Article Synopsis

  • High protein intake, often seen as healthy, may activate mTOR signaling in macrophages, linked to ischaemic cardiovascular disease.
  • Clinical studies reveal that leucine is the main amino acid triggering mTOR activation in macrophages, with significant effects only seen with protein intake over roughly 25g per meal.
  • Research indicates that protein intake above 22% of dietary energy can promote atherosclerosis in male mice, highlighting the cardiovascular risks of excessive dietary protein.

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Article Abstract

High protein intake is common in western societies and is often promoted as part of a healthy lifestyle; however, amino-acid-mediated mammalian target of rapamycin (mTOR) signalling in macrophages has been implicated in the pathogenesis of ischaemic cardiovascular disease. In a series of clinical studies on male and female participants ( NCT03946774 and NCT03994367 ) that involved graded amounts of protein ingestion together with detailed plasma amino acid analysis and human monocyte/macrophage experiments, we identify leucine as the key activator of mTOR signalling in macrophages. We describe a threshold effect of high protein intake and circulating leucine on monocytes/macrophages wherein only protein in excess of ∼25 g per meal induces mTOR activation and functional effects. By designing specific diets modified in protein and leucine content representative of the intake in the general population, we confirm this threshold effect in mouse models and find ingestion of protein in excess of ∼22% of dietary energy requirements drives atherosclerosis in male mice. These data demonstrate a mechanistic basis for the adverse impact of excessive dietary protein on cardiovascular risk.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11448845PMC
http://dx.doi.org/10.1038/s42255-024-00984-2DOI Listing

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