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Abstract
Enhancing placental insulin-like growth factor (IGF) availability appears to be an attractive strategy for improving outcomes in fetal growth restriction (FGR). Our approach was the novel use of [Leu(27)]IGF-II, a human IGF-II analog that binds the IGF-II clearance receptor IGF-IIR in fetal growth-restricted (FGR) mice. We hypothesized that the impact of [Leu(27)]IGF-II infusion in C57BL/6J (wild-type) and endothelial nitric oxide synthase knockout (eNOS(-/-); FGR) mice would be to enhance fetal growth and investigated this from mid- to late gestation; 1 mg·kg(-1)·day(-1) [Leu(27)]IGF-II was delivered via a subcutaneous miniosmotic pump from E12.5 to E18.5. Fetal and placental weights recorded at E18.5 were used to generate frequency distribution curves; fetuses
Original language | English |
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Pages (from-to) | E24-E31 |
Journal | American journal of physiology. Endocrinology and metabolism |
Volume | 310 |
Issue number | 1 |
DOIs | |
Publication status | Published - 1 Jan 2016 |
Keywords
- [Leu27]insulin-like growth factor II
- endothelial nitric oxide synthase knockout
- fetal growth restriction
- insulin-like growth factor
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Dive into the research topics of 'The impact of a human IGF-II analog ([Leu27]IGF-II) on fetal growth in a mouse model of fetal growth restriction'. Together they form a unique fingerprint.Projects
- 1 Finished
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Foetal Growth Restriction: A Failure of Placental Adaptation in Response to Foetal Nutrient Demand.
Dilworth, M. (PI)
1/09/13 → 31/08/18
Project: Research