1,721,021 research outputs found
Seizing opportunities and navigating the challenges of spaceflight research as an early career researcher
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Nrf2 deficiency induces skeletal muscle mitochondrial dysfunction: a proteomics/bioinformatics approach.
No full textDietary manipulations for health and the prevention and management of disease: An editorial
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Skeletal muscle immobilisation-induced atrophy: mechanistic insights from human studies
No full textPeriods of skeletal muscle disuse lead to rapid declines in muscle mass (atrophy), which is fundamentally underpinned by an imbalance between muscle protein synthesis (MPS) and muscle protein breakdown (MPB). The complex interplay of molecular mechanisms contributing to the altered regulation of muscle protein balance during disuse have been investigated but rarely synthesised in the context of humans. This narrative review discusses human models of muscle disuse and the ensuing inversely exponential rate of muscle atrophy. The molecular processes contributing to altered protein balance are explored, with a particular focus on growth and breakdown signalling pathways, mitochondrial adaptations and neuromuscular dysfunction. Finally, key research gaps within the disuse atrophy literature are highlighted providing future avenues to enhance our mechanistic understanding of human disuse atrophy.</p
Critical variables regulating age-related anabolic responses to protein nutrition in skeletal muscle
No full textProtein nutrition is critical for the maintenance of skeletal muscle mass across the lifecourse and for the growth of muscle in response to resistance exercise - both acting via the stimulation of protein synthesis. The transient anabolic response to protein feeding may vary in magnitude and duration, depending on, e.g., timing, dose, amino acid composition and delivery mode, which are in turn influenced by physical activity and age. This review aims to: (i) summarise the fundamental metabolic responses of muscle to protein feeding, (ii) discuss key variables regulating muscle anabolic responses to protein feeding, and (iii) explore how these variables can be optimised for muscle anabolism in response to physical activity and ageing.</p
Understanding the complex relationship between amino acid absorption kinetics and postprandial muscle protein synthesis rates in healthy adults and critically ill patients
No full textPurpose of review: protein digestion and amino acid absorption kinetics are quantifiable metrics commonly utilized to determine the quality of a protein source. This review critically evaluates recent evidence (primarily from studies that provided commonly consumed protein-rich foods) regarding the relationship between in vivo protein digestion and amino acid absorption rates with the postprandial stimulation of muscle protein synthesis (MPS), with an emphasis on healthy adults and critically ill patients.Recent findings: ingested protein sources that elicit moderate amino acid bioavailability, including leucine, stimulate MPS rates to a comparable extent as protein sources that elicit high amino acid bioavailability in healthy young adults. Amino acid absorption kinetics appear to be modulated in critically ill patients, leading to a marked reduction in postprandial MPS rates. Preliminary studies demonstrate that enteral feeding of high dose free amino acids increase amino acid bioavailability to a greater extent than intact protein, leading to a positive whole-body net protein balance in critically ill patients. However, in practice, the high osmolarity of free amino acids leads to a high prevalence of diarrhoea and thus limits the clinical application of this intervention.Summary: the enteral provision of free amino acids represents a theoretical, but not practically-relevant, clinical nutrition strategy to mitigate the catabolic response to critical illness. Future studies are warranted to establish targeted protein/amino acid-based interventions to mitigate skeletal muscle atrophy during the metabolic care of critically ill patients.</p
Space omics research in Europe: Contributions, geographical distribution and ESA member state funding schemes
No full textThe European research community, via European Space Agency (ESA) spaceflight opportunities, has significantly contributed toward our current understanding of spaceflight biology. Recent molecular biology experiments include "omic" analysis, which provides a holistic and systems level understanding of the mechanisms underlying phenotypic adaptation. Despite vast interest in, and the immense quantity of biological information gained from space omics research, the knowledge of ESA-related space omics works as a collective remains poorly defined due to the recent exponential application of omics approaches in space and the limited search capabilities of pre-existing records. Thus, a review of such contributions is necessary to clarify and promote the development of space omics among ESA and ESA state members. To address this gap, in this review, we i) identified and summarized omics works led by European researchers, ii) geographically described these omics works, and iii) highlighted potential caveats in complex funding scenarios among ESA member states
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