IGF-1 infusion to fetal sheep increases organ growth but not by stimulating nutrient transfer to the fetus.
Stremming. Jane J; Heard. Sara S; White. Alicia A; Chang. Eileen I EI; Shaw. Steven C SC; Wesolowski. Stephanie R SR; Jonker. Sonnet S SS; Rozance. Paul J PJ; Brown. Laura D LD
Key Findings
- LR3 IGF‑1 increased weights of specific fetal organs (heart, adrenal, spleen) without raising overall fetal weight
- Umbilical amino‑acid uptake and fetal plasma amino‑acid levels were lower in the IGF‑1 group
- Myoblast (muscle precursor) proliferation was higher with IGF‑1, despite unchanged blood flow and nutrient transfer
Practical Outcomes
- For biohackers, this study shows that IGF‑1 can drive organ‑specific growth without increasing nutrient supply, but it’s a fetal sheep model and not directly applicable to adult humans. It doesn’t provide a usable dosing protocol or safety data for supplementation, so it has limited practical relevance for longevity or performance enhancement.
Summary
Giving a short‑acting IGF‑1 variant (LR3 IGF‑1) to unborn sheep for a week made some organs like the heart and adrenal gland a bit bigger, but it didn’t make the whole fetus heavier and didn’t boost blood flow or nutrient delivery from the placenta. In fact, the fetuses took up fewer amino acids, yet they still grew those organs, likely because they used the available nutrients more efficiently.
Abstract
Insulin-like growth factor-1 (IGF-1) is an important fetal growth factor. However, the role of fetal IGF-1 in increasing placental blood flow, nutrient transfer, and nutrient availability to support fetal growth and protein accretion is not well understood. Catheterized fetuses from late gestation pregnant sheep received an intravenous infusion of LR3 IGF-1 (LR3 IGF-1; <i>n</i> = 8) or saline (SAL; <i>n</i> = 8) for 1 wk. Sheep then underwent a metabolic study to measure uterine and umbilical blood flow, nutrient uptake rates, and fetal protein kinetic rates. By the end of the infusion, fetal weights were not statistically different between groups (SAL: 3.260 ± 0.211 kg, LR3 IGF-1: 3.682 ± 0.183; <i>P</i> = 0.15). Fetal heart, adrenal gland, and spleen weights were higher (<i>P</i> < 0.05), and insulin was lower in LR3 IGF-1 (<i>P</i> < 0.05). Uterine and umbilical blood flow and umbilical uptake rates of glucose, lactate, and oxygen were similar between groups. Umbilical amino acid uptake rates were lower in LR3 IGF-1 (<i>P</i> < 0.05) as were fetal concentrations of multiple amino acids. Fetal protein kinetic rates were similar. LR3 IGF-1 skeletal muscle had higher myoblast proliferation (<i>P</i> < 0.05). In summary, LR3 IGF-1 infusion for 1 wk into late gestation fetal sheep increased the weight of some fetal organs. However, because umbilical amino acid uptake rates and fetal plasma amino acid concentrations were lower in the LR3 IGF-1 group, we speculate that animals treated with LR3 IGF-1 can efficiently utilize available nutrients to support organ-specific growth in the fetus rather than by stimulating placental blood flow or nutrient transfer to the fetus.<b>NEW & NOTEWORTHY</b> After a 1-wk infusion of LR3 IGF-1, late gestation fetal sheep had lower umbilical uptake rates of amino acids, lower fetal arterial amino acid and insulin concentrations, and lower fetal oxygen content; however, LR-3 IGF-1-treated fetuses were still able to effectively utilize the available nutrients and oxygen to support organ growth and myoblast proliferation.
Study Information
pubmed
2021
2021-01-11T00:00:00.000Z
10.1152/ajpendo.00453.2020
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