Hepatic autophagy contributes to the metabolic response to dietary protein restriction
Open accessAbstract
Autophagy is an essential cellular response which acts to release stored cellular substrates during nutrient restriction, and particularly plays a key role in the cellular response to amino acid restriction. However, there has been limited work testing whether the induction of autophagy is required for adaptive metabolic responses to dietary protein restriction in the whole animal. Here, we found that moderate dietary protein restriction led to a series of metabolic changes in rats, including increases in food intake and energy expenditure, the downregulation of hepatic fatty acid synthesis gene expression and reduced markers of hepatic mitochondrial number. Importantly, these effects were also associated with an induction of hepatic autophagy. To determine if the induction of autophagy contributes to these metabolic effects, we tested the metabolic response to dietary protein restriction in BCL2-AAA mice, which bear a genetic mutation that impairs autophagy induction. Interestingly, BCL2-AAA mice exhibit exaggerated responses in terms of both food intake and energy expenditure, whereas the effects of protein restriction on hepatic metabolism were significantly blunted. These data demonstrate that restriction of dietary protein is sufficient to trigger hepatic autophagy, and that disruption of autophagy significantly alters both hepatic and whole animal metabolic response to dietary protein restriction.
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Low-protein diets induce hyperphagia, particularly in rodent models.
“a number of studies demonstrate that low-protein diets induce hyperphagia, particularly in rodent models”
From FGF21 and the physiological regulation of macronutrient preference (2020) · cites this paper as [76]
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References 44 · Cited by 36
- Authors
- Henagan, T. M., Laeger, T., Navard, A. M., Albarado, D., Noland, R. C., Stadler, K., Elks, C. M., Burk, D., & Morrison, C. D.
- Affiliations
- Pennington Biomedical Research Center (US)
- Corresponding author
- Morrison, Christopher D.
- ORCID
- Venue
- Metabolism
- Publisher
- Elsevier BV
- Published
- 2016-06
- Volume
- 65
- Issue
- 6
- Pages
- 805-815
- ISSN
- 0026-0495 (ISSN-L)
- PMC
- PMC4867053
- OpenAlex
- W2291233794
- Cited by
- 36
- References
- 44
- Citations by year
- 2026: 3 · 2025: 2 · 2024: 3 · 2023: 3 · 2022: 5 · 2021: 4 · 2020: 5 · 2019: 4 · 2018: 6 · 2017: 1
- FWCI
- 3.43
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Metabolism (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Civil War Book Review (submittedVersion)
- Funders
- National Institute of General Medical Sciences (P20GM103528, P30GM118430)
- National Institute of Diabetes and Digestive and Kidney Diseases (R01DK081563, R01DK105032, T32DK064584, P30DK072476)
- National Center for Research Resources (P20RR021945)
- Topics
- Health Sciences › Medicine › Epidemiology › Autophagy in Disease and Therapy
- Health Sciences › Medicine › Physiology › Dietary Effects on Health
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Keywords
- hepatic autophagy, protein restriction, dietary intake, energy expenditure, hepatic fatty acid synthesis, liver mitochondria, amino acid restriction, nutrient restriction
- MeSH terms
- Animals, Autophagy, Eating, Energy Metabolism, Liver, Male, Mutation, Protein Deficiency, Rats, Sprague-Dawley, Diet, Protein-Restricted, Mice, Rats
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