(3):255-63. doi: 10.1016/j.placenta.2011.01.007. Epub 2011 Feb 3.

Abstract

Multiparous ewes received 100% (control, C, n = 13) or 50% (nutrient restricted, NR, n = 14) of NRC dietary requirements from d28-d78 of gestation. On d78, 5 C and 6 NR ewes were necropsied. The remaining 8 C and 8 NR ewes were fed to 100% of NRC from d78-d135 and necropsied. Maternal blood was collected at both necropsies and at weekly intervals for assay of glucose, insulin and leptin. Fetal blood was collected at d78 and d135 necropsies for assay of glucose and lipids. Cotyledonary (COT) tissue was evaluated for protein and mRNA expression [fatty acid transporter (FATP)1, FATP4, CD36, glucose transporter (GLUT)1 and GLUT3], mRNA expression only [placenta fatty acid binding protein (FABPpm) and lipoprotein lipase (LPL)], or expression of phosphorylated and total protein forms [AMP kinase (AMPK)α, acetyl-CoA carboxylase (ACC), extracellular signal-regulated kinase (Erk)1/2, mammalian target of rapamycin (mTOR) and protein kinase B (Akt)]. On d78, but not d135, placental and fetal weights were reduced (P < 0.05) in NR vs. C ewes. Maternal circulating glucose, insulin and leptin levels were decreased in NR vs. C ewes on d78 (P < 0.05) but similar at d135. Fetal blood glucose and triglyceride levels were lower in NR vs. C ewes (P < 0.05) on d78, but similar on d135. On d78, GLUT1, FATP4, CD36 mRNA and protein expression levels, FABPpm mRNA level, and leptin protein level were all increased (P < 0.05) in COT of NR vs. C ewes. AMPK, ACC, and Erk1/2 activities were also increased (P < 0.05) in NR vs. C COT on d78. In contrast, only FATP4 was increased (P < 0.05) at both the mRNA and protein levels in COT of NR realimented vs. C ewes on d135. These data demonstrate placental adaptation to maternal NR through increasing nutrient transporter production and growth signaling activity.

摘要

多胎母羊在妊娠第 28-78 天接受了 NRC 饮食需求的 100%(对照组,C,n=13)或 50%(营养限制,NR,n=14)。在第 78 天,5 只 C 组和 6 只 NR 组母羊被安乐死。其余 8 只 C 组和 8 只 NR 组母羊从第 78 天到第 135 天喂食至 100%的 NRC,并被安乐死。在两次剖检时和每周采集一次母羊血液,以检测葡萄糖、胰岛素和瘦素。在第 78 天和第 135 天剖检时采集胎儿血液,以检测葡萄糖和脂质。评估胎盘中的蛋白和 mRNA 表达[脂肪酸转运蛋白(FATP)1、FATP4、CD36、葡萄糖转运蛋白(GLUT)1 和 GLUT3]、仅 mRNA 表达[胎盘脂肪酸结合蛋白(FABPpm)和脂蛋白脂肪酶(LPL)]或磷酸化和总蛋白形式的表达[AMP 激酶(AMPK)α、乙酰辅酶 A 羧化酶(ACC)、细胞外信号调节激酶(Erk)1/2、雷帕霉素哺乳动物靶标(mTOR)和蛋白激酶 B(Akt)]。在第 78 天,但不在第 135 天,NR 组与 C 组母羊的胎盘和胎儿重量均降低(P<0.05)。NR 组母羊的循环葡萄糖、胰岛素和瘦素水平在第 78 天低于 C 组(P<0.05),但在第 135 天相似。在第 78 天,NR 组与 C 组母羊的胎儿血糖和甘油三酯水平均较低(P<0.05),但在第 135 天相似。在第 78 天,NR 组与 C 组母羊的 GLUT1、FATP4、CD36 mRNA 和蛋白表达水平、FABPpm mRNA 水平和瘦素蛋白水平均升高(P<0.05)。在第 78 天,NR 组母羊的 AMPK、ACC 和 Erk1/2 活性也升高(P<0.05)。相比之下,只有 FATP4 在第 135 天 NR 组母羊的胎盘中同时在 mRNA 和蛋白水平上增加(P<0.05)。这些数据表明,胎盘通过增加营养转运蛋白的产生和生长信号活性来适应母体 NR。

