Ostojic Sergej M, Ostojic Jelena, Drid Patrik, Vranes Milan, Jovanov Pavle
Faculty of Sport and PE, University of Novi Sad, Novi Sad, Serbia; University of Belgrade School of Medicine, Belgrade, Serbia.
University Clinical Center of Vojvodina, Novi Sad, Serbia.
Nutrition. 2017 Jan;33:149-156. doi: 10.1016/j.nut.2016.06.001. Epub 2016 Jun 8.
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.
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.
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.
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.
胍基乙酸(GAA)是一种实验性膳食添加剂,在能量需求较高的组织中可能作为肌酸来源。在本病例研究中,我们评估了5名健康男性口服GAA 8周期间,脑白质、灰质、小脑和丘脑的肌酸水平,并监测了干预副作用的发生率和严重程度。
在干预的前4周,志愿者每天补充36mg/kg体重(BW)的GAA;之后,GAA剂量滴定至每日≤60mg/kg BW。在基线、第4周和第8周,参与者接受脑磁共振波谱检查、临床化学研究以及关于副作用发生率和严重程度的开放式问卷调查。
补充GAA后,小脑、白质和灰质中的脑肌酸水平以相似的方式增加,4周后报告初始增加10.7%,在第4至8周随访中进一步上升(7.7%)(P<0.05)。丘脑肌酸水平在4周后下降6.5%(P=0.02),8周后非显著增加8%(P=0.09)。在8周随访时,GAA使所有评估脑区的N-乙酰天门冬氨酸水平升高(P<0.05)。在干预期间,没有参与者报告任何神经系统不良事件(如癫痫发作、刺痛、抽搐)。
补充GAA导致人脑肌酸池出现区域依赖性增加。这可能与恢复以低脑肌酸和肌酸合成功能性酶机制为特征的疾病中的细胞生物能量学有关,这些疾病包括神经退行性疾病、脑肿瘤或脑血管疾病。