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Published on: August 21, 2017
Postprandial increase of oleoylethanolamide mobilization in small intestine of the Burmese python (Python molurus)
Giuseppe Astarita1, Bryan C Rourke, Johnnie B Andersen
1Dept. of Psychiatry and Human Behavior, Univ. of California, Irvine, CA, USA.
Oleoylethanolamide (OEA), a lipid mediator, significantly increases in python intestines after feeding, suggesting a conserved role in satiety across vertebrates. This finding highlights OEA
Area of Science:
- Comparative Physiology
- Lipid Metabolism
- Gastrointestinal Endocrinology
Background:
- Oleoylethanolamide (OEA) is an endogenous lipid mediator known to inhibit feeding in rodents by activating the PPAR-alpha receptor.
- In rodents, intestinal OEA levels rise post-feeding, contributing to satiety.
- Burmese pythons exhibit extreme feeding patterns and significant post-meal physiological changes.
Purpose of the Study:
- To investigate if feeding-induced OEA mobilization occurs in Burmese pythons (Python molurus).
- To explore the potential evolutionary conservation of OEA's role in energy intake regulation.
Main Methods:
- Measurement of OEA levels in the gastrointestinal tract of fasted and fed pythons using liquid chromatography/mass spectrometry (LC/MS).
- Analysis of N-acyl phosphatidylethanolamine species as potential OEA precursors.
- Quantification of various fatty-acid ethanolamides (FAEs) in python intestines.
Main Results:
- A dramatic, nearly 300-fold increase in small intestinal OEA levels was observed in fed pythons compared to fasted ones.
- Increased levels of OEA precursors (N-acyl phosphatidylethanolamines) suggest in situ OEA biosynthesis.
- Elevated levels of saturated, mono-, and diunsaturated FAEs were found in fed pythons' small intestines.
Conclusions:
- Feeding stimulates significant OEA mobilization in the Burmese python's gastrointestinal tract.
- The presence of OEA and related FAEs in pythons indicates a potentially widespread role for these lipid messengers across vertebrate groups.
- OEA may represent an evolutionarily ancient mechanism for regulating energy intake.
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