Maternal obesity depresses essential fatty acid transport in the placenta
孕妇肥胖会抑制胎盘中必需脂肪酸的转运
基本信息
- 批准号:8847576
- 负责人:
- 金额:$ 23.46万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2013
- 资助国家:美国
- 起止时间:2013-05-01 至 2017-04-30
- 项目状态:已结题
- 来源:
- 关键词:5&apos-AMP-activated protein kinaseAcidsAdolescentAdultAnimal ModelAnimalsAnti-Inflammatory AgentsAnti-inflammatoryAntioxidantsArachidonic AcidsAreaBiomedical ResearchBirthBlood VesselsBody mass indexC-reactive proteinCD36 geneCardiovascular DiseasesCardiovascular systemChildChronic DiseaseClinical ResearchCoronary heart diseaseDataDepressed moodDevelopmentDietDietary Essential Fatty AcidDiseaseElderlyEnvironmentEpidemicEssential Fatty AcidsFatty AcidsFatty LiverFatty acid glycerol estersFemaleFetal DevelopmentFetusFutureGenderGene ExpressionGoalsGrowthHealthHealth Care CostsHealth SciencesHeart ResearchHumanImmunohistochemistryIn VitroIncidenceIndiumInflammationInflammatoryInstitutionInterleukin-1Interleukin-8InvestigationJapanese PopulationKineticsLabelLeadLifeLipidsLiteratureLiverMacacaMeasuresMediatingMetabolic syndromeMetabolismModelingMolecular BiologyMonkeysMothersMyocardiumNeonatalNeurologicNewborn InfantNutrientNutritional ScienceObesityOleic AcidsOperative Surgical ProceduresOregonOutcomeOverweightPathologyPerinatalPerinatal mortality demographicsPhysiologyPlacentaPlayPopulationPregnancyPrenatal NutritionPrevalencePrimary Cell CulturesPrimatesPropertyProtein Kinase InhibitorsResearchResearch InstituteResearch MethodologyResearch PersonnelResearch TrainingRiskRoleScientistStable Isotope LabelingStearic AcidsThird Pregnancy TrimesterTissuesTracerTrainingTraining ProgramsTranslational ResearchTumor Necrosis Factor-alphaUnited StatesUniversitiesWomanWorkabstractingadverse outcomeboyscardiovascular disorder riskcareercytokinedesignexperiencefatty acid transportfetalfetus nutritiongirlshigh riskin uteroin vivomalemother nutritionnonhuman primatenutritionoffspringplacental transferpregnantprogramsprotein kinase inhibitorrapid growthreceptorresponsesensorsextranslational studyuptake
项目摘要
Project Abstract
The candidate's five-year career goal is to become an independent investigator in the areas of maternal nutrition
and placental nutrient transport and metabolism. Her long-term career objective is to build a strong translational
research program, utilizing appropriate animal models and human investigations to study the effect of maternal
pre-pregnancy nutrition on placental growth and function, neonatal health, and the offspring's risk of future
cardiovascular disease. It is becoming increasingly clear that the placenta plays a key role in the origin of
adverse fetal outcomes resulting from maternal over- or under-nutrition. In keeping with this view, the placenta is
an important element in the origins of adult chronic disease.
The candidate has a strong scientific background in molecular biology, immunohistochemistry, primary
cell culture and small and large animal surgery. She has gained expertise in fetal physiology (especially of the
cardiovascular system) and is well-versed in the literature surrounding the developmental origins of health and
cardiovascular disease. Additional training is required however before she can achieve her career goal of
becoming an independent investigator in maternal-fetal health. The proposed training program has been
designed to provide: 1) training in placental physiology and research methodologies, 2) experience in nutritional
science and research methodologies and 3) in-depth training in human investigation. The Oregon Health and
Science University is an ideal environment for this training. It offers its strong reputation as a leading biomedical
research and training institution; the Heart Research Center is internationally recognized for its work in fetal
physiology and the developmental origins of health and disease; the Oregon National Primate Research Center
is internationally recognized for its translational research in pregnancy and the Oregon Clinical and Translational
Research Institute is dedicated to the development of successful trainees and young investigators in
translational and clinical research.
