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Oral aversion to dietary sugar, ethanol and glycerol correlates with alterations in specific hepatic metabolites in a mouse model of human citrin deficiency.
- Source :
-
Molecular genetics and metabolism [Mol Genet Metab] 2017 Apr; Vol. 120 (4), pp. 306-316. Date of Electronic Publication: 2017 Feb 14. - Publication Year :
- 2017
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Abstract
- Mice carrying simultaneous homozygous mutations in the genes encoding citrin, the mitochondrial aspartate-glutamate carrier 2 (AGC2) protein, and mitochondrial glycerol-3-phosphate dehydrogenase (mGPD), are a phenotypically representative model of human citrin (a.k.a., AGC2) deficiency. In this study, we investigated the voluntary oral intake and preference for sucrose, glycerol or ethanol solutions by wild-type, citrin (Ctrn)-knockout (KO), mGPD-KO, and Ctrn/mGPD double-KO mice; all substances that are known or suspected precipitating factors in the pathogenesis of human citrin deficiency. The double-KO mice showed clear suppressed intake of sucrose, consuming less with progressively higher concentrations compared to the other mice. Similar observations were made when glycerol or ethanol were given. The preference of Ctrn-KO and mGPD-KO mice varied with the different treatments; essentially no differences were observed for sucrose, while an intermediate intake or similar to that of the double-KO mice was observed for glycerol and ethanol. We next examined the hepatic glycerol 3-phosphate, citrate, citrulline, lysine, glutamate and adenine nucleotide levels following forced enteral administration of these solutions. A strong correlation between the simultaneous increased hepatic glycerol 3-phosphate and decreased ATP or total adenine nucleotide content and observed aversion of the mice during evaluation of their voluntary preferences was found. Overall, our results suggest that the aversion observed in the double-KO mice to these solutions is initiated and/or mediated by hepatic metabolic perturbations, resulting in a behavioral response to increased hepatic cytosolic NADH and a decreased cellular adenine nucleotide pool. These findings may underlie the dietary predilections observed in human citrin deficient patients.<br /> (Copyright © 2017 Elsevier Inc. All rights reserved.)
- Subjects :
- Adenosine Triphosphate metabolism
Amino Acid Transport Systems, Acidic genetics
Animals
Antiporters genetics
Disease Models, Animal
Glycerolphosphate Dehydrogenase genetics
Glycerophosphates metabolism
Humans
Mice
Mice, Knockout
Citrullinemia metabolism
Dietary Sucrose administration & dosage
Ethanol administration & dosage
Glycerol administration & dosage
Liver chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 1096-7206
- Volume :
- 120
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Molecular genetics and metabolism
- Publication Type :
- Academic Journal
- Accession number :
- 28259708
- Full Text :
- https://doi.org/10.1016/j.ymgme.2017.02.004