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Tolerability and pharmacokinetics of oxaloacetate 100mg capsules in Alzheimer's subjects

机译:草酸乙酸100mg胶囊在阿尔茨海默氏症患者中的耐受性和药代动力学

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Bioenergetics and bioenergetic-related functions are altered in Alzheimer's disease (AD) subjects. These alterations represent therapeutic targets and provide an underlying rationale for modifying brain bioenergetics in AD-affected persons. Preclinical studies in cultured cells and mice found that administering oxaloacetate (OAA), a Krebs cycle and gluconeogenesis intermediate, enhanced bioenergetic fluxes and upregulated some brain bioenergetic infrastructure-related parameters. We therefore conducted a study to provide initial data on the tolerability and pharmacokinetics of OAA in AD subjects. Six AD subjects received OAA 100 mg capsules twice a day for one month. The intervention was well-tolerated. Blood level measurements following ingestion of a 100 mg OAA capsule showed modest increases in OAA concentrations, but pharmacokinetic analyses were complicated by relatively high amounts of endogenous OAA. We conclude that OAA 100 mg capsules twice per day for one month are safe in AD subjects but do not result in a consistent and clear increase in the OAA blood level, thus necessitating future clinical studies to evaluate higher doses.
机译:在阿尔茨海默氏病(AD)受试者中,生物能学和与生物能相关的功能发生了改变。这些改变代表了治疗目标,并为改变受AD影响的人的大脑生物能学提供了基本原理。在培养的细胞和小鼠中进行的临床前研究发现,施用草酰乙酸(OAA),Krebs循环和糖异生中间体可以增强生物能通量并上调一些与脑部生物能基础设施相关的参数。因此,我们进行了一项研究,以提供有关OAA对AD受试者的耐受性和药代动力学的初步数据。六个AD受试者每天两次接受OAA 100 mg胶囊,持续一个月。干预耐受性良好。摄入100 mg OAA胶囊后的血药浓度测量显示OAA浓度适度增加,但是由于相对大量的内源性OAA而使药代动力学分析复杂化。我们得出的结论是,在AD受试者中,每天两次OAA 100毫克胶囊对于一个月的受试者是安全的,但不会导致OAA血药浓度持续而明显的增加,因此有必要进行进一步的临床研究以评估更高的剂量。

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