Department of Biopharmaceutics and Pharmaceutical Technology, University of Greifswald, 17489 Greifswald, Germany.
Institute of Nutritional Medicine, University Hospital Schleswig-Holstein, Campus Lübeck, University of Lübeck, 23538 Lübeck, Germany.
Nutrients. 2023 Apr 12;15(8):1852. doi: 10.3390/nu15081852.
(1) Background: Spermidine is a biogenic polyamine that plays a crucial role in mammalian metabolism. As spermidine levels decline with age, spermidine supplementation is suggested to prevent or delay age-related diseases. However, valid pharmacokinetic data regarding spermidine remains lacking. Therefore, for the first time, the present study investigated the pharmacokinetics of oral spermidine supplementation. (2) Methods: This study was designed as a randomized, placebo-controlled, triple-blinded, two-armed crossover trial with two 5-day intervention phases separated by a washout phase of 9 days. In 12 healthy volunteers, 15 mg/d of spermidine was administered orally, and blood and saliva samples were taken. Spermidine, spermine, and putrescine were quantified by liquid chromatography-mass spectrometry (LC-MS/MS). The plasma metabolome was investigated using nuclear magnetic resonance (NMR) metabolomics. (3) Results: Compared with a placebo, spermidine supplementation significantly increased spermine levels in the plasma, but it did not affect spermidine or putrescine levels. No effect on salivary polyamine concentrations was observed. (4) Conclusions: This study's results suggest that dietary spermidine is presystemically converted into spermine, which then enters systemic circulation. Presumably, the in vitro and clinical effects of spermidine are at least in part attributable to its metabolite, spermine. It is rather unlikely that spermidine supplements with doses <15 mg/d exert any short-term effects.
(1) 背景:亚精胺是一种生物源性多胺,在哺乳动物代谢中起着至关重要的作用。随着年龄的增长,亚精胺水平下降,因此建议补充亚精胺以预防或延缓与年龄相关的疾病。然而,关于亚精胺的药代动力学数据仍然缺乏。因此,本研究首次考察了口服亚精胺补充的药代动力学。
(2) 方法:该研究设计为随机、安慰剂对照、三盲、双臂交叉试验,两个 5 天干预阶段之间有 9 天的洗脱期。在 12 名健康志愿者中,每天口服 15mg 亚精胺,并采集血样和唾液样。采用液相色谱-质谱联用(LC-MS/MS)定量分析亚精胺、精胺和腐胺。采用核磁共振(NMR)代谢组学研究血浆代谢组。
(3) 结果:与安慰剂相比,亚精胺补充显著增加了血浆中的精胺水平,但对亚精胺或腐胺水平没有影响。唾液多胺浓度没有观察到变化。
(4) 结论:本研究结果表明,膳食亚精胺在进入全身循环之前被预先转化为精胺。推测亚精胺的体外和临床作用至少部分归因于其代谢产物精胺。剂量<15mg/d 的亚精胺补充剂不太可能产生任何短期作用。