4.7 Article

Obesity- and sex-related metabolism of arginine and nitric oxide in adults

Journal

AMERICAN JOURNAL OF CLINICAL NUTRITION
Volume 116, Issue 6, Pages 1610-1620

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1093/ajcn/nqac277

Keywords

morbid obesity; arginine; citrulline; nitric oxide; stable tracer; whole-body production; protein breakdown

Funding

  1. internal Texas A&M University grants

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This study aimed to investigate the association between obesity, sex, and sex-by-obesity interaction on whole-body arginine kinetics. The findings suggest that alterations in arginine metabolism are present in morbid obesity, but further research is needed to explore the factors related to these changes.
Background There is growing interest in the supplementation of arginine (Arg) and citrulline (Cit) in obesity due to their potential anti-obesogenic and anti-inflammatory properties. However, there is no consensus on the metabolic changes in Arg kinetics in obesity. Objectives This exploratory cross-sectional study aimed to investigate the association between obesity, sex, and sex-by-obesity interaction on whole-body Arg kinetics in a large group of human subjects. Methods We studied 83 nonobese [BMI (kg/m(2)) <30] and 80 morbidly obese (BMI >30) middle-aged individuals (40% males) enrolled in the MEDIT (Metabolism of Disease with Isotope Tracers) trial. After body-composition measurement by DXA, we collected arterial(ized) blood samples for amino acid (AA) concentrations, markers of inflammation [high-sensitivity C-reactive protein (hs-CRP)], liver function, and glucose in a postabsorptive state. We administered a pulse of AA stable tracers and measured whole-body production (WBP) of Arg, Cit, ornithine (Orn), phenylalanine, and tyrosine, and calculated their clearance (disposal capacity) and metabolite interconversions [markers for NO and de novo Arg production, systemic Arg hydrolysis, and whole-body protein breakdown (wbPB)]. We measured plasma enrichments by LC-MS/MS and statistics by Fisher's exact test or analysis of (co)variance. Significance was set at P Results Obese individuals were normoglycemic and characterized by low-grade inflammation (P < 0.0001) and greater wbPB (P = 0.0298). We found lower plasma Cit concentration (P < 0.0001) in the obese group but no differences in the WBP of Arg, Cit, and Orn. Furthermore, we observed overproduction of NO (P < 0.0001) in obesity but lower de novo Arg production (P = 0.0007). The WBP of Arg was lower in females for almost all Arg-related AAs, except for plasma Cit and NO production. Conclusions Alterations in Arg metabolism are present in morbid obesity. Further studies are needed to investigate if these changes could be related to factors such as increased Arg requirement in obesity or metabolic adaptation.

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