One in five women who deliver in the United States is obese (body mass index (BMI) of >30 kg/m2). This
condition is associated with both short- and long-term adverse consequences for mother and her baby. Such
babies are at risk for developing chronic diseases including adult-onset coronary heart disease and the
metabolic syndrome. Our preliminary data show that male offspring of overweight and obese mothers have lower
levels of docosaehexanoic acid - a long chain polyunsaturated (LC-PUFA) derivative of essential fatty acids - than
female offspring, while no differences in LC-PUFA levels exist between male and female offspring of lean women. Such
deficiencies lead to neurological and vascular pathologies in the newborn. All of the essential LC-PUFA that are
acquired by the fetus are actively transported across the placental barrier. The effect of maternal obesity on
placental delivery of LC-PUFA to the fetus is unknown. Due to their rapid growth in utero, boys invest less in placental
growth than girls and are at a greater risk of undernourishment and poor outcomes in response to stressful conditions.
Maternal obesity exposes the placental-fetal unit to pro-inflammatory molecules. Inflammatory cytokines inhibit fatty
acid uptake in the liver, muscle and heart. The effect of inflammatory cytokines on placental transport is not known. It is
also unknown whether male fetuses and their placentas are more sensitive than females to maternal obesity and
inflammation. The overall goal of this proposal is to determine the degree to which maternal obesity alters
gender-specific fatty acid transport in the placenta.
Studies will be conducted in our non-human primate model of maternal obesity from which we will
establish the relationship between obesity and 3rd trimester placental fatty acid transport in vivo using stable
isotope-labeled fatty acid tracers. Complementary studies in women will determine the degree to which maternal
BMI and fetal sex alter placental lipid uptake. The roles of inflammatory cytokines in altering fatty acid uptake
kinetics will be determined in placental tissue isolated from lean women with male or female offspring. These
translational studies will determine the effect of maternal obesity, fetal sex and inflammatory cytokines on
placental fat transport in a human population.
Upon completion of the proposed studies, we will have determined 1) the degree to which maternal
obesity alters uptake and transport of LC-PUFA in the late gestation non-human primate placenta, 2) the
effect of fetal gender on placental LC-PUFA uptake in women at term and 3) mechanisms by which
