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Culturing and Measuring Fetal and Newborn Murine Long Bones
Published on: April 26, 2019
Intrauterine programming of bone. Part 1: alteration of the osteogenic environment
S A Lanham1, C Roberts, C Cooper
1Bone and Joint Research Group, Developmental Origins of Health and Disease, University of Southampton, Southampton, SO16 6YD, UK. S.A.Lanham@soton.ac.uk.
Insights
Maternal protein restriction during pregnancy alters offspring bone development, leading to lasting changes in bone biochemistry and skeletal programming. This highlights the critical role of in utero nutrition on long-term bone health.
Area of Science:
- Developmental biology
- Nutritional science
- Skeletal biology
Background:
- Epidemiological studies suggest skeletal growth is programmed during intrauterine and early postnatal life.
- This study investigates the effects of maternal protein insufficiency on skeletal development in a rat model.
- Osteoporosis is believed to be partly programmed in utero.
Purpose of the Study:
- To investigate the long-term effects of maternal protein restriction during pregnancy on offspring skeletal development.
- To analyze bone biochemistry and serum markers in offspring exposed to a low protein diet in utero.
- To understand the consequences of altered in utero diet on later life skeletal health.
Main Methods:
- Rat dams were fed either an 18% (control) or 9% (low protein) diet during pregnancy.
- Offspring were studied at various time points: 4, 8, 12, 16, 20, and 47 weeks of age.
- Bone biochemistry and serum markers (alkaline phosphatase, IGF-1, osteocalcin, 25-OH vitamin D) were analyzed.
Main Results:
- Offspring of protein-restricted dams showed altered alkaline phosphatase activity, peaking earlier (4 weeks) compared to controls (8-20 weeks).
- Serum IGF-1 was lower in female offspring at 4 weeks.
- Serum osteocalcin was higher in both male and female offspring at 4 weeks, and serum 25-OH vitamin D was lower in males at later time points.
Conclusions:
- A low protein diet in utero significantly affected the osteogenic environment in offspring.
- These effects on skeletal development persisted into late adulthood.
- Early life nutritional environment plays a key role in programming skeletal development with lifelong consequences.
Unlabelled:
Osteoporosis is believed to partly be programmed in utero. Rat dams were given a low protein diet during pregnancy and 135 offspring studied at different ages. Bone biochemistry showed altered characteristics. Altered in utero diet has consequences for later life.
Introduction:
Epidemiological studies suggest skeletal growth is programmed during intrauterine and early postnatal life. We have investigated this in a rat model of maternal protein insufficiency.
Methods:
Dams received either 18% w/w (control) or 9% w/w (low protein) diet during pregnancy, and the offspring were studied at selected time points (4, 8, 12, 16, 20, 47 weeks).
Results:
Alkaline phosphatase activity in controls reached peak levels from 8 to 20 weeks of age. In contrast, restricted diet offspring were at peak levels from 4 weeks of age. Peak levels were similar in both groups. Serum IGF-1 levels were lower in female restricted diet offspring at 4 weeks of age, and serum osteocalcin was significantly higher at 4 weeks of age in male and female offspring from mothers fed the restricted diet, whereas serum 25-OH vitamin D was significantly lower in restricted diet males at 8, 12, and 20 weeks of age.
Conclusions:
These data indicate that a low protein diet in utero affected the osteogenic environment in the offspring with effects that persist into late adulthood. These results indicate the key role of the nutritional environment in early development on programming of skeletal development with implicit consequences in later life.
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