短期摄入硝酸肌酸和肌酸酐对健康成人肌酸药代动力学和安全性生物标志物的影响

Sergej M. Ostojic, V. Štajer, N. Todorovic, Marijana Ranisavljev, Bogdan Andjelic, J. Panić, Alexandros Nikolaidis, Ron Kramer, Milan Vraneš
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引用次数: 0

摘要

本研究旨在评估不同剂量的硝酸肌酸-肌酸酐干预对健康人的药代动力学和安全性的影响。10 名年轻成年人(平均年龄 26.1 ± 5.0 岁;5 名女性)自愿参加了这项双盲、交叉、随机对照试验。参与者被随机分配接受低剂量硝酸肌酸-肌酐混合物(CN-CRN-Low;1.5 克硝酸肌酸和 1.5 克肌酐)、高剂量硝酸肌酸-肌酐混合物(CN-CRN-High;3 克硝酸肌酸和 3 克肌酐)或 1.在单剂量药代动力学实验和为期 14 天的安全性试验中,CN-CRN-Low 和 CN-CRN-High 干预方案的分布容积和总清除率均高于 CONTROL 干预方案(P < 0.05)。此外,与其他干预措施相比,CN-CRN-高干预措施显示出明显更高的肌酸最大血清浓度(P < 0.05)。在所有干预措施中,血清胱抑素 C 水平保持不变(P = 0.65),没有参与者出现胱抑素 C 浓度异常或其他安全性生物标志物发生重大变化。还需要进一步研究,以探索硝酸肌酸-肌酸补充剂在不同临床和运动人群中对功能和表现的潜在益处。
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Effects of Short-Term Creatine Nitrate Plus Creatinine Intake on Creatine Pharmacokinetics and Safety Biomarkers in Healthy Adults
A blend of creatine nitrate and creatinine has demonstrated promising bioavailability; however, prior studies have not thoroughly examined its pharmacokinetics and safety profiles, particularly its impact on kidney stress indicators, such as serum cystatin C. This study aimed to assess the effects of varying doses of creatine nitrate-creatinine intervention on pharmacokinetics and safety in healthy humans. Ten young adults (mean age 26.1 ± 5.0 years; 5 females) volunteered for this double-blind, crossover, randomized controlled trial. The participants were randomly assigned to receive either a low-dose creatine nitrate-creatinine mixture (CN-CRN-Low; 1.5 g of creatine nitrate and 1.5 g of creatinine), a high-dose creatine nitrate-creatinine mixture (CN-CRN-High; 3 g of creatine nitrate and 3 g of creatinine), or 1.5 g of creatine nitrate (CONTROL) in both a single-dose pharmacokinetics experiment, and a 14-day safety trial. Both CN-CRN-Low and CN-CRN-High interventions displayed increased volume of distribution and total clearance compared to the CONTROL intervention (P < 0.05) in a single-dose pharmacokinetics experiment. Additionally, the CN-CRN-High intervention showed significantly higher creatine maximum serum concentrations compared to the other interventions (P < 0.05). Serum cystatin C levels remained unchanged across all interventions (P = 0.65), with no participants experiencing abnormal cystatin C concentrations or major changes in other safety biomarkers. The present study demonstrates dose-specific utilization of creatine nitrate-creatinine intervention, with the mixture induced no kidney damage. Further studies are needed to explore the potential functional and performance benefits of creatine nitrate-creatinine supplementation in diverse clinical and athletic cohorts.
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