Please use this identifier to cite or link to this item: https://open.uns.ac.rs/handle/123456789/17191
Title: Dietary guanidinoacetic acid increases brain creatine levels in healthy men
Authors: Ostojić, Sergej 
Ostojić, Jelena 
Drid, Patrik 
Vraneš, Milan 
Jovanov, Pavle 
Keywords: Cerebellum;Gray matter;White matter;Creatine synthesis;MR spectroscopy;Side effects
Issue Date: 2017
Journal: Nutrition
Abstract: Objective Guanidinoacetic acid (GAA) is an experimental dietary additive that might act as a creatine source in tissues with high-energy requirements. In this case study, we evaluated brain levels of creatine in white matter, gray matter, cerebellum, and thalamus during 8 wk oral GAA administration in five healthy men and monitored the prevalence and severity of side effects of the intervention. Methods Volunteers were supplemented daily with 36 mg/kg body weight (BW) of GAA for the first 4 wk of the intervention; afterward GAA dosage was titrated ≤60 mg/kg BW of GAA daily. At baseline, 4, and 8 wk, the participants underwent brain magnetic resonance spectroscopy, clinical chemistry studies, and open-ended questionnaire for side-effect prevalence and severity. Results Brain creatine levels increased in similar fashion in cerebellum, and white and gray matter after GAA supplementation, with an initial increase of 10.7% reported after 4 wk, and additional upsurge (7.7%) from the weeks 4 to 8 follow-up (P < 0.05). Thalamus creatine levels decreased after 4 wk for 6.5% (P = 0.02), and increased nonsignificantly after 8 wk for 8% (P = 0.09). GAA induced an increase in N-acetylaspartate levels at 8-wk follow-up in all brain areas evaluated (P < 0.05). No participants reported any neurologic adverse event (e.g., seizures, tingling, convulsions) during the intervention. Conclusions Supplemental GAA led to a region-dependent increase of the creatine pool in the human brain. This might be relevant for restoring cellular bioenergetics in disorders characterized by low brain creatine and functional enzymatic machinery for creatine synthesis, including neurodegenerative diseases, brain tumors, or cerebrovascular disease.
URI: https://open.uns.ac.rs/handle/123456789/17191
ISSN: 0899-9007
DOI: (BISIS)102982
(BISIS)102982
(BISIS)102982
10.1016/j.nut.2016.06.001
(BISIS)102982
(BISIS)102982
Appears in Collections:FSFV Publikacije/Publications
FINS Publikacije/Publications

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