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Protein breakdown, synthesis, net balance, and Phe splanchnic extraction were calculated before and at the end of the enteral feeding period, using equations for steady-state whole-body protein kinetics.
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Synthesis maps utilizing only spatial or narrative arrangement alone or in combination were less popular options, but a breakdown of synthesis map scores and scores for organization indicates that all organizational schemes were conducive to successful synthesis map creation.
This loss is mostly driven by an increased muscle protein breakdown, whereas synthesis rates are on average not changed [1].
A proper balance of lipid breakdown and synthesis is essential for achieving energy homeostasis as alterations in either of these processes can lead to pathological states such as obesity.
Although the underlying mechanisms involved in the development of muscle atrophy are poorly understood, an imbalance between protein breakdown and synthesis, in favour of the former, plays an important role in this process [6].
Muscle atrophy depends on the balance between protein breakdown, protein synthesis rates, and apoptosis.
It is plausible that the observed regulation of genes linked to lipid breakdown or synthesis could be due to oxidative stress.
This methodology allows for a direct measurement of the impact of a feeding regimen on in vivo protein breakdown, protein synthesis, protein balance and amino acid oxidation.
However, a previous study has suggested that low-grade inflammation disturbs the balance between protein breakdown and synthesis and is thereby associated with muscle size in dialysis patients [ 21].
One of these (Additional file 5) included upregulated transcripts involved in glycolysis, the Calvin cycle, pectin breakdown, tryptophan synthesis and the wound response, whereas another (Additional file 6) included downregulated transcripts involved in AsA peroxidation, glucuronoside metabolism and glutathione metabolism.
Although the biochemical pathways engaged in the development of muscle atrophy are poorly understood, an imbalance between protein breakdown and synthesis, in favor of the former, is believed to play a role in this process [ 4].
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