inflammatory cytokines suppress placental fatty acid uptake in vitro.
项目摘要
候选人的五年职业目标是成为产妇营养领域的独立调查员
胎盘营养物质的运输和代谢。她的长期职业目标是建立一个强大的翻译
研究计划,利用适当的动物模型和人体调查来研究母体的影响
孕前营养对胎盘生长和功能、新生儿健康及后代未来风险的影响
心血管疾病。越来越清楚的是,胎盘在胎盘的起源中起着关键作用。
母亲营养过多或营养不足造成的不良胎儿结局。与这一观点一致,胎盘是
成人慢性病起源中的一个重要因素。
应聘者在分子生物学、免疫组织化学、初级
细胞培养和大小动物外科手术。她获得了胎儿生理学方面的专业知识(特别是
心血管系统),精通关于健康和健康的发育起源的文献
心血管疾病。然而,在她能够实现她的职业目标之前,还需要额外的培训
成为母婴健康领域的独立调查者。拟议的培训计划已被
旨在提供:1)胎盘生理学和研究方法的培训,2)营养方面的经验
科学和研究方法以及3)人类调查方面的深入培训。俄勒冈州卫生与公众服务部
理工科大学是这种培训的理想环境。它提供了作为领先的生物医学的强大声誉
研究和培训机构;心脏研究中心因其在胎儿方面的工作而得到国际认可
生理学与健康和疾病的发育起源;俄勒冈州国家灵长类研究中心
因其在怀孕和俄勒冈州临床和翻译方面的翻译研究而得到国际认可
研究院致力于培养成功的实习生和年轻的研究人员
翻译和临床研究。
在美国分娩的女性中,有五分之一患有肥胖症(体重指数为30公斤/平方米)。这
这种情况与母亲及其婴儿的短期和长期不良后果有关。是这样的
婴儿有患慢性疾病的风险,包括成人起病的冠心病和
代谢综合征。我们的初步数据显示,超重和肥胖母亲的男性后代的体重较低
二十二碳己酸--一种必需脂肪酸的长链多不饱和(LC-PUFA)衍生物--的水平
雌性后代的LC-PUFA水平没有差异,而瘦身女性后代之间的LC-PUFA水平没有差异。是这样的
缺乏症会导致新生儿的神经和血管病变。所有基本的LC-PUFA都是
由胎儿获得的物质会主动地通过胎盘屏障运输。母体肥胖对母体健康的影响
LC-PUFA通过胎盘进入胎儿的情况尚不清楚。由于他们在子宫内的快速生长,男孩在胎盘上的投资较少
儿童比女孩发育更快,营养不良的风险更大,应对紧张状况的结果也更差。
母亲肥胖使胎盘-胎儿单位暴露于促炎分子。炎性细胞因子抑制脂肪
肝脏、肌肉和心脏的酸性摄取。炎性细胞因子对胎盘转运的影响尚不清楚。它是
也不知道男性胎儿和他们的胎盘是否比女性对母亲肥胖和
发炎。这项提案的总体目标是确定母亲肥胖改变的程度。
特定性别的脂肪酸在胎盘中的运输。
我们将在母体肥胖的非人类灵长类动物模型中进行研究,我们将从
应用STRATE建立体内肥胖与妊娠晚期胎盘脂肪酸转运的关系
同位素标记的脂肪酸示踪剂。对妇女的补充性研究将确定产妇的
体重指数和胎儿性别改变胎盘脂肪摄取。炎性细胞因子在改变脂肪酸摄取中的作用
将从有男性或女性后代的瘦弱女性身上分离出胎盘组织,以确定动力学。这些
翻译研究将确定母亲肥胖、胎儿性别和炎性细胞因子对
人类人群中的胎盘脂肪运输。
在完成拟议的研究后,我们将确定1)产妇
肥胖改变妊娠晚期非人类灵长类胎盘对LC-PUFA的摄取和转运,2)
胎儿性别对足月胎盘LC-PUFA摄取的影响及其机制
炎性细胞因子在体外抑制胎盘脂肪酸摄取。
项目成果
期刊论文数量(8)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Placental oleic acid uptake is lower in male offspring of obese women.
- DOI:10.1016/j.placenta.2013.03.009
- 发表时间:2013-06
- 期刊:
- 影响因子:3.8
- 作者:Brass, E.;Hanson, E.;O'Tierney-Ginn, P. F.
- 通讯作者:O'Tierney-Ginn, P. F.
IFPA Meeting 2013 Workshop Report I: diabetes in pregnancy, maternal dyslipidemia in pregnancy, oxygen in placental development, stem cells and pregnancy pathology.
- DOI:10.1016/j.placenta.2013.11.010
- 发表时间:2014-02
- 期刊:
- 影响因子:3.8
- 作者:M. Abumaree;S. Alahari;C. Albrecht;I. Aye;S. Bainbridge;S. Chauvin;V. Clifton;G. Desoye;L. Ermini;D. Giuffrida;C. Graham;Q. Huang;B. Kalionis;S. Lager;L. Leach;Y. Li;M. Litvack;A. Nuzzo;M. Moretto-Zita;P. O’Tierney-Ginn;T. Powell;A. Rolfo;C. Salomon;A. Serov;M. Westwood;H. Yung;G. Lash
- 通讯作者:M. Abumaree;S. Alahari;C. Albrecht;I. Aye;S. Bainbridge;S. Chauvin;V. Clifton;G. Desoye;L. Ermini;D. Giuffrida;C. Graham;Q. Huang;B. Kalionis;S. Lager;L. Leach;Y. Li;M. Litvack;A. Nuzzo;M. Moretto-Zita;P. O’Tierney-Ginn;T. Powell;A. Rolfo;C. Salomon;A. Serov;M. Westwood;H. Yung;G. Lash
Placental Impact of Dietary Supplements: More Than Micronutrients.
