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Sirtuin 4 controls leucine metabolism and insulin secretion by reversing effects of reactive metabolites

2018· article· en· W3176437258 on OpenAlexaboutno aff
Frank K. Huynh, Kristin A. Anderson, J. Darren Stuart, Zhihong Lin, Matthew D. Hirschey

Bibliographic record

VenueThe FASEB Journal · 2018
Typearticle
Languageen
FieldMedicine
TopicSirtuins and Resveratrol in Medicine
Canadian institutionsnot available
FundersNational Institute on AgingNational Institutes of HealthAmerican Heart AssociationEllison Medical Foundation
KeywordsLeucineInsulinMetabolismInternal medicineEndocrinologyCarbohydrate metabolismBiologyNAD+ kinaseGlucose homeostasisSecretionBiochemistryChemistryInsulin resistanceAmino acidEnzymeMedicine

Abstract

fetched live from OpenAlex

Sirtuins are a family of conserved NAD + ‐dependent enzymes that remove a variety of post‐translational acyl lysine modifications. By performing this deacylation function, sirtuins can regulate several aspects of metabolism and aging. Recently, we discovered new post‐translational modifications (PTMs) that can be removed by sirtuin 4 (SIRT4). Interestingly, these PTMs can be generated by reactive metabolites produced during leucine oxidation and in the absence of SIRT4, these PTMs accumulate on and inhibit enzymes in the leucine oxidation pathway. These observations suggest that SIRT4 is a key regulator of leucine metabolism through a novel mechanism that responds to levels of reactive metabolites. Accordingly, we found that SIRT4KO mice have dysregulated leucine metabolism. As a consequence of this, SIRT4KO mice have elevated leucine‐stimulated insulin secretion. Long‐term stimulation of insulin secretion by leucine over time in SIRT4KO mice led to elevated plasma insulin levels even in the basal state. This chronic elevation of insulin was associated with an acceleration of aging‐induced insulin resistance in SIRT4KO mice. Interestingly, when leucine was administered as a bolus with glucose, insulin secretion was synergistically increased more than 3‐fold over glucose or leucine alone in aged SIRT4KO mice. Importantly, this elevated insulin secretion resulted in total normalization of glucose tolerance to resemble that of a young mouse and despite extremely high insulin levels, there was no sign of dangerous hypoglycemia. Thus, our data reveal that short‐term inhibition of SIRT4 potentially has therapeutically relevant effects on leucine metabolism and insulin secretion, but a long‐term loss of SIRT4 can drive inappropriate hyperinsulinemia and lead to insulin resistance. Taken together, our data reveal a novel mechanism of metabolic control involving reactive metabolites and position SIRT4 as a key regulator of leucine metabolism and insulin secretion. Support or Funding Information We would like to acknowledge funding support from the American Heart Association grants 12SDG8840004 and 12IRG9010008, The Ellison Medical Foundation, the National Institutes of Health and the NIA grant R01AG045351, and the Duke Pepper Older Americans Independence Center (OAIC) Program in Aging Research supported by the National Institute of Aging (P30AG028716‐01). FKH was supported by an American Diabetes Association/Canadian Diabetes Association Post‐doctoral Fellowship (PF‐3‐13‐4342‐FH). This abstract is from the Experimental Biology 2018 Meeting. There is no full text article associated with this abstract published in The FASEB Journal .

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: Bench or experimental
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.001
Threshold uncertainty score0.004

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0000.001
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.001
Insufficient payload (model declined to judge)0.0010.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.008
GPT teacher head0.253
Teacher spread0.245 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designBench or experimental
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations0
Published2018
Admission routes1
Has abstractyes

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