Please use this identifier to cite or link to this item: https://open.uns.ac.rs/handle/123456789/7880
Title: Serum creatine, creatinine and total homocysteine concentration-time profiles after a single oral dose of guanidinoacetic acid in humans
Authors: Ostojić, Sergej 
Niess, Barbara
Stojanović , Marko 
Idrizovic, Kemal
Issue Date: Jan-2014
Journal: Journal of Functional Foods
Abstract: Guanidinoacetic acid (GAA) is a suitable feed additive yet its possible application in human nutrition as a food supplement requires preliminary pharmacokinetics data. The aim of the present study was to explore the effects of an acute oral dose of GAA on serum GAA, creatine (Cr), creatinine (Crn), and total homocysteine (T-Hcy) concentration-time profiles and urinary excretion rates of GAA, Cr and Crn. Twenty-four young healthy participants (age 22.3. ±. 1.3. years; 12 males and 12 females) voluntarily ingested a single dose of GAA (2.4. g) or placebo (inulin) followed by the serial measurement of serum GAA, Cr, Crn and T-Hcy and urinary GAA, Cr and Crn concentration within the next 24. h. In response to GAA ingestion a substantial rise in serum GAA and Cr concentration was observed occurring 1. h after the ingestion (peak value of 144.9. ±. 24.8. μmol/L and 65.5. ±. 18.6. μmol/L, respectively). The Crn serum profile for 24. h was not affected by 2.4. g GAA ingestion, showing a peak value of 90.1. ±. 12.2. μmol/L 1. h post-administration. A single dose of GAA induced a notable rise in serum T-Hcy by about 40%. The peak value was observed 12. h post administration (13.1. ±. 2.1. μmol/L). Urinary excretion for GAA and Cr peaked after 4. h (453.1. ±. 235.0. mg/L and 40.8. ±. 33.3. mg/L, respectively). Crn excretion in urine remained unchanged after GAA administration. In conclusion, orally ingested GAA was readily bioavailable and was transformed to Cr. Serum T-Hcy kinetics proofed to be sensitive to acute GAA intake. Trial identification: clinicaltrials.gov number NCT01133899.
URI: https://open.uns.ac.rs/handle/123456789/7880
ISSN: 1756-4646
DOI: 10.1016/j.jff.2013.12.004
Appears in Collections:FSFV Publikacije/Publications

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