- DOI:10.1016/j.clinthera.2020.11.017
- 发表时间:2021-03
- 期刊:
- 影响因子:3.2
- 作者:Rasool A;Alvarado-Flores F;O'Tierney-Ginn P
- 通讯作者:O'Tierney-Ginn P
Let's Talk About Sex: Placentas' Central Role in Sexually Dimorphic Responses to the Maternal Milieu.
- DOI:10.1210/clinem/dgaa683
- 发表时间:2020-12-01
- 期刊:
- 影响因子:0
- 作者:O'Tierney-Ginn P
- 通讯作者:O'Tierney-Ginn P
Fatty acid transporter expression and regulation is impaired in placental macrovascular endothelial cells in obese women.
肥胖女性胎盘大血管内皮细胞中脂肪酸转运蛋白的表达和调节受损。
- DOI:10.1080/14767058.2017.1397119
- 发表时间:2019
- 期刊:
- 影响因子:0
- 作者:Yang,Xiaohua;Glazebrook,Patricia;Ranasinghe,GeraldineC;Haghiac,Maricela;Calabuig-Navarro,Virtu;Minium,Judi;O'Tierney-Ginn,Perrie
- 通讯作者:O'Tierney-Ginn,Perrie
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
数据更新时间:{{ journalArticles.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ monograph.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ sciAawards.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ conferencePapers.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ patent.updateTime }}
Perrie F O'Tierney-Ginn其他文献
Perrie F O'Tierney-Ginn的其他文献
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
{{ truncateString('Perrie F O'Tierney-Ginn', 18)}}的其他基金
Administrative Supplement to Placental miRNA profiles associated with maternal insulin resistance and fetal adiposity: maternal-placental crosstalk
与母体胰岛素抵抗和胎儿肥胖相关的胎盘 miRNA 谱的行政补充:母体-胎盘串扰
- 批准号:
9911807 - 财政年份:2019
- 资助金额:
$ 23.46万 - 项目类别:
Placental lipid metabolism impacts fetal adiposity and is programmed by the maternal metabolic milieu in early pregnancy
胎盘脂质代谢影响胎儿肥胖,并受妊娠早期母体代谢环境影响
- 批准号:
9397888 - 财政年份:2017
- 资助金额:
$ 23.46万 - 项目类别:
Maternal Metabolic Markers of infant Adiposity (MAMMA) Study supplement)
婴儿肥胖的母体代谢标志物 (MAMMA) 研究补充品)
- 批准号:
10591672 - 财政年份:2017
- 资助金额:
$ 23.46万 - 项目类别:
Placental lipid metabolism impacts fetal adiposity and is programmed by the maternal metabolic milieu in early pregnancy
胎盘脂质代谢影响胎儿肥胖,并受妊娠早期母体代谢环境影响
- 批准号:
10201689 - 财政年份:2017
- 资助金额:
$ 23.46万 - 项目类别:
Maternal obesity depresses essential fatty acid transport in the placenta
孕妇肥胖会抑制胎盘中必需脂肪酸的转运
- 批准号:
8643321 - 财政年份:2013
- 资助金额:
$ 23.46万 - 项目类别:
Maternal obesity depresses essential fatty acid transport in the placenta
孕妇肥胖会抑制胎盘中必需脂肪酸的转运
- 批准号:
8706701 - 财政年份:2013
- 资助金额:
