耐受性
正电子发射断层摄影术
生物能学
药代动力学
医学
神经退行性变
柠檬酸合酶
谷胱甘肽
认知
药理学
人脑
内科学
心理学
疾病
不利影响
核医学
化学
精神科
生物化学
线粒体
酶
作者
Eric D. Vidoni,In‐Young Choi,Phil Lee,Gregory A. Reed,Na Zhang,Joseph Pleen,Jonathan D. Mahnken,Jonathan Clutton,Annette M. Becker,Erica Sherry,Rebecca Bothwell,Heidi Anderson,Robert A. Harris,William M. Brooks,Heather Wilkins,Lisa Mosconi,Jeffrey M. Burns,Russell H. Swerdlow
摘要
Brain bioenergetics are defective in Alzheimer's disease (AD). Preclinical studies find oxaloacetate (OAA) enhances bioenergetics, but human safety and target engagement data are lacking.We orally administered 500 or 1000 mg OAA, twice daily for 1 month, to AD participants (n = 15 each group) and monitored safety and tolerability. To assess brain metabolism engagement, we performed fluorodeoxyglucose positron emission tomography (FDG PET) and magnetic resonance spectroscopy before and after the intervention. We also assessed pharmacokinetics and cognitive performance.Both doses were safe and tolerated. Compared to the lower dose, the higher dose benefited FDG PET glucose uptake across multiple brain regions (P < .05), and the higher dose increased parietal and frontoparietal glutathione (P < .05). We did not demonstrate consistent blood level changes and cognitive scores did not improve.1000 mg OAA, taken twice daily for 1 month, is safe in AD patients and engages brain energy metabolism.
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