相似文献

1
Upregulation of growth signaling and nutrient transporters in cotyledons of early to mid-gestational nutrient restricted ewes.
Placenta. 2011 Mar;32(3):255-63. doi: 10.1016/j.placenta.2011.01.007. Epub 2011 Feb 3.
3
Maternal obesity markedly increases placental fatty acid transporter expression and fetal blood triglycerides at midgestation in the ewe.
Am J Physiol Regul Integr Comp Physiol. 2010 Nov;299(5):R1224-31. doi: 10.1152/ajpregu.00309.2010. Epub 2010 Sep 15.
7
Periconceptional nutrient restriction in the ewe alters MAPK/ERK1/2 and PI3K/Akt growth signaling pathways and vascularity in the placentome.
Placenta. 2007 Nov-Dec;28(11-12):1192-9. doi: 10.1016/j.placenta.2007.05.004. Epub 2007 Jun 21.
8

引用本文的文献

3
Placental adaptations supporting fetal growth during normal and adverse gestational environments.
Exp Physiol. 2023 Mar;108(3):371-397. doi: 10.1113/EP090442. Epub 2022 Dec 9.
4
Chronic Hypoxia in Ovine Pregnancy Recapitulates Physiological and Molecular Markers of Preeclampsia in the Mother, Placenta, and Offspring.
Hypertension. 2022 Jul;79(7):1525-1535. doi: 10.1161/HYPERTENSIONAHA.122.19175. Epub 2022 May 9.
5
Ruminant Placental Adaptation in Early Maternal Undernutrition: An Overview.
Front Vet Sci. 2021 Oct 20;8:755034. doi: 10.3389/fvets.2021.755034. eCollection 2021.
8
Placental adaptations in a nonhuman primate model of gestational protein restriction.
J Dev Orig Health Dis. 2021 Dec;12(6):908-914. doi: 10.1017/S204017442000121X. Epub 2020 Dec 14.
9
Stimulation of soluble guanylate cyclase diminishes intrauterine growth restriction in a rat model of placental ischemia.
Am J Physiol Regul Integr Comp Physiol. 2021 Feb 1;320(2):R149-R161. doi: 10.1152/ajpregu.00234.2020. Epub 2020 Nov 11.

本文引用的文献

1
Maternal obesity and overnutrition alter fetal growth rate and cotyledonary vascularity and angiogenic factor expression in the ewe.
Am J Physiol Regul Integr Comp Physiol. 2010 Jul;299(1):R249-58. doi: 10.1152/ajpregu.00498.2009. Epub 2010 Apr 28.
2
Adaptations in placental phenotype support fetal growth during undernutrition of pregnant mice.
J Physiol. 2010 Feb 1;588(Pt 3):527-38. doi: 10.1113/jphysiol.2009.181214. Epub 2009 Nov 30.
3
AMPK as a mediator of hormonal signalling.
J Mol Endocrinol. 2010 Feb;44(2):87-97. doi: 10.1677/JME-09-0063. Epub 2009 Jul 22.
4
Maternal obesity accelerates fetal pancreatic beta-cell but not alpha-cell development in sheep: prenatal consequences.
Am J Physiol Regul Integr Comp Physiol. 2009 Sep;297(3):R835-43. doi: 10.1152/ajpregu.00072.2009. Epub 2009 Jul 15.
6
Transport of fatty acids across the human placenta: a review.
Prog Lipid Res. 2009 Jan;48(1):52-61. doi: 10.1016/j.plipres.2008.11.001. Epub 2008 Nov 12.
7
Long-chain polyunsaturated fatty acid (LC-PUFA) transfer across the placenta.
Clin Nutr. 2008 Oct;27(5):685-93. doi: 10.1016/j.clnu.2008.05.010. Epub 2008 Jul 18.
9
Hypothalamic fatty acid metabolism: a housekeeping pathway that regulates food intake.
Bioessays. 2007 Mar;29(3):248-61. doi: 10.1002/bies.20539.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验