$ 23.46万 - 项目类别:
Maternal obesity depresses essential fatty acid transport in the placenta
孕妇肥胖会抑制胎盘中必需脂肪酸的转运
- 批准号:
8257957 - 财政年份:2011
- 资助金额:
$ 23.46万 - 项目类别:
Maternal obesity depresses essential fatty acid transport in the placenta
孕妇肥胖会抑制胎盘中必需脂肪酸的转运
- 批准号:
8111040 - 财政年份:2011
- 资助金额:
$ 23.46万 - 项目类别:
相似海外基金
Pharmacological targeting of AMP-activated protein kinase for immune cell regulation in Type 1 Diabetes
AMP 激活蛋白激酶对 1 型糖尿病免疫细胞调节的药理学靶向
- 批准号:
2867610 - 财政年份:2023
- 资助金额:
$ 23.46万 - 项目类别:
Studentship
Establishing AMP-activated protein kinase as a regulator of adipose stem cell plasticity and function in health and disease
建立 AMP 激活蛋白激酶作为脂肪干细胞可塑性和健康和疾病功能的调节剂
- 批准号:
BB/W009633/1 - 财政年份:2022
- 资助金额:
$ 23.46万 - 项目类别:
Fellowship
Determining the role of AMP-activated protein kinase in the integration of skeletal muscle metabolism and circadian biology
确定 AMP 激活蛋白激酶在骨骼肌代谢和昼夜节律生物学整合中的作用
- 批准号:
532989-2019 - 财政年份:2021
- 资助金额:
$ 23.46万 - 项目类别:
Postdoctoral Fellowships
Metabolic control of integrin membrane traffic by AMP-activated protein kinase controls cell migration.
AMP 激活的蛋白激酶对整合素膜运输的代谢控制控制着细胞迁移。
- 批准号:
459043 - 财政年份:2021
- 资助金额:
$ 23.46万 - 项目类别:
Studentship Programs
Determining the role of AMP-activated protein kinase in the integration of skeletal muscle metabolism and circadian biology
确定 AMP 激活蛋白激酶在骨骼肌代谢和昼夜节律生物学整合中的作用
- 批准号:
532989-2019 - 财政年份:2020
- 资助金额:
$ 23.46万 - 项目类别:
Postdoctoral Fellowships
The Role of AMP-activated Protein Kinase in GVHD-causing T Cells
AMP 激活的蛋白激酶在引起 GVHD 的 T 细胞中的作用
- 批准号:
10561642 - 财政年份:2019
- 资助金额:
$ 23.46万 - 项目类别:
Determining the role of AMP-activated protein kinase in the integration of skeletal muscle metabolism and circadian biology
确定 AMP 激活蛋白激酶在骨骼肌代谢和昼夜节律生物学整合中的作用
- 批准号:
532989-2019 - 财政年份:2019
- 资助金额:
$ 23.46万 - 项目类别:
Postdoctoral Fellowships
Treating Diabetic Inflammation using AMP-Activated Protein Kinase Activators
使用 AMP 激活的蛋白激酶激活剂治疗糖尿病炎症
- 批准号:
2243045 - 财政年份:2019
- 资助金额:
$ 23.46万 - 项目类别:
Studentship
The Role of AMP-activated Protein Kinase in GVHD-causing T Cells
AMP 激活的蛋白激酶在引起 GVHD 的 T 细胞中的作用
- 批准号:
10359032 - 财政年份:2019
- 资助金额:
$ 23.46万 - 项目类别:
Investigating the therapeutic potential of AMP-activated protein kinase in myotonic dystrophy type 1
研究 AMP 激活蛋白激酶在 1 型强直性肌营养不良中的治疗潜力
- 批准号:
428988 - 财政年份:2019
- 资助金额:
$ 23.46万 - 项目类别:
Studentship Programs