Cited by 183Regulation of Appetite and ObesityHypothalamic control of reproductive hormonesBiochemical Analysis and Sensing Techniques

Amino acids inhibit Agrp gene expression via an mTOR-dependent mechanism

Open access
Morrison, Christopher D., Xi, Xiaochun, White, Christy L., Ye, Jianping, Martin, Roy J.·2007·American Journal of Physiology-Endocrinology and Metabolism

Abstract

Metabolic fuels act on hypothalamic neurons to regulate feeding behavior and energy homeostasis, but the signaling mechanisms mediating these effects are not fully clear. Rats placed on a low-protein diet (10% of calories) exhibited increased food intake (P < 0.05) and hypothalamic Agouti-related protein (Agrp) gene expression (P = 0.002). Direct intracerebroventricular injection of either an amino acid mixture (RPMI 1640) or leucine alone (1 mug) suppressed 24-h food intake (P < 0.05), indicating that increasing amino acid concentrations within the brain is sufficient to suppress food intake. To define a cellular mechanism for these direct effects, GT1-7 hypothalamic cells were exposed to low amino acids for 16 h. Decreasing amino acid availability increased Agrp mRNA levels in GT1-7 cells (P < 0.01), and this effect was attenuated by replacement of the amino acid leucine (P < 0.05). Acute exposure to elevated amino acid concentrations increased ribosomal protein S6 kinase phosphorylation via a rapamycin-sensitive mechanism, suggesting that amino acids directly stimulated mammalian target of rapamycin (mTOR) signaling. To test whether mTOR signaling contributes to amino acid inhibition of Agrp gene expression, GT1-7 cells cultured in either low or high amino acids for 16 h and were also treated with rapamcyin (50 nM). Rapamycin treatment increased Agrp mRNA levels in cells exposed to high amino acids (P = 0.01). Taken together, these observations indicate that amino acids can act within the brain to inhibit food intake and that a direct, mTOR-dependent inhibition of Agrp gene expression may contribute to this effect.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1152/ajpendo.00675.2006

Cites

36 of 36 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Cites

Flagged first, then by citations

Cited by

Sorted by citations

Authors
Morrison, C. D., Xi, X., White, C. L., Ye, J., & Martin, R. J.
Affiliations
Pennington Biomedical Research Center (US)
Venue
American Journal of Physiology-Endocrinology and Metabolism
Published
2007-07
Volume
293
Issue
1
Pages
E165-E171
ISSN
  • 0193-1849 (ISSN-L)
  • 1522-1555
OpenAlex
W2015145490
Cited by
183
References
36
Citations by year
2026: 5 · 2025: 5 · 2024: 4 · 2023: 5 · 2022: 6 · 2021: 4 · 2020: 15 · 2019: 7 · 2018: 9 · 2017: 10 · 2016: 13 · 2015: 7 · 2014: 7 · 2013: 11 · 2012: 16
FWCI
6.53
Type
journal article
Language
en
Open access
Locations
  • American Journal of Physiology-Endocrinology and Metabolism (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
Funders
  • National Institutes of Health
  • National Institute of General Medical Sciences (P20GM103528, P30GM118430)
  • National Institute of Diabetes and Digestive and Kidney Diseases (P30DK072476)
  • National Institute of Neurological Disorders and Stroke (NS-051570, R03NS051570)
  • National Center for Research Resources (RR 021945, P20RR021945)
Topics
  • Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Regulation of Appetite and Obesity
  • Health Sciences › Medicine › Reproductive Medicine › Hypothalamic control of reproductive hormones
  • Health Sciences › Nursing › Nutrition and Dietetics › Biochemical Analysis and Sensing Techniques
Keywords
amino acids, agouti-related protein, mTOR signaling, leucine, food intake regulation, hypothalamic neurons, GT1-7 cells, S6K, rapamycin, low-protein diet, energy homeostasis
MeSH terms
Amino Acids, Animals, Cells, Cultured, Eating, Gene Expression Regulation, Hypothalamus, Male, Protein Kinases, Signal Transduction, Rats, Sprague-Dawley, Diet, Protein-Restricted, Intercellular Signaling Peptides and Proteins, Rats, Agouti-Related Protein, TOR Serine-Threonine Kinases

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review