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Metabolic Evidence for Adaptation to a High Protein Diet in Rats
Open accessAbstract
This study was designed to assess the effects of long-term adaptation to a high protein diet on energy intake, body weight gain, body composition and splanchnic metabolic indicators in rats. For this purpose, adult male Wistar rats were fed either a 50 g/100 g dry matter (DM) protein diet (P50 group) or a 14 g/100 g DM protein diet (P14 group) for 21 d. These two groups were compared with a P14 pair-fed (P14-pf) group that consumed the same daily energy as the P50 group. The energy intake of the P50 group was 16 +/- 1% less than that of the P14 group (P < 0.05), and the P50 group had significantly lower body weight. The P50 group had significantly less adipose tissue compared with both P14 and P14-pf rats. The activities of the brush border membrane enzymes, neutral aminopeptidase and gamma-glutamyl transferase, were significantly higher in the P50 group than in the P14 rats. Similarly, the activities of alanine aminotransferase, arginase and serine dehydratase were significantly higher in the liver of P50 rats compared with P14 rats. Both amino acid transporter system A and X(A,G-) activities, measured in freshly isolated hepatocytes, were significantly higher in the P50 group (8- and 1.5-fold, P < 0.05, respectively) compared with the P14 group. The 1.5-fold increase in the steady-state activity of X(A,G-) was accompanied by a doubling of EAAT2 mRNA, involved in the system X(A,G-). This study provides confirmation that specific biochemical and molecular adaptive processes of the splanchnic area are involved in the response to variations in the protein content of the diet.
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“some studies suggest that rats will consume and grow rather well on high-protein diets if given sufficient time to adapt to the diet”
From FGF21 and the physiological regulation of macronutrient preference (2020) · cites this paper as [66]
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“As expected (42), control animals fed a high-protein diet (Fig. 5C, D) exhibited decreased body weight gain, food intake, and other body composition parameters compared with control animals fed normal diet (Fig. 5A, B).”
From Anabolic effect of plant brassinosteroid (2011) · cites this paper as [42]
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“%) in the BBM by HPD, verifying findings of previously published studies (8, 11–13 , 27 ).”
FoxO transcription factors couple the urea cycle and gluconeogenesis by controlling Ass1Preprint
Karkoutly, S., Takeuchi, Y., Saber, Z. M., Tao, D., Mendsaikhan, T., Saikawa, R., Aita, Y., Murayama, Y., Shikama, A., Masuda, Y., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2025.12.22.695746
FoxO transcription factors coordinate the urea cycle and gluconeogenesis by controlling Ass1
Karkoutly, S., Takeuchi, Y., Saber, Z. M., Tao, D., Mendsaikhan, T., Saikawa, R., Aita, Y., Murayama, Y., Shikama, A., Masuda, Y., et al. (2026) · iScience · doi:10.1016/j.isci.2026.117399
“9–13 Also known as the ornithine cycle, the urea cycle is a liver-specific pathway that comprises five core enzymes: carbamoyl-phosphate synthetase 1 (CPS1), ornithine transcarbamylase (OTC), argininosuccinate synthetase (ASS1), argininosuccinate lyase (ASL), and arginase 1 (ARG1).”
Metadata
- Authors
- Jean, C., Rome, S., Mathé, V., Huneau, J.-F., Aattouri, N., Fromentin, G., Achagiotis, C. L., & Tomé, D.
- Affiliations
- Physiologie de la Nutrition et du Comportement Alimentaire (FR)
- Corresponding author
- Tomé, Daniel
- Venue
- The Journal of Nutrition
- Publisher
- Elsevier BV
- Published
- 2001-01
- Volume
- 131
- Issue
- 1
- Pages
- 91-98
- ISSN
- 0022-3166 (ISSN-L)
- OpenAlex
- W1918271356
- Cited by
- 189
- References
- 52
- Citations by year
- 2026: 1 · 2025: 8 · 2024: 4 · 2023: 6 · 2022: 5 · 2021: 9 · 2020: 9 · 2019: 7 · 2018: 10 · 2017: 11 · 2016: 9 · 2015: 4 · 2014: 2 · 2013: 6 · 2012: 13
- FWCI
- 13.79
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Journal of Nutrition (publishedVersion)
- PubMed (publishedVersion)
- HAL (submittedVersion)
- Topics
- Life Sciences › Agricultural and Biological Sciences › Animal Science and Zoology › Animal Nutrition and Physiology
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diet, Metabolism, and Disease
- Health Sciences › Nursing › Nutrition and Dietetics › Muscle metabolism and nutrition
- Keywords
- high-protein diet, energy intake, weight gain, body composition, adipose tissue, splanchnic metabolism, brush border enzymes, gamma-glutamyl transferase, amino acid transporters, system A, hepatocytes
- MeSH terms
- Adaptation, Physiological, Animals, Body Composition, Carrier Proteins, Dietary Proteins, Energy Metabolism, Enzymes, Intestines, Liver, Male, Metabolism, Weight Gain, Rats, Wistar, Receptors, Glutamate, Receptors, Neurotransmitter, Amino Acid Transport Systems, Amino Acid Transport System X-AG, Excitatory Amino Acid Transporter 2, Symporters, Glutamate Plasma Membrane Transport Proteins, Rats
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