Physiological and pharmacokinetic effects of oral 1,3-dimethylamylamine administration in men.

IF 2.9 3区 医学 Q2 Medicine
Brian K Schilling, Kelley G Hammond, Richard J Bloomer, Chaela S Presley, Charles R Yates
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引用次数: 20

Abstract

Background: 1,3-dimethylamylamine (DMAA) has been a component of dietary supplements and is also used within "party pills," often in conjunction with alcohol and other drugs. Ingestion of higher than recommended doses results in untoward effects including cerebral hemorrhage. To our knowledge, no studies have been conducted to determine both the pharmacokinetic profile and physiologic responses of DMAA.

Methods: Eight men reported to the lab in the morning following an overnight fast and received a single 25 mg oral dose of DMAA. Blood samples were collected before and through 24 hours post-DMAA ingestion and analyzed for plasma DMAA concentration using high-performance liquid chromatography-mass spectrometry. Resting heart rate, blood pressure, and body temperature was also measured.

Results: One subject was excluded from the data analysis due to abnormal DMAA levels. Analysis of the remaining seven participants showed DMAA had an oral clearance of 20.02 ± 5 L∙hr⁻¹, an oral volume of distribution of 236 ± 38 L, and terminal half-life of 8.45 ± 1.9 hr. Lag time, the delay in appearance of DMAA in the circulation following extravascular administration, varied among participants but averaged approximately 8 minutes (0.14 ± 0.13 hr). The peak DMAA concentration for all subjects was observed within 3-5 hours following ingestion and was very similar across subjects, with a mean of ~70 ng∙mL⁻¹. Heart rate, blood pressure, and body temperature were largely unaffected by DMAA treatment.

Conclusions: These are the first data to characterize the oral pharmacokinetic profile of DMAA. These findings indicate a consistent pattern of increase across subjects with regards to peak DMAA concentration, with peak values approximately 15-30 times lower than those reported in case studies linking DMAA intake with adverse events. Finally, a single 25 mg dose of DMAA does not meaningfully impact resting heart rate, blood pressure, or body temperature.

Trial registration: NCT01765933.

Abstract Image

Abstract Image

Abstract Image

男性口服1,3-二甲胺的生理和药代动力学影响。
背景:1,3-二甲氨基胺(DMAA)一直是膳食补充剂的一种成分,也用于“派对药丸”中,通常与酒精和其他药物一起使用。摄入超过推荐剂量会导致包括脑出血在内的不良影响。据我们所知,目前还没有研究确定DMAA的药代动力学特征和生理反应。方法:8名男性在禁食一晚后,于早上到实验室报到,并接受单次口服剂量25 mg的DMAA。在摄入DMAA前和摄入后24小时内采集血样,采用高效液相色谱-质谱法分析血浆DMAA浓度。静息心率、血压和体温也被测量。结果:1例受试者因DMAA水平异常被排除在数据分析之外。对其余7名参与者的分析显示,DMAA的口服清除率为20.02±5 L∙hr⁻¹,口服容积分布为236±38 L,终末半衰期为8.45±1.9小时。延迟时间,即血管外给药后DMAA在循环中出现的延迟,在参与者中有所不同,但平均约为8分钟(0.14±0.13小时)。所有受试者的峰值DMAA浓度在摄入后3-5小时内观察到,并且在受试者之间非常相似,平均为~70 ng∙mL⁻¹。心率、血压和体温在很大程度上不受DMAA治疗影响。结论:这是第一个描述DMAA口服药代动力学特征的数据。这些研究结果表明,在DMAA峰值浓度方面,受试者之间存在一致的增加模式,峰值比将DMAA摄入与不良事件联系起来的案例研究中报告的峰值低约15-30倍。最后,单次25mg剂量的DMAA对静息心率、血压或体温没有显著影响。试验注册:NCT01765933。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Pharmacology & Toxicology
BMC Pharmacology & Toxicology PHARMACOLOGY & PHARMACY-TOXICOLOGY
CiteScore
4.40
自引率
0.00%
发文量
0
审稿时长
12 weeks
期刊介绍: BMC Pharmacology and Toxicology is an open access, peer-reviewed journal that considers articles on all aspects of chemically defined therapeutic and toxic agents. The journal welcomes submissions from all fields of experimental and clinical pharmacology including clinical trials and toxicology.
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