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Published on: April 29, 2015
Jejunal function and plasma amino acid concentrations in the segmental trisomic Ts65Dn mouse
J A Cefalu1, W J Croom, E J Eisen
1Department of Animal Science, North Carolina State University, Raleigh 27695-7621, USA.
Summary
Mice with trisomy for MMU 16 (Ts65Dn) exhibit altered digestive function and amino acid metabolism. These mice show differences in oxygen consumption and jejunal morphology compared to controls.
Area of Science:
- Genetics
- Physiology
- Biochemistry
Background:
- The Ts65Dn mouse model is trisomic for the distal portion of MMU 16.
- Understanding jejunal function and amino acid metabolism is crucial for physiological studies.
Purpose of the Study:
- To investigate differences in jejunal function and plasma amino acid concentrations between Ts65Dn mice and diploid controls.
- To assess O2 consumption, glucose uptake, and jejunal morphology in Ts65Dn mice.
Main Methods:
- Comparison of whole-body and intestinal O2 consumption between Ts65Dn and control mice.
- Measurement of jejunal glucose uptake and plasma amino acid concentrations.
- Histomorphometric analysis of jejunal mucosa.
Main Results:
- Ts65Dn mice showed lower O2 consumption per gram of fasted body weight.
- No significant differences in active or passive glucose uptake were observed.
- Ts65Dn mice exhibited higher apparent energetic efficiency of jejunal active glucose uptake.
- Shorter villus height and decreased villus circumference were noted in Ts65Dn mice.
- Elevated plasma concentrations of tyrosine, phenylalanine, valine, leucine, isoleucine, and citrulline were found in Ts65Dn mice.
- Lower plasma hydroxyproline concentrations were detected in Ts65Dn mice.
Conclusions:
- Ts65Dn mice display anomalies in digestive function, including altered oxygen consumption and jejunal morphology.
- Significant differences in plasma amino acid profiles suggest metabolic disturbances in Ts65Dn mice.
- These findings highlight the physiological impact of trisomy on MMU 16 in mice.

