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The Use of Gas Chromatography to Analyze Compositional Changes of Fatty Acids in Rat Liver Tissue during Pregnancy
Published on: March 13, 2014
Selective changes to phosphatidylcholine and phosphatidylethanolamine molecular species in the developing fetal
Graham C Burdge1, Anthony D Postle
1Institute of Human Nutrition, School of Medicine, University of Southampton, Southampton, UK. g.c.burdge@soton.ac.uk
Insights
Fetal liver phospholipid composition, including phosphatidylcholine (PC) and phosphatidylethanolamine (PE), changes selectively with gestational age. These developmental shifts in liver PC and PE species are largely independent of maternal fatty acid supply.
Area of Science:
- Biochemistry
- Developmental Biology
- Lipidomics
Background:
- Membrane phospholipid molecular species composition critically impacts integral protein function and cellular signaling.
- Understanding developmental changes in fetal lipid profiles is essential for assessing metabolic health and developmental trajectories.
Purpose of the Study:
- To investigate the impact of advancing gestational age on the molecular species composition of fetal guinea pig liver phosphatidylcholine (PC) and phosphatidylethanolamine (PE).
- To analyze the changes in plasma PC molecular species composition during fetal development.
- To determine if maternal fatty acid supply influences these developmental changes.
Main Methods:
- Fetal guinea pig livers and plasma were collected at regular intervals (every 5 days from 40 to 65 days of gestation, and at term - 68 days).
- Hepatic and plasma PC and PE molecular species were quantified using electrospray ionization mass spectrometry.
- Statistical analysis was performed to identify significant changes in lipid species concentrations relative to gestational age.
Main Results:
- Increasing gestational age led to selective alterations in specific hepatic PC and PE molecular species.
- The ratio of sn-1 18:0 to sn-1 16:0 species increased in liver PC but not PE.
- Concentrations of 1-O-alkyl-2-acyl PC species decreased significantly during specific gestational periods, while 1-O-alkenyl-2-acyl PE species showed a transient increase.
- PC and PE sn-2 18:2n-6 species concentrations tripled from day 40 to term, with differential increases observed for specific PC and PE species.
- Plasma PC composition mirrored the changes observed in hepatic PC.
Conclusions:
- Fetal liver PC and PE molecular species composition undergo differential regulation during development.
- These developmental changes appear to be largely independent of maternal fatty acid supply.
- The findings highlight the intricate control over lipid metabolism during late gestation.
Abstract:
The molecular species composition of membrane phospholipids influences the activities of integral proteins and cell signalling pathways. We determined the effect of increasing gestational age on fetal guinea pig liver phosphatidylcholine (PC) and phosphatidylethanolamine (PE), and plasma PC molecular species composition. The livers were collected from fetuses (n = 5/time point) at 5 day intervals between 40 and 65 days of gestation, and at term (68 days). Hepatic PC and PE molecular species composition was determined by electrospray ionisation mass spectrometry. An increasing gestational age was accompanied by selective changes in individual molecular species. The proportion of the sn-1 18:0 species increased relative to the sn-1 16:0 species in liver PC, but not PE, with an increasing gestational age. 1-O-alkyl-2-acyl PC species concentrations decreased significantly between 40 and 45 days of gestation (40%), and 65 and 68 days (54%). Total 1-O-alkenyl-2-acyl PE species concentration increased between days 60 and 65, due to a rise in 1-O-16:0 alkyl/20:4 content, and then decreased until term. Between day 40 and term, PC and PE sn-2 18:2n-6 species concentrations increased 3-fold. PC16:0/18:2 increased gradually throughout gestation, while PC18:0/18:2 content only increased after day 65. The overall increase in PE18:2n-6 content was due to PE18:0/18:2 alone. The composition of plasma PC essentially reflected hepatic PC. Overall, these data suggest differential regulation of hepatic PC and PE molecular species composition during development which is essentially independent of the maternal fatty acid supply.
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