Literature DB >> 19050051

Potassium bicarbonate attenuates the urinary nitrogen excretion that accompanies an increase in dietary protein and may promote calcium absorption.

Lisa Ceglia1, Susan S Harris, Steven A Abrams, Helen M Rasmussen, Gerard E Dallal, Bess Dawson-Hughes.   

Abstract

CONTEXT: Protein is an essential component of muscle and bone. However, the acidic byproducts of protein metabolism may have a negative impact on the musculoskeletal system, particularly in older individuals with declining renal function.
OBJECTIVE: We sought to determine whether adding an alkaline salt, potassium bicarbonate (KHCO3), allows protein to have a more favorable net impact on intermediary indices of muscle and bone conservation than it does in the usual acidic environment.
DESIGN: We conducted a 41-d randomized, placebo-controlled, double-blind study of KHCO3 or placebo with a 16-d phase-in and two successive 10-d metabolic diets containing low (0.5 g/kg) or high (1.5 g/kg) protein in random order with a 5-d washout between diets.
SETTING: The study was conducted in a metabolic research unit. PARTICIPANTS: Nineteen healthy subjects ages 54-82 yr participated. INTERVENTION: KHCO3 (up to 90 mmol/d) or placebo was administered for 41 d. MAIN OUTCOME MEASURES: We measured 24-h urinary nitrogen excretion, IGF-I, 24-h urinary calcium excretion, and fractional calcium absorption.
RESULTS: KHCO3 reduced the rise in urinary nitrogen excretion that accompanied an increase in protein intake (P = 0.015) and was associated with higher IGF-I levels on the low-protein diet (P = 0.027) with a similar trend on the high-protein diet (P = 0.050). KHCO3 was also associated with higher fractional calcium absorption on the low-protein diet (P = 0.041) with a similar trend on the high-protein diet (P = 0.064).
CONCLUSIONS: In older adults, KHCO3 attenuates the protein-induced rise in urinary nitrogen excretion, and this may be mediated by IGF-I. KHCO3 may also promote calcium absorption independent of the dietary protein content.

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Year:  2008        PMID: 19050051      PMCID: PMC2730228          DOI: 10.1210/jc.2008-1796

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


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