bioRxiv Science⌕ Search

bioRxiv · 10.1101/2024.03.25.586077

Suboptimal refeeding compensates stunting in a mouse model of juvenile malnutrition

Abstract

BackgroundEarly life, particularly after weaning, is the most rapid period of growth in mammals, and this growth is highly dependent on adequate nutrition. Protein-energy malnutrition (PEM) during this critical window can lead to stunting and wasting, which have long-term health consequences. ObjectiveThis study aimed to develop a mouse model of juvenile PEM to assess the effects of refeeding with various diets and interventions on growth recovery, including the impact of probiotic supplementation and suboptimal refeeding diets. MethodsJuvenile C57Bl/6J mice were fed a low-protein diet (LPD, 5% kcal from protein) starting at postnatal day 14 (P14) to induce malnutrition. Following weaning, both male and female mice were refed an optimal diet (Altromin 1310, 27% kcal from protein) at different times ranging from P28 to P56. In a second intervention, male mice were supplemented during refeeding with Lactiplantibacillus plantarum WJL (LpWJL), a probiotic known to stimulate growth in malnourished conditions. A final group of malnourished male mice were refed with a Western diet (WD, 34.5% kcal from fat; 15.3% kcal from protein) or a modified Western diet (MWD, 34.2% kcal from fat; 7.5% kcal from protein) to model suboptimal refeeding. ResultsRefeeding with an optimal diet fully restored growth in female mice, but male mice exhibited persistent stunting despite nutritional rehabilitation. LpWJL treatment during refeeding did not enhance systemic growth in males. In contrast, refeeding with WD or MWD restored body length but impaired glucose metabolism, particularly in mice refed MWD after PEM. LpWJL exacerbated glucose intolerance in the suboptimal refeeding groups. ConclusionSex-dependent differences exist in the recovery from early-life malnutrition, with males showing incomplete growth recovery despite optimal refeeding. Suboptimal diets, while compensating for stunting, impair glucose metabolism, especially when protein intake is insufficient. Probiotic supplementation with LpWJL did not improve growth outcomes.

Source connections

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Thoumas, J.-L., Cavaroc, A., Sery, D., Leulier, F., De Vadder, F.. 2024-03-25. Suboptimal refeeding compensates stunting in a mouse model of juvenile malnutrition. https://doi.org/10.1101/2024.03.25.586077

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Hypothalamic Farnesoid X Receptor deficiency alters energy balance by modulating hepatic glucose production and adipose tissue metabolism through central insulin signaling.

Objectives: The bile acid nuclear receptor Farnesoid X Receptor (FXR, NR1H4) is a major regulator of metabolism and energy homeostasis in peripheral organs. It modulates bile acid, glucose, and lipid metabolism, as well as fat mass and body weight. However, FXR is also expressed in the brain, particularly in the hypothalamus, a key center for the regulation of energy homeostasis. Although one study has demonstrated a role for brain FXR activation in energy balance, its specific hypothalamic role is still unknown. Here, we examined the role of FXR in the mediobasal hypothalamus in the regulation of energy balance. Methods: We used a genetic approach combined with metabolic phenotyping to determine the effect of FXR invalidation in the mediobasal hypothalamus on metabolic parameters involved in the central regulation of energy homeostasis. Results: Our results demonstrate that hypothalamic FXR deficiency induces a positive energy balance, resulting in a reduction in energy expenditure due to alterations in glucose metabolism accompanied by structural changes in white adipose tissues. Conclusion: This study uncovers a previously unrecognized role for hypothalamic FXR in the central homeostatic control of energy balance, providing new insights into its contribution to peripheral glucose metabolism and adipose tissue structural remodeling.

physiology↗

Rad and Phospholamban are Key Drivers of the Ventricular Adrenergic Response and Stress-Induced Arrhythmia

The adrenergic response is a fundamental mechanism that regulates heart rate (chronotropy), cardiac contractility (inotropy) and relaxation (lusitropy). Adrenergic stress is also a recognized trigger of arrhythmia in disease. Yet, our understanding of the underlying molecular basis remains incomplete. Protein kinase A (PKA) and the calcium/calmodulin-dependent kinase II (CaMKII) phosphorylate multiple targets proposed to participate in the adrenergic response, including the GTP-binding protein Rad, phospholamban (PLB) and ryanodine receptor 2 (RyR2). Here we demonstrate that phosphorylation of both Rad and PLB is necessary for inotropy and lusitropy. We show that changes in cardiac contractility and relaxation are primarily dependent on intracellular calcium handling. Finally, we report that Rad and PLB control stress-induced arrhythmogenesis, despite the phosphorylation of other pro-arrhythmic targets. We have identified the essential molecular components of the adrenergic response, resolving a long-standing debate in cardiac excitation-contraction coupling and refining current models of sympathetic regulation in health and disease.

physiology↗

Light-cycle time-restricted feeding remodels a hidden layer of the cardiac transcriptome through sex-specific transcript switching

Light-cycle time-restricted feeding disrupts daily cardiovascular and thermoregulatory rhythms, but the molecular effects of light-cycle time-restricted feeding on the heart have been measured only at the level of total gene expression. We used Oxford Nanopore long-read RNA sequencing to resolve the full-length ventricular transcriptome from male and female mice under ad libitum feeding or light-cycle time-restricted feeding across the 24-hour cycle. Greater than 20% of cardiac transcripts represent unannotated variants of known genes absent from the current GENCODE reference annotation. Light-cycle time-restricted feeding reorganizes transcript usage across hundreds of genes, including genes encoding splicing regulators, largely without changing total gene expression. The genes affected are sex-specific, with fewer than 2% of changes shared at the gene, transcript, and transcript-usage levels. We show that transcript-level regulation is a previously underrecognized component of the cardiac response to altered feeding behavior, undetected by conventional short-read approaches.

